Synergistical Dual Strategies Based on in Situ-Converted Heterojunction and Reduction-Induced Surface Oxygen Vacancy for Enhanced Photoelectrochemical Performance of TiO2
Synergistical Dual Strategies Based on in Situ-Converted Heterojunction and Reduction-Induced Surface Oxygen Vacancy for Enhanced Photoelectrochemical Performance of TiO2
复制标题
基于原位转换异质结和还原诱导表面氧空位的协同双重策略增强 TiO2 的光电化学性能
DOI:
10.1021/acsami.9b12537
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发表时间:
2019-10-09
影响因子:
9.5
通讯作者:
Yan, Xiaohong
中科院分区:
文献类型:
--
作者:
He, Yanfang;Wang, Peipei;Yan, Xiaohong
Identifying effective means to improve the charge separation performance assisted by adequate surface reaction represents a significant challenge for developing a highly efficient TiO2 photoanode. Here we report a structural synergistic strategy between a close contact heterojunction and a surface oxygen vacancy to significantly boost the charge separation efficiency and charge injection efficiency of TiO2 nanowires (NWs) in PEC water splitting. To accomplish this task, a TiO2/SrTiO3 (TiO2/STO) heterojunction was first constructed by in situ conversion, resulting in close contact between interface, promoting separation of the photoinduced charge carriers, which increased charge separation efficiency by 107% compared to TiO2. After the amorphous layer established on the surface of the SrTiO3 coating, the resulting TiO2/SrTiO3/r-SrTiO3 (TiO2/STO/r-STO) improved the light absorption property of the photoelectrodes and boosted the ability to adsorb the reactant hydroxide ions, resulting in charge injection efficiency improvement by 67.3% compared with pure TiO2. This complementary modification for enhancing charge separation and boosting the surface reaction demonstrates a significant capacity to improve the photoelectrochemical (PEC) performance of one photoanode, which could be instructive for other fields including photocatalysis and PEC carbon dioxide reduction.