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Corresponding Author

Peng Rao (raopeng@hainanu.edu.cn);
Ying Liang (liangying@hainanu.edu.cn);
Xin-Long Tian (tianxl@hainanu.edu.cn)

Abstract

Development of robust electrocatalyst for oxygen reduction reaction (ORR) in a seawater electrolyte is the key to realize seawater electrolyte-based zinc-air batteries (SZABs). Herein, constructing a local electric field coupled with chloride ions (Cl) fixation strategy in dual single-atom catalysts (DSACs) was proposed, and the resultant catalyst delivered considerable ORR performance in a seawater electrolyte, with a high half-wave potential (E1/2) of 0.868 V and a good maximum power density (Pmax) of 182 mW·cm−2 in the assembled SZABs, much higher than those of the Pt/C catalyst (E1/2: 0.846 V; Pmax: 150 mW·cm−2). The in-situ characterization and theoretical calculations revealed that the Fe sites have a higher Cl adsorption affinity than the Co sites, and preferentially adsorbs Cl in a seawater electrolyte during the ORR process, and thus constructs a low-concentration Cl local microenvironment through the common-ion exclusion effect, which prevents Cl adsorption and corrosion in the Co active centers, achieving impressive catalytic stability. In addition, the directional charge movement between Fe and Co atomic pairs establishes a local electric field, optimizing the adsorption energy of Co sites for oxygen-containing intermediates, and further improving the ORR activity.

Graphical Abstract

Keywords

Seawater zinc-air battery, Oxygen reduction reaction, Local electric field, Chloride ion fixation strategy, Single- atom catalyst

Creative Commons License

Creative Commons Attribution 4.0 International License
This work is licensed under a Creative Commons Attribution 4.0 International License.

Publication Date

2025-09-28

Online Available Date

2025-06-03

Revised Date

2025-05-21

Received Date

2025-04-14

JOE2504132-Supporting Information.pdf (1867 kB)
Local Electric Fields Coupled with Cl− Fixation Strategy for Improving Seawater Oxygen Reduction Reaction Performance - Supporting Information

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