Strengthening Bonding Interaction of a (Co0.91V0.09)3(BTC)2 Metal–Organic Framework with BiVO4 Photoanodes Enabling Ultrastable Photoelectrochemical Water Oxidation

IF 15.8 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
ACS Nano Pub Date : 2025-04-17 DOI:10.1021/acsnano.5c01111
Liangcheng Xu, Yingjuan Zhang, Boyan Liu, Kang Wan, Xin Wang, Tingsheng Wang, Lianzhou Wang, Songcan Wang, Wei Huang
{"title":"Strengthening Bonding Interaction of a (Co0.91V0.09)3(BTC)2 Metal–Organic Framework with BiVO4 Photoanodes Enabling Ultrastable Photoelectrochemical Water Oxidation","authors":"Liangcheng Xu, Yingjuan Zhang, Boyan Liu, Kang Wan, Xin Wang, Tingsheng Wang, Lianzhou Wang, Songcan Wang, Wei Huang","doi":"10.1021/acsnano.5c01111","DOIUrl":null,"url":null,"abstract":"Although the oxygen evolution reaction (OER) activity of BiVO<sub>4</sub> photoanodes has been significantly enhanced, achieving long-term photostability is still challenging due to the gradual dissolution of V<sup>5+</sup> during photoelectrochemical (PEC) water splitting. Herein, we deliberately generate ligand defects in a (Co<sub>0.91</sub>V<sub>0.09</sub>)<sub>3</sub>(BTC)<sub>2</sub> metal–organic framework (CoV-MOF) that creates more undercoordinated sites, forming strong chemical bonds with BiVO<sub>4</sub>. Consequently, the dissolution of V<sup>5+</sup> from BiVO<sub>4</sub> during PEC water splitting can be effectively suppressed, leading to significantly enhanced stability. The optimized Co<sub>3</sub>O<sub>4</sub>/CoV-MOF/BiVO<sub>4</sub> photoanode exhibits a high photocurrent density of 6.0 mA cm<sup>–2</sup> at 1.23 V vs the reversible hydrogen electrode (RHE). Impressively, the photoanode can stably operate for 500 h at 0.6 V vs RHE under AM 1.5 G illumination. This work demonstrates the proof-of-concept of anchoring V<sup>5+</sup> in BiVO<sub>4</sub> photoanodes achieving ultrastable PEC water splitting.","PeriodicalId":21,"journal":{"name":"ACS Nano","volume":"24 1","pages":""},"PeriodicalIF":15.8000,"publicationDate":"2025-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Nano","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1021/acsnano.5c01111","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

Although the oxygen evolution reaction (OER) activity of BiVO4 photoanodes has been significantly enhanced, achieving long-term photostability is still challenging due to the gradual dissolution of V5+ during photoelectrochemical (PEC) water splitting. Herein, we deliberately generate ligand defects in a (Co0.91V0.09)3(BTC)2 metal–organic framework (CoV-MOF) that creates more undercoordinated sites, forming strong chemical bonds with BiVO4. Consequently, the dissolution of V5+ from BiVO4 during PEC water splitting can be effectively suppressed, leading to significantly enhanced stability. The optimized Co3O4/CoV-MOF/BiVO4 photoanode exhibits a high photocurrent density of 6.0 mA cm–2 at 1.23 V vs the reversible hydrogen electrode (RHE). Impressively, the photoanode can stably operate for 500 h at 0.6 V vs RHE under AM 1.5 G illumination. This work demonstrates the proof-of-concept of anchoring V5+ in BiVO4 photoanodes achieving ultrastable PEC water splitting.

Abstract Image

(Co0.91V0.09)3(BTC)2金属有机骨架与BiVO4光阳极强化键合作用,实现超稳定的光电化学水氧化
尽管BiVO4光阳极的析氧反应(OER)活性显著增强,但由于V5+在光电化学(PEC)水分解过程中逐渐溶解,实现长期光稳定性仍然具有挑战性。在此,我们故意在(Co0.91V0.09)3(BTC)2金属-有机框架(CoV-MOF)中产生配体缺陷,从而产生更多的欠协调位点,与BiVO4形成强化学键。因此,在PEC水裂解过程中,可以有效抑制BiVO4中V5+的溶解,从而显著提高稳定性。与可逆氢电极(RHE)相比,优化后的Co3O4/CoV-MOF/BiVO4光阳极在1.23 V时具有6.0 mA cm-2的高光电流密度。令人印象深刻的是,光阳极可以在0.6 V vs RHE下在AM 1.5 G照明下稳定工作500小时。这项工作证明了锚定V5+在BiVO4光阳极中实现超稳定PEC水分解的概念验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
ACS Nano
ACS Nano 工程技术-材料科学:综合
CiteScore
26.00
自引率
4.10%
发文量
1627
审稿时长
1.7 months
期刊介绍: ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信