Knowledge and attitudes on anemia and menstrual health among Malaysian female university students

Bibliographic Details
Title: Knowledge and attitudes on anemia and menstrual health among Malaysian female university students
Authors: Kai Ting Mok, Satvinder Kaur, Yee-How Say, Siti Sabariah Bahari, Chirawat Paratthakonkun, Trias Mahmudiono, Nurliyana Abdul Razak
Source: Scientific Reports, Vol 14, Iss 1, Pp 1-10 (2024)
Publisher Information: Nature Portfolio, 2024.
Publication Year: 2024
Collection: LCC:Medicine
LCC:Science
Subject Terms: Anemia, Knowledge, Attitude, Menstrual health, Preventive health, Women’s health, Medicine, Science
More Details: Abstract Anemia is a significant public health concern, particularly among young female adults due to its potential impact on reproductive health. This study investigated the association between anemia-related knowledge, attitudes, menstrual health, and anemia status among Malaysian university students. This was a cross-sectional study named “SCARF” - Study to Combat Anemia - Research for Female Students, involving 674 university students in Malaysia. Anemia status was determined based on haemoglobin level, while knowledge, attitude and menstrual health were measured using validated questionnaires. The mean menarche age of students in this study was 12.1 ± 1.21 years. Students who were anemic had significantly longer menstrual cycle duration (P = 0.034) and more days with heavy flow (P = 0.038). Most students had poor knowledge (44.5%) and attitudes (84.1%) towards anemia. Students with good knowledge were 1.1 times more likely to have better anemia status compared to those with poor knowledge (95% CI: 1.0–1.2, P = 0.049). This study highlighted a lack of practical application of the knowledge to dietary habits. Collaborative efforts between educators and healthcare providers are crucial in developing a comprehensive strategy, such as interventions to prioritise educational initiatives and practical support to enhance overall menstrual health among female students.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2045-2322
Relation: https://doaj.org/toc/2045-2322
DOI: 10.1038/s41598-024-76655-9
Access URL: https://doaj.org/article/d2ec399a02894449bef7dfd538fbb7bc
Accession Number: edsdoj.2ec399a02894449bef7dfd538fbb7bc
Database: Directory of Open Access Journals
Full text is not displayed to guests.
FullText Links:
  – Type: pdflink
    Url: https://content.ebscohost.com/cds/retrieve?content=AQICAHjPtM4BHU3ZchRwgzYmadcigk49r9CVlbU7V5F6lgH7WwEigxnghHQphW65Ke7STQ-LAAAA4jCB3wYJKoZIhvcNAQcGoIHRMIHOAgEAMIHIBgkqhkiG9w0BBwEwHgYJYIZIAWUDBAEuMBEEDL6ly1aTXCQh23B6VgIBEICBmgZ4gQY8B4d35aHUlTvBX1X95NeIl82IwQMZgAqoqOC89bp0zrzeTbdNxgO0RIzvZSJfQ7--uOeYRRWu431aTxvtCbVZ3O6uQU11fg6OTGUJy6tSCcAZeloTufp3ZqS1X7n8jNwAu20-mTVrKkSlt9tPs6wq6CBUhULzzPnp1azBIxw_SklWs1LsHv6_FK9lfXFbLqX4end7pRU=
Text:
  Availability: 1
  Value: <anid>AN0174800147;[fkqs]13jan.24;2024Jan17.06:48;v2.2.500</anid> <title id="AN0174800147-1">Room temperature wafer bonding through conversion of polysilazane into SiO2 </title> <sbt id="AN0174800147-2">Introduction</sbt> <p>Room temperature wafer bonding is a desirable approach for the packaging and assembly of diverse electronic devices. The formation of SiO 2 layer at the bonding interface is crucial for a reliable wafer bonding as represented by conventional bonding techniques such as hydrophilic bonding and glass frit bonding. This paper reports a novel concept of room temperature wafer bonding based on the conversion of polysilazane to SiO 2 at the bonding interface. As polysilazane is converted to SiO 2 by hydrolysis, in this work, adsorbed water is introduced to the bonding interface by plasma treatment, thereby facilitating the formation of SiO 2 at the wafer bonding interface. The experimental results indicate that the adsorbed water from the plasma treatment diffuses into the polysilazane layer and facilitates its hydrolysis and conversion. The proposed method demonstrates the successful wafer bonding at room temperature with high bond strength without interfacial voids. This technique will provide a new approach of bonding wafers at room temperature for electronics packaging.</p> <p>Wafer bonding technology has evolved significantly, particularly in the field of electronic applications manufactured at the wafer level to achieve high throughput. This advancement is especially critical for the packaging and assembly of MEMS devices, optical systems, and CMOS applications. Among these, wafer bonding of Si and Si-based materials is widely adapted for various applications including the packaging of MEMS sensors[<reflink idref="bib1" id="ref1">1</reflink>], optical system sealing[<reflink idref="bib2" id="ref2">2</reflink>], microchannel devices[<reflink idref="bib3" id="ref3">3</reflink>], and 3D stacking of memory and logic devices[<reflink idref="bib4" id="ref4">4</reflink>].</p> <p>The formation of a <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> layer at the bonding interface is the fundamental and highly effective approach for wafer bonding. One of the representing methods in this regard is hydrophilic bonding, where the Si surface containing physisorbed water and chemisorbed OH groups forms hydrogen and molecular bonds at the bonding interface[<reflink idref="bib5" id="ref5">5</reflink>],[<reflink idref="bib6" id="ref6">6</reflink>]. In order to enhance the bonding quality and lower the process temperature, plasma treatments typically using <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>O</mtext><mn>2</mn></msub></math> </ephtml> or <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>N</mtext><mn>2</mn></msub></math> </ephtml> gas are widely employed to render Si bonding surfaces hydrophilic, facilitating water adsorption. Subsequent post-bonding annealing at 200-600 <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><mrow><msup><mrow /><mo>∘</mo></msup><mtext>C</mtext></mrow></math> </ephtml> promotes Si oxidation at the bonding interface, thereby increasing the bond strength[<reflink idref="bib7" id="ref7">7</reflink>],[<reflink idref="bib8" id="ref8">8</reflink>].</p> <p>In the field of MEMS packaging, glass frit bonding is also widely adapted through the formation of an <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> interface using low-melting-point glass pastes[<reflink idref="bib9" id="ref9">9</reflink>],[<reflink idref="bib10" id="ref10">10</reflink>]. Here, the bonding surfaces are coated with such glass pastes, and thermo compression bonding at 350-600 <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><mrow><msup><mrow /><mo>∘</mo></msup><mtext>C</mtext></mrow></math> </ephtml> induces adhesion between the substrates through the reflowed glass layer. Hence, the formation of the <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> layer at the bonding interface is pivotal for ensuring mechanical reliability.</p> <p>However, the bonding process temperature is a crucial factor in industrial applications. Elevated temperatures can deteriorate device performance and the bonding interface's reliability due to mismatches in the coefficient of thermal expansion between substrates. Consequently, low-temperature bonding, particularly at room temperature, is needed to accommodate next-generation electronics.