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基于La(1-x)Sr(x)CoO(3-δ)钙钛矿电催化剂的水电解

Water electrolysis on La(1-x)Sr(x)CoO(3-δ) perovskite electrocatalysts.

作者信息

Mefford J Tyler, Rong Xi, Abakumov Artem M, Hardin William G, Dai Sheng, Kolpak Alexie M, Johnston Keith P, Stevenson Keith J

机构信息

Department of Chemistry, The University of Texas at Austin, Austin, Texas 78712, USA.

Department of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.

出版信息

Nat Commun. 2016 Mar 23;7:11053. doi: 10.1038/ncomms11053.

Abstract

Perovskite oxides are attractive candidates as catalysts for the electrolysis of water in alkaline energy storage and conversion systems. However, the rational design of active catalysts has been hampered by the lack of understanding of the mechanism of water electrolysis on perovskite surfaces. Key parameters that have been overlooked include the role of oxygen vacancies, B-O bond covalency, and redox activity of lattice oxygen species. Here we present a series of cobaltite perovskites where the covalency of the Co-O bond and the concentration of oxygen vacancies are controlled through Sr(2+) substitution into La(1-x)Sr(x)CoO(3-δ) . We attempt to rationalize the high activities of La(1-x)Sr(x)CoO(3-δ) through the electronic structure and participation of lattice oxygen in the mechanism of water electrolysis as revealed through ab initio modelling. Using this approach, we report a material, SrCoO2.7, with a high, room temperature-specific activity and mass activity towards alkaline water electrolysis.

摘要

钙钛矿氧化物作为碱性储能和转换系统中水电解的催化剂具有吸引力。然而,由于对钙钛矿表面水电解机理缺乏了解,活性催化剂的合理设计受到了阻碍。被忽视的关键参数包括氧空位的作用、B-O键的共价性以及晶格氧物种的氧化还原活性。在此,我们展示了一系列钴酸盐钙钛矿,其中通过将Sr(2+) 取代到La(1-x)Sr(x)CoO(3-δ) 中来控制Co-O键的共价性和氧空位浓度。我们试图通过从头算模型揭示的电子结构和晶格氧在水电解机理中的参与来解释La(1-x)Sr(x)CoO(3-δ) 的高活性。使用这种方法,我们报道了一种材料SrCoO2.7,它对碱性水电解具有高的室温比活性和质量活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/153f/4814573/d039dea66878/ncomms11053-f1.jpg

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