Interfacial charge transfer in carbon nitride heterojunctions monitored by optical methods

Emma Mitchell , Abigail Law , Robert Godin
{"title":"Interfacial charge transfer in carbon nitride heterojunctions monitored by optical methods","authors":"Emma Mitchell ,&nbsp;Abigail Law ,&nbsp;Robert Godin","doi":"10.1016/j.jphotochemrev.2021.100453","DOIUrl":null,"url":null,"abstract":"<div><p>Solar energy conversion is inciting tremendous research efforts in many fields due to the vast potential of sunlight as a sustainable energy source. For solar energy to become widely used and become a major component of our energy mix, energy storage on large scales must be addressed and the components used must be abundant. Artificial photosynthesis to produce solar fuels holds promise as a way to convert solar energy into storable energy. Organic photocatalysts have rapidly established themselves as a viable alternative to inorganic systems. Organic photocatalyst can be prepared from inexpensive precursors and offer a synthetic versatility and tunability that can be exploited to improve efficiencies. Carbon nitride (CN<sub>x</sub>) has emerged as a leading organic photocatalyst with advantageous chemical and photo stabilities. Recombination of photogenerated electrons and holes limit the efficiency of CN<sub>x</sub> materials below levels necessary to become a viable energy production system. To improve the efficiency and key characteristics such as light harvesting, charge carrier lifetime, and interfacial rate of charge transfer, a second material is put in contact with CN<sub>x</sub> to form a heterojunction. While there are many examples of heterojunctions improving the photocatalytic activity beyond that of the isolated CN<sub>x</sub>, we are still lacking the deep understanding of charge carrier dynamics necessary to rationalize the improvements and design optimal junctions. This review covers the studies of CN<sub>x</sub> heterojunctions that have used optical methods to monitor the charge carrier dynamics. Time-resolved photoluminescence (TRPL) is the most common technique used and there are many examples that have used transient absorption spectroscopy (TAS) to probe the charge carrier dynamics. However, attempting to link the lifetime change to the activity differences does not yield a clear trend. It is likely that the reactive charges are not consistently being monitored and is obscuring the expected correlations. Both shorter and longer charge carrier lifetimes can be observed with both TRPL and TAS techniques and can be interpreted as arising from interfacial charge separation. Even when the same materials are used in the junction there is no consistency in observing a shorter or longer lifetime. The holistic view of charge carrier dynamics in CN<sub>x</sub> heterojunctions presented here intends to identify overarching themes from a wide range of CN<sub>x</sub>-containing systems and help take stock of where our current understanding stands. More specific spectral assignments and linking the observed lifetimes to certain photophysical or photochemical processes are needed to build models to help us understand the links between the charge carrier dynamics and the activity. These are crucial to develop general strategies that will lead to optimal CN<sub>x</sub> heterojunctions.</p></div>","PeriodicalId":376,"journal":{"name":"Journal of Photochemistry and Photobiology C: Photochemistry Reviews","volume":"49 ","pages":"Article 100453"},"PeriodicalIF":12.8000,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"14","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Photochemistry and Photobiology C: Photochemistry Reviews","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1389556721000526","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 14