</p> <p>Regarding to the formation of <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> , the conversion of polysilazane into <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> is a distinctive characteristic, represented by perhydropolysilazane (PHPS) <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><mrow><mo stretchy="false">(</mo><msub><mrow><mo stretchy="false">(</mo><msub><mtext>SiH</mtext><mn>2</mn></msub><mtext>NH</mtext><mo stretchy="false">)</mo></mrow><mtext>n</mtext></msub><mo stretchy="false">)</mo></mrow></math> </ephtml> , which undergoes hydrolysis when it interacts with water. This reaction leads to the formation of <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> , along with the release of byproducts such as <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>NH</mtext><mn>3</mn></msub></math> </ephtml> and <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>H</mtext><mn>2</mn></msub></math> </ephtml> ( <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><mrow><msub><mtext>SiH</mtext><mn>2</mn></msub><mtext>NH</mtext><mspace width="0.166667em" /><mo>+</mo><mspace width="0.166667em" /><mn>2</mn><msub><mtext>H</mtext><mn>2</mn></msub><mtext>O</mtext><mspace width="0.166667em" /><mo>-</mo><mo>></mo><mspace width="0.166667em" /><msub><mtext>SiO</mtext><mn>2</mn></msub><mspace width="0.166667em" /><mo>+</mo><mspace width="0.166667em" /><msub><mtext>NH</mtext><mn>3</mn></msub><mspace width="0.166667em" /><mo>+</mo><mspace width="0.166667em" /><mn>2</mn><msub><mtext>H</mtext><mn>2</mn></msub></mrow></math> </ephtml> )[<reflink idref="bib11" id="ref11">11</reflink>],[<reflink idref="bib12" id="ref12">12</reflink>].</p> <p>PHPS can be converted into <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> through various methods, including annealing within the temperature range of 200-1000 <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><mrow><msup><mrow /><mo>∘</mo></msup><mtext>C</mtext></mrow></math> </ephtml> [<reflink idref="bib12" id="ref13">12</reflink>],[<reflink idref="bib13" id="ref14">13</reflink>], infrared (IR) irradiation[<reflink idref="bib14" id="ref15">14</reflink>]–[<reflink idref="bib16" id="ref16">16</reflink>], treatment with pH-controlled chemicals[<reflink idref="bib17" id="ref17">17</reflink>], and exposure to moisture[<reflink idref="bib18" id="ref18">18</reflink>],[<reflink idref="bib19" id="ref19">19</reflink>]. Since PHPS forms <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> membrane by simple approaches compared to vacuum process such as chemical vapor deposition (CVD), PHPS is widely adapted to the coating of polymer films and metals[<reflink idref="bib20" id="ref20">20</reflink>]–[<reflink idref="bib22" id="ref21">22</reflink>] and interlayer dielectrics[<reflink idref="bib23" id="ref22">23</reflink>],[<reflink idref="bib24" id="ref23">24</reflink>].</p> <p>It is worth noting that the PHPS conversion into <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> proceeds even at room temperature in the presence of water[<reflink idref="bib11" id="ref24">11</reflink>],[<reflink idref="bib13" id="ref25">13</reflink>],[<reflink idref="bib25" id="ref26">25</reflink>],[<reflink idref="bib26" id="ref27">26</reflink>]. Hence, the conversion of PHPS to <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> holds the potential for creating a bonding interface consisting of <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> at room temperature, by introducing <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><mrow><msub><mtext>H</mtext><mn>2</mn></msub><mtext>O</mtext></mrow></math> </ephtml> at the PHPS interface, for instance, through the use of plasma hydrophilic treatment.</p> <p>Based on this concept, this study proposes a novel approach of room temperature wafer bonding by forming <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> bonding interface utilizing the PHPS conversion. The plasma hydrophilic treatment is applied to the Si wafer surface or the PHPS layer, thereby introducing adsorbed water to facilitate the PHPS conversion at the bonding interface. This is followed by wafer bonding via PHPS, leading to the formation of a <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> bonding interface at room temperature.</p> <p>To investigate the proposed wafer bonding process via PHPS, two approaches were explored. The first approach involved utilizing the PHPS layer as a source of water and oxygen for the conversion of the PHPS bonding interface. In this case, the PHPS layers on the bonding pair wafers were directly subjected to plasma hydrophilic treatment. Wafer bonding was then performed via both side PHPS layers on the both of bonding pair wafers. The effects of plasma treatment were examined by comparing conditions where both sides, one side, or none of the PHPS layers underwent plasma treatment.</p> <p>In the second approach, plasma treatment was applied to the Si wafer surfaces. This scenario involved plasma hydrophilic treatment that facilitated water adsorption on the Si wafer surfaces, followed by the PHPS coating on the Si wafers. This implies that the PHPS receives water not from the ambient air but from the Si wafer surface. Subsequently, wafer bonding was performed via one side PHPS layer using the PHPS-coated wafer and the plasma-treated Si wafer. For comparison, wafer bonding was also performed via one side PHPS layer without plasma treatment to the wafer surface.</p> <hd id="AN0174800147-3">Results</hd> <p>In order to investigate the PHPS conversion into <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> at room temperature by plasma hydrophilic treatment, chemical components of the PHPS coating on wafers were analyzed by x-ray photoelectron spectroscopy (XPS). Figure 1 presents the XPS core spectra of the PHPS surface before and after <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>N</mtext><mn>2</mn></msub></math> </ephtml> plasma treatment. When the PHPS layer is just coated, oxygen peak is not observed, accompanied by a significant peak of nitrogen. The silicon peak at around 101.3 eV indicates silicon nitride[<reflink idref="bib27" id="ref28">27</reflink>],[<reflink idref="bib28" id="ref29">28</reflink>]. This is attributed to the intrinsic composition of PHPS[<reflink idref="bib16" id="ref30">16</reflink>],[<reflink idref="bib29" id="ref31">29</reflink>],[<reflink idref="bib30" id="ref32">30</reflink>]. However, when the PHPS layer is treated with plasma, an increase in the oxygen peak and a decrease in the nitrogen peak are significant. Moreover, the silicon peak shifts towards a higher binding energy around 103.5 eV, indicating the presence of silicon oxide[<reflink idref="bib27" id="ref33">27</reflink>],[<reflink idref="bib28" id="ref34">28</reflink>]. Since the <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>N</mtext><mn>2</mn></msub></math> </ephtml> plasma itself does not contain <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><mrow><msub><mtext>H</mtext><mn>2</mn></msub><mtext>O</mtext></mrow></math> </ephtml> and <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>O</mtext><mn>2</mn></msub></math> </ephtml> , it is suggested that the water adsorbs on the PHPS surface after the plasma treatment. Subsequently, the PHPS layer consumes the adsorbed water present on its hydrophilic surface for the conversion reaction.