Structural and Electrochemical Identification of CoFe Pnictide Catalysts Affecting the Performance of the Oxygen Evolution Reaction. Issue 3 (7th March 2023)

• Record Type: Journal Article
• Authors: Lee, Ui Young; Jeong, Dong In; Choi, Hyung Wook; Kim, Jiwon; Kang, Bong Kyun; Yoon, Dae Ho
• Is Part Of: Journal of the Electrochemical Society. Volume 170:Issue 3(2023)
• Publication Date: 2023-03-07
• Subjects: Electrochemistry -- Periodicals; 541.3705
• DOI: 10.1149/1945-7111/acbee9
• Languages: English
• ISSNs: 0013-4651

Abstract

Abstract : The advance of efficient electrocatalysts for electrochemical water splitting is highly significant for the energy conversion system, but is hindered by the high overpotential of the oxygen evolution reaction (OER) by four-electron transfer. Herein, we report a variation of transition metal compound based on the Co–Fe Prussian blue analogue (PBA) precursor. CoP/FeP, Co2 N/Fe3 N, and CoFe catalysts are synthesized in N2 atmosphere by phosphorization, nitridation, and calcination, respectively. After phosphorization, the synthesized mesoporous CoP/FeP nanocubes contribute to the improvement of the electrocatalyst performance by maintaining the shape of the precursor. The mesoporous structure of the CoP/FeP catalyst enhanced the electrochemically active surface area (ECSA) than other Co2 N/Fe3 N and CoFe catalysts, resulting in better OER performance with an overpotential of 279 mV at a current density of 10 mA∙cm −2, a Tafel slope of 74 mV∙dec −1, and good stability for 24 h with only 5.64% degradation in alkaline solution (1.0 M KOH).