Phosphorene Co-catalyst Advancing Highly Efficient Visible-Light Photocatalytic Hydrogen Production

被引:314
作者
Ran, Jingrun [1 ]
Zhu, Bicheng [2 ]
Qiao, Shi-Zhang [1 ]
机构
[1] Univ Adelaide, Sch Chem Engn, Adelaide, SA 5005, Australia
[2] Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, 122 Luoshi Rd, Wuhan 430070, Hubei, Peoples R China
基金
澳大利亚研究理事会;
关键词
co-catalysts; density functional calculations; hydrogen production; phosphorene; photocatalysis; CADMIUM SULFIDE NANOCOMPOSITE; BLACK PHOSPHORUS; SEMICONDUCTOR; EVOLUTION; NANOSHEETS; GAP;
D O I
10.1002/anie.201703827
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Transitional metals are widely used as co-catalysts boosting photocatalytic H-2 production. However; metal-based co-catalysts suffer from high cost, limited abundance and detrimental environment impact. To date, metal-free co-catalyst is rarely reported. Here we for the first time utilized density functional calculations to guide the application of phosphorene as a high-efficiency metal-free co-catalyst for CdS, Zn0.8Cd0.2S or ZnS. Particularly, phosphorene modified CdS shows a high apparent quantum yield of 34.7 % al 420 nm. This outstanding activity arises from the strong, electronic coupling between phosphorene and CdS, as well as the favorable band structure, high charge mobility and massive active sites of phosphorene, supported by computations and advanced characterizations, for example, synchrotron-based X-ray absorption near edge spectroscopy. This work brings new opportunities to prepare highly-active, cheap and green photocatalysts.
引用
收藏
页码:10373 / 10377
页数:5
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