</p> <p>Graph: Figure 1XPS core spectra of the PHPS surfaces before and after the N2 plasma hydrophilic treatment for (a) O1s, (b) N1s, and (c) Si2p peaks.</p> <p>The stitched IR images of the typical bonded wafers with PHPS layers are depicted in Fig. 2. These images reveal the presence of interfacial voids, which appear as patterns with interference fringes. Basically the bonding interface shows a good adhesion without significant interfacial voids except the bonding via both side PHPS layer with both side plasma treatment (Fig. 2 (<bold>a</bold>)). Due to the high viscosity of PHPS before its conversion to <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> , good adhesion is achieved through the PHPS layers. Additionally, it is indicated that submicron-sized particles can become embedded within the soft PHPS layers[<reflink idref="bib17" id="ref35">17</reflink>],[<reflink idref="bib31" id="ref36">31</reflink>].</p> <p>Conversely, bonding via both sides plasma-treated PHPS layers results in large interfacial voids, as shown in Fig. 2 (<bold>a</bold>). As indicated by the XPS analysis, plasma treatment converts the PHPS surface to hard <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> . However, since the spin-coated PHPS layer does not possess a smooth and flat surface, the converted <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> surface does not fully compensate for surface asperities, leading to lower quality adhesion.</p> <p>Graph: Figure 2Stitched IR images of the bonded wafers via PHPS. (a) Bonding via both side PHPS layers with plasma treatment for both PHPS layers, (b) bonding via both side PHPS layers with plasma treatment for one PHPS layer, (c) bonding via both side PHPS layers without plasma treatment, (d) bonding via one side PHPS layers with plasma treatment, and (e) bonding via one side PHPS layers without plasma treatment.</p> <p>The results of the bond strength measurements obtained through blade insertion tests are presented in Fig. 3. For the bonding via both side PHPS layers, the bond strength is low when both PHPS layers are subjected to plasma treatment or when plasma treatment is not performed, yielding bond strengths of 0.64 J/m <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msup><mrow /><mn>2</mn></msup></math> </ephtml> and 0.30 J/m <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msup><mrow /><mn>2</mn></msup></math> </ephtml> , respectively. In the scenario where both sides of the PHPS layers undergo plasma treatment, both surfaces are converted into <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> with surface asperities. Consequently, weak adhesion and a low bond strength result, which aligns with the results of the IR observations. In cases where plasma treatment is not performed, an insufficient supply of water at the bonding interface prevents the PHPS layers from conversion, resulting in a low bond strength.</p> <p>Conversely, when only one side of the PHPS layers is treated with plasma, a significantly improved bond strength of 5.54 J/m <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msup><mrow /><mn>2</mn></msup></math> </ephtml> is achieved. In this case, the bonding interface features the adhesive PHPS layer in contact with the hydrophilic PHPS layer. The hydrophilic layer with adsorbed water facilitates the conversion of the untreated PHPS layer into <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> . As a result, both strong adhesion and high bond strength are attained.</p> <p>In the cases of the bondings via the single side PHPS layer, when wafer bonding is conducted without the plasma hydrophilic treatment, the resulting bond strength measures 1.07 J/m <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msup><mrow /><mn>2</mn></msup></math> </ephtml> . In contrast, bonding with plasma treatment exhibits a significantly improved bond strength of 6.02 J/m <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msup><mrow /><mn>2</mn></msup></math> </ephtml> . Consistent with the bonding using both side PHPS layers, the plasma treatment introduces adsorbed water to the PHPS layer, thereby promoting its conversion to a mechanically stable <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> interface at room temperature.</p> <p>Graph: Figure 3Bond strength γ of the bonded wafers via PHPS layers at room temperature.</p> <p>Figure 4(a) shows the cross-sectional scanning electron microscopic (SEM) images of the bonding interface for the Si wafers bonded using PHPS layers on both sides with one side subjected to plasma treatment. In the low magnification image, the bonding interface appears uniform and devoid of voids. At higher magnification, the bonding interface is seen to consist of PHPS layers, each with a thickness of 0.4 <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><mi mathvariant="normal">μ</mi></math> </ephtml> m, resulting in a total thickness of 0.8 <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><mi mathvariant="normal">μ</mi></math> </ephtml> m. For the bonding via single side PHPS layer with plasma treatment shown in Fig. 4(b), a uniform and void-free bonding interface is also clearly visible, with the thickness of the PHPS layer measuring 0.4 <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><mi mathvariant="normal">μ</mi></math> </ephtml> m, consistent with the thickness observed in the bonding using double side PHPS layers.</p> <p>Graph: Figure 4Cross-sectional SEM observation of the bonding interface of (a) both side PHPS layers with one side plasma treatment and (b) one side PHPS layer with plasma treatment.</p> <p>Energy dispersive x-ray spectroscopy (EDX) analysis was performed across the bonding interface, and the results are presented in Fig. 5. For the bonding via double side PHPS layers with one side plasma, the presence of O and N is detected at the interface of the PHPS layers, while the Si signal is relatively lower compared to the bulk Si area. This can be attributed to the lower density of Si atoms in the converted PHPS layers. Moreover, the O intensity appears to be uniformly distributed across the PHPS layers, while the N intensity is relatively weak on the left side of the PHPS layers but as strong as O on the right side.</p> <p>This distribution of N intensity is attributed to the differing treatment of the two PHPS layers. Specifically, the left side PHPS layer in Fig. 5(a) is treated with plasma, while the right side is not. The dominant O signal on the left side is consistent with the PHPS conversion by plasma treatment, while the strong N signal on the right side suggests that the PHPS layer in this region is partially converted to <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> .