| Literature DB >> 31550415 |
Jianwen Huang1, Yaoyao Li1, Yadong Zhang2, Gaofeng Rao1, Chunyang Wu1, Yin Hu1, Xianfu Wang1, Ruifeng Lu3, Yanrong Li1, Jie Xiong1.
Abstract
The oxygen evolution reaction (OER) has been explored extensively for reliable hydrogen supply to boost the energy conversion efficiency. The superior OER performance of newly developed non-noble metal electrocatalysts has concealed the identification of the real active species of the catalysts. Now, the critical active phase in nickel-based materials (represented by NiNPS) was directly identified by observing the dynamic surface reconstruction during the harsh OER process via combining in situ Raman tracking and ex situ microscopy and spectroscopy analyses. The irreversible phase transformation from NiNPS to α-Ni(OH)2 and reversible phase transition between α-Ni(OH)2 and γ-NiOOH prior to OER demonstrate γ-NiOOH as the key active species for OER. The hybrid catalyst exhibits 48-fold enhanced catalytic current at 300 mV and remarkably reduced Tafel slope to 46 mV dec-1 , indicating the greatly accelerated catalytic kinetics after surface evolution.Entities:
Keywords: in situ Raman tracking; oxygen evolution; oxyhydroxide intermediate; pre-catalysts; surface reconstruction
Year: 2019 PMID: 31550415 DOI: 10.1002/anie.201910716
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336