电催化剂
催化作用
析氧
钌
兴奋剂
溶解
耐久性
材料科学
钙钛矿(结构)
化学工程
无机化学
化学
纳米技术
结晶学
物理化学
电化学
有机化学
电极
复合材料
工程类
光电子学
作者
M. Retuerto,L. Pascual,Federico Calle‐Vallejo,Pilar Ferrer,Diego Gianolio,Alejandro Pereira,Álvaro García,Jorge Torrero,M. T. Fernández‐Díaz,P. Benčok,M.A. Peña,J.L.G. Fierro,Sergio Rojas
标识
DOI:10.1038/s41467-019-09791-w
摘要
Abstract The design of active and durable catalysts for the H 2 O/O 2 interconversion is one of the major challenges of electrocatalysis for renewable energy. The oxygen evolution reaction (OER) is catalyzed by SrRuO 3 with low potentials (ca. 1.35 V RHE ), but the catalyst’s durability is insufficient. Here we show that Na doping enhances both activity and durability in acid media. DFT reveals that whereas SrRuO 3 binds reaction intermediates too strongly, Na doping of ~0.125 leads to nearly optimal OER activity. Na doping increases the oxidation state of Ru, thereby displacing positively O p-band and Ru d-band centers, weakening Ru-adsorbate bonds. The enhanced durability of Na-doped perovskites is concomitant with the stabilization of Ru centers with slightly higher oxidation states, higher dissolution potentials, lower surface energy and less distorted RuO 6 octahedra. These results illustrate how high OER activity and durability can be simultaneously engineered by chemical doping of perovskites.
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