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题名: Mechanistic studies of photocatalytic reaction of methanol for hydrogen production on Pt/TiO2 by in situ Fourier transform IR and time-resolved IR spectroscopy
作者: Chen, Tao;  Feng, Zhaochi;  Wu, Guopeng;  Shi, Jianying;  Ma, Guijun;  Ying, Pinliang;  Li, Can
通讯作者: 李灿
刊名: JOURNAL OF PHYSICAL CHEMISTRY C
发表日期: 2007-06-07
DOI: 10.1021/jp071022b
卷: 111, 期:22, 页:8005-8014
收录类别: SCI
文章类型: Article
部门归属: 5
项目归属: 503
产权排名: 1;1
WOS标题词: Science & Technology ;  Physical Sciences ;  Technology
类目[WOS]: Chemistry, Physical ;  Nanoscience & Nanotechnology ;  Materials Science, Multidisciplinary
研究领域[WOS]: Chemistry ;  Science & Technology - Other Topics ;  Materials Science
英文摘要: The anaerobic photocatalytic reaction of methanol on Pt/TiO2 catalyst was studied by in situ Fourier transform IR and time-resolved IR spectroscopy. For the Pt/TiO2 catalysts reduced at high temperature, the capacity of methanol adsorption decreases with the increase of the Pt loading, indicating that Pt particles or atoms occupy some of the active sites on TiO2 for methanol adsorption. Surface species CH2O(a), CH2OO(a), and HCOO(a) are derived from the photocatalytic reaction of methanol on Pt/TiO2. The increase of gas-phase methanol or water accelerates the photoreaction and improves the activity of H-2 production. When the catalysts are exposed to methanol, the strong electronic absorption on nanosecond to second time scale is observed, indicating that a great amount of long-lived electrons are produced in TiO2-based photocatalysts after band gap excitation. The decay rate of the long-lived electrons correlates well with the activity of H-2 production. These results show that the long-lived electrons contribute to the H-2 generation and the decays of the long-lived electrons on millisecond to second time scale in Pt/TiO2 are ascribed to the reaction for H-2 evolution: e(tr)(-)[Pt] + H+-> H center dot -> 1/2H(2). The function of the molecularly adsorbed methanol or water is found to mediate the proton transfer on the TiO2 surface. The activities of H-2 production under steady-state irradiation conditions were also measured, and it is deduced that the yield of the long-lived electrons could be responsible for the activity of H-2 production.
关键词[WOS]: INFRARED-ABSORPTION SPECTROSCOPY ;  DIFFUSE-REFLECTANCE SPECTROSCOPY ;  ELECTRON-PARAMAGNETIC-RESONANCE ;  PHOTOGENERATED ELECTRONS ;  CARRIER DYNAMICS ;  AQUEOUS-SOLUTION ;  TIO2 PARTICLES ;  FT-IR ;  NANOCRYSTALLINE TIO2 ;  CHARGE SEPARATION
语种: 英语
原文出处: 查看原文
WOS记录号: WOS:000246842400027
Citation statistics: 
内容类型: 期刊论文
URI标识: http://cas-ir.dicp.ac.cn/handle/321008/99685
Appears in Collections:中国科学院大连化学物理研究所_期刊论文

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作者单位: 1.Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China

Recommended Citation:
Chen, Tao,Feng, Zhaochi,Wu, Guopeng,et al. Mechanistic studies of photocatalytic reaction of methanol for hydrogen production on Pt/TiO2 by in situ Fourier transform IR and time-resolved IR spectroscopy[J]. JOURNAL OF PHYSICAL CHEMISTRY C,2007,111(22):8005-8014.
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