Efficient Photocatalytic Hydrogen Evolution via Band Alignment Tailoring: Controllable Transition from Type-I to Type-II

被引:51
作者
Cheng, Zhongzhou [1 ,2 ]
Wang, Fengmei [2 ,3 ]
Shifa, Tofik Ahmed [2 ,3 ]
Jiang, Chao [1 ]
Liu, Quanlin [1 ]
He, Jun [2 ]
机构
[1] Univ Sci & Technol, Sch Mat Sci & Engn, Beijing 100083, Peoples R China
[2] Natl Ctr Nanosci & Technol, CAS Key Lab Nanosyst & Hierarch Fabricat, CAS Ctr Excellence Nanosci, Beijing 100190, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
ceria; cerium sulfide; heterostructures; SnS2; water splitting; ENERGY-CONVERSION; WATER; SNS2; PERFORMANCE; GRAPHENE; GENERATION; NANOPARTICLES; NANOSHEETS;
D O I
10.1002/smll.201702163
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Considering the sizable band gap and wide spectrum response of tin disulfide (SnS2), ultrathin SnS2 nanosheets are utilized as solar-driven photocatalyst for water splitting. Designing a heterostructure based on SnS2 is believed to boost their catalytic performance. Unfortunately, it has been quite challenging to explore a material with suitable band alignment using SnS2 nanomaterials for photocatalytic hydrogen generation. Herein, a new strategy is used to systematically tailor the band alignment in SnS2 based heterostructure to realize efficient H-2 production under sunlight. A Type-I to Type-II band alignment transition is demonstrated via introducing an interlayer of Ce2S3, a potential photocatalyst for H-2 evolution, between SnS2 and CeO2. Subsequently, this heterostructure demonstrates tunability in light absorption, charge transfer kinetics, and material stability. The optimized heterostructure (SnS2-Ce2S3-CeO2) exhibits an incredibly strong light absorption ranging from deep UV to infrared light. Significantly, it also shows superior hydrogen generation with the rate of 240 mu mol g(-1) h(-1) under the illumination of simulated sunlight with a very good stability.
引用
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页数:7
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