Hou Tianyi, Liu Borui, Sun Xiaohong, Fan Anran, Xu Zhongkai, Cai Shu, Zheng Chunming, Yu Guihua, Tricoli Antonio
School of Materials Science and Engineering, Key Laboratory of Advanced Ceramics and Machining Technology of Ministry of Education, Tianjin University, Tianjin 300072, China.
Research School of Electrical, Energy, and Materials Engineering, Nanotechnology Research Laboratory, Australian National University, Canberra, Australian Capital Territory 2601, Australia.
ACS Nano. 2021 Apr 27;15(4):6735-6746. doi: 10.1021/acsnano.0c10121. Epub 2021 Mar 19.
Transition-metal sulfides (TMSs) powered by conversion and/or alloying reactions are considered to be promising anode materials for advanced lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs). However, the limited electronic conductivity and large volume expansion severely hinder their practical application. Herein, we report a covalent coupling strategy for TMS-based anode materials using amide linkages to bind TMSs and carbon nanotubes (CNTs). In the synthesis, the thiourea acts as not only the capping agent for morphology control but also the linking agent for the covalent coupling. As a proof of concept, the covalently coupled ZnS/CNT composite (CC-ZnS/CNT) has been prepared, with ZnS nanoparticles (∼10 nm) tightly anchored on CNT bundles. The compact ZnS-CNT heterojunctions are greatly beneficial to facilitating the electron/ion transfer and ensuring structural stability. Due to the strong coupling interaction between ZnS and CNTs, the composite presents prominent pseudocapacitive behavior and highly reversible electrochemical processes, thus leading to superior long-term stability and excellent rate capability, delivering reversible capacities of 333 mAh g at 2 A g over 4000 cycles for LIBs and 314 mAh g at 5 A g after 500 cycles for SIBs. Consequently, CC-ZnS/CNT exhibits great competence for applications in LIBs and SIBs, and the covalent coupling strategy is proposed as a promising approach for designing high-performance anode materials.
由转化和/或合金化反应驱动的过渡金属硫化物(TMSs)被认为是用于先进锂离子电池(LIBs)和钠离子电池(SIBs)的有前景的负极材料。然而,有限的电子导电性和大体积膨胀严重阻碍了它们的实际应用。在此,我们报道了一种基于TMS的负极材料的共价偶联策略,使用酰胺键将TMSs与碳纳米管(CNTs)结合。在合成过程中,硫脲不仅作为形貌控制的封端剂,还作为共价偶联的连接剂。作为概念验证,制备了共价偶联的ZnS/CNT复合材料(CC-ZnS/CNT),其中ZnS纳米颗粒(约10 nm)紧密锚定在CNT束上。紧密的ZnS-CNT异质结极大地有利于促进电子/离子转移并确保结构稳定性。由于ZnS和CNTs之间的强耦合相互作用,该复合材料呈现出突出的赝电容行为和高度可逆的电化学过程,从而导致优异的长期稳定性和出色的倍率性能,在LIBs中以2 A g的电流密度循环4000次时可逆容量为333 mAh g,在SIBs中以5 A g的电流密度循环500次后可逆容量为314 mAh g。因此,CC-ZnS/CNT在LIBs和SIBs应用中表现出很大的优势,并且共价偶联策略被提出作为设计高性能负极材料的一种有前景的方法。