</p> <p>The EDX line profile across the bonding interface of the single PHPS layer is illustrated in Fig. 5(b). At the PHPS layer area, the Si intensity is lower, while the presence of O and N is detected at the bonding interface. In comparison to the bonding utilizing both side PHPS layers as shown in Fig. 5(a), the composition of the PHPS layer appears to distribute more uniformly across the bonding interface, and the N intensity is closer to the background level. This suggests a more uniform conversion of the PHPS layer to <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> than the bonding via both side PHPS layers. Given that the single PHPS layer at the bonding interface is situated between hydrophilic Si surfaces, the adsorbed water diffuses into the PHPS layer from both sides. As a result, the conversion of PHPS to <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> proceeds more uniformly than the bonding via both sides PHPS layers.</p> <p>Furthermore, the N signal in EDX can be partly attributed to the byproducts of <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>NH</mtext><mn>3</mn></msub></math> </ephtml> resulting from the PHPS conversion. Given that N is generally spread throughout the PHPS layers, it suggests the diffusion of <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>NH</mtext><mn>3</mn></msub></math> </ephtml> and <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>H</mtext><mn>2</mn></msub></math> </ephtml> byproducts into the PHPS layer. As the converted PHPS into <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> has an amorphous structure, both <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>NH</mtext><mn>3</mn></msub></math> </ephtml> and <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>H</mtext><mn>2</mn></msub></math> </ephtml> are expected to diffuse similarly to <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><mrow><msub><mtext>H</mtext><mn>2</mn></msub><mtext>O</mtext></mrow></math> </ephtml> .</p> <p>Graph: Figure 5EDX line profile across the bonding interface via (a) both side PHPS layers with one side plasma treatment and (b) single side PHPS layer with plasma treatment.</p> <p>To investigate the PHPS conversion at the bonding interface, XPS analysis was performed on the debonded surface for both the bondings using both side PHPS layers and a single side PHPS layer, with and without plasma treatment. The atomic ratio of O and N was calculated from the O1s and N1s peaks for each condition, as illustrated in Fig. 6.</p> <p>For bonding via both side PHPS layers without plasma treatment, the N ratio was 0.88, suggesting that the N in the PHPS molecules was slightly replaced by O from the natural adsorption of water on the Si wafers[<reflink idref="bib32" id="ref37">32</reflink>]. However, when one of the both side PHPS layers was treated with plasma, the N ratio decreased to 0.50, indicating that the adsorbed water from the plasma treatment replaced the N at the bonding interface.</p> <p>On the other hand, the debonded surface with a single side PHPS layer also exhibited a high N ratio of 0.75 without plasma treatment. Similarly to bonding via both side PHPS layers, plasma treatment reduced the N ratio to 0.30 for bonding via a single side PHPS layer. As indicated by the cross-sectional EDX analysis, the single PHPS layer is sandwiched between the hydrophilic Si surfaces. The conversion of the single side PHPS layer proceeded further due to the relatively larger amount of water present at the bonding interface, as the amount of PHPS was half of that in the bonding via both side PHPS layers. Consequently, the replacement of N by O proceeded more largely compared to the bonding via double side PHPS layers.</p> <p>Graph: Figure 6Atomic ratio of O and N on the debonded wafer surface of the bonding via both and one side PHPS layers with and without plasma treatment.</p> <hd id="AN0174800147-4">Discussion</hd> <p>Based on the experimental results, we propose a room temperature bonding mechanism as illustrated in Fig. 7. For bonding with both-side PHPS layers, the plasma treatment initiates the conversion of one PHPS layer to <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> , facilitated by adsorbed water, as confirmed by the XPS analysis. Following the bonding of the plasma-treated PHPS layer with the untreated PHPS layer, the latter adheres to the substrates due to its ability to deform and compensate for surface asperities, as evidenced by IR imaging of the bonding interface. Subsequently, the water from the plasma-treated PHPS layer diffuses into the untreated PHPS layer, proceeding the hydrolysis of the untreated PHPS layer[<reflink idref="bib29" id="ref38">29</reflink>]. As the condensation polymerization of Si-OH groups proceeds and enhances the bond strength even at room temperature[<reflink idref="bib6" id="ref39">6</reflink>],[<reflink idref="bib33" id="ref40">33</reflink>],[<reflink idref="bib34" id="ref41">34</reflink>], <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> is formed at the bonding interface proceeds, resulting in a increased bond strength. The plasma-treated PHPS layer serves as a source of water and oxygen, supporting this conversion process, as indicated by cross-sectional EDX analysis.</p> <p>In the case of bonding with a single PHPS layer, the PHPS layer is coated on the hydrophilic surface with adsorbed water, thus facilitating PHPS conversion including hydrolysis step starting from the rear side. It has also been reported that the adsorbed water on the substrates react with the PHPS layer coated on the substrate[<reflink idref="bib32" id="ref42">32</reflink>]. This conversion is driven by the diffusion of the adsorbed water originating from the Si surface into the PHPS layer. Concurrently, the PHPS layer serves as an adhesive during the bonding of the PHPS-coated wafer to the uncoated wafer. Given that the surface of the uncoated wafer is also hydrophilic due to adsorbed water, water similarly diffuses into the PHPS layer from the front side. Consequently, the PHPS layer, situated between two hydrophilic Si surfaces, undergoes more uniform conversion into <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> compared to bonding via PHPS layers on both sides, as supported by the EDX analysis.</p> <p>Compared to other wafer bonding techniques, the wafer bonding via PHPS is comparable to water glass bonding[<reflink idref="bib35" id="ref43">35</reflink>]–[<reflink idref="bib37" id="ref44">37</reflink>] and sol-gel bonding[<reflink idref="bib38" id="ref45">38</reflink>]–[<reflink idref="bib40" id="ref46">40</reflink>]. Both of these techniques involve bonding through a liquid precursor of <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> , followed by an annealing step to create the bonding interface composed of <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> . However, a fundamental distinction lies in the mechanism of transformation to <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> . In sol-gel or water glass bonding, the conversion to <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> occurs through condensation polymerization, necessitating annealing to eliminate <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><mrow><msub><mtext>H</mtext><mn>2</mn></msub><mtext>O</mtext></mrow></math> </ephtml> from the bonding interface. In contrast, the proposed method utilizing a PHPS layer achieves the formation of the <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> bonding interface through hydrolysis, allowing for bonding at room temperature without the need for annealing.