A Template Editing Strategy to Create Interlayer-Confined Active Species for Efficient and Durable Oxygen Evolution Reaction

© 2022 Wiley-VCH GmbH.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 35(2023), 2 vom: 07. Jan., Seite e2203420
1. Verfasser: Liu, Depei (VerfasserIn)
Weitere Verfasser: Yan, Yuandong, Li, Hu, Liu, Duanduan, Yang, Yandong, Li, Taozhu, Du, Yu, Yan, Shicheng, Yu, Tao, Zhou, Wei, Cui, Peixin, Zou, Zhigang
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2023
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article Ni hydroxides interlayer-confined active species oxygen evolution reaction template editing strategy
Beschreibung
Zusammenfassung:© 2022 Wiley-VCH GmbH.
Substantial overpotentials and insufficient and unstable active sites of oxygen evolution reaction (OER) electrocatalysts limit their efficiency and stability in OER-related energy conversion and storage technologies. Here, a template editing strategy is proposed to graft highly active catalytic species onto highly conductive rigid frameworks to tackle this challenge. As a successful attempt, two types of NiO6 units of layered Ni BDC (BDC stands for 1,4-benzenedicarboxylic acid) metal organic frameworks are selectively edited by chemical etching-assisted electroxidation to create layered γ-NiOOH with intercalated Ni-O species. In such an interlayer-confined intercalated architecture, the large interlayer space with high ion permeability offers an ideal reaction region to sufficiently expose the OER active sites comprising high-density intercalated Ni-O species, which also suppresses the undesirable γ to β phase transformation, thus exhibiting efficient and durable OER activity. As a result, water oxidation can occur at an extremely low overpotential of 130 mV and affords 1000 h stability at 100 mA cm-2 . The strategy conceptually shows the possibility of achieving stable homogeneous-like catalysis in heterogeneous catalysis
Beschreibung:Date Completed 13.01.2023
Date Revised 13.01.2023
published: Print-Electronic
Citation Status PubMed-not-MEDLINE
ISSN:1521-4095
DOI:10.1002/adma.202203420