Enhanced H2 evolution of TiO2 with efficient multiple electrons transfer modified by tiny CuOx–NiO bimetallic oxides
Enhanced H2 evolution of TiO2 with efficient multiple electrons transfer modified by tiny CuOx–NiO bimetallic oxides
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DOI:
10.1016/j.ijhydene.2018.03.083
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发表时间:
2018-04
影响因子:
7.2
通讯作者:
Meng Zhang;Runze Sun;Gaoyuan Long;Chidong Zhou;Yanfang Zhou;Mengxia Chen;Xiuying Huang;Gaorui Han-Gaor
中科院分区:
文献类型:
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作者:
Meng Zhang;Runze Sun;Gaoyuan Long;Chidong Zhou;Yanfang Zhou;Mengxia Chen;Xiuying Huang;Gaorui Han-Gaor
CuOx–NiO bimetallic oxides modified TiO2catalysts were prepared via a precipitation-photoreduction approach for photocatalytic H2production. 0.9%Cu0.1%Ni/TiO2exhibited the highest H2evolution rate (about 55.4 μmol/g/min) under UV–visible light irradiation (350–780 nm), which is higher than the sum of CuOx/TiO2and NiO/TiO2catalyst. Cu species exhibited more reducing valence state including Cu0when deposited on NiO/TiO2compared with deposited on TiO2. The polyvalent Cu species lead to enhanced photocurrent and reduced transfer resistance confirmed by photoelectron chemical analysis. CuOx–NiO modification of the TiO2surface is beneficial for the photoexcited electron transfer, which suppresses electrons recombination. The lifetime of photoexcited electrons was enhanced greatly from 1.16 (TiO2) to 5.15 ns (CuOx–NiO/TiO2). A multiple electrons transfer mechanism for polyvalent bimetallic oxides co-modified TiO2was proposed based on careful analysis. This work demonstrated a polyvalent bimetallic oxides modified TiO2system with efficient photocatalytic H2production which can provide some insightful understanding for bimetallic metal oxides co-catalyst design and H2evolution mechanism.