Cao Bin, Liu Huan, Zhang Xin, Zhang Peng, Zhu Qizhen, Du Huiling, Wang Lianli, Zhang Rupeng, Xu Bin
State Key Laboratory of Organic-Inorganic Composites, Beijing Key Laboratory of Electrochemical Process and Technology for Materials, Beijing University of Chemical Technology, Beijing, 100029, People's Republic of China.
College of Materials Science and Engineering, Xi'an University of Science and Technology, Xi'an, 710054, People's Republic of China.
Nanomicro Lett. 2021 Sep 26;13(1):202. doi: 10.1007/s40820-021-00728-x.
ZnS has great potentials as an anode for lithium storage because of its high theoretical capacity and resource abundance; however, the large volume expansion accompanied with structural collapse and low conductivity of ZnS cause severe capacity fading and inferior rate capability during lithium storage. Herein, 0D-2D ZnS nanodots/TiCT MXene hybrids are prepared by anchoring ZnS nanodots on TiCT MXene nanosheets through coordination modulation between MXene and MOF precursor (ZIF-8) followed with sulfidation. The MXene substrate coupled with the ZnS nanodots can synergistically accommodate volume variation of ZnS over charge-discharge to realize stable cyclability. As revealed by XPS characterizations and DFT calculations, the strong interfacial interaction between ZnS nanodots and MXene nanosheets can boost fast electron/lithium-ion transfer to achieve excellent electrochemical activity and kinetics for lithium storage. Thereby, the as-prepared ZnS nanodots/MXene hybrid exhibits a high capacity of 726.8 mAh g at 30 mA g, superior cyclic stability (462.8 mAh g after 1000 cycles at 0.5 A g), and excellent rate performance. The present results provide new insights into the understanding of the lithium storage mechanism of ZnS and the revealing of the effects of interfacial interaction on lithium storage performance enhancement.
硫化锌因其高理论容量和资源丰富性而具有作为锂存储负极的巨大潜力;然而,硫化锌在锂存储过程中伴随结构坍塌的大体积膨胀和低电导率会导致严重的容量衰减和较差的倍率性能。在此,通过在MXene和MOF前驱体(ZIF-8)之间进行配位调制,随后进行硫化,将硫化锌纳米点锚定在TiCT MXene纳米片上,制备了0D-2D硫化锌纳米点/TiCT MXene杂化物。与硫化锌纳米点耦合的MXene基底可以协同适应硫化锌在充放电过程中的体积变化,以实现稳定的循环性能。XPS表征和DFT计算表明,硫化锌纳米点与MXene纳米片之间的强界面相互作用可以促进快速的电子/锂离子转移,从而实现优异的锂存储电化学活性和动力学。因此,所制备的硫化锌纳米点/MXene杂化物在30 mA g下表现出726.8 mAh g的高容量、优异的循环稳定性(在0.5 A g下1000次循环后为462.8 mAh g)和出色的倍率性能。目前的结果为理解硫化锌的锂存储机制以及揭示界面相互作用对锂存储性能增强的影响提供了新的见解。