通过氧化锌纳米形状的表面重构调节 CO2 到 CO 的电催化还原反应

IF 6.7 3区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Journal of Science: Advanced Materials and Devices Pub Date : 2024-05-22 DOI:10.1016/j.jsamd.2024.100748
Mustapha Umar , Mohammed Yousef Aljezan , Ismail Abdulazeez , Abduljamiu O. Amao , Saheed A. Ganiyu , Khalid Alhooshani
{"title":"通过氧化锌纳米形状的表面重构调节 CO2 到 CO 的电催化还原反应","authors":"Mustapha Umar ,&nbsp;Mohammed Yousef Aljezan ,&nbsp;Ismail Abdulazeez ,&nbsp;Abduljamiu O. Amao ,&nbsp;Saheed A. Ganiyu ,&nbsp;Khalid Alhooshani","doi":"10.1016/j.jsamd.2024.100748","DOIUrl":null,"url":null,"abstract":"<div><p>The electrocatalytic conversion of carbon dioxide (CO<sub>2</sub>) into valuable chemicals presents a promising strategy for closing the carbon cycle. In this study, we synthesized zinc (Zn) catalysts through hydrothermal methods using either polyvinylpyrrolidone (PVP) or cetyltrimethylammonium bromide (CTAB) as stabilizing agents. These catalysts proved highly efficient in converting CO<sub>2</sub> into carbon monoxide (CO). Our findings revealed that ZnO, synthesized with different morphologies—namely, nanoneedles (ZnO-NN) and nanorods (ZnO-NR)—underwent significant electro-reconstruction, ultimately leading to the formation of hexagonal metallic Zn crystals, regardless of their initial characteristics. Utilizing ex-situ operando techniques, we elucidated that metallic Zn serves as the active phase for the CO<sub>2</sub>-to-CO conversion process. In a comparison, ZnO-NN catalysts demonstrated superior selectivity and stability, achieving 91.3% CO selectivity at a potential of −0.88 V vs. RHE (Reversible Hydrogen Electrode) due to the facile transformation of ZnO to metallic Zn. Remarkably, these catalysts maintained this level of performance for more than 17 h. Conversely, ZnO-NR catalysts exhibited a lower CO selectivity of 62.5% at a relatively higher potential of −0.98 V vs RHE.</p></div>","PeriodicalId":17219,"journal":{"name":"Journal of Science: Advanced Materials and Devices","volume":null,"pages":null},"PeriodicalIF":6.7000,"publicationDate":"2024-05-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2468217924000790/pdfft?md5=34a1ccd46db23f96f70243172df40fc4&pid=1-s2.0-S2468217924000790-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Modulating the electrocatalytic reduction of CO2 to CO via surface reconstruction of ZnO nanoshapes\",\"authors\":\"Mustapha Umar ,&nbsp;Mohammed Yousef Aljezan ,&nbsp;Ismail Abdulazeez ,&nbsp;Abduljamiu O. Amao ,&nbsp;Saheed A. Ganiyu ,&nbsp;Khalid Alhooshani\",\"doi\":\"10.1016/j.jsamd.2024.100748\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The electrocatalytic conversion of carbon dioxide (CO<sub>2</sub>) into valuable chemicals presents a promising strategy for closing the carbon cycle. In this study, we synthesized zinc (Zn) catalysts through hydrothermal methods using either polyvinylpyrrolidone (PVP) or cetyltrimethylammonium bromide (CTAB) as stabilizing agents. These catalysts proved highly efficient in converting CO<sub>2</sub> into carbon monoxide (CO). Our findings revealed that ZnO, synthesized with different morphologies—namely, nanoneedles (ZnO-NN) and nanorods (ZnO-NR)—underwent significant electro-reconstruction, ultimately leading to the formation of hexagonal metallic Zn crystals, regardless of their initial characteristics. Utilizing ex-situ operando techniques, we elucidated that metallic Zn serves as the active phase for the CO<sub>2</sub>-to-CO conversion process. In a comparison, ZnO-NN catalysts demonstrated superior selectivity and stability, achieving 91.3% CO selectivity at a potential of −0.88 V vs. RHE (Reversible Hydrogen Electrode) due to the facile transformation of ZnO to metallic Zn. Remarkably, these catalysts maintained this level of performance for more than 17 h. Conversely, ZnO-NR catalysts exhibited a lower CO selectivity of 62.5% at a relatively higher potential of −0.98 V vs RHE.</p></div>\",\"PeriodicalId\":17219,\"journal\":{\"name\":\"Journal of Science: Advanced Materials and Devices\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":6.7000,\"publicationDate\":\"2024-05-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2468217924000790/pdfft?md5=34a1ccd46db23f96f70243172df40fc4&pid=1-s2.0-S2468217924000790-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Science: Advanced Materials and Devices\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2468217924000790\",\"RegionNum\":3,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Science: Advanced Materials and Devices","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2468217924000790","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

