Anatase TiO2(001)-(1 x 4) Surface Is Intrinsically More Photocatalytically Active than the Rutile TiO2(110)-(1 x 1) Surface

被引:24
作者
Xiong, Feng [1 ]
Yin, Li-Li [2 ,3 ]
Lin, Fei [2 ,3 ]
Wu, Zongfang [1 ]
Wang, Zhengming [1 ]
Sun, Guanghui [1 ]
Xu, Hong [1 ]
Chai, Peng [1 ]
Gong, Xue-Qing [2 ,3 ]
Huang, Weixin [1 ]
机构
[1] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale,Dept Chem Phys, Key Lab Surface & Interface Chem & Energy Catalys, Anhui Higher Educ Inst,CAS Key Lab Mat Energy Con, Jinzhai Rd 96, Hefei 230026, Anhui, Peoples R China
[2] East China Univ Sci & Technol, Key Lab Adv Mat, Ctr Computat Chem, Meilong Rd 130, Shanghai 200237, Peoples R China
[3] East China Univ Sci & Technol, Sch Chem & Mol Engn, Res Inst Ind Catalysis, Meilong Rd 130, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
INITIO MOLECULAR-DYNAMICS; 001; FACETS; TIO2; PHOTOCATALYSIS; CHARGE SEPARATION; OXYGEN; O-2; PHOTODESORPTION; SCIENCE; MECHANISMS; ADSORPTION;
D O I
10.1021/acs.jpcc.9b06319
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Aligning the intrinsic photocatalytic activities of various types of TiO2 facets is of great importance and interest in TiO2 photocatalysis. Herein, we report a comparative study of the intrinsic photocatalytic activities of anatase TiO2(001)-(1 x 4) and rutile TiO2(110)-(1 x 1) surfaces probed by photostimulated desorption of O-2 with combined thermal desorption spectroscopy, photostimulated desorption spectroscopy, and density functional theory calculations. Photostimulated desorption behavior of O-2 depends on both TiO2 surface structures and O-2 adsorption configurations. O-2 species adsorbed on the anatase TiO2(001)-(1 x 4) surface exhibit a higher intrinsic photostimulated desorption reactivity than those on the rutile TiO2(110)-(1 x 1) surface, which can be associated with their electronic structures and subsequent hole transfer processes from TiO2. These results provide, for the first time, direct and unambiguous experimental evidence for the higher intrinsic photocatalytic activity of the anatase TiO2(001) facet than those of other TiO2 facets and highlight the key role of structures of both TiO2 surfaces and adsorbed species in TiO2 photocatalysis.
引用
收藏
页码:24558 / 24565
页数:8
相关论文
共 56 条
[1]   Light-induced charge separation in anatase TiO2 particles [J].
Berger, T ;
Sterrer, M ;
Diwald, O ;
Knözinger, E ;
Panayotov, D ;
Thompson, TL ;
Yates, JT .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (13) :6061-6068
[2]   IMPROVED TETRAHEDRON METHOD FOR BRILLOUIN-ZONE INTEGRATIONS [J].
BLOCHL, PE ;
JEPSEN, O ;
ANDERSEN, OK .
PHYSICAL REVIEW B, 1994, 49 (23) :16223-16233
[3]   Introduction: Titanium Dioxide (TiO2) Nanomaterials [J].
Chen, Xiaobo ;
Selloni, Annabella .
CHEMICAL REVIEWS, 2014, 114 (19) :9281-+
[4]   The surface science of titanium dioxide [J].
Diebold, U .
SURFACE SCIENCE REPORTS, 2003, 48 (5-8) :53-229
[5]   Thermally-driven processes on rutile TiO2(110)-(1 x 1): A direct view at the atomic scale [J].
Dohnalek, Zdenek ;
Lyubinetsky, Igor ;
Rousseau, Roger .
PROGRESS IN SURFACE SCIENCE, 2010, 85 (5-8) :161-205
[6]   Electron-energy-loss spectra and the structural stability of nickel oxide: An LSDA+U study [J].
Dudarev, SL ;
Botton, GA ;
Savrasov, SY ;
Humphreys, CJ ;
Sutton, AP .
PHYSICAL REVIEW B, 1998, 57 (03) :1505-1509
[7]   TiO2 photocatalysis and related surface phenomena [J].
Fujishima, Akira ;
Zhang, Xintong ;
Tryk, Donald A. .
SURFACE SCIENCE REPORTS, 2008, 63 (12) :515-582
[8]   Reactivity of anatase TiO2 nanoparticles:: The role of the minority (001) surface [J].
Gong, XQ ;
Selloni, A .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (42) :19560-19562
[9]   Nonaqueous Synthesis of TiO2 Nanocrystals Using TiF4 to Engineer Morphology, Oxygen Vacancy Concentration, and Photocatalytic Activity [J].
Gordon, Thomas R. ;
Cargnello, Matteo ;
Paik, Taejong ;
Mangolini, Filippo ;
Weber, Ralph T. ;
Fornasiero, Paolo ;
Murray, Christopher B. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2012, 134 (15) :6751-6761
[10]   Accurate description of van der Waals complexes by density functional theory including empirical corrections [J].
Grimme, S .
JOURNAL OF COMPUTATIONAL CHEMISTRY, 2004, 25 (12) :1463-1473