Carbon dots bridged Zn0.5Cd0.5S with interfacial amide bond facilitating electron transfer for efficient photocatalytic hydrogen peroxide production

IF 20.2 1区 化学 Q1 CHEMISTRY, PHYSICAL Applied Catalysis B: Environmental Pub Date : 2024-01-10 DOI:10.1016/j.apcatb.2024.123721
Ting Tang , Jiwu Zhao , Yongli Shen , Fan Yang , Shuang Yao , Changhua An
{"title":"Carbon dots bridged Zn0.5Cd0.5S with interfacial amide bond facilitating electron transfer for efficient photocatalytic hydrogen peroxide production","authors":"Ting Tang ,&nbsp;Jiwu Zhao ,&nbsp;Yongli Shen ,&nbsp;Fan Yang ,&nbsp;Shuang Yao ,&nbsp;Changhua An","doi":"10.1016/j.apcatb.2024.123721","DOIUrl":null,"url":null,"abstract":"<div><p>Photocatalytic H<sub>2</sub>O<sub>2</sub><span> production has gained significant attention as an environmentally friendly approach. The key is to explore efficient photocatalysts with sufficient active sites and excellent electron transfer capacity. Herein, we propose a novel approach by incorporating carbon dots (CDs) on ethylenediamine capped Zn</span><sub>0.5</sub>Cd<sub>0.5</sub>S, which was bridged with an interfacial amide bond. Smooth transfer of photoinduced electrons from Zn<sub>0.5</sub>Cd<sub>0.5</sub>S to carbon dots via a high-speed electron channel is afforded by interfacial amide bond. A remarkable H<sub>2</sub>O<sub>2</sub><span> yield with a rate of 252 μmol/h and an apparent quantum yield (AQY) of 31 % at 400 nm is achieved. Photoelectrochemical analysis and density function theory (DFT) calculation reveal CDs with abundant oxygenous functional groups as active sites, boosting activity and selectivity. This interfacial engineering strategy with the acceleration of electrons transfer and enhanced 2e</span><sup>-</sup> selectivity can be applied to advanced photocatalytic systems for the achievement of valuable organics, environmental purification and new energy carriers.</p></div>","PeriodicalId":244,"journal":{"name":"Applied Catalysis B: Environmental","volume":"346 ","pages":"Article 123721"},"PeriodicalIF":20.2000,"publicationDate":"2024-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied Catalysis B: Environmental","FirstCategoryId":"1","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0926337324000328","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: 0

Abstract

Photocatalytic H2O2 production has gained significant attention as an environmentally friendly approach. The key is to explore efficient photocatalysts with sufficient active sites and excellent electron transfer capacity. Herein, we propose a novel approach by incorporating carbon dots (CDs) on ethylenediamine capped Zn0.5Cd0.5S, which was bridged with an interfacial amide bond. Smooth transfer of photoinduced electrons from Zn0.5Cd0.5S to carbon dots via a high-speed electron channel is afforded by interfacial amide bond. A remarkable H2O2 yield with a rate of 252 μmol/h and an apparent quantum yield (AQY) of 31 % at 400 nm is achieved. Photoelectrochemical analysis and density function theory (DFT) calculation reveal CDs with abundant oxygenous functional groups as active sites, boosting activity and selectivity. This interfacial engineering strategy with the acceleration of electrons transfer and enhanced 2e- selectivity can be applied to advanced photocatalytic systems for the achievement of valuable organics, environmental purification and new energy carriers.

Abstract Image

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
碳点桥接 Zn0.5Cd0.5S,其界面酰胺键可促进电子转移,从而高效光催化生产过氧化氢
光催化 H2O2 生产作为一种环境友好型方法受到了广泛关注。关键在于探索具有足够活性位点和出色电子传递能力的高效光催化剂。在此,我们提出了一种新方法,即在乙二胺封端的 Zn0.5Cd0.5S 上加入碳点(CD),并以界面酰胺键作为桥接。界面酰胺键使光诱导电子通过高速电子通道从 Zn0.5Cd0.5S 顺利转移到碳点。在 400 纳米波长下,H2O2 产率高达 252 μmol/h,表观量子产率 (AQY) 为 31%。光电化学分析和密度函数理论(DFT)计算显示,CD 具有丰富的含氧官能团作为活性位点,从而提高了活性和选择性。这种加速电子转移和提高 2e- 选择性的界面工程策略可应用于先进的光催化系统,以实现有价值的有机物、环境净化和新能源载体。
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
Applied Catalysis B: Environmental
Applied Catalysis B: Environmental 环境科学-工程:化工
CiteScore
38.60
自引率
6.30%
发文量
1117
审稿时长
24 days
期刊介绍: Applied Catalysis B: Environment and Energy (formerly Applied Catalysis B: Environmental) is a journal that focuses on the transition towards cleaner and more sustainable energy sources. The journal's publications cover a wide range of topics, including: 1.Catalytic elimination of environmental pollutants such as nitrogen oxides, carbon monoxide, sulfur compounds, chlorinated and other organic compounds, and soot emitted from stationary or mobile sources. 2.Basic understanding of catalysts used in environmental pollution abatement, particularly in industrial processes. 3.All aspects of preparation, characterization, activation, deactivation, and regeneration of novel and commercially applicable environmental catalysts. 4.New catalytic routes and processes for the production of clean energy, such as hydrogen generation via catalytic fuel processing, and new catalysts and electrocatalysts for fuel cells. 5.Catalytic reactions that convert wastes into useful products. 6.Clean manufacturing techniques that replace toxic chemicals with environmentally friendly catalysts. 7.Scientific aspects of photocatalytic processes and a basic understanding of photocatalysts as applied to environmental problems. 8.New catalytic combustion technologies and catalysts. 9.New catalytic non-enzymatic transformations of biomass components. The journal is abstracted and indexed in API Abstracts, Research Alert, Chemical Abstracts, Web of Science, Theoretical Chemical Engineering Abstracts, Engineering, Technology & Applied Sciences, and others.
期刊最新文献
Conversion of CO2 to higher alcohols on K-CuZnAl/Zr-CuFe composite Effects of the chemical states of N sites and mesoporosity of N-doped carbon supports on single-atom Ru catalysts during CO2-to-formate conversion Visible-light responsive TiO2 for the complete photocatalytic decomposition of volatile organic compounds (VOCs) and its efficient acceleration by thermal energy Controlled doping of ultralow amounts Ru on Ni cathode for PEMWE: Experimental and theoretical elucidation of enhanced performance Mesoporous zeolite ZSM-5 confined Cu nanoclusters for efficient selective catalytic reduction of NOx by NH3
×
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