Authors

Document Type

Article

Corresponding Author(s)

Tingyu Lu([email protected]);
Dongmei Sun([email protected]);
Yawen Tang([email protected])

Abstract

Designing efficient and durable electrocatalysts for the oxygen evolution reaction (OER) is critical for advancing sustainable electrochemical energy conversion and storage technologies such as rechargeable Zinc-Air Battery (ZAB). Herein, we fabricate a heterostructured OER catalyst composed of CoS2 and Co3O4 nanosheets supported on nitrogen-doped carbon nanofibers (hereafter denoted as CoS2/Co3O4@CFs) through the anion engineering. Experimental results demonstrate that the in-situ selective sulfidation constructs abundant CoS2/Co3O4 heterointerfaces, enabling the synergistic regulation of electronic structure and active-site distribution. The O-to-S anion substitution modulates the interfacial electronic properties and establishes a pronounced work-function difference, where CoS2 exhibits a higher work function than Co3O4. This difference drives interfacial charge redistribution and the formation of a built-in electric field, which may modulate the local adsorption environment of oxygenated intermediates and thereby contribute to the enhanced OER kinetics. Therefore, CoS2/Co3O4@CFs delivers superior OER activity with a low overpotential of 304 mV A at 10 mA⋅cm-2, along with remarkable long-term durability in alkaline electrolyte. Furthermore, when employed as the air cathode in a ZAB, the CoS2/Co3O4@CFs demonstrates excellent rechargeability, favorable rate capability, and stable cycling performance. This work highlights anion-induced in-situ topochemical transformation strategy for regulating interfacial electron redistribution, providing insights into the rational design of high-performance cobalt-based electrocatalysts.

Graphical Abstract

Keywords

non-precious electrocatalysts, anion-engineered topochemical transformation, schottky heterostructure, oxygen evolution reaction, zinc-air battery

Online Date

9-22-2026

2606151-SI.pdf (1627 kB)

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