Robustly photogenerating H2 in water using FeP/CdS catalyst under solar irradiation

被引:106
作者
Cheng, Huanqing [1 ,2 ,3 ]
Lv, Xiao-Jun [1 ,2 ]
Cao, Shuang [1 ,2 ]
Zhao, Zong-Yan [4 ]
Chen, Yong [1 ,2 ]
Fu, Wen-Fu [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Tech Inst Phys & Chem, Key Lab Photochem Convers & Optoelect Mat, Beijing 100190, Peoples R China
[2] Chinese Acad Sci, Tech Inst Phys & Chem, HKU CAS Joint Lab New Mat, Beijing 100190, Peoples R China
[3] Yunnan Normal Univ, Coll Chem & Chem Engn, Kunming 650092, Peoples R China
[4] Kunming Univ Sci & Technol, Fac Mat Sci & Engn, Kunming 650093, Peoples R China
基金
北京市自然科学基金;
关键词
PHOTOCATALYTIC HYDROGEN EVOLUTION; PHOSPHIDE NANOPARTICLES; NICKEL PHOSPHIDE; NANOWIRE ARRAYS; EFFICIENT; GRAPHENE; CATHODE; CDS; COCATALYSTS; FE;
D O I
10.1038/srep19846
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Photosplitting water for H-2 production is a promising, sustainable approach for solar-to-chemical energy conversion. However, developing low-cost, high efficient and stable photocatalysts remains the major challenge. Here we report a composite photocatalyst consisting of FeP nanoparticles and CdS nanocrystals (FeP/CdS) for photogenerating H-2 in aqueous lactic acid solution under visible light irradiation. Experimental results demonstrate that the photocatalyst is highly active with a H-2-evolution rate of 202000 mu mol h(1) g(1) for the first 5 h (106000 mu mol h(-1) g(-1) under natural solar irradiation), which is the best H-2 evolution activity, even 3-fold higher than the control in situ photodeposited Pt/CdS system, and the corresponding to an apparent quantum efficiency of over 35% at 520 nm. More important, we found that the system exhibited excellent stability and remained effective after more than 100 h in optimal conditions under visible light irradiation. A wide-ranging analysis verified that FeP effectively separates the photoexcited charge from CdS and showed that the dual active sites in FeP enhance the activity of FeP/CdS photocatalysts.
引用
收藏
页数:10
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