</p> <p>Regarding to the conventional direct bonding of Si or <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> , wafer bonding via PHPS exhibits a comparable bonding quality. In conventional hydrophilic bonding of Si or <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> with plasma hydrophilic treatment, the bond strength typically increases with post-bonding annealing. For Si/Si and <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> / <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> wafer bonding, the typical bond strength <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><mi mathvariant="normal">γ</mi></math> </ephtml> is less than 1 J/m <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msup><mrow /><mn>2</mn></msup></math> </ephtml> without post-bonding annealing[<reflink idref="bib6" id="ref47">6</reflink>],[<reflink idref="bib41" id="ref48">41</reflink>]. The bond strength <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><mi mathvariant="normal">γ</mi></math> </ephtml> increases to over 2 J/m <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msup><mrow /><mn>2</mn></msup></math> </ephtml> after annealing at temperatures no lower than 300 <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><mrow><msup><mrow /><mo>∘</mo></msup><mtext>C</mtext></mrow></math> </ephtml> . Despite the conventional hydrophilic wafer bonding requiring a heating step for a robust bonding interface, wafer bonding via PHPS achieves a high bond strength without annealing.</p> <p>In addition, conventional hydrophilic wafer bonding is often associated with concerns about bubble formation at the bonding interface. Post-bonding annealing in hydrophilic bonding facilitates the condensation polymerization of Si-OH at the bonding interface. This process generates byproducts such as <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>H</mtext><mn>2</mn></msub></math> </ephtml> and residual <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><mrow><msub><mtext>H</mtext><mn>2</mn></msub><mtext>O</mtext></mrow></math> </ephtml> , resulting in the formation of bubbles and voids at the bonding interface[<reflink idref="bib41" id="ref49">41</reflink>],[<reflink idref="bib42" id="ref50">42</reflink>]. In contrast, wafer bonding via PHPS, as depicted in Fig. 2, does not exhibit the formation of bubbles, contributing to an improved bonding quality.</p> <p>Graph: Figure 7The room temperature wafer bonding mechanism via (a) both side PHPS layers with plasma treatment for one side PHPS layer and (b) one side PHPS layer with plasma treatment.</p> <hd id="AN0174800147-5">Conclusions</hd> <p>In this paper, we investigated and demonstrated wafer bonding via PHPS at room temperature. Through the strategic use of plasma hydrophilic treatment on either the Si surface or the PHPS layer, we have effectively facilitated the conversion of PHPS into a robust bonding interface composed of <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> . This approach achieves the bond strength exceeding 5 J/m <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msup><mrow /><mn>2</mn></msup></math> </ephtml> and the void-free bonding interfaces, which are attributed to the combined effects of PHPS adhesion and <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> formation. The XPS and EDX analysis also suggest the bonding mechanism that the adsorbed water by hydrophilic plasma treatment diffuses into the PHPS layer which results in the partial conversion of PHPS into <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>SiO</mtext><mn>2</mn></msub></math> </ephtml> , contributing to the robust bonding interface. This technique will provide a new approach for the wafer bonding at room temperature for electronics packaging.</p> <hd id="AN0174800147-6">Methods</hd> <p>4 inch Si wafers, with a thickness of 525 <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><mi mathvariant="normal">μ</mi></math> </ephtml> m, were utilized for the wafer bonding experiments. A 20 wt% solution of PHPS in dibutyl ether solvent was purchased.</p> <p>In the case of the wafer bonding via both side PHPS layers, first, the wafers were coated with PHPS solution by spin coating at 2000 rpm for 20 s. The coated PHPS layers underwent a baking process on a hot plate at 100 <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><mrow><msup><mrow /><mo>∘</mo></msup><mtext>C</mtext></mrow></math> </ephtml> for 5 min to volatilize the solvent. This baking step completely removes the solvent from the PHPS layer[<reflink idref="bib32" id="ref51">32</reflink>],[<reflink idref="bib43" id="ref52">43</reflink>], that is also supported by XPS and EDX analysis (data not shown). Sequentially, the PHPS layers were treated with <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>N</mtext><mn>2</mn></msub></math> </ephtml> plasma with 150 W power for 60 s to induce hydrophilicity on the PHPS layer's surface. After the surface treatment, the PHPS-coated surfaces of the Si wafers were manually brought into contact under ambient air conditions at room temperature. For comparison, wafer bonding was also conducted with plasma treatment applied to both sides of the PHPS layers, one side of the PHPS layers, and without any plasma treatment.</p> <p>In the case of the wafer bonding via one side PHPS layer, one wafer of a bonding pair was coated with PHPS. First, the bonding pair of Si wafers were treated with <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>O</mtext><mn>2</mn></msub></math> </ephtml> plasma followed by <ephtml> <math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mtext>N</mtext><mn>2</mn></msub></math> </ephtml> plasma to enhance water adsorption[<reflink idref="bib44" id="ref53">44</reflink>],[<reflink idref="bib45" id="ref54">45</reflink>], with both treatments conducted at a power of 150 W for 60 s each. After the plasma treatment, the wafers underwent a DI water rinse and were subsequently spin-dried. Following these surface preparations, the PHPS solution was spin-coated onto the one of the treated Si wafer pair, and solvent volatilization was conducted under the same conditions as described earlier. Finally, the Si wafer coated with PHPS and the uncoated wafer were bonded together in the ambient air at room temperature. The wafer bonding was also performed without the plasma hydrophilic treatment of Si wafers for comparison.</p> <p>The PHPS layer underwent analysis using XPS to investigate surface compositions. The bonding quality was evaluated by IR imaging of the bonded wafers and bond strength measurements using the blade test[<reflink idref="bib46" id="ref55">46</reflink>]. The properties of the cross-sectional bonding interface were observed using SEM with EDX.</p> <hd id="AN0174800147-7">Acknowledgements</hd> <p>This work is supported by the Amada foundation, Tokyo Ohka Foundation for The Promotion of Science and Technology, and JSPS KAKENHI Grant Number JP23K13554.</p> <hd id="AN0174800147-8">Author contributions</hd> <p>K.T. designed and carried out the experiments, analyzed the experimental results, and wrote the manuscript. K.T., T.S., and E.H. discussed results, commented on, and edited the manuscript.