Self-organized TiO2 nanotube arrays with uniform platinum nanoparticles for highly efficient water splitting

被引:68
|
作者
Lai, Yuekun [1 ,2 ,3 ,4 ]
Gong, Jiaojiao [1 ,2 ]
Lin, Changjian [1 ,2 ]
机构
[1] Xiamen Univ, State Key Lab Phys Chem Solid Surfaces, Xiamen 361005, Peoples R China
[2] Xiamen Univ, Coll Chem & Chem Engn, Xiamen 361005, Peoples R China
[3] Univ Munster, Inst Phys, D-48149 Munster, Germany
[4] Univ Munster, Ctr Nanotechnol CeNTech, D-48149 Munster, Germany
基金
中国国家自然科学基金;
关键词
TiO2 nanotube arrays; Multi-step electrochemical anodization; Pt nanoparticles; Photoelectrochemical activity; Organic additive; Hydrogen production; ANODIZED TUBULAR TITANIA; PHOTOCATALYTIC ACTIVITY; HYDROGEN GENERATION; SOLAR-CELLS; THIN-FILMS; FABRICATION; ENERGY; PHOTOELECTROLYSIS; PHOTOANODE; H-2;
D O I
10.1016/j.ijhydene.2012.01.078
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
Highly efficient water splitting electrode based on uniform platinum (Pt) nanoparticles on self-organized TiO2 nanotube arrays (TNTAs) was prepared by a combination of multi-step electrochemical anodization with facile photoreduction process. Uniform platinum (Pt) nanoparticles with an average diameter of 8 nm are distributed homogeneously on nanoporous top layer and underneath TiO2 nanotube wall. In comparison to pristine TNTAs, Pt@TNTAs show substantially enhanced photocurrent density and the incident photon-to-current conversion efficiency (IPCE) in the entire wavelength window. The maximum photocurrent density and IPCE from the optimized Pt@TNTAs photoelectrode (Pt, similar to 1.57 wt%) were about 24.2 mA cm(-2) and 87.9% at 350 nm, which is much higher than that of the pure nanotubes sample (16.3 mA cm(-2) and 67.3%). The resultant Pt@TNTAs architecture exhibited significantly enhanced photoelectrochemical activities for solar water splitting with hydrogen evolution rate up to 495 mu mol h(-1) cm(-2) in 2 M Na2CO3 + 0.5 M ethylene glycol under the optimal external bias of -0.3 V-SCE. Copyright (C) 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:6438 / 6446
页数:9
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