Carbon dots enhanced interfacial electron storage and transfer of iron phosphide for productively photocatalytic water splitting

被引:3
|
作者
Si, Honglin [1 ]
Li, Zenan [1 ]
Zhang, Tianyang [1 ]
Fan, Zhenglong [1 ]
Huang, Hui [1 ]
Liu, Yang [1 ]
Kang, Zhenhui [1 ,2 ]
机构
[1] Soochow Univ, Inst Funct Nano & Soft Mat FUNSOM, Jiangsu Key Lab Carbon Based Funct Mat & Devices, 199 Renai Rd, Suzhou 215123, Jiangsu, Peoples R China
[2] Macau Univ Sci & Technol, Macao Inst Mat Sci & Engn MIMSE, MUST SUDA Joint Res Ctr Adv Funct Mat, Taipa 999078, Macao, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Carbon dots; FeP; Photocatalytic hydrogen evolution; Transient photovoltage; QUANTUM DOTS; VISIBLE-LIGHT; HYDROGEN-PRODUCTION; EFFICIENT; NANOCOMPOSITES;
D O I
10.1016/j.apsusc.2023.159153
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Iron phosphide (FeP), as a low-cost and high-performance phosphide, not only has good stability but also possesses broad optical absorption, which can be used as a visible light or even near-infrared photocatalyst. How-ever, their limited photocatalytic performance arises from the rapid charge recombination and a scarcity of active sites. Here, FeP was modified by introducing carbon dots (CDs), and the photocatalytic performance for H2 production of CDs/FeP reached 33.85 mu mol/h/g, which improved significantly compared to that of the pristine FeP (6.65 mu mol/h/g). The catalytic reaction goes through a 4-electron passway, which generates O2 and H2 simultaneously. CDs can not merely accelerate the interfacial charge delivery rate, but also can rapidly store photogenerated electrons, reducing the recombination of electrons and holes to improve the photocatalytic performance of FeP. This work provides a new perspective on enhancing the photocatalytic water activity of phosphides by improving electron transfer at the phosphide interface.
引用
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页数:9
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