Abstract

Solar energy conversion is inciting tremendous research efforts in many fields due to the vast potential of sunlight as a sustainable energy source. For solar energy to become widely used and become a major component of our energy mix, energy storage on large scales must be addressed and the components used must be abundant. Artificial photosynthesis to produce solar fuels holds promise as a way to convert solar energy into storable energy. Organic photocatalysts have rapidly established themselves as a viable alternative to inorganic systems. Organic photocatalyst can be prepared from inexpensive precursors and offer a synthetic versatility and tunability that can be exploited to improve efficiencies. Carbon nitride (CNx) has emerged as a leading organic photocatalyst with advantageous chemical and photo stabilities. Recombination of photogenerated electrons and holes limit the efficiency of CNx materials below levels necessary to become a viable energy production system. To improve the efficiency and key characteristics such as light harvesting, charge carrier lifetime, and interfacial rate of charge transfer, a second material is put in contact with CNx to form a heterojunction. While there are many examples of heterojunctions improving the photocatalytic activity beyond that of the isolated CNx, we are still lacking the deep understanding of charge carrier dynamics necessary to rationalize the improvements and design optimal junctions. This review covers the studies of CNx heterojunctions that have used optical methods to monitor the charge carrier dynamics. Time-resolved photoluminescence (TRPL) is the most common technique used and there are many examples that have used transient absorption spectroscopy (TAS) to probe the charge carrier dynamics. However, attempting to link the lifetime change to the activity differences does not yield a clear trend. It is likely that the reactive charges are not consistently being monitored and is obscuring the expected correlations. Both shorter and longer charge carrier lifetimes can be observed with both TRPL and TAS techniques and can be interpreted as arising from interfacial charge separation. Even when the same materials are used in the junction there is no consistency in observing a shorter or longer lifetime. The holistic view of charge carrier dynamics in CNx heterojunctions presented here intends to identify overarching themes from a wide range of CNx-containing systems and help take stock of where our current understanding stands. More specific spectral assignments and linking the observed lifetimes to certain photophysical or photochemical processes are needed to build models to help us understand the links between the charge carrier dynamics and the activity. These are crucial to develop general strategies that will lead to optimal CNx heterojunctions.

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
用光学方法监测氮化碳异质结的界面电荷转移
由于太阳能作为一种可持续能源的巨大潜力,太阳能转换正在许多领域激起巨大的研究努力。要使太阳能得到广泛应用,成为我国能源结构的重要组成部分,必须解决大规模储能问题,并保证所使用的组件丰富。人工光合作用生产太阳能燃料有望将太阳能转化为可储存的能源。有机光催化剂已迅速成为无机系统的可行替代品。有机光催化剂可以由廉价的前体制备,并提供合成的多功能性和可调节性,可以用来提高效率。氮化碳(CNx)已成为一种主要的有机光催化剂,具有良好的化学和光稳定性。光生电子和空穴的重组限制了CNx材料的效率,使其低于成为可行的能源生产系统所必需的水平。为了提高效率和关键特性,如光收集、电荷载流子寿命和电荷转移的界面速率,将第二种材料与CNx接触以形成异质结。虽然有许多异质结比分离的CNx更能提高光催化活性的例子,但我们仍然缺乏对载流子动力学的深刻理解,从而使改进和设计最佳结变得合理。本文综述了利用光学方法监测载流子动力学的CNx异质结的研究。时间分辨光致发光(TRPL)是最常用的技术,利用瞬态吸收光谱(TAS)探测载流子动力学的例子很多。然而,试图将寿命变化与活动差异联系起来并不能得出明确的趋势。很可能反应性电荷没有被持续监测,并且模糊了预期的相关性。TRPL和TAS技术都可以观察到较短和较长的载流子寿命,并且可以解释为由界面电荷分离引起。即使在结中使用相同的材料,也没有观察到更短或更长寿命的一致性。本文提出的CNx异质结中载流子动力学的整体观点旨在从广泛的含CNx系统中确定总体主题,并帮助评估我们目前的理解。需要更具体的光谱分配和将观察到的寿命与某些光物理或光化学过程联系起来,以建立模型,帮助我们理解载流子动力学与活性之间的联系。这些对于开发导致最佳CNx异质结的一般策略至关重要。
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
CiteScore
21.90
自引率
0.70%
发文量
36
审稿时长
47 days
期刊介绍: The Journal of Photochemistry and Photobiology C: Photochemistry Reviews, published by Elsevier, is the official journal of the Japanese Photochemistry Association. It serves as a platform for scientists across various fields of photochemistry to communicate and collaborate, aiming to foster new interdisciplinary research areas. The journal covers a wide scope, including fundamental molecular photochemistry, organic and inorganic photochemistry, photoelectrochemistry, photocatalysis, solar energy conversion, photobiology, and more. It provides a forum for discussing advancements and promoting collaboration in the field of photochemistry.
期刊最新文献
Biophotonics and nanorobotics for biomedical imaging, biosensing, drug delivery, and therapy Photocatalytic water splitting reaction: The pathway from semiconductors to MOFs Boron doped nanomaterials for photocatalysis Fluorescent fluorinated materials: A novel material for application in photodynamic therapy and designing chemical sensors Editorial Board
×
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