纳米笼
法拉第效率
硫黄
氧化还原
碳纤维
电化学
材料科学
化学工程
电解质
氮气
电子转移
化学
电极
无机化学
复合数
催化作用
有机化学
冶金
工程类
物理化学
复合材料
作者
Tianming Liu,Guocheng Lv,Meng Liu,Xiaoya Cui,Hao Liu,Haodong Li,Changchun Zhao,Longfei Wang,Juchen Guo,Libing Liao
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-10-30
卷期号:18 (45): 31559-31568
标识
DOI:10.1021/acsnano.4c13092
摘要
Aluminum–sulfur batteries (ASBs) are emerging as promising energy storage systems due to their safety, low cost, and high theoretical capacity. However, it remains a challenge to overcome voltage hysteresis and short cycle life in the sulfur/Al2S3 conversion reaction, which hinders the development of ASBs. Here, we studied a high-voltage ASB system based on sulfur oxidation in an AlCl3/urea electrolyte. Nitrogen-doped hollow nanocages (HNCs) synthesized from MOF precursors were rationally designed as sulfur/carbon composite electrodes (S@HNC), and the impact of the nitrogen species on the electrochemical performance of sulfur electrodes was systematically investigated. The S@HNC-900 achieved efficient conversion at 1.9 V, delivering a stable capacity of 197.3 mA h g–1 and a Coulombic efficiency of 93.28% after 100 cycles. Furthermore, the S@HNC-900 electrode exhibited exceptional rate capacity and 800th long-term cycling stability, retaining a capacity of 87.1 mA h g–1 at 500 mA g–1. Ex situ XPS and XRD characterizations elucidated the redox mechanism, revealing a four-electron transfer process (S/AlSCl7) at the S@HNC-900 electrode. Density functional theory calculations demonstrated that pyridinic nitrogen-enriched HNC-900 significantly enhanced the sulfur conversion reaction and facilitated the adsorption of sulfur intermediates (SCl3+) on the carbon interface. This work provides critical insights into the high-voltage sulfur redox mechanism and establishes a foundation for the rational design of carbon-based electrocatalysts for the enhancement of ASB performance.
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