Direct conversion of two-dimensional ZIF-L film to porous ZnO nano-sheet film and its performance as photoanode in dye-sensitized solar cell

被引:53
作者
Liu, Qi [1 ,2 ]
Low, Ze-Xian [1 ]
Feng, Yi [1 ]
Leong, Sookwan [1 ]
Zhong, Zhaoxiang [1 ]
Yao, Jianfeng [1 ]
Hapgood, Karen [1 ]
Wang, Huanting [1 ]
机构
[1] Monash Univ, Dept Chem Engn, Clayton, Vic 3800, Australia
[2] Anhui Polytech Univ, Wuhu 241000, Peoples R China
基金
澳大利亚研究理事会;
关键词
ZnO; Zeolitic imidazolate framework; Film; Direct conversion; Photoanode; ZEOLITIC IMIDAZOLATE FRAMEWORKS; METAL-ORGANIC FRAMEWORKS; CARBON; ARRAYS; NANOCOMPOSITE; NANOWIRES; GROWTH;
D O I
10.1016/j.micromeso.2014.03.023
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A zeolitic imidazolate framework-L (ZIF-L) film with a leaf-like morphology was successfully fabricated on FTO substrate in aqueous solution at room temperature on a large-scale. This ZIF-L film with a thickness of similar to 4 mu m was composed of highly uniform nanosheets of 100-150 nm in thickness, which stood nearly perpendicularly on the substrate. A porous ZnO nanosheet film was subsequently obtained by simply calcining the ZIF-L film at 550 degrees C for 0.5 h. The resulting ZnO nanosheets presented a curved petal-like morphology, which was composed of interconnected nanoparticles. The ZnO film with a thickness of only about 4 mu m showed highly crystalline and well-defined porous features. An overall light conversion efficiency of 2.52% was achieved by using this thin porous ZnO nanosheet film as a photoanode in dye-sensitized solar cell (DSSC), significantly better than that derived from the film of ZnO nanorods with similar thickness (1.27%). The superior performance of the DSSC with porous ZnO nanosheet is attributed to the following: (1) the high surface area leads to a higher dye loading; (2) the nanopores enable more efficient electrolyte diffusion and rapid adsorption of the dye, thereby reducing the chances of formation of Zn2+/dye aggregates; and (3) increased light-harvesting efficiency. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:1 / 7
页数:7
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