Visible- Light- Induced Generation of H2 by Nanocomposites of Few- Layer TiS2 and TaS2 with CdS Nanoparticles

被引:39
作者
Gupta, Uttam [1 ,2 ]
Rao, Bolla Govinda [1 ,2 ]
Maitra, Urmimala [1 ,2 ]
Prasad, B. E. [1 ,2 ]
Rao, C. N. R. [1 ,2 ]
机构
[1] Jawaharlal Nehru Ctr Adv Sci Res, Chem & Phys Mat Unit, New Chem Unit, Bangalore 560064, Karnataka, India
[2] Jawaharlal Nehru Ctr Adv Sci Res, Int Ctr Mat Sci, Bangalore 560064, Karnataka, India
关键词
graphene; layered chalcogenides; photocatalysis; turnover frequency; water splitting; PHOTOCATALYTIC H-2-PRODUCTION PERFORMANCE; HYDROGEN-PRODUCTION; H-2; EVOLUTION; GRAPHENE; WATER; IRRADIATION; COMPOSITES; PRINCIPLES; NANOSHEETS; MOS2;
D O I
10.1002/asia.201301537
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Graphene analogues of TaS2 and TiS2 (3-4layers), prepared by Li intercalation followed by exfoliation in water, were characterized. Nanocomposites of CdS with few-layer TiS2 and TaS2 were employed for the visible-light-induced H-2 evolution reaction (HER). Benzyl alcohol was used as the sacrificial electron donor, which was oxidized to benzaldehyde during the reaction. Few-layer TiS2 is a semiconductor with a band gap of 0.7eV, and its nanocomposite with CdS showed an activity of 1000molh(-1)g(.)(-1) The nanocomposite of few-layer TaS2, in contrast, gave rise to higher activity of 2320molh(-1)g(-1), which was attributed to the metallic nature of few-layer TaS2. The amount of hydrogen evolved after 20 and 16h for the CdS/TiS2 and CdS/TaS2 nanocomposites was 14833 and 28132mol, respectively, with turnover frequencies of 0.24 and 0.57h(-1), respectively.
引用
收藏
页码:1311 / 1315
页数:5
相关论文
共 36 条
[2]  
[Anonymous], 2013, ANGEW CHEM, DOI DOI 10.1002/ANGE.201306918
[3]   Titanium dioxide nanomaterials: Synthesis, properties, modifications, and applications [J].
Chen, Xiaobo ;
Mao, Samuel S. .
CHEMICAL REVIEWS, 2007, 107 (07) :2891-2959
[4]   First principles study of structural, vibrational and electronic properties of graphene-like MX2 (M=Mo, Nb, W, Ta; X=S, Se, Te) monolayers [J].
Ding, Yi ;
Wang, Yanli ;
Ni, Jun ;
Shi, Lin ;
Shi, Siqi ;
Tang, Weihua .
PHYSICA B-CONDENSED MATTER, 2011, 406 (11) :2254-2260
[5]   Bulk and surface electronic structure of 1T-TiS2 and 1T-TiSe2 [J].
Fang, CM ;
deGroot, RA ;
Haas, C .
PHYSICAL REVIEW B, 1997, 56 (08) :4455-4463
[6]   A kinetic study of CdS photocorrosion by intensity modulated photocurrent and photoelectrochemical impedance spectroscopy [J].
Fermín, DJ ;
Ponomarev, EA ;
Peter, LM .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1999, 473 (1-2) :192-203
[7]   ELECTROCHEMICAL PHOTOLYSIS OF WATER AT A SEMICONDUCTOR ELECTRODE [J].
FUJISHIMA, A ;
HONDA, K .
NATURE, 1972, 238 (5358) :37-+
[8]   Highly Durable N-Doped Graphene/CdS Nanocomposites with Enhanced Photocatalytic Hydrogen Evolution from Water under Visible Light Irradiation [J].
Jia, Li ;
Wang, Dong-Hong ;
Huang, Yu-Xi ;
Xu, An-Wu ;
Yu, Han-Qin .
JOURNAL OF PHYSICAL CHEMISTRY C, 2011, 115 (23) :11466-11473
[9]   Single crystal CdS nanowires with high visible-light photocatalytic H2-production performance [J].
Jin, Jian ;
Yu, Jiaguo ;
Liu, Gang ;
Wong, Po Keung .
JOURNAL OF MATERIALS CHEMISTRY A, 2013, 1 (36) :10927-10934
[10]   Heterogeneous photocatalyst materials for water splitting [J].
Kudo, Akihiko ;
Miseki, Yugo .
CHEMICAL SOCIETY REVIEWS, 2009, 38 (01) :253-278