Crystalline phase-dependent photocatalytic water splitting for hydrogen generation on KNbO3 submicro-crystals

被引:76
作者
Yan, Lisha [1 ,3 ]
Zhang, Jun [2 ]
Zhou, Xuemei [1 ]
Wu, Xiaoxing [1 ]
Lan, Jinyao [1 ]
Wang, Yinshu [3 ]
Liu, Gang [1 ]
Yu, Jiaguo [2 ]
Zhi, Linjie [1 ]
机构
[1] Natl Ctr Nanosci & Technol, Beijing 100190, Peoples R China
[2] Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, Wuhan 430070, Peoples R China
[3] Beijing Normal Univ, Dept Phys, Beijing 100875, Peoples R China
基金
中国国家自然科学基金;
关键词
Hydrothermal; Perovskite; Potassium niobate; Submicro-crystals; Water splitting; ELECTRONIC-STRUCTURE; SHAPE CONTROL; SEMICONDUCTOR; NANOCRYSTALS; NANOWIRES; PHOTOELECTRON; COMPOSITES; NANOSHEETS; GRAPHENE;
D O I
10.1016/j.ijhydene.2013.01.028
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
Potassium niobate (KNbO3) submicro-crystals with cubic and orthorhombic phases were hydrothermally prepared and characterized by powder X-ray diffraction, micro-Raman spectroscopy, Fourier transform infrared spectroscopy, nitrogen adsorption desorption, diffuse reflectance UV visible spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy, and high-resolution transmission electron microscopy. The photocatalytic performance of the as-prepared KNbO3 samples was evaluated toward H-2 generation from an aqueous methanol solution under UV. The surface area-normalized rate of H-2 production over submicro-cubes with cubic phase is two times larger than that of submicro-rods with orthorhombic phase. In addition, both cubic and orthorhombic KNbO3 submicro-crystals showed much higher reactivity than commercial KNbO3 bulk-like powders. The underlying mechanism was discussed in terms of crystal structure and electronic structure. The results from this study are potentially applicable to a range of perovskites useful in water splitting as well as other areas of heterogeneous photocatalysis. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:3554 / 3561
页数:8
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