</p> <hd id="AN0174800147-9">Data availability</hd> <p>The datasets used and/or analyzed during the current study available from the corresponding author on reasonable request.</p> <hd id="AN0174800147-10">Competing interests</hd> <p>The authors declare no competing interests.</p> <hd id="AN0174800147-11">Publisher's note</hd> <p>Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.</p> <ref id="AN0174800147-12"> <title> References </title> <blist> <bibl id="bib1" idref="ref1" type="bt">1</bibl> <bibtext> Howlader M, Okada H, Kim T, Itoh T, Suga T. Wafer level surface activated bonding tool for mems packaging. J. Electrochem. Soc. 2004; 151: G461-G467. 1:CAS:528:DC%2BD2cXlvVKjurw%3D. 10.1149/1.1758723</bibtext> </blist> <blist> <bibl id="bib2" idref="ref2" type="bt">2</bibl> <bibtext> Higurashi E, Chino D, Suga T, Sawada R. Au-Au surface-activated bonding and its application to optical microsensors with 3-D structure. IEEE J. Sel. Top. Quantum Electron. 2009; 15: 1500-1505. 2009IJSTQ.15.1500H. 1:CAS:528:DC%2BD1MXht12qsLzN. 10.1109/JSTQE.2009.2020812</bibtext> </blist> <blist> <bibl id="bib3" idref="ref3" type="bt">3</bibl> <bibtext> Takeuchi K. Microfluidic chip connected to porous microneedle array for continuous isf sampling. Drug Deliv. Transl. Res. 2022; 12: 435-443. 1:CAS:528:DC%2BB38XksFaqtrY%3D. 10.1007/s13346-021-01050-0. 34739717</bibtext> </blist> <blist> <bibl id="bib4" idref="ref4" type="bt">4</bibl> <bibtext> Fujino, M, Takahashi, K, Araga, Y. & Kikuchi, K. 300 mm wafer-level hybrid bonding for cu/interlayer dielectric bonding in vacuum. Jpn. J. Appl. Phys. 59, SBBA02. https://doi.org/10.7567/1347-4065/ab4b2b (2019).</bibtext> </blist> <blist> <bibl id="bib5" idref="ref5" type="bt">5</bibl> <bibtext> Ventosa C. Hydrophilic low-temperature direct wafer bonding. J. Appl. Phys. 2008; 104. 2008JAP.104l3524V. 10.1063/1.3040701</bibtext> </blist> <blist> <bibl id="bib6" idref="ref6" type="bt">6</bibl> <bibtext> Fournel F. Water stress corrosion in bonded structures. ECS J. Solid State Sci. Technol. 2015; 4: P124-P130. 1:CAS:528:DC%2BC2MXmtVagtrc%3D. 10.1149/2.0031505jss</bibtext> </blist> <blist> <bibl id="bib7" idref="ref7" type="bt">7</bibl> <bibtext> Howlader MR, Itoh H, Suga T, Kim M. Sequential plasma activated process for silicon direct bonding. ECS Trans. 2006; 3: 191-202. 1:CAS:528:DC%2BD2sXmslOksrc%3D. 10.1149/1.2357070</bibtext> </blist> <blist> <bibl id="bib8" idref="ref8" type="bt">8</bibl> <bibtext> Takeuchi, K. & Suga, T. Quantification of wafer bond strength under controlled atmospheres. Jpn. J. Appl. Phys. 61, SF1010. https://doi.org/10.35848/1347-4065/ac5e49 (2022).</bibtext> </blist> <blist> <bibl id="bib9" idref="ref9" type="bt">9</bibl> <bibtext> Knechtel R. Glass frit bonding: An universal technology for wafer level encapsulation and packaging. Microsyst. Technol. 2005; 12: 63-68. 1:CAS:528:DC%2BD28XitVSmtA%3D%3D. 10.1007/s00542-005-0022-x</bibtext> </blist> <blist> <bibtext> Knechtel R, Wiemer M, Frömel J. Wafer level encapsulation of microsystems using glass frit bonding. Microsyst. Technol. 2006; 12: 468-472. 1:CAS:528:DC%2BD28XivVCgtrk%3D. 10.1007/s00542-005-0036-4</bibtext> </blist> <blist> <bibtext> Nakajima K, Uchiyama H, Kitano T, Kozuka H. Conversion of solution-derived perhydropolysilazane thin films into silica in basic humid atmosphere at room temperature. J. Am. Ceram. Soc. 2013; 96: 2806-2816. 1:CAS:528:DC%2BC3sXhsVektLrE. 10.1111/jace.12513</bibtext> </blist> <blist> <bibtext> Günthner, M, Wang, K, Bordia, R. K. & Motz, G. Conversion behaviour and resulting mechanical properties of polysilazane-based coatings. J. Eur. Ceram. Soc. 32, 1883–1892. https://doi.org/10.1016/j.jeurceramsoc.2011.09.005 (2012)</bibtext> </blist> <blist> <bibtext> Kozuka H, Fujita M, Tamoto S. Polysilazane as the source of silica: The formation of dense silica coatings at room temperature and the new route to organic–inorganic hybrids. J. Sol–Gel Sci. Technol. 2008; 48: 148-155. 1:CAS:528:DC%2BD1cXhtFejurzP. 10.1007/s10971-008-1793-1</bibtext> </blist> <blist> <bibtext> Lee J-S, Oh J-H, Moon S-W, Sul W-S, Kim S-D. A technique for converting perhydropolysilazane to SiOx at low temperature. Electrochem. Solid-State Lett. 2009; 13: H23. 1:CAS:528:DC%2BD1MXhsVWqs77L. 10.1149/1.3264092</bibtext> </blist> <blist> <bibtext> Morlier A, Cros S, Garandet J-P, Alberola N. Structural properties of ultraviolet cured polysilazane gas barrier layers on polymer substrates. Thin Solid Films. 2014; 550: 85-89. 2014TSF.550.85M. 1:CAS:528:DC%2BC3sXhslGls7vM. 10.1016/j.tsf.2013.10.140</bibtext> </blist> <blist> <bibtext> Baek JJ. Intense pulsed uv light treatment to design functional optical films from perhydropolysilazane: An alternative to conventional heat treatment processes. J. Mater. Sci. 2022; 57: 254-273. 2022JMatS.57.254B. 1:CAS:528:DC%2BB38Xlt1emsw%3D%3D. 10.1007/s10853-021-06598-3</bibtext> </blist> <blist> <bibtext> Wang W-Y. Rapid conversion of perhydropolysilazane into thin silica coating at low temperature. Chin. J. Polym. Sci. 2023. 10.1007/s10118-023-2959-6</bibtext> </blist> <blist> <bibtext> Müller S, de Hazan Y, Penner D. Effect of temperature, humidity and aminoalkoxysilane additive on the low temperature curing of polyorganosilazane coatings studied by ir spectroscopy, gravimetric and evolved gas analysis. Prog. Organ. Coat. 2016; 97: 133-145. 1:CAS:528:DC%2BC28Xlt1GitbY%3D. 10.1016/j.porgcoat.2016.03.021</bibtext> </blist> <blist> <bibtext> Chavez R, Ionescu E, Balan C, Fasel C, Riedel R. Effect of ambient atmosphere on crosslinking of polysilazanes. J. Appl. Polym. Sci. 2011; 119: 794-802. 1:CAS:528:DC%2BC3cXhsFygtr7F. 10.1002/app.32777</bibtext> </blist> <blist> <bibtext> Akutsu, K. et al. Investigation of structure of a thin SiO2 layer as an antifouling and corrosion-resistant coating. J. Ceram. Soc. Jpn. 124, 172–176. https://doi.org/10.2109/jcersj2.15153 (2016).</bibtext> </blist> <blist> <bibtext> Günthner M. Advanced coatings on the basis of Si(C)N precursors for protection of steel against oxidation. J. Eur. Ceram. Soc. 2009; 29: 2061-2068. 2009sree.book..G. 1:CAS:528:DC%2BD1MXls1ehtbY%3D. 10.1016/j.jeurceramsoc.2008.11.013</bibtext> </blist> <blist> <bibtext> Hu, L, Li, M, Xu, C. & Luo, Y. Perhydropolysilazane derived silica coating protecting kapton from atomic oxygen attack. Thin Solid Films 520, 1063–1068. https://doi.org/10.1016/j.tsf.2011.10.011 (2011).</bibtext> </blist> <blist> <bibtext> Park K-S, Ko P-S, Kim S-D. Effects of N2O plasma treatment on perhydropolysilazane spin-on-dielectrics for inter-layer-dielectric applications. Thin Solid Films. 2014; 551: 57-60. 2014TSF.551.57P. 1:CAS:528:DC%2BC3sXhvFKgs7jM. 10.1016/j.tsf.2013.11.104</bibtext> </blist> <blist> <bibtext> Kim S-D, Ko P-S, Park K-S. Perhydropolysilazane spin-on dielectrics for inter-layer-dielectric applications of sub-30 nm silicon technology. Semicond. Sci. Technol. 2013; 28. 2013SeScT.28c5008K. 1:CAS:528:DC%2BC3sXlslCiu7w%3D. 10.1088/0268-1242/28/3/035008</bibtext> </blist> <blist> <bibtext> Bauer F. Preparation of moisture curable polysilazane coatings: part I. Elucidation of low temperature curing kinetics by ft-ir spectroscopy. Prog. Organ. Coat. 2005; 53: 183-190. 