Lei Huanhao, Zuo Jinning, Lu Jia, Ma Ziqiang, Wang Yuke, Dai Wangqi, Cheng Xinyu, Xia Huikang, Fu Zhengwen
Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Department of Chemistry, College of Smart Materials and Future Energy, Fudan University, Shanghai, 200433, P. R. China.
Nano Science and Technology Institute, University of Science and Technology of China, Suzhou, 215123, P. R. China.
Adv Mater. 2025 Jun 25:e2507962. doi: 10.1002/adma.202507962.
Pristine metal-organic frameworks (MOFs) with their excellent cycling stability and high capacity are considered as promising next-generation anode materials for advanced high-performance lithium-ion batteries. Despite extensive efforts to improve initial Coulombic efficiency (ICE) via electrochemical prelithiation, the fundamental processes governing transition metals (TMs) dissolution and associated degradation mechanisms in MOFs-based full cells remain unclear. In this study, crystalline cobalt-nickel bimetallic metal-organic frameworks CoNi-MOF (CoNi-Benzene dicarboxylic MOFs), specifically derived from benzene dicarboxylic (BDC) ligands, are selected as the target material for investigation. A solid-state corrosion (SSC) strategy for prelithiating MOFs anodes with corrosion of lithium metal is proposed for the first time. The full cell with prelithiated MOFs anode achieves an energy density of 493 Wh kg and demonstrates superior cycling stability with 83.3% capacity retention after 240 cycles at 0.2 C. The SSC prelithiation strategy effectively passivates Co/Ni nanoparticles, reducing Ni dissolution percentage by an order of magnitude (from 15.32% to 1.16%), which is identified as the key factor underpinning the enhanced full cell performance. This study underscores the practical applicability of MOFs-based anodes prelithiated by the SSC strategy for achieving high-energy-density and long-cycling lithium-ion batteries.
具有出色循环稳定性和高容量的原始金属有机框架(MOF)被认为是用于先进高性能锂离子电池的有前途的下一代负极材料。尽管人们通过电化学预锂化在提高初始库仑效率(ICE)方面付出了巨大努力,但基于MOF的全电池中过渡金属(TM)溶解的基本过程以及相关的降解机制仍不清楚。在本研究中,选择了特别由苯二甲酸(BDC)配体衍生而来的结晶钴镍双金属金属有机框架CoNi-MOF(CoNi-苯二甲酸MOF)作为研究的目标材料。首次提出了一种通过锂金属腐蚀对MOF负极进行预锂化的固态腐蚀(SSC)策略。采用预锂化MOF负极的全电池实现了493 Wh/kg的能量密度,并在0.2 C下循环240次后表现出优异的循环稳定性,容量保持率为83.3%。SSC预锂化策略有效地钝化了Co/Ni纳米颗粒,将Ni的溶解百分比降低了一个数量级(从15.32%降至1.16%),这被认为是全电池性能增强的关键因素。本研究强调了通过SSC策略预锂化的基于MOF的负极在实现高能量密度和长循环锂离子电池方面的实际适用性。