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用于锂硫电池中电催化多硫化物转化的碳化钼纳米结构

Molybdenum carbide nanostructures for electrocatalytic polysulfide conversion in lithium-polysulfide batteries.

作者信息

Wu Yunling, Deng Jun, Zhou Yuan, Huang Yang, Li Yanguang

机构信息

Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Soochow University, Suzhou 215123, China.

出版信息

Nanoscale Horiz. 2020 Mar 1;5(3):501-506. doi: 10.1039/c9nh00618d. Epub 2019 Nov 18.

Abstract

Introduction of appropriate cathode electrocatalysts in lithium-sulfur or lithium-polysulfide batteries can accelerate the polysulfide interconversion and suppress the shuttle effect. However, improvements are often limited especially under high sulfur loading. Herein, we prepare molybdenum carbide nanostructures and investigate their potential as the cathode electrocatalyst for lithium-polysulfide batteries. The product is prepared by the self-polymerization of dopamine in the presence of MoO ions, followed by high-temperature carburization. It features ultrasmall α-MoC nanoparticles uniformly dispersed on a hierarchical carbonaceous support. Polysulfide adsorption experiments and electrochemical measurements show that this material has a strong surface affinity toward polysulfides, and can greatly enhance their conversion rate, in particular the LiS↔ LiS/LiS conversion. When assessed as the cathode electrocatalyst, it enables lithium-polysulfide batteries with large specific capacity (up to 1400 mA h g), impressive rate capability (800 mA h g at 3200 mA g) and excellent cycling stability even at high sulfur loading.

摘要

在锂硫或锂多硫化物电池中引入合适的阴极电催化剂可以加速多硫化物的相互转化并抑制穿梭效应。然而,改进往往受到限制,特别是在高硫负载情况下。在此,我们制备了碳化钼纳米结构,并研究了它们作为锂多硫化物电池阴极电催化剂的潜力。该产物通过多巴胺在MoO离子存在下的自聚合制备,随后进行高温渗碳。它具有均匀分散在分级碳质载体上的超小α-MoC纳米颗粒。多硫化物吸附实验和电化学测量表明,这种材料对多硫化物具有很强的表面亲和力,并且可以大大提高它们的转化率,特别是LiS↔LiS/LiS的转化。当作为阴极电催化剂进行评估时,它能使锂多硫化物电池具有大的比容量(高达1400 mA h g)、令人印象深刻的倍率性能(在3200 mA g下为800 mA h g)以及即使在高硫负载下也具有出色的循环稳定性。

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