Microwave-assisted synthesis of C-doped TiO2 and ZnO hybrid nanostructured materials as quantum-dots sensitized solar cells

被引:35
作者
Rangel-Mendez, Jose R. [1 ]
Matos, Juan [2 ]
Chazaro-Ruiz, Luis F. [1 ]
Gonzalez-Castillo, Ana C. [1 ]
Barrios-Yanez, Guillermo [1 ]
机构
[1] IPICYT, Environm Sci Div, Camino Presa San Jose 2055,Col Lomas 4a Secc, San Luis Potosi 78216, Mexico
[2] Univ Concepcion, UDT, Biomat Dept, Ave Cordillera,2634,Parque Ind Coronel, Coronel, Bio Bio, Chile
关键词
C-doped materials; Microwave-synthesis; TiO2; ZnO; Quantum-dots; Solar cells; HOLLOW SPHERES; ELECTRIC-FIELD; THIN-FILMS; CARBON; DYE; PHOTOCATALYSIS; ANATASE; NANO; WETTABILITY; DEGRADATION;
D O I
10.1016/j.apsusc.2017.10.236
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
The microwave-assisted solvothermal synthesis of C-doped TiO2 and ZnO hybrid materials was performed. Saccharose, titanium isopropoxide and zinc acetate were used as organic and inorganic sources for the synthesis. The influence of temperature and reaction time on the textural and optoelectronic properties of the hybrid materials was verified. Carbon quantum-dots of TiO2 and ZnO nanostructured spheres were obtained in a second pot by controlled calcination steps of the precursor hybrid materials. A carefully characterization by adsorption-desorption N-2 isotherms, XRD, XPS, SEM, UV-vis/DR and electro-and photo-electrochemistry properties of the carbon quantum-dots TiO2 and ZnO spheres was performed. The photoelectrochemical activity of TiO2-C and ZnO-C films proved to be dependent on the conditions of synthesis. It was found a red-shift in the energy band gap of the semiconductors with values of 3.02 eV and 3.13 eV for the TiO2-C and ZnO-C, respectively, clearly lower than those on bare semiconductors, which is associated with the C-doping effect. From the photo-electrochemistry characterization of C-doped TiO2 and ZnO films can be concluded that the present materials have potential applications as photoelectrodes for quantum-dots sensitized solar cells. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:744 / 755
页数:12
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