多硫化物
异质结
材料科学
氧化还原
介孔材料
纳米技术
电子流
电子
光电子学
化学
电极
催化作用
电解质
生物化学
物理
物理化学
量子力学
冶金
作者
Jinji Lan,Shu Zhang,Le Yang,Chunjun Chen,Huilei Wu,Liubin Feng,Dong‐Li An,Jiajia Chen
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-08-26
标识
DOI:10.1021/acsnano.5c09873
摘要
Due to the high solubility and multielectron transfer capabilities of polysulfides, aqueous polysulfide redox flow batteries (PS-RFBs) have emerged as promising candidates for large-scale energy storage, offering both low cost and high capacity. However, the sluggish electrochemical kinetics of polysulfides leads to significantly high polarization and low energy efficiency. Here, we tailor a two-dimensional ordered mesoporous nitrogen-doped carbon@MoS2 (Meso-NC@MoS2) heterojunction with a sandwich-like nanostructure to accelerate the redox kinetics of polysulfides. The in-plane electric field in Meso-NC@MoS2 optimizes polysulfide adsorption and establishes a directional charge transfer channel, thereby enhancing electron transport from Meso-NC@MoS2 to S42– and consequently improving the reaction kinetics activity of S42– on the electrocatalyst. As a result, the Meso-NC@MoS2 based PS-RFBs exhibit a reduction in charging overpotential of approximately 377 mV compared to blank carbon felt, while the battery energy efficiency increases from 42.28% to 85.75% at 20 mA cm–2. Additionally, the battery can demonstrate a high-power density of 112 mW cm–2, as well as operating for up to 3200 cycles in 30 days with a high Coulombic efficiency of 99.9% at 60 mA cm–2.
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