Du Wenqing, Liu Jiawei, Zeb Akif, Lin Xiaoming
Guangzhou Key Laboratory of Materials for Energy Conversion and Storage, Key Laboratory of Theoretical Chemistry of Environment, Ministry of Education, School of Chemistry, South China Normal University, Guangzhou 510006, PR China.
ACS Appl Mater Interfaces. 2022 Aug 24;14(33):37652-37666. doi: 10.1021/acsami.2c06897. Epub 2022 Aug 12.
In recent years, transition metal oxides have been considered as the most promising anode materials due to their high theoretical capacity, low price, and abundant natural reserves. Among them, zinc manganate is used as an electrode material for anodes, whose application is mostly hindered due to its poor ionic/electronic conductivity. In this work, a series of ZnMnO (ZMO) are synthesized by a hydrothermal technique coordinated with a metal-organic framework-based high-temperature calcination process for their application as an anode in lithium-ion batteries (LIBs). Meanwhile, this study systematically explores the influence of carbon doping and the types of organic ligands and oxygen vacancies on the electrochemical properties of the synthesized ZMO. Density functional theory (DFT) calculations and experimental investigations reveal that the introduction of carbon and oxygen vacancies can enhance electronic conductivity, more active sites and faster Li adsorption, resulting in better electrochemical performances. As expected, all ZMOs with carbon doping (PMA-ZMO, MI-ZMO, and BDC-ZMO) derived from 1,2,4,5-benzenetetracarboxylic acid, 2-methylimidazole, and 1,4-dicarboxybenzene achieve outstanding electrochemical performance. Meanwhile, the introduction of oxygen vacancies can enhance the electronic conductivity and can significantly reduce the activation energy of Li transport, thereby accelerating the Li diffusion kinetics in the lithiation/delithiation process. Furthermore, an optimal ZMO anode material synthesized by 2-methylimidazole delivers a high reversible capacity of 1174.7 mA h g after 300 cycles at 0.1 A g and 600 mA h g at 0.5 A g after 300 cycles. After high-rate charge and discharge cycles, the specific capacity rapidly recovers to a value greater than the initial value, which proves the unusual activation and thereby an excellent rate property of the electrode. Hence, we conclude that ZMO provides potential application prospects as an anode electrode material for LIBs.
近年来,过渡金属氧化物因其高理论容量、低价格和丰富的天然储量而被认为是最有前途的负极材料。其中,锰酸锌用作负极的电极材料,但其应用大多因离子/电子导电性差而受阻。在本工作中,通过水热技术与基于金属有机框架的高温煅烧过程相结合,合成了一系列ZnMnO(ZMO),用于锂离子电池(LIBs)负极。同时,本研究系统地探讨了碳掺杂、有机配体类型和氧空位对合成的ZMO电化学性能的影响。密度泛函理论(DFT)计算和实验研究表明,碳和氧空位的引入可以提高电子导电性、增加更多活性位点并加快锂吸附,从而产生更好的电化学性能。正如预期的那样,所有由1,2,4,5-苯四甲酸、2-甲基咪唑和1,4-二羧基苯衍生的碳掺杂ZMO(PMA-ZMO、MI-ZMO和BDC-ZMO)都具有出色的电化学性能。同时,氧空位的引入可以提高电子导电性,并能显著降低锂传输的活化能,从而加速锂化/脱锂过程中的锂扩散动力学。此外,由2-甲基咪唑合成的最佳ZMO负极材料在0.1 A g下循环300次后可逆容量高达1174.7 mA h g,在0.5 A g下循环300次后为600 mA h g。经过高倍率充放电循环后,比容量迅速恢复到大于初始值的值,这证明了电极具有异常的活化作用,从而具有优异的倍率性能。因此,我们得出结论,ZMO作为LIBs的负极电极材料具有潜在的应用前景。