Abdelghafar Fatma, Xu Xiaomin, Jiang San Ping, Shao Zongping
WA School of Mines: Minerals, Energy and Chemical Engineering (WASM-MECE), Curtin University, Perth, WA, 6102, Australia.
Department of Evaluation and Analysis, Egyptian Petroleum Research Institute, Cairo, 11727, Egypt.
ChemSusChem. 2024 Aug 12;17(15):e202301534. doi: 10.1002/cssc.202301534. Epub 2024 Apr 6.
The development of advanced electrolysis technologies such as anion exchange membrane water electrolyzer (AEMWE) is central to the vision of a sustainable energy future. Key to the realization of such AEMWE technology lies in the exploration of low-cost and high-efficient catalysts for facilitating the anodic oxygen evolution reaction (OER). Despite tremendous efforts in the fundamental research, most of today's OER works are conducted under room temperature, which deviates significantly with AEMWE's operating temperature (50-80 °C). To bridge this gap, it is highly desirable to obtain insights into the OER catalytic behavior at elevated temperatures. Herein, using the well-known perovskite catalyst BaSrCoFeO (BSCF) as a proof of concept, the effect of temperature on the variation in OER catalytic activity and stability is evaluated. It is found that the BSCF's activity increases with increasing temperature due to enhanced lattice oxygen participation promoting the lattice oxygen-mediated OER process. Further, surface amorphization and cation leaching of BSCF become more pronounced as temperature increases, causing a somewhat attenuated OER stability. These new understandings of the fundamental OER catalysis over perovskite materials at industrial-relevant temperature conditions are expected to have strong implications for the research of OER catalysts to be deployed in practical water electrolyzers.
诸如阴离子交换膜水电解槽(AEMWE)等先进电解技术的发展对于可持续能源未来的愿景至关重要。实现此类AEMWE技术的关键在于探索用于促进阳极析氧反应(OER)的低成本、高效催化剂。尽管在基础研究方面付出了巨大努力,但当今大多数OER研究工作是在室温下进行的,这与AEMWE的工作温度(50 - 80°C)有显著偏差。为了弥合这一差距,非常有必要深入了解高温下的OER催化行为。在此,以著名的钙钛矿催化剂BaSrCoFeO(BSCF)作为概念验证,评估了温度对OER催化活性和稳定性变化的影响。研究发现,由于晶格氧参与增强促进了晶格氧介导的OER过程,BSCF的活性随温度升高而增加。此外,随着温度升高,BSCF的表面非晶化和阳离子浸出变得更加明显,导致OER稳定性有所减弱。这些关于工业相关温度条件下钙钛矿材料上基本OER催化作用的新认识预计将对应用于实际水电解槽的OER催化剂研究产生重大影响。