Physical Insights into Band Bending in Pristine and Co-Pi-Modified BiVO4 Photoanodes with Dramatically Enhanced Solar Water Splitting Efficiency

被引:23
作者
Kandiel, Tarek A. [1 ,2 ]
Ahmed, Mahmoud G. [3 ]
Ahmed, Amira Y. [3 ]
机构
[1] King Fahd Univ Petr & Minerals KFUPM, Dept Chem, Dhahran 31261, Saudi Arabia
[2] KFUPM, KA CARE Energy Res & Innovat Ctr ERIC, Dhahran 31261, Saudi Arabia
[3] Sohag Univ, Fac Sci, Dept Chem, Sohag 82524, Egypt
关键词
MODULATED PHOTOCURRENT SPECTROSCOPY; PHOTOELECTROCHEMICAL WATER; SURFACE RECOMBINATION; OXIDATION; HYDROGEN; ARRAYS; PHOTOCATHODES; ELECTRODES; FILMS; IRON;
D O I
10.1021/acs.jpclett.0c01419
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
Herein, a novel method is introduced to synthesize 3D hierarchically assembled BiVO4 nanosheet photoanodes. Despite the fact that the obtained photoanodes inherit the intrinsic properties of 2D and 3D structures, they generate low photocurrent under simulated solar light at 1.0 sun. Upon modification with the cobalt-phosphate (Co-Pi) cocatalyst, the photocurrent is dramatically enhanced from 0.41 to 3.32 mA cm(-2) at 1.23 V-RHE. Charge-transfer kinetic studies by intensity-modulated photocurrent spectroscopy indicated that the low photocurrent response is mainly due to the high density of surface states, which pin the Fermi level and suspend the band bending. The Co-Pi loading passivates these surface states, unpins the Fermi level, and thus resumes the band bending. It also greatly enhances the rate constant of charge transfer and the overall efficiency, evincing that Co-Pi exhibits a dual function (i.e., passivation and catalysis). The current results explicitly disclose the role of the Co-Pi cocatalyst in photoelectrochemical solar water splitting on BiVO4.
引用
收藏
页码:5015 / 5020
页数:6
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