纳米结构v掺杂Fe2O3上的Pt助催化剂纳米层促进光电化学水氧化

Hardy Shuwanto, Hairus Abdullah, Young Ku, Jenni Lie
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引用次数: 0

摘要

采用一种缺陷的掺杂Fe2O3体系,以Pt为助催化剂进行了光电化学(PEC)水氧化。通过XPS和EPR分析揭示了VFPt-2.5光阳极所含的缺陷。有趣的是,通过SEM和TEM分析,电沉积的v掺杂α-Fe2O3的形貌为纳米级,平均直径为~ 12 nm,厚度为300 nm。在1 M KOH电解质溶液(pH = 14)中,当外加偏压为1.23 VRHE时,VFPt-2.5光阳极的起始电位达到0.22 VRHE,光电流密度达到2.5 mA/cm2。VFPt-2.5计算的IPCE和ABPE值分别为~ 37%和0.85%。VFPt-2.5//Pt产生的氧和氢分别为82和170 μmol。VFPt-2.5的稳定性达到95.2%,表明Pt可以帮助克服导致电荷复合的表面态的反向效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Pt Co-catalyst nanolayer on nanostructured V-doped Fe2O3 for boosting photoelectrochemical water oxidation

Pt Co-catalyst nanolayer on nanostructured V-doped Fe2O3 for boosting photoelectrochemical water oxidation

A defective system of V-doped Fe2O3 with Pt as a cocatalyst was employed for photoelectrochemical (PEC) water oxidation. The contained defects in VFPt-2.5 photoanode were revealed by XPS and EPR analyses. Interestingly, the morphology of electrodeposited V-doped α-Fe2O3 is observed to be nanosized with an average diameter size of ∼12 nm and thickness of 300 nm by SEM and TEM analyses. Under light irradiation, VFPt-2.5 photoanode achieved a remarkable onset potential of 0.22 VRHE and a photocurrent density of 2.5 mA/cm2 with an applied external bias at 1.23 VRHE in 1 M KOH electrolyte solution (pH = 14). The calculated IPCE and ABPE values of VFPt-2.5 were ∼37% and 0.85%, respectively. The generated oxygen and hydrogen by VFPt-2.5//Pt were found to be 82 and 170 μmol. The stability of VFPt-2.5 reached 95.2% revealing that Pt could help to overcome the reversed effect of surface states that cause the charge recombination.

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