Dong Feifei, Li Lu, Kong Ziqi, Xu Xiaomin, Zhang Yaping, Gao Zhenghui, Dongyang Biaokui, Ni Meng, Liu Quanbing, Lin Zhan
Guangzhou Key Laboratory of Clean Transportation Energy Chemistry, School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou Higher Education Mega Center, Guangzhou, 510006, P. R. China.
WA School of Mines: Minerals, Energy and Chemical Engineering (WASM-MECE), Curtin University, Perth, WA, 6102, Australia.
Small. 2021 Jan;17(2):e2006638. doi: 10.1002/smll.202006638. Epub 2020 Dec 16.
Developing robust and highly efficient electrocatalysts for oxygen evolution reaction (OER) is critical for renewable, secure, and emission-free energy technologies. Perovskite Ba Sr Co Fe O (BSCF) has emerged as a promising OER electrocatalyst with desirable intrinsic activity. Inspired by the factor that substituting in transition-metal sublattice of the perovskite can further optimize the OER activity, herein, nickel-substituted BSCF is adopted, that is, Ba Sr Co Fe Ni O (x = 0.05, 0.1, 0.2, denoted as BSCFNx, x = 5, 10, 20, respectively), as efficient and stable OER catalysts in alkaline solution. The phase structure, microchemistry, oxygen vacancy, and electrochemical activity of such samples are well-investigated. Endowed with an overpotential of only 278 mV at 10 mA cm and a Tafel slope of merely 47.98 mV dec , BSCFN20 exhibits the optimum OER activity. When constructing a two-electrode cell with BSCFN20 as anode and Pt/C as cathode (BSCFN20||Pt/C) for water splitting, it only requires a voltage of 1.63 V to achieve 50 mA cm , and the BSCFN20||Pt/C remains stable within 80 h at 10 mA cm , superior to the state-of-the-art RuO ||Pt/C counterpart. This work provides a feasible strategy for designing stable and highly active perovskite electrocatalysts for future energy storage and conversion.
开发用于析氧反应(OER)的稳健且高效的电催化剂对于可再生、安全且无排放的能源技术至关重要。钙钛矿BaSrCoFeO(BSCF)已成为一种具有理想本征活性的有前景的OER电催化剂。受钙钛矿过渡金属亚晶格中的取代可进一步优化OER活性这一因素的启发,本文采用镍取代的BSCF,即BaSrCoFeNiO(x = 0.05、0.1、0.2,分别表示为BSCFNx,x = 5、10、20),作为碱性溶液中高效且稳定的OER催化剂。对这些样品的相结构、微观化学、氧空位和电化学活性进行了充分研究。BSCFN20在10 mA cm时的过电位仅为278 mV,塔菲尔斜率仅为47.98 mV dec,表现出最佳的OER活性。当构建以BSCFN20为阳极、Pt/C为阴极的双电极电解槽(BSCFN20||Pt/C)用于水分解时,仅需1.63 V的电压即可达到50 mA cm,并且BSCFN20||Pt/C在10 mA cm下80 h内保持稳定,优于目前最先进的RuO||Pt/C。这项工作为设计用于未来能量存储和转换的稳定且高活性的钙钛矿电催化剂提供了一种可行的策略。