赤铁矿
钝化
光电流
分解水
材料科学
表面状态
可逆氢电极
化学工程
纳米技术
电极
光电子学
化学
曲面(拓扑)
电化学
物理化学
冶金
光催化
催化作用
几何学
工程类
参比电极
数学
图层(电子)
生物化学
作者
Qingjiang Zhao,Pengda Huang,Dong Hu,Tianbao Li,Bingshe Xu
标识
DOI:10.1002/cptc.202300013
摘要
Abstract Hematite is considered a promising photoanode material for solar water splitting; however, its photoelectrochemical (PEC) water splitting performance is limited by a high‐density surface state. In this study, we achieved passivation of a hematite surface using In 2 O 3 nanoparticles. We characterized the passivation effect by analyzing the Mott‐Schottky curves. The resulting compound exhibited a negative shift of 0.1 eV in the onset potential compared to pure hematite, strongly indicating that the defect surface state of hematite was effectively passivated. Furthermore, the addition of NiFe(OH) x as a cocatalyst enhanced the oxygen evolution reaction kinetics. The optimal Ti−Fe 2 O 3 /In 2 O 3 /NiFe(OH) x compound photoanode achieved a superior photocurrent density of 2.6 mA cm −2 at 1.23 V vs. RHE, which is more than six times that of pure hematite (0.41 mA cm −2 ). This finding highlights a potential avenue for overcoming the issue of a high surface‐state density as the limiting condition for photoelectrodes.
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