Visualizing Ultrafast Photogenerated Electron and Hole Separation in Facet-Engineered Bismuth Vanadate Crystals

IF 14.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Fengke Sun, Yuting Deng, Jing Leng, Ming Shi, Can Li, Shengye Jin, Rengui Li* and Wenming Tian*, 
{"title":"Visualizing Ultrafast Photogenerated Electron and Hole Separation in Facet-Engineered Bismuth Vanadate Crystals","authors":"Fengke Sun,&nbsp;Yuting Deng,&nbsp;Jing Leng,&nbsp;Ming Shi,&nbsp;Can Li,&nbsp;Shengye Jin,&nbsp;Rengui Li* and Wenming Tian*,&nbsp;","doi":"10.1021/jacs.4c1096210.1021/jacs.4c10962","DOIUrl":null,"url":null,"abstract":"<p >Photogenerated charge separation is pivotal for effecting efficient photocatalytic reactions. Understanding this process with spatiotemporal resolution is vital for devising highly efficient photocatalysts. Here, we employed pump–probe transient reflection microscopy to directly observe the temporal and spatial evolution of photogenerated electrons and holes on the surface of facet-engineered bismuth vanadate (BiVO<sub>4</sub>) crystals. The findings suggest that the anisotropic built-in field of BiVO<sub>4</sub> crystals propels the separation of photogenerated electrons and holes toward different facets through a two-step process across varying time scales. Photogenerated electrons and holes undergo ultrafast separation within ∼6 ps, with electrons transforming into localized small polarons toward the {010} facets of truncated BiVO<sub>4</sub> octahedral crystals. However, the photogenerated holes prolong their separation up to ∼2000 ps in a drift–diffusion manner before ultimately accumulating on the {120} facets. This work provides a comprehensive visualization of spatiotemporal charge separation at the nano/microscale on semiconductor photocatalysts, which is beneficial for understanding the photocatalysis mechanism.</p>","PeriodicalId":49,"journal":{"name":"Journal of the American Chemical Society","volume":"146 45","pages":"31106–31113 31106–31113"},"PeriodicalIF":14.4000,"publicationDate":"2024-10-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the American Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/jacs.4c10962","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

Photogenerated charge separation is pivotal for effecting efficient photocatalytic reactions. Understanding this process with spatiotemporal resolution is vital for devising highly efficient photocatalysts. Here, we employed pump–probe transient reflection microscopy to directly observe the temporal and spatial evolution of photogenerated electrons and holes on the surface of facet-engineered bismuth vanadate (BiVO4) crystals. The findings suggest that the anisotropic built-in field of BiVO4 crystals propels the separation of photogenerated electrons and holes toward different facets through a two-step process across varying time scales. Photogenerated electrons and holes undergo ultrafast separation within ∼6 ps, with electrons transforming into localized small polarons toward the {010} facets of truncated BiVO4 octahedral crystals. However, the photogenerated holes prolong their separation up to ∼2000 ps in a drift–diffusion manner before ultimately accumulating on the {120} facets. This work provides a comprehensive visualization of spatiotemporal charge separation at the nano/microscale on semiconductor photocatalysts, which is beneficial for understanding the photocatalysis mechanism.

Abstract Image

可视化刻面工程钒酸铋晶体中的超快光生电子和空穴分离
光生电荷分离是实现高效光催化反应的关键。了解这一过程的时空分辨率对于设计高效光催化剂至关重要。在这里,我们采用泵浦探针瞬态反射显微镜直接观察了钒酸铋(BiVO4)晶体表面光生电子和空穴的时空演变。研究结果表明,BiVO4 晶体的各向异性内置场推动光生电子和空穴在不同时间尺度上通过两步过程向不同刻面分离。光生电子和空穴在 6 ps 内发生超快分离,电子转变为局部小极子,朝向截断的 BiVO4 八面体晶体的 {010} 面。然而,光生空穴以漂移扩散的方式将其分离时间延长至 ∼ 2000 ps,最终聚集在{120}面上。这项研究全面展示了半导体光催化剂在纳米/微米尺度上的时空电荷分离,有助于理解光催化机理。
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
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
×
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