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The roles of various Ni species over SnO2 in enhancing the photocatalytic properties for hydrogen generation under visible light irradiation
被引:26
作者:
Du, Quanchao
[1
,2
]
Lu, Gongxuan
[1
]
机构:
[1] Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金:
美国国家科学基金会;
关键词:
Photocatalysis;
Hydrogen evolution;
Ni(OH)(2);
Ni2O3;
PN junction;
Visible light irradiation;
CONGO RED;
WATER;
OXIDE;
NANOSHEETS;
NANOTUBES;
NI(OH)(2);
EVOLUTION;
METAL;
FILM;
D O I:
10.1016/j.apsusc.2014.03.043
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070305 [高分子化学与物理];
摘要:
The photocatalysts containing various nickel species were successfully fabricated via loading Ni(OH)(2) and/or Ni2O3 species on the surface of SnO2 nanoparticles, and their roles in the photo-absorb ability, photo-induced charge transfer and photocatalytic hydrogen evolution performances were also investigated under visible light irradiation. Pt/Ni2O3-SnO2 catalyst was not active for hydrogen evolution reaction, while the photocatalytic hydrogen evolution rates of Pt/Ni(OH)(2)-SnO2 and Pt/Ni(OH)(2)-Ni2O3-SnO2 were 0.9 and 10.8 pinol g(-1) h(-1), respectively. It indicated that the photocatalytic activity of Pt/Ni(OH)(2)-Ni2O3-SnO2 catalyst had been improved evidently in the presence of Ni-2 O-3. The UV-vis DRS results showed that Ni(OH)(2) enhanced light absorption of catalyst significantly in visible light region. The i-t curves confirmed that the co-existence of Ni(OH)(2) and Ni2O3 improved significantly the photocurrent of Pt/Ni(OH)(2)-Ni2O3-SnO2 photo-electrode. In addition, the long term experiments revealed that Pt/Ni(OH)(2)-Ni2O3-SnO2 catalyst was quite stable under given conditions. A proposed reaction mechanism for hydrogen evolution was also present. (C) 2014 Elsevier B.V. All rights reserved.
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页码:235 / 241
页数:7
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