Document Type

Article

Corresponding Author(s)

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

Abstract

The development of robust electrocatalyst for oxygen reduction reaction (ORR) in seawater electrolyte is the key to realize the seawater electrolyte-based zinc-air batteries (SZABs). Herein, constructing a local electric field coupled with Cl fixation strategy in dual single-atom catalysts (DSACs) is proposed, and the resultant catalyst delivers considerable ORR performance in seawater electrolyte, with a high half-wave potential (E1/2) of 0.868 V and a good maximum power density (Pmax) of 182 mW cm2 in the assembled SZABs, much higher than those of the Pt/C catalyst (E1/2: 0.846 V; Pmax: 150 mW cm2). The in-situ characterization and theoretical calculations reveal that the Fe sites have a higher Cl adsorption affinity than the Co sites, preferentially adsorbs Cl in seawater electrolyte during the ORR process, thus constructs a low-concentration Cl local microenvironment through the common-ion exclusion effect, which prevents Cl adsorption and corrosion the Co active centers, achieving impressive catalytic stability. In addition, the directional charge movement between Fe and Co atomic pairs constructs 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 batteries, Oxygen reduction reaction, Local electric fields, Cl− fixation strategy, Single-atom catalysts

Online Date

6-3-2025

2504132-SI.pdf (1091 kB)

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