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探索钙钛矿氟化物向超快析氧的动态自重构

Probing Dynamic Self-Reconstruction on Perovskite Fluorides toward Ultrafast Oxygen Evolution.

作者信息

Zhang Jing, Ye Yu, Wang Zhenbin, Xu Yin, Gui Liangqi, He Beibei, Zhao Ling

机构信息

Faculty of Materials Science and Chemistry, China University of Geosciences, Wuhan, 430074, China.

State Key Laboratory of Geological Processes and Mineral Resources, China University of Geosciences, Wuhan, 430074, China.

出版信息

Adv Sci (Weinh). 2022 Sep;9(27):e2201916. doi: 10.1002/advs.202201916. Epub 2022 Jul 22.

Abstract

Exploring low cost, highly active, and durable electrocatalysts for oxygen evolution reaction (OER) is of prime importance to boost energy conversion efficiency. Perovskite fluorides are emerging as alternative electrocatalysts for OER, however, their intrinsically active sites during real operation are still elusive. Herein, the self-reconstruction on newly designed NiFe coupled perovskite fluorides during OER process is demonstrated. In situ Raman spectroscopy, ex situ X-ray absorption spectroscopy, and theoretical calculation reveal that Fe incorporation can significantly activate the self-reconstruction of perovskite fluorides and efficiently lower the energy barrier of OER. Benefiting from self-reconstruction and low energy barrier, the KNi Fe F @nickel foam (KNFF2@NF) electrocatalyst delivers an ultralow overpotential of 258 mV to afford 100 mA cm and an excellent durability for 100 h, favorably rivaling most the state-of-the-art OER electrocatalysts. This protocol provides the fundamental understanding on OER mechanism associated with surface reconstruction for perovskite fluorides.

摘要

探索低成本、高活性且耐用的析氧反应(OER)电催化剂对于提高能量转换效率至关重要。钙钛矿氟化物正成为OER的替代电催化剂,然而,它们在实际运行过程中的本征活性位点仍然难以捉摸。在此,展示了新设计的镍铁耦合钙钛矿氟化物在OER过程中的自重构。原位拉曼光谱、非原位X射线吸收光谱和理论计算表明,铁的掺入可以显著激活钙钛矿氟化物的自重构,并有效降低OER的能垒。受益于自重构和低能垒,泡沫镍负载的KNiFeF(KNFF2@NF)电催化剂提供258 mV的超低过电位以实现100 mA cm,并且具有100小时的优异耐久性,与大多数最先进的OER电催化剂相比具有优势。该方案提供了对与钙钛矿氟化物表面重构相关的OER机制的基本理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c331/9507342/c0d5298c73c3/ADVS-9-2201916-g006.jpg

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