1:CAS:528:DC%2BD2MXks1Wiu7Y%3D. 10.1016/j.porgcoat.2005.02.006</bibtext> </blist> <blist> <bibtext> Zhan Y, Grottenmüller R, Li W, Javaid F, Riedel R. Evaluation of mechanical properties and hydrophobicity of room-temperature, moisture-curable polysilazane coatings. J. Appl. Polym. Sci. 2021; 138: 50469. 1:CAS:528:DC%2BB3MXhsFGktbk%3D. 10.1002/app.50469</bibtext> </blist> <blist> <bibtext> Sun X, Liu HT, Cheng HF. Oxidation behavior of silicon nitride fibers obtained from polycarbosilane fibers via electron beam irradiation curing. RSC Adv. 2017; 7: 47833-47839. 2017RSCAd.747833S. 1:CAS:528:DC%2BC2sXhs1ChsLrP. 10.1039/C7RA09056K</bibtext> </blist> <blist> <bibtext> Diéguez L. Optical gratings coated with thin Si3N4 layer for efficient immunosensing by optical waveguide lightmode spectroscopy. Biosensors. 2012; 2: 114-126. 1:CAS:528:DC%2BC38XnvFWnt70%3D. 10.3390/bios2020114. 25585707. 4263575</bibtext> </blist> <blist> <bibtext> Qi H. The atomic oxygen erosion resistance effect and mechanism of the perhydropolysilazane-derived siox coating used on polymeric materials in space environment. Polymers. 2022; 14: 66. 1:CAS:528:DC%2BB38XitFOmtbo%3D. 10.3390/polym14020322</bibtext> </blist> <blist> <bibtext> Biesuz M. First synthesis of silicon nanocrystals in amorphous silicon nitride from a preceramic polymer. Nanotechnology. 2019; 30. 2019Nanot.30y5601B. 1:CAS:528:DC%2BC1MXhtlGmu7jM. 10.1088/1361-6528/ab0cc8. 30836334</bibtext> </blist> <blist> <bibtext> Shimomura, J. et al. The effect of thermal treatment on conversion to silica of silica/polymethylmethacrylate hybrid films prepared by sol–gel method using perhydropolysilazane. Trans. Mater. Res. Soc. Jpn.33, 993–996. https://doi.org/10.14723/tmrsj.33.993 (2008).</bibtext> </blist> <blist> <bibtext> Niizeki T. Structural study of silica coating thin layers prepared from perhydropolysilazane: Substrate dependence and water penetration structure. Coatings. 2016. 10.3390/coatings6040064</bibtext> </blist> <blist> <bibtext> Howlader MMR. Sequential plasma-activated bonding mechanism of silicon/silicon wafers. J. Microelectromech. Syst. 2010; 19: 840-848. 2780308. 1:CAS:528:DC%2BC3cXhtFajt7nK. 10.1109/JMEMS.2010.2049731</bibtext> </blist> <blist> <bibtext> Wang C, Higurashi E, Suga T. Void-free room-temperature silicon wafer direct bonding using sequential plasma activation. Jpn. J. Appl. Phys. 2008; 47: 2526-2530. 2008JaJAP.47.2526W. 1:CAS:528:DC%2BD1cXlsl2mtrk%3D. 10.1143/jjap.47.2526</bibtext> </blist> <blist> <bibtext> Lin HC, Chang KL, Pickrell GW, Hsieh KC, Cheng KY. Low temperature wafer bonding by spin on glass. J. Vac. Sci. Technol. B Microelectron. Nanometer Struct. Process. Meas. Phenom. 2002; 20: 752-754. 2002JVSTB.20.752L. 1:CAS:528:DC%2BD38XisFymtbs%3D. 10.1116/1.1464832</bibtext> </blist> <blist> <bibtext> Puers R, Cozma A. Bonding wafers with sodium silicate solution. J. Micromech. Microeng. 1997; 7: 114-117. 1997JMiMi.7.114P. 1:CAS:528:DyaK2sXntVGlsbc%3D. 10.1088/0960-1317/7/3/008</bibtext> </blist> <blist> <bibtext> Xu Y, Wang S-K, Yao P, Wang Y, Chen D. An air-plasma enhanced low-temperature wafer bonding method using high-concentration water glass adhesive layer. Appl. Surf. Sci. 2020; 500. 1:CAS:528:DC%2BC1MXhvFeqsL7I. 10.1016/j.apsusc.2019.144007</bibtext> </blist> <blist> <bibtext> Barbé C. Sol–gel bonding of silicon wafers: Part 1: Influence of the processing temperature on final bond morphology and interfacial energy. Thin Solid Films. 2005; 488: 153-159. 2005TSF.488.153B. 1:CAS:528:DC%2BD2MXms1OmsLk%3D. 10.1016/j.tsf.2005.04.108</bibtext> </blist> <blist> <bibtext> Barbé C. Sol–gel bonding of silicon wafers: Part 2. Influence of the sol-gel chemistry on bond morphology and interfacial energy. Thin Solid Films. 2005; 488: 160-166. 2005TSF.488.160B. 1:CAS:528:DC%2BD2MXms1OmsLY%3D. 10.1016/j.tsf.2005.04.109</bibtext> </blist> <blist> <bibtext> Tan CM, Deng SS, Wei J, Yu WB. Mechanism of sol-gel intermediate layer low temperature wafer bonding. J. Phys. D Appl. Phys. 2005; 38: 1308. 2005JPhD.38.1308T. 1:CAS:528:DC%2BD2MXjvFSmsLg%3D. 10.1088/0022-3727/38/8/031</bibtext> </blist> <blist> <bibtext> Masteika V, Kowal J, Braithwaite NSJ, Rogers T. A review of hydrophilic silicon wafer bonding. ECS J. Solid State Sci. Technol. 2014; 3: Q42-Q54. 1:CAS:528:DC%2BC2cXls1Sls78%3D. 10.1149/2.007403jss</bibtext> </blist> <blist> <bibtext> Le Tiec Y. Water management on semiconductor surfaces. Microelectron. Eng. 2011; 88: 3432-3436. 10.1016/j.mee.2010.10.017</bibtext> </blist> <blist> <bibtext> Ohishi T, Yamazaki Y. Formation and gas barrier characteristics of polysilazane-derived silica coatings formed by excimer light irradiation on pet films with vacuum evaporated silica coatings. Mater. Sci. Appl. 2016; 8: 1-14</bibtext> </blist> <blist> <bibtext> He R, Yamauchi A, Suga T. Sequential plasma activation methods for hydrophilic direct bonding at sub-200 C. Jpn. J. Appl. Phys. 2018; 57: 02BD03. 1:CAS:528:DC%2BC1cXhsFKmsrrO. 10.7567/jjap.57.02bd03</bibtext> </blist> <blist> <bibtext> Takeuchi K, Mu F, Yamauchi A, Suga T. Sequential plasma activation for low temperature bonding of aluminosilicate glass. ECS J. Solid State Sci. Technol. 2021; 10. 2021JSSST.10e4007T. 1:CAS:528:DC%2BB3MXhtlOjs73F. 10.1149/2162-8777/abfd4b</bibtext> </blist> <blist> <bibtext> Maszara WP, Goetz G, Caviglia A, McKitterick JB. Bonding of silicon wafers for silicon-on-insulator. J. Appl. Phys. 1988; 64: 4943-4950. 1988JAP.64.4943M. 1:CAS:528:DyaL1MXkvFehug%3D%3D. 10.1063/1.342443</bibtext> </blist> </ref> <aug> <p>By Kai Takeuchi; Tadatomo Suga and Eiji Higurashi</p> <p>Reported by Author; Author; Author</p> </aug> <nolink nlid="nl1" bibid="bib10" firstref="ref10"></nolink> <nolink nlid="nl2" bibid="bib11" firstref="ref11"></nolink> <nolink nlid="nl3" bibid="bib12" firstref="ref12"></nolink> <nolink nlid="nl4" bibid="bib13" firstref="ref14"></nolink> <nolink nlid="nl5" bibid="bib14" firstref="ref15"></nolink> <nolink nlid="nl6" bibid="bib16" firstref="ref16"></nolink> <nolink nlid="nl7" bibid="bib17" firstref="ref17"></nolink> <nolink nlid="nl8" bibid="bib18" firstref="ref18"></nolink> <nolink nlid="nl9" bibid="bib19" firstref="ref19"></nolink> <nolink nlid="nl10" bibid="bib20" firstref="ref20"></nolink> <nolink nlid="nl11" bibid="bib22" firstref="ref21"></nolink> <nolink nlid="nl12" bibid="bib23" firstref="ref22"></nolink> <nolink nlid="nl13" bibid="bib24" firstref="ref23"></nolink> <nolink nlid="nl14" bibid="bib25" firstref="ref26"></nolink> <nolink nlid="nl15" bibid="bib26" firstref="ref27"></nolink> <nolink nlid="nl16" bibid="bib27" firstref="ref28"></nolink> <nolink nlid="nl17" bibid="bib28" firstref="ref29"></nolink> <nolink nlid="nl18" bibid="bib29" firstref="ref31"></nolink> <nolink nlid="nl19" bibid="bib30" firstref="ref32"></nolink> <nolink nlid="nl20" bibid="bib31" firstref="ref36"></nolink> <nolink nlid="nl21" bibid="bib32" firstref="ref37"></nolink> <nolink nlid="nl22" bibid="bib33" firstref="ref40"></nolink> <nolink nlid="nl23" bibid="bib34" firstref="ref41"></nolink> <nolink nlid="nl24" bibid="bib35" firstref="ref43"></nolink> <nolink nlid="nl25" bibid="bib37" firstref="ref44"></nolink> <nolink nlid="nl26" bibid="bib38" firstref="ref45"></nolink> <nolink nlid="nl27" bibid="bib40" firstref="ref46"></nolink> <nolink nlid="nl28" bibid="bib41" firstref="ref48"></nolink> <nolink nlid="nl29" bibid="bib42" firstref="ref50"></nolink> <nolink nlid="nl30" bibid="bib43" firstref="ref52"></nolink> <nolink nlid="nl31" bibid="bib44" firstref="ref53"></nolink> <nolink nlid="nl32" bibid="bib45" firstref="ref54"></nolink> <nolink nlid="nl33" bibid="bib46" firstref="ref55"></nolink>
