Interfacial Electronic Regulation of V-Doped CdS/NiS2 Heterostructures for Enhanced Visible-Light Photocatalytic Hydrogen Evolution

IF 5.5 3区 材料科学 Q2 CHEMISTRY, PHYSICAL ACS Applied Energy Materials Pub Date : 2026-10-12 Epub Date: 2026-09-26 DOI:10.1021/acsaem.6c02534
Yong Zhao, Qian Chen, Jianfeng Huang, Dewei Chu, Mengfan Niu, Faliang Luo, Haijun Ma, Liyun Cao, Junle Dong, Liangliang Feng
{"title":"Interfacial Electronic Regulation of V-Doped CdS/NiS2 Heterostructures for Enhanced Visible-Light Photocatalytic Hydrogen Evolution","authors":"Yong Zhao,&nbsp;Qian Chen,&nbsp;Jianfeng Huang,&nbsp;Dewei Chu,&nbsp;Mengfan Niu,&nbsp;Faliang Luo,&nbsp;Haijun Ma,&nbsp;Liyun Cao,&nbsp;Junle Dong,&nbsp;Liangliang Feng","doi":"10.1021/acsaem.6c02534","DOIUrl":null,"url":null,"abstract":"<p>Photocatalytic hydrogen evolution represents a promising approach for sustainable solar-to-hydrogen conversion; however, the practical application of CdS photocatalysts is still limited by inefficient charge separation and poor stability. Herein, a V-doped CdS/NiS<sub>2</sub> (VCN) heterostructured photocatalyst was successfully constructed via a facile, in situ hydrothermal strategy for interfacial electronic regulation. The optimized VCN-1 photocatalyst achieves a hydrogen evolution rate of 8704.8 μmol g<sup>–1</sup> h<sup>–1</sup> under visible-light irradiation, which is approximately 133.7 times higher than that of pristine CdS. This enhanced photocatalytic performance is attributed to the synergistic effects of NiS<sub>2</sub> coupling and V doping. The CdS/NiS<sub>2</sub> heterojunction facilitates interfacial electron transfer, while V doping modulates the electronic structure and promotes charge migration. In addition, the VCN-1 photocatalyst maintains stable hydrogen evolution performance during repeated photocatalytic cycles. This work provides an effective strategy for regulating heterointerfaces and electronic structures toward the development of efficient CdS-based photocatalysts for solar energy conversion.</p>","PeriodicalId":4,"journal":{"name":"ACS Applied Energy Materials","volume":"9 19","pages":"13203–13213"},"PeriodicalIF":5.5000,"publicationDate":"2026-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Energy Materials","FirstCategoryId":"88","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsaem.6c02534","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/9/26 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Photocatalytic hydrogen evolution represents a promising approach for sustainable solar-to-hydrogen conversion; however, the practical application of CdS photocatalysts is still limited by inefficient charge separation and poor stability. Herein, a V-doped CdS/NiS2 (VCN) heterostructured photocatalyst was successfully constructed via a facile, in situ hydrothermal strategy for interfacial electronic regulation. The optimized VCN-1 photocatalyst achieves a hydrogen evolution rate of 8704.8 μmol g–1 h–1 under visible-light irradiation, which is approximately 133.7 times higher than that of pristine CdS. This enhanced photocatalytic performance is attributed to the synergistic effects of NiS2 coupling and V doping. The CdS/NiS2 heterojunction facilitates interfacial electron transfer, while V doping modulates the electronic structure and promotes charge migration. In addition, the VCN-1 photocatalyst maintains stable hydrogen evolution performance during repeated photocatalytic cycles. This work provides an effective strategy for regulating heterointerfaces and electronic structures toward the development of efficient CdS-based photocatalysts for solar energy conversion.

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
v掺杂CdS/NiS2异质结构的界面电子调控增强可见光光催化析氢
光催化析氢是一种有前途的可持续太阳能制氢转化方法;然而,CdS光催化剂的实际应用仍然受到电荷分离效率低和稳定性差的限制。本文通过原位水热策略成功构建了v掺杂CdS/NiS2 (VCN)异质结构光催化剂,用于界面电子调节。优化后的VCN-1光催化剂在可见光下的析氢速率为8704.8 μmol g-1 h-1,是原始CdS的133.7倍左右。这种增强的光催化性能归因于NiS2偶联和V掺杂的协同作用。CdS/NiS2异质结有利于界面电子转移,而V掺杂调节了电子结构,促进了电荷迁移。此外,VCN-1光催化剂在多次光催化循环中保持稳定的析氢性能。这项工作为调控异质界面和电子结构提供了一种有效的策略,以开发高效的基于cd的太阳能转换光催化剂。
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 去求助
来源期刊
ACS Applied Energy Materials
ACS Applied Energy Materials Materials Science-Materials Chemistry
CiteScore
10.30
自引率
6.20%
发文量
1368
期刊介绍: ACS Applied Energy Materials is an interdisciplinary journal publishing original research covering all aspects of materials, engineering, chemistry, physics and biology relevant to energy conversion and storage. The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrate knowledge in the areas of materials, engineering, physics, bioscience, and chemistry into important energy applications.
期刊最新文献
Issue Publication Information Issue Editorial Masthead Leveraging Chirality-Induced Spin Selectivity to Enhance the Production of Reactive Oxygen Species In-Situ-Polymerized Higher-Performance Poly(Ionic Liquid) Solid Polymer Electrolyte Enabling a Stable Interface for Lithium Metal Batteries Mixed Triple-Cation Tin and Lead Bromide Perovskites: Bridging Atomic Structure, Lattice Dynamics, and Stability
wanfang
×
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学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
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