External field induced piezo-photocatalytic hydrogen evolution for BiFeO3@CdS heterojunction

IF 5.5 2区 材料科学 Q1 MATERIALS SCIENCE, CHARACTERIZATION & TESTING
Zongzhi Yue, Ze Wu, Jinwei Zhang, Dapeng Hong, Yanyang Zhang, Lianwei Shan
{"title":"External field induced piezo-photocatalytic hydrogen evolution for BiFeO3@CdS heterojunction","authors":"Zongzhi Yue,&nbsp;Ze Wu,&nbsp;Jinwei Zhang,&nbsp;Dapeng Hong,&nbsp;Yanyang Zhang,&nbsp;Lianwei Shan","doi":"10.1016/j.matchar.2025.115544","DOIUrl":null,"url":null,"abstract":"<div><div>In this work, we synthesized S-type BiFeO<sub>3</sub>@CdS heterojunction piezo-photocatalysts through an innovative core-shell structure design. Their efficient hydrogen evolution performances were systematically investigated under the synergistic effect of ultrasound and visible light irradiation. The core-shell-structured BiFeO<sub>3</sub>@CdS-1 exhibits a remarkable piezo-photocatalytic hydrogen evolution rate of 1704 μmol g<sup>−1</sup> within 4 h, which is 4.19 and 8.52 times higher than those achieved under sole light irradiation and piezoelectric conditions, respectively. Comprehensive characterizations (XPS, SPV, and electrochemical analyses etc) confirm the formation of efficient charge transfer channels at the heterojunction interface, thereby promoting the spatial separation of electron-hole pairs. By combining density functional theory (DFT) calculations, we demonstrate that the piezoelectricity-induced built-in electric field and the interfacial electric field of the heterojunction significantly reduces the energy barrier for the hydrogen evolution reaction and enhanced carrier separation efficiency. This work presents a novel strategy for designing highly efficient and stable hydrogen evolution catalysts through the integration of interface engineering and piezo-photocatalysis.</div></div>","PeriodicalId":18727,"journal":{"name":"Materials Characterization","volume":"229 ","pages":"Article 115544"},"PeriodicalIF":5.5000,"publicationDate":"2025-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Materials Characterization","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1044580325008332","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, CHARACTERIZATION & TESTING","Score":null,"Total":0}
引用次数: 0

Abstract

In this work, we synthesized S-type BiFeO3@CdS heterojunction piezo-photocatalysts through an innovative core-shell structure design. Their efficient hydrogen evolution performances were systematically investigated under the synergistic effect of ultrasound and visible light irradiation. The core-shell-structured BiFeO3@CdS-1 exhibits a remarkable piezo-photocatalytic hydrogen evolution rate of 1704 μmol g−1 within 4 h, which is 4.19 and 8.52 times higher than those achieved under sole light irradiation and piezoelectric conditions, respectively. Comprehensive characterizations (XPS, SPV, and electrochemical analyses etc) confirm the formation of efficient charge transfer channels at the heterojunction interface, thereby promoting the spatial separation of electron-hole pairs. By combining density functional theory (DFT) calculations, we demonstrate that the piezoelectricity-induced built-in electric field and the interfacial electric field of the heterojunction significantly reduces the energy barrier for the hydrogen evolution reaction and enhanced carrier separation efficiency. This work presents a novel strategy for designing highly efficient and stable hydrogen evolution catalysts through the integration of interface engineering and piezo-photocatalysis.

Abstract Image

BiFeO3@CdS异质结外场诱导压电光催化析氢
在这项工作中,我们通过创新的核壳结构设计合成了s型BiFeO3@CdS异质结压电光催化剂。在超声和可见光的协同作用下,系统地研究了它们的高效析氢性能。核壳结构BiFeO3@CdS-1在4 h内具有1704 μmol g−1的压电光催化析氢速率,分别是单光照射和压电条件下的4.19和8.52倍。综合表征(XPS, SPV和电化学分析等)证实在异质结界面处形成了有效的电荷转移通道,从而促进了电子-空穴对的空间分离。结合密度泛函理论(DFT)计算,我们证明了压电诱导的内置电场和异质结的界面电场显著降低了析氢反应的能垒,提高了载流子分离效率。本研究提出了一种结合界面工程和压电光催化设计高效稳定析氢催化剂的新策略。
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
Materials Characterization
Materials Characterization 工程技术-材料科学:表征与测试
CiteScore
7.60
自引率
8.50%
发文量
746
审稿时长
36 days
期刊介绍: Materials Characterization features original articles and state-of-the-art reviews on theoretical and practical aspects of the structure and behaviour of materials. The Journal focuses on all characterization techniques, including all forms of microscopy (light, electron, acoustic, etc.,) and analysis (especially microanalysis and surface analytical techniques). Developments in both this wide range of techniques and their application to the quantification of the microstructure of materials are essential facets of the Journal. The Journal provides the Materials Scientist/Engineer with up-to-date information on many types of materials with an underlying theme of explaining the behavior of materials using novel approaches. Materials covered by the journal include: Metals & Alloys Ceramics Nanomaterials Biomedical materials Optical materials Composites Natural Materials.
×
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:604180095
Book学术官方微信