Mesoporous Co x Sn (1– x ) O 2 as an efficient oxygen evolution catalyst support for SPE water electrolyzer

Author:

Chen Gang1ORCID,Li Jiakun12,Lv Hong32,Wang Sen32,Zuo Jian32,Zhu Lihua1

Affiliation:

1. College of Materials and Engineering, Hunan University, Changsha, Hunan 410082, People's Republic of China

2. Clean Energy Automotive Engineering Center, Tongji University, Shanghai 201804, People's Republic of China

3. School of Automotive Studies, Tongji University, Shanghai 201804, People's Republic of China

Abstract

SPE water electrolysis is a promising method of hydrogen production owing to its multiple strengths, including its high efficiency, high product purity and excellent adaptability. However, the overpotential of the oxygen evolution reaction process and consumption of Ir during charging in SPE water electrolysis will inevitably result in large energy loss and then high cost. Under these circumstances, we propose a novel 40IrO 2 /Co x Sn (1− x ) O 2 ( x = 0.1, 0.2, 0.3) anode catalyst, where the Co x Sn (1− x ) O 2 support is synthesized by a hydrothermal method and IrO 2 is synthesized by a modified Adams fusion method. After modifying the component of Co x Sn (1− x ) O 2 , the 40IrO 2 /Co x Sn (1− x ) O 2 exhibits an increased specific surface area, electrical conductivity and surface active sites. Moreover, a single cell is fabricated by Pt/C as cathode catalyst, 40IrO 2 /Co x Sn (1− x ) O 2 as anode catalyst and Nafion 117 membrane as electrolyte. The 40IrO 2 /Co 0.2 Sn 0.8 O 2 exhibits the lowest overpotential (1.748 V at 1000 mA cm −2 ), and only 0.18 mV h −1 of voltage increased for 100 h durability test at 1000 mA cm −2 . Consequently, Co x Sn (1− x ) O 2 is a promising anode electrocatalyst support for an SPE water electrolyzer.

Funder

National High-tech R&D Program of China

Fundamental Research Funds for the Central Universities

National Nature Science Foundation of China

Publisher

The Royal Society

Subject

Multidisciplinary

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