期刊
JOURNAL OF MATERIALS CHEMISTRY A
卷 7, 期 8, 页码 3828-3841出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c8ta11456k
关键词
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资金
- National Natural Science Foundation of China [21676213, 21476183]
- China Postdoctoral Science Foundation [2016M600809]
- Natural Science Basic Research Plan in Shaanxi Province of China [2017JM2026, 2018JM5020]
- Graduate Student Innovation Funds of Northwest University [YYB17015]
Two-dimensional (2D) layered heterostructures have attracted substantial attention in recent years as promising platforms for the direct conversion of renewable solar energy to chemical fuels due to their unique optoelectronic, transport, and interfacial properties. The rational structural design and tailored synthesis of semiconductor heterojunctions are critical to explore and achieve well-defined photocatalytic systems. Herein, we propose a design strategy for ultrathin 2D FeS-FeSe2 lateral heterostructures to achieve rapid spatial migration of photogenerated charge carriers and to facilitate favorable kinetics of target surface redox reactions for photocatalysis. The resultant composites have superior photocatalytic H-2 generation activity (2071.1 mmol g(-1) h(-1)) without any noble metal as a cocatalyst under sunlight and show marked photocatalytic durability after a continuous test for 20 h under alkaline conditions. In particular, we have found, for the first time, that the irradiated FeS-FeSe2 is active for producing H2O2 by the two-electron reduction of O-2 in the photocatalytic degradation process of phenol solution. A series of mechanistic studies on photocatalysis clearly demonstrates that the pronounced photocatalytic performance of the 2D lateral heterojunction nanosheets could be a result of increased carrier density, longer electron lifetime and higher hole injection efficiency as well as a stepwise two-electron/two-step reduction pathway.
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