Evaluation of A-Site Ba2+-Deficient Ba1−xCo0.4Fe0.4Zr0.1Y0.1O3−δ Oxides as Electrocatalysts for Efficient Hydrogen Evolution Reaction

• Main Authors: Xiangnan Li, Liqing He, Xiongwei Zhong, Jie Zhang, Shijing Luo, Wendi Yi, Luozheng Zhang, Manman Hu, Jun Tang, Xianyong Zhou, Xingzhong Zhao, Baomin Xu
• Format: Article
• Language: English
• Published: Hindawi-Wiley 2018-01-01
• Series: Scanning
• Online Access: http://dx.doi.org/10.1155/2018/1341608
• ISSN: 0161-0457; 1932-8745

Exploring earth-abundant and cost-effective catalysts with high activity and stability for a hydrogen evolution reaction (HER) is of great importance to practical applications of alkaline water electrolysis. Here, we report on A-site Ba2+-deficiency doping as an effective strategy to enhance the electrochemical activity of BaCo0.4Fe0.4Zr0.1Y0.1O3−δ for HER, which is related to the formation of oxygen vacancies around active Co/Fe ions. By comparison with the benchmarking Ba0.5Sr0.5Co0.8Fe0.2O3−δ, one of the most spotlighted perovskite oxides, the Ba0.95Co0.4Fe0.4Zr0.1Y0.1O3−δ oxide has lower overpotential and smaller Tafel slope. Furthermore, the Ba0.95Co0.4Fe0.4Zr0.1Y0.1O3−δ catalyst is ultrastable in an alkaline solution. The enhanced HER performance originated from the increased active atoms adjacent to oxygen vacancies on the surface of the Ba0.95Co0.4Fe0.4Zr0.1Y0.1O3−δ catalyst induced by Ba2+-deficiency doping. The low-coordinated active atoms and adjacent oxygen ions may play the role of heterojunctions that synergistically facilitate the Volmer process and thus render stimulated HER catalytic activity. The preliminary results suggest that Ba2+-deficiency doping is a feasible method to tailor the physical and electrochemical properties of perovskite, and that Ba0.95Co0.4Fe0.4Zr0.1Y0.1O3−δ is a potential catalyst for HER.