High catalytic activity of oxygen-induced (200) surface of Ta2O5 nanolayer towards durable oxygen evolution reaction

被引:34
作者
Xiao, Wen [1 ,2 ]
Huang, Xiaolei [1 ]
Song, Wendong [2 ]
Yang, Yong [1 ]
Herng, Tun Seng [1 ]
Xue, Jun Min [1 ]
Peng, Yuan Ping [3 ]
Ding, Jun [1 ]
机构
[1] Natl Univ Singapore, Dept Mat Sci & Engn, Singapore 117575, Singapore
[2] ASTAR, Data Storage Inst, 4 Fusionopolis Way, Singapore 138635, Singapore
[3] Natl Univ Singapore, Dept Phys, Singapore 117542, Singapore
基金
新加坡国家研究基金会;
关键词
Oxygen evolution reaction; Ta2O5; catalysis; DFT calculations; Pulsed laser deposition; Oxygen control; Surface modulation; GENERALIZED GRADIENT APPROXIMATION; MESOPOROUS TANTALUM OXIDE; FUEL-CELL; PHOTOCATALYTIC ACTIVITY; THERMAL TA2O5; WATER; REDUCTION; ELECTROCATALYSTS; NANOCRYSTALS; ELECTROLYSIS;
D O I
10.1016/j.nanoen.2016.04.020
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
Efficient and durable catalysts towards oxygen evolution reaction (OER) are highly desirable for renewable energy technologies. Herein, we develop a new, efficient, economical and durable Ta2O5 OER catalyst by controlling oxygen environment to induce the active OER catalytic surface. Stable surface structures of Ta2O5 and their onset overpotentials towards OER are calculated via systematic DFT simulations. Oxygen site on the stable (200) surface of Ta2O5 is explicitly identified as the most active OER site, possessing a small calculated onset overpotential of 0.25 V. In addition, using the simulated oxygen rich condition, we successfully grow a (200)-surface-exposed Ta2O5 nanolayer on a carbon cloth by oxygen-controlled pulsed laser deposition. In accordance to the simulation, the designated (200) surface exhibits high OER activity with an onset overpotential of 0.29 V and overpotential of 0.385 V at 10 mA/cm(2). The oxygen-controlled surface modulation to activate catalytic activity provides a novel strategy for effective development of metal-oxide catalysts for clean energy technologies. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:60 / 67
页数:8
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