Suppr超能文献

制备双相氧化物电催化剂以促进析氧反应的过掺杂策略

Overdoping Strategy for Preparing a Two-Phase Oxide Electrocatalyst to Boost Oxygen Evolution Reaction.

作者信息

Cai Jian, Quan Wei, Chen Tianyi, Ye Daixin, Zhao Hongbin, Wu Chengzhang

机构信息

Department of Physics, College of Sciences & Institute for Sustainable Energy, Shanghai University, Shanghai, 200444, P. R. China.

State Key Laboratory of Advanced Special Steel & Shanghai Key Laboratory of Advanced Ferrometallurgy & College of Materials Science and Engineering, Shanghai University, Shanghai, 200444, P. R. China.

出版信息

Chem Asian J. 2022 Jun 1;17(11):e202200127. doi: 10.1002/asia.202200127. Epub 2022 Apr 14.

Abstract

The oxygen evolution reaction is of great significance to the production of hydrogen from high efficiency electrolytic water, hydrogen oxygen fuel cell and other energy conversion devices, but there are many challenges such as high cost, low efficiency and poor stability of catalysts. Among non-precious metal catalysts, oxide has its unique advantages. We used overdoping strategy to prepare two-phase oxide electrocatalyst SrCo Fe Mo O (SCFM ) containing double perovskite and Co O with excellent OER electrocatalytic activity and stability in alkaline solution. It required an overpotential of 361.7 mV to reach a 10 mA cm current density and its performance only degrades by 3.48% after 1000 CV cycles accelerated stability tests, whose electrochemical performance is superior to that of single-phase double perovskites and undoped perovskites. SrCo Fe O (SCF) ordinary perovskite is doped with slightly molybdenum (Mo), and then the ordinary perovskite turns into double perovskite because of the polyvalence characteristics of Mo. When Mo is overdoped, Co O phase was precipitated while Mo entered perovskite phase. This process causes lattice distortion and makes the surface electronic structure benign changes. Furthermore, the microscopic morphology of the material surface and the valence state of cobalt element are changed, thereby improving the microenvironment of the electrochemical process.

摘要

析氧反应对于从高效电解水、氢氧燃料电池及其他能量转换装置中制氢具有重要意义,但存在诸多挑战,如催化剂成本高、效率低和稳定性差等。在非贵金属催化剂中,氧化物具有其独特优势。我们采用过掺杂策略制备了含双钙钛矿的两相氧化物电催化剂SrCoFeMoO(SCFM)以及在碱性溶液中具有优异析氧反应电催化活性和稳定性的CoO。达到10 mA cm电流密度需要361.7 mV的过电位,并且在1000次循环伏安加速稳定性测试后其性能仅下降3.48%,其电化学性能优于单相双钙钛矿和未掺杂的钙钛矿。SrCoFeO(SCF)普通钙钛矿被微量钼(Mo)掺杂,然后由于Mo的多价特性普通钙钛矿转变为双钙钛矿。当Mo过掺杂时,CoO相析出而Mo进入钙钛矿相。这一过程导致晶格畸变并使表面电子结构发生良性变化。此外,材料表面的微观形貌和钴元素的价态发生改变,从而改善了电化学过程的微环境。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验