Understanding the role of nickel–iron (oxy)hydroxide (NiFeOOH) electrocatalysts on hematite photoanodes. Issue 2 (17th December 2020)

• Record Type: Journal Article
• Authors: Lee, Jihye; Seo, Daye; Won, Sunghwan; Chung, Taek Dong
• Is Part Of: Sustainable energy & fuels. Volume 5:Issue 2(2021)
• Page Start: 501
• Page End: 508
• Publication Date: 2020-12-17
• Subjects: Renewable energy sources -- Periodicals; Fuel cells -- Periodicals; Electric batteries -- Periodicals; Electrochemistry -- Periodicals; 660.297
• DOI: 10.1039/d0se01500h
• Languages: English
• ISSNs: 2398-4902

Abstract

Abstract : A NiFeOOH electrocatalyst prepared by photo-assisted anodic deposition on hematite performs a dual function: increasing the water oxidation kinetics and suppressing surface charge recombination. Abstract : Hematite (α-Fe2 O3 ) modified with a nickel–iron (oxy)hydroxide (NiFeOOH) electrocatalyst is among the most promising photoanodes for photoelectrochemical water splitting. Previous studies have demonstrated that a NiFeOOH overlayer on the α-Fe2 O3 photoanode enhances the photoelectrochemical performance; however, the mechanism underlying this improvement remains poorly understood. In this paper, we report on how the NiFeOOH overlayer affects the energetics of the photoanode and the kinetics of surface charge carriers as a function of NiFeOOH thickness. It was found that a thin NiFeOOH film not only reduced surface charge recombination but also increased the water oxidation kinetics. This result is in conflict with earlier studies asserting that surface modification of semiconductor electrodes with oxide-based electrocatalysts does not affect the water oxidation kinetics. The distinctive dual-function character of the NiFeOOH overlayer arises from the combination of the remarkable catalytic activity of NiFeOOH and the properties of photo-assisted electrodeposition. However, thick NiFeOOH films lead to a substantial decrease in photocurrent owing to the low conductivity of the segregated FeOOH phase in the film.