A-Site Cation-Ordering Layered Perovskite EuBa0.5Sr0.5Co2- x Fe x O5+δ as Highly Active and Durable Electrocatalysts for Oxygen Evolution Reaction

Xiu Wang; Yingnan Dou; Ying Xie; Jingping Wang; Tian Xia; Lihua Huo; Hui Zhao

doi:10.1021/acsomega.0c01383

A-Site Cation-Ordering Layered Perovskite EuBa_0.5Sr_0.5Co_{2- x} Fe _x O_5+δ as Highly Active and Durable Electrocatalysts for Oxygen Evolution Reaction

ACS Omega. 2020 May 20;5(21):12501-12515. doi: 10.1021/acsomega.0c01383. eCollection 2020 Jun 2.

Authors

Xiu Wang¹, Yingnan Dou¹, Ying Xie¹, Jingping Wang², Tian Xia¹, Lihua Huo¹, Hui Zhao¹

Affiliations

¹ Key Laboratory of Functional Inorganic Materials Chemistry, Ministry of Education, School of Chemistry, Chemical Engineering and Materials, Heilongjiang University, Harbin 150080, Heilongjiang, People's Republic of China.
² Key Laboratory of Superlight Material and Surface Technology, Ministry of Education, College of Materials Science and Chemical Engineering, Harbin Engineering University, Harbin 150001, Heilongjiang, People's Republic of China.

Abstract

The developments of high-performance and tolerant catalysts may enable more sustainable energy in the future, especially toward water oxidation. Herein, we report A-site cation-ordering layered perovskite EuBa_0.5Sr_0.5Co_2-x Fe _x O_5+δ (EBSCFx) (x = 0.2-0.6) electrocatalysts. When evaluated for oxygen evolution reaction (OER) in alkaline media, EuBa_0.5Sr_0.5Co_1.6Fe_0.4O_5+δ (EBSCF0.4) exhibits the best catalytic activity among all of these catalysts, as evidenced by the lowest overpotential of 420 mV at a current density of 10 mA cm^-2. Notably, the catalytic activity of EBSCF0.4 is better than that of commercial IrO₂ at the overpotential >460 mV. Furthermore, the EBSCF0.4-20RuO₂ (involving 20 wt % RuO₂) composite catalyst is developed and gives an overpotential as low as 390 mV at 50 mA cm^-2, which is even superior to commercial RuO₂. For overall water splitting, an electrolysis voltage of merely 1.47 V is achieved at 10 mA cm^-2 in an electrolyzer employing EBSCF0.4-20RuO₂ as bifunctional catalysts, with exceptional durability for 24 h. Such a performance outperforms state-of-the-art IrO₂∥Pt/C and RuO₂∥Pt/C couples. According to density functional theory (DFT) calculations, the unique catalytic properties of EBSCF0.4 may benefit from highly active Fe sites with octahedral coordination, and the synergistic effects of Fe and Ru sites in the composite catalyst accelerate the electrochemical water oxidation.