Wang Chan, Zhang Pengfei, Li Jiatong, Wang Rui, Yang Changheng, Yu Fushuai, Zhao Xuening, Zhao Kaichen, Zheng Xiaoyan, Zhang Huigang, Yang Tao
Shaanxi Key Laboratory for Theoretical Physics Frontiers, Institute of Modern Physics, Northwest University, Xi'an, 710127, People's Republic of China.
Shaanxi Key Laboratory of Degradable Biomedical Materials, School of Chemical and Engineering, Institute of Low-Carbon Technology Application, Northwest University, Xi'an, 710069, People's Republic of China.
Nanomicro Lett. 2025 Jul 18;18(1):7. doi: 10.1007/s40820-025-01849-3.
Lithium-sulfur (Li-S) batteries require efficient catalysts to accelerate polysulfide conversion and mitigate the shuttle effect. However, the rational design of catalysts remains challenging due to the lack of a systematic strategy that rationally optimizes electronic structures and mesoscale transport properties. In this work, we propose an autogenously transformed CoWO/WO heterojunction catalyst, integrating a strong polysulfide-adsorbing intercalation catalyst with a metallic-phase promoter for enhanced activity. CoWO effectively captures polysulfides, while the CoWO/WO interface facilitates their S-S bond activation on heterogenous catalytic sites. Benefiting from its directional intercalation channels, CoWO not only serves as a dynamic Li-ion reservoir but also provides continuous and direct pathways for rapid Li-ion transport. Such synergistic interactions across the heterojunction interfaces enhance the catalytic activity of the composite. As a result, the CoWO/WO heterostructure demonstrates significantly enhanced catalytic performance, delivering a high capacity of 1262 mAh g at 0.1 C. Furthermore, its rate capability and high sulfur loading performance are markedly improved, surpassing the limitations of its single-component counterparts. This study provides new insights into the catalytic mechanisms governing Li-S chemistry and offers a promising strategy for the rational design of high-performance Li-S battery catalysts.
锂硫(Li-S)电池需要高效催化剂来加速多硫化物转化并减轻穿梭效应。然而,由于缺乏合理优化电子结构和中尺度传输性能的系统策略,催化剂的合理设计仍然具有挑战性。在这项工作中,我们提出了一种自生转变的CoWO₄/WO₃异质结催化剂,它将强吸附多硫化物的插层催化剂与金属相促进剂相结合以提高活性。CoWO₄有效地捕获多硫化物,而CoWO₄/WO₃界面促进其在异质催化位点上的S-S键活化。得益于其定向插层通道,CoWO₄不仅作为动态锂离子储存库,还为快速锂离子传输提供连续且直接的途径。这种跨异质结界面的协同相互作用增强了复合材料的催化活性。结果,CoWO₄/WO₃异质结构表现出显著增强的催化性能,在0.1 C下提供1262 mAh g的高容量。此外,其倍率性能和高硫负载性能得到明显改善,超越了其单组分对应物的局限性。本研究为控制锂硫化学的催化机制提供了新见解,并为高性能锂硫电池催化剂的合理设计提供了一种有前景的策略。