Catalytic oxidation of formaldehyde on surface of H-TiO2/H-C-TiO2 without light illumination at room temperature

被引:104
作者
Zeng, Lei [1 ]
Song, Wulin [1 ,2 ]
Li, Minghui [1 ]
Zeng, Dawen [1 ]
Xie, Changsheng [1 ]
机构
[1] Huazhong Univ Sci & Technol, State Key Lab Mat Proc & Die & Mould Technol, Wuhan 430074, Peoples R China
[2] Huazhong Univ Sci & Technol, Analyt & Testing Ctr, Wuhan 430074, Peoples R China
基金
中国国家自然科学基金;
关键词
Hydrogenated TiO2; Non-light-illumination catalysis; Room temperature catalysis; Oxygen vacancy; Formaldehyde; TIO2 NANOWIRE ARRAYS; PHOTOCATALYTIC ACTIVITY; HYDROGENATED TIO2; OXYGEN VACANCIES; MESOPOROUS TIO2; DOPED TITANIA; WATER; DEFECTS; BLACK; PHOTOOXIDATION;
D O I
10.1016/j.apcatb.2013.09.013
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
A modified TiO2 was prepared by short-time annealing in low concentration of hydrogen gas at low temperature and ordinary pressure. As a result, the hydrogenated TiO2 (H-TiO2) and hydrogenated carbon-doped TiO2 (H-C-TiO2) could decompose gaseous formaldehyde without light irradiation at room temperature. Compared with pure TiO2, the H-TiO2 and H-C-TiO2 were allowed to introduce more oxygen vacancies and surface hydroxyl groups, which had crucial contribution to catalytic oxidation of gaseous formaldehyde in the dark. Moreover, the existence of oxygen vacancies and surface hydroxyl groups were confirmed by XPS and EPR. Oxygen vacancies could efficiently govern O-2 adsorption by trapping O-2 molecules on defect sites and producing active oxygen species. The surface hydroxyl groups could facilitate the adsorption of O-2 molecules and remove carbonate species which could block the catalytic active sites. Based on these results, a novel mechanism of gaseous formaldehyde decomposed by hydrogenated TiO2 in the dark was proposed. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:490 / 498
页数:9
相关论文
共 47 条
[1]   Vanadia-titania thin films for photocatalytic degradation of formaldehyde in sunlight [J].
Akbarzadeh, Rokhsareh ;
Umbarkar, Shubhangi B. ;
Sonawane, Ravindra S. ;
Takle, Srikant ;
Dongare, Mohan K. .
APPLIED CATALYSIS A-GENERAL, 2010, 374 (1-2) :103-109
[2]   Formaldehyde/methanol combustion on alumina-supported manganese-palladium oxide catalyst [J].
Alvarez-Galván, MC ;
Pawelec, B ;
O'Shea, VAD ;
Fierro, JLG ;
Arias, PL .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2004, 51 (02) :83-91
[3]   Nanostructured TiO2 films with 2 eV optical gaps [J].
Barborini, E ;
Conti, AM ;
Kholmanov, I ;
Piseri, P ;
Podestà, A ;
Milani, P ;
Cepek, C ;
Sakho, O ;
Macovez, R ;
Sancrotti, M .
ADVANCED MATERIALS, 2005, 17 (15) :1842-+
[4]   Increasing Solar Absorption for Photocatalysis with Black Hydrogenated Titanium Dioxide Nanocrystals [J].
Chen, Xiaobo ;
Liu, Lei ;
Yu, Peter Y. ;
Mao, Samuel S. .
SCIENCE, 2011, 331 (6018) :746-750
[5]   Theoretical assessment of the catalytic (Pt/TiO2) oxidation of formaldehyde at ambient temperature [J].
Dewil, R ;
Everaert, K ;
Baeyens, J .
CATALYSIS COMMUNICATIONS, 2005, 6 (12) :793-795
[6]   N-Doped TiO2 Nanofibers Deposited by Electrospinning [J].
Di Camillo, Daniela ;
Ruggieri, Fabrizio ;
Santucci, S. ;
Lozzi, Luca .
JOURNAL OF PHYSICAL CHEMISTRY C, 2012, 116 (34) :18427-18431
[7]   The power of EPR techniques in revealing active sites in heterogeneous photocatalysis: The case of anion doped TiO2 [J].
Fittipaldi, Maria ;
Gatteschi, Dante ;
Fornasiero, Paolo .
CATALYSIS TODAY, 2013, 206 :2-11
[8]   XPS study of copper-doped carbon aerogels [J].
Fu, RW ;
Yoshizawa, N ;
Dresselhaus, MS ;
Dresselhaus, G ;
Satcher, JH ;
Baumann, TF .
LANGMUIR, 2002, 18 (26) :10100-10104
[9]   ELECTROCHEMICAL PHOTOLYSIS OF WATER AT A SEMICONDUCTOR ELECTRODE [J].
FUJISHIMA, A ;
HONDA, K .
NATURE, 1972, 238 (5358) :37-+
[10]  
Fujishima A., 2000, J PHOTOCH PHOTOBIO C, V1, P1, DOI DOI 10.1016/S1389-5567(00)00002-2