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优化吸附-催化协同作用以加速室温钠硫电池中的硫转化动力学

Optimizing Adsorption-Catalysis Synergy to Accelerate Sulfur Conversion Kinetics in Room-Temperature Na-S Batteries.

作者信息

Shi Yujie, Zhang Limou, Wang Ting, Ma Runze, Wang Dongjiao, Fu Yujun, Du RuiPu, Zhang Junfei, Liu Dequan, Wu Liang, Li Weihan, Wu Ying, He Deyan

机构信息

School of Materials and Energy, and LONGi Institute of Future Technology, Lanzhou University, Lanzhou, 730000, China.

School of Mathematics and Physics, Lanzhou Jiaotong University, Lanzhou, 730000, China.

出版信息

Small. 2025 Jun;21(24):e2502257. doi: 10.1002/smll.202502257. Epub 2025 Apr 25.

Abstract

Room-temperature sodium-sulfur (RT Na-S) batteries are expected to become the next-generation energy storage system due to their ultrahigh theoretically energy density of 1274 Wh kg, abundant sulfur resource, and low cost. However, practical application is hindered by challenges of severe shuttle effect and sluggish S conversion kinetics. In this study, a series of nano-sized nickel-based chalcogenides are designed and fabricated as electrocatalysts for S cathode. The p orbitals originated from different anions show great effect on the partial-filled d orbital of the metal Ni site, which further regulates the electronic states of the catalytic site. Theoretical and experimental results confirm the excellent electrocatalytic performance of NiSe electrocatalyst with low reaction energy barriers, moderate adsorption capability, and strong catalytic conversion ability, consistent with Sabatier's principle. The optimized NiSe catalyst presents a high reversible capacity of 720.4 mAh g with excellent durability over 200 cycles at 0.2 A g retained a capacity of 401.4 mAh g after 1000 cycles at 2 A g in RT Na-S batteries. This work presents the balancing of adsorption and catalytic conversion toward polysulfides via the modulation of d/p orbitals of active sites.

摘要

室温钠硫(RT Na-S)电池因其理论能量密度高达1274瓦时/千克、硫资源丰富且成本低廉,有望成为下一代储能系统。然而,严重的穿梭效应和缓慢的硫转化动力学等挑战阻碍了其实际应用。在本研究中,设计并制备了一系列纳米级镍基硫族化物作为硫正极的电催化剂。源自不同阴离子的p轨道对金属镍位点的部分填充d轨道有显著影响,进而调节催化位点的电子态。理论和实验结果证实了NiSe电催化剂具有优异的电催化性能,反应能垒低、吸附能力适中且催化转化能力强,符合萨巴蒂尔原理。优化后的NiSe催化剂在室温钠硫电池中表现出720.4毫安时/克的高可逆容量,在0.2安/克的电流密度下循环200次具有优异的耐久性,在2安/克的电流密度下循环1000次后仍保留401.4毫安时/克的容量。这项工作通过调节活性位点的d/p轨道实现了对多硫化物吸附和催化转化的平衡。

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