Mg-doped Ta3N5 nanorods coated with a conformal CoOOH layer for water oxidation: bulk and surface dual modification of photoanodes

被引:59
作者
Pei, Lang [1 ]
Xu, Zhe [1 ]
Shi, Zhan [2 ]
Zhu, Heng [1 ]
Yan, Shicheng [1 ]
Zou, Zhigang [1 ,2 ]
机构
[1] Nanjing Univ, Coll Engn & Appl Sci, Collaborat Innovat Ctr Adv Microstruct, Ecomat & Renewable Energy Res Ctr, 22 Hankou Rd, Nanjing 210093, Jiangsu, Peoples R China
[2] Nanjing Univ, Dept Phys, Natl Lab Solid State Microstruct, Jiangsu Key Lab Nano Technol, 22 Hankou Rd, Nanjing 210093, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
SOLAR; SEMICONDUCTOR; PERFORMANCE; TRANSPORT; ARRAYS; PHOTOCATALYST; HYDROGEN;
D O I
10.1039/c7ta06227c
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
Charge separation/transfer and photocorrosion are two major factors limiting the photoelectrochemical (PEC) applications of the Ta3N5 photocatalyst. Herein, we have fabricated Ta3N5 single-crystal nanorods with Mg doping by flux-assisted crystal growth, aiming to shorten the charge transport distance and increase the electrical conductivity. The optimized Mg-doped Ta3N5 photoanodes exhibit an unprecedented PEC water splitting activity with an AM 1.5G photocurrent of 1.5 mA cm(-2) at 1.23 V-RHE. The high performance is attributed to the fact that the bulk modification, Mg doping, can induce oxygen-impurity surface states as effective electron trap centers, thus increasing the electrical conductivity of Ta3N5 and charge separation efficiency. After a conformal surface modification with CoOOH by a simple electrodeposition method as a water oxidation electrocatalyst to improve the hole extraction and reaction kinetics, the Mg-doped Ta3N5 photoanodes afford an over 4-fold increase in photocurrent (ca. 6.5 mA cm(-2) at 1.23 VRHE) and about 70% retention of the initial photocurrent after 70 min irradiation at 1.0 VRHE. Our results testify that the bulk and surface co-modification is an effective route to develop high-performance PEC water splitting devices.
引用
收藏
页码:20439 / 20447
页数:9
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