Hierarchy and delithiation regulations on mesoporous LiCoO2 nanosheets for boosted water oxidation electrocatalysis. (December 2021)

• Record Type: Journal Article
• Authors: Dai, Zhengfei; Liu, Yaoda; Liang, Tingting; Lenus, Syama; Liu, Qianyi; Zhang, Xu; Vijayakumar, Paranthaman
• Is Part Of: Applied materials today. Volume 25(2021)
• Publication Date: 2021-12
• Subjects: LiCoO2 -- Hierarchical structures -- Chemical delithiation -- Electrocatalysts -- Oxygen evolution reaction; Materials science -- Periodicals; Materials -- Research -- Periodicals; 620.1105
• DOI: 10.1016/j.apmt.2021.101241
• Languages: English
• ISSNs: 2352-9407

Abstract

Highlights: Mesoporous LiCoO2 hierarchical nanostructures were controllably synthesized. The LiCoO2 structure was further chemically delithiated to activate the Co 4+ /Co 3+ pair. The delithiated LiCo0.72 O2 exhibited a low overpotential of 289 mV at 10 mA cm −2 . The role of chemical delithiation on LiCoO2 for OER was revealed by DFT calculations. ABSTRACT: Layered lithium cobaltite (LiCoO2 ) is currently an emerging low-cost and active electrocatalyst in oxygen evolution reaction (OER) with good stability. However, most of its OER catalytic studies are mainly based on aggregated LiCoO2 powder, and thus construction of distinct LiCoO2 nanostructures would be the primary quest for OER performance optimization. In this work, mesoporous LiCoO2 hierarchical nanosheets were hydrothermally synthesized on carbon cloth and then chemically delithiated for OER electrocatalysis. Two types of LiCoO2 hierarchical nanostructures, including sheet-on-rod and sheet-on-sheet features, have been prepared and compared for OER activity. The LiCoO2 sheet-on-sheet structure with higher OER performance was further chemically delithiated towards Li1-x CoO2 to activate the Co 4+ /Co 3+ pair and boost the OER process. As a result, the delithiated LiCo0.72 O2 catalyst delivers an outstanding and durable catalytic performance toward OER in alkaline solution, including an overpotential of 289 mV at 10 mA cm −2, small Tafel slope, and low charge transfer resistance. First-principle calculations indicate that the delithiation can change the electronic state of the LiCoO2 system, and the water oxidation can be promoted by optimizing the adsorption Gibbs free energy of OER intermediates. The present investigation paves an interesting avenue for the rational design of highly efficient LiCoO2 water oxidation catalysts. Graphical abstract: Image, graphical abstract Delithiated mesoporous LiCoO2 hierarchical nanosheets with activated Co 4+ /Co 3+ pair enable the boosted water dissociation kinetics and preferable electrocatalytic properties for oxygen evolution reaction.