通过电催化将二氧化碳(CO2)转化为有价值的化学物质是实现碳循环的一项前景广阔的战略。在本研究中,我们使用聚乙烯吡咯烷酮(PVP)或十六烷基三甲基溴化铵(CTAB)作为稳定剂,通过水热法合成了锌(Zn)催化剂。事实证明,这些催化剂能高效地将二氧化碳转化为一氧化碳(CO)。我们的研究结果表明,以不同形态合成的氧化锌--即纳米针(ZnO-NN)和纳米棒(ZnO-NR)--会发生显著的电重构,最终形成六方金属锌晶体,无论其初始特性如何。利用原位操作技术,我们阐明了金属锌是 CO2 到 CO 转化过程中的活性相。相比之下,ZnO-NN 催化剂表现出更高的选择性和稳定性,在 -0.88 V 电位与 RHE(可逆氢电极)相比时,由于 ZnO 易于转化为金属 Zn,CO 选择性达到 91.3%。相反,ZnO-NR 催化剂在相对较高的 -0.98 V 电位(相对于 RHE)下的 CO 选择性较低,仅为 62.5%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Modulating the electrocatalytic reduction of CO2 to CO via surface reconstruction of ZnO nanoshapes

The electrocatalytic conversion of carbon dioxide (CO2) into valuable chemicals presents a promising strategy for closing the carbon cycle. In this study, we synthesized zinc (Zn) catalysts through hydrothermal methods using either polyvinylpyrrolidone (PVP) or cetyltrimethylammonium bromide (CTAB) as stabilizing agents. These catalysts proved highly efficient in converting CO2 into carbon monoxide (CO). Our findings revealed that ZnO, synthesized with different morphologies—namely, nanoneedles (ZnO-NN) and nanorods (ZnO-NR)—underwent significant electro-reconstruction, ultimately leading to the formation of hexagonal metallic Zn crystals, regardless of their initial characteristics. Utilizing ex-situ operando techniques, we elucidated that metallic Zn serves as the active phase for the CO2-to-CO conversion process. In a comparison, ZnO-NN catalysts demonstrated superior selectivity and stability, achieving 91.3% CO selectivity at a potential of −0.88 V vs. RHE (Reversible Hydrogen Electrode) due to the facile transformation of ZnO to metallic Zn. Remarkably, these catalysts maintained this level of performance for more than 17 h. Conversely, ZnO-NR catalysts exhibited a lower CO selectivity of 62.5% at a relatively higher potential of −0.98 V vs RHE.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Science: Advanced Materials and Devices
Journal of Science: Advanced Materials and Devices Materials Science-Electronic, Optical and Magnetic Materials
CiteScore
11.90
自引率
2.50%
发文量
88
审稿时长
47 days
期刊介绍: In 1985, the Journal of Science was founded as a platform for publishing national and international research papers across various disciplines, including natural sciences, technology, social sciences, and humanities. Over the years, the journal has experienced remarkable growth in terms of quality, size, and scope. Today, it encompasses a diverse range of publications dedicated to academic research. Considering the rapid expansion of materials science, we are pleased to introduce the Journal of Science: Advanced Materials and Devices. This new addition to our journal series offers researchers an exciting opportunity to publish their work on all aspects of materials science and technology within the esteemed Journal of Science. With this development, we aim to revolutionize the way research in materials science is expressed and organized, further strengthening our commitment to promoting outstanding research across various scientific and technological fields.
期刊最新文献
Harnessing ambient sound: Different approaches to acoustic energy harvesting using triboelectric nanogenerators A novel carbon quantum dot (CQD) synthesis method with cost-effective reactants and a definitive indication: Hot bubble synthesis (HBBBS) Pt/ZnO and Pt/few-layer graphene/ZnO Schottky devices with Al ohmic contacts using Atlas simulation and machine learning Photothermal impacts induced by laser pulse in a 2D semiconducting medium with temperature-dependent properties under strain–temperature rate-dependent theory Comparative analysis of microlens array formation in fused silica glass by laser: Femtosecond versus picosecond pulses
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1