期刊
CHEMSUSCHEM
卷 7, 期 12, 页码 3426-3434出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cssc.201402574
关键词
heterogeneous catalysis; hydrogen; nickel; photochemistry; water splitting
资金
- Australian Research Council (ARC) [DP1095861, DP130104459]
The application of various earth-abundant Ni species, such as NiS, Ni, Ni(OH)(2), and NiO, as a co-catalyst in a ZnxCd1-xS system for visible-light photocatalytic H-2 production was investigated for the first time. The loading of Ni or NiS enhanced the photocatalytic activity of ZnxCd1-xS because they could promote the electron transfer at the interface with ZnxCd1-xS and catalyze the H-2 evolution. Surprisingly, Ni(OH)(2)-loaded ZnxCd1-xS exhibits a very high photocatalytic H-2-production rate of 7160 mu mol h(-1) g(-1) with a quantum efficiency of 29.5% at 420 nm, which represents one of the most efficient metal sulfide photocatalysts without a Pt co-catalyst to date. This outstanding activity arises from the pronounced synergetic effect between Ni(OH)(2) and metallic Ni formed in situ during the photocatalytic reaction. However, the loading of NiO deactivated the activity of ZnxCd1-xS because of their unmatched conduction band positions. This paper reports the optimization of the ZnxCd1-xS system by selecting an appropriate Ni-based co-catalyst, Ni(OH)(2), from a series of Ni species to achieve the highest photocatalytic H-2-production activity for the first time and also reveals the roles of these Ni species in the photocatalytic activity.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据