CustomLinks:
  – Url: https://resolver.ebsco.com/c/xy5jbn/result?sid=EBSCO:edsdoj&genre=article&issn=20452322&ISBN=&volume=14&issue=1&date=20241001&spage=1&pages=1-10&title=Scientific Reports&atitle=Knowledge%20and%20attitudes%20on%20anemia%20and%20menstrual%20health%20among%20Malaysian%20female%20university%20students&aulast=Kai%20Ting%20Mok&id=DOI:10.1038/s41598-024-76655-9
    Name: Full Text Finder (for New FTF UI) (s8985755)
    Category: fullText
    Text: Find It @ SCU Libraries
    MouseOverText: Find It @ SCU Libraries
  – Url: https://doaj.org/article/d2ec399a02894449bef7dfd538fbb7bc
    Name: EDS - DOAJ (s8985755)
    Category: fullText
    Text: View record from DOAJ
    MouseOverText: View record from DOAJ
Header DbId: edsdoj
DbLabel: Directory of Open Access Journals
An: edsdoj.2ec399a02894449bef7dfd538fbb7bc
RelevancyScore: 1047
AccessLevel: 3
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 1047.2685546875
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: Knowledge and attitudes on anemia and menstrual health among Malaysian female university students
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AR" term="%22Kai+Ting+Mok%22">Kai Ting Mok</searchLink><br /><searchLink fieldCode="AR" term="%22Satvinder+Kaur%22">Satvinder Kaur</searchLink><br /><searchLink fieldCode="AR" term="%22Yee-How+Say%22">Yee-How Say</searchLink><br /><searchLink fieldCode="AR" term="%22Siti+Sabariah+Bahari%22">Siti Sabariah Bahari</searchLink><br /><searchLink fieldCode="AR" term="%22Chirawat+Paratthakonkun%22">Chirawat Paratthakonkun</searchLink><br /><searchLink fieldCode="AR" term="%22Trias+Mahmudiono%22">Trias Mahmudiono</searchLink><br /><searchLink fieldCode="AR" term="%22Nurliyana+Abdul+Razak%22">Nurliyana Abdul Razak</searchLink>
– Name: TitleSource
  Label: Source
  Group: Src
  Data: Scientific Reports, Vol 14, Iss 1, Pp 1-10 (2024)
– Name: Publisher
  Label: Publisher Information
  Group: PubInfo
  Data: Nature Portfolio, 2024.
– Name: DatePubCY
  Label: Publication Year
  Group: Date
  Data: 2024
– Name: Subset
  Label: Collection
  Group: HoldingsInfo
  Data: LCC:Medicine<br />LCC:Science
– Name: Subject
  Label: Subject Terms
  Group: Su
  Data: <searchLink fieldCode="DE" term="%22Anemia%22">Anemia</searchLink><br /><searchLink fieldCode="DE" term="%22Knowledge%22">Knowledge</searchLink><br /><searchLink fieldCode="DE" term="%22Attitude%22">Attitude</searchLink><br /><searchLink fieldCode="DE" term="%22Menstrual+health%22">Menstrual health</searchLink><br /><searchLink fieldCode="DE" term="%22Preventive+health%22">Preventive health</searchLink><br /><searchLink fieldCode="DE" term="%22Women%27s+health%22">Women’s health</searchLink><br /><searchLink fieldCode="DE" term="%22Medicine%22">Medicine</searchLink><br /><searchLink fieldCode="DE" term="%22Science%22">Science</searchLink>
– Name: Abstract
  Label: Description
  Group: Ab
  Data: Abstract Anemia is a significant public health concern, particularly among young female adults due to its potential impact on reproductive health. This study investigated the association between anemia-related knowledge, attitudes, menstrual health, and anemia status among Malaysian university students. This was a cross-sectional study named “SCARF” - Study to Combat Anemia - Research for Female Students, involving 674 university students in Malaysia. Anemia status was determined based on haemoglobin level, while knowledge, attitude and menstrual health were measured using validated questionnaires. The mean menarche age of students in this study was 12.1 ± 1.21 years. Students who were anemic had significantly longer menstrual cycle duration (P = 0.034) and more days with heavy flow (P = 0.038). Most students had poor knowledge (44.5%) and attitudes (84.1%) towards anemia. Students with good knowledge were 1.1 times more likely to have better anemia status compared to those with poor knowledge (95% CI: 1.0–1.2, P = 0.049). This study highlighted a lack of practical application of the knowledge to dietary habits. Collaborative efforts between educators and healthcare providers are crucial in developing a comprehensive strategy, such as interventions to prioritise educational initiatives and practical support to enhance overall menstrual health among female students.
– Name: TypeDocument
  Label: Document Type
  Group: TypDoc
  Data: article
– Name: Format
  Label: File Description
  Group: SrcInfo
  Data: electronic resource
– Name: Language
  Label: Language
  Group: Lang
  Data: English
– Name: ISSN
  Label: ISSN
  Group: ISSN
  Data: 2045-2322
– Name: NoteTitleSource
  Label: Relation
  Group: SrcInfo
  Data: https://doaj.org/toc/2045-2322
– Name: DOI
  Label: DOI
  Group: ID
  Data: 10.1038/s41598-024-76655-9
– Name: URL
  Label: Access URL
  Group: URL
  Data: <link linkTarget="URL" linkTerm="https://doaj.org/article/d2ec399a02894449bef7dfd538fbb7bc" linkWindow="_blank">https://doaj.org/article/d2ec399a02894449bef7dfd538fbb7bc</link>
– Name: AN
  Label: Accession Number
  Group: ID
  Data: edsdoj.2ec399a02894449bef7dfd538fbb7bc
PLink https://login.libproxy.scu.edu/login?url=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsdoj&AN=edsdoj.2ec399a02894449bef7dfd538fbb7bc
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1038/s41598-024-76655-9
    Languages:
      – Text: English
    PhysicalDescription:
      Pagination:
        PageCount: 10
        StartPage: 1
    Subjects:
      – SubjectFull: Anemia
        Type: general
      – SubjectFull: Knowledge
        Type: general
      – SubjectFull: Attitude
        Type: general
      – SubjectFull: Menstrual health
        Type: general
      – SubjectFull: Preventive health
        Type: general
      – SubjectFull: Women’s health
        Type: general
      – SubjectFull: Medicine
        Type: general
      – SubjectFull: Science
        Type: general
    Titles:
      – TitleFull: Knowledge and attitudes on anemia and menstrual health among Malaysian female university students
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Kai Ting Mok
      – PersonEntity:
          Name:
            NameFull: Satvinder Kaur
      – PersonEntity:
          Name:
            NameFull: Yee-How Say
      – PersonEntity:
          Name:
            NameFull: Siti Sabariah Bahari
      – PersonEntity:
          Name:
            NameFull: Chirawat Paratthakonkun
      – PersonEntity:
          Name:
            NameFull: Trias Mahmudiono
      – PersonEntity:
          Name:
            NameFull: Nurliyana Abdul Razak
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 01
              M: 10
              Type: published
              Y: 2024
          Identifiers:
            – Type: issn-print
              Value: 20452322
          Numbering:
            – Type: volume
              Value: 14
            – Type: issue
              Value: 1
          Titles:
            – TitleFull: Scientific Reports
              Type: main
ResultId 1