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探索四方钨青铜结构钒铌氧化物中的镁嵌入

Probing Mg Intercalation in the Tetragonal Tungsten Bronze Framework VNbO.

作者信息

Johnson Ian D, Nolis Gene, McColl Kit, Wu Yimin A, Thornton Daisy, Hu Linhua, Yoo Hyun Deog, Freeland John W, Corà Furio, Cockcroft Jeremy K, Parkin Ivan P, Klie Robert F, Cabana Jordi, Darr Jawwad A

机构信息

Department of Chemistry, University College London, 20 Gower Street, London WC1H 0AJ, U.K.

Department of Chemistry, University of Illinois at Chicago, Chicago, Illinois 60607, United States.

出版信息

Inorg Chem. 2020 Jul 20;59(14):9783-9797. doi: 10.1021/acs.inorgchem.0c01013. Epub 2020 Jul 7.

DOI:10.1021/acs.inorgchem.0c01013
PMID:32633981
Abstract

While commercial Li-ion batteries offer the highest energy densities of current rechargeable battery technologies, their energy storage limit has almost been achieved. Therefore, there is considerable interest in Mg batteries, which could offer increased energy densities in comparison to Li-ion batteries if a high-voltage electrode material, such as a transition-metal oxide, can be developed. However, there are currently very few oxide materials which have demonstrated reversible and efficient Mg insertion and extraction at high voltages; this is thought to be due to poor Mg diffusion kinetics within the oxide structural framework. Herein, the authors provide conclusive evidence of electrochemical insertion of Mg into the tetragonal tungsten bronze VNbO, with a maximum reversible electrochemical capacity of 75 mA h g, which corresponds to a magnesiated composition of MgVNbO. Experimental electrochemical magnesiation/demagnesiation revealed a large voltage hysteresis with charge/discharge (1.12 V vs Mg/Mg); when magnesiation is limited to a composition of MgVNbO, this hysteresis can be reduced to only 0.5 V. Hybrid-exchange density functional theory (DFT) calculations suggest that a limited number of Mg sites are accessible via low-energy diffusion pathways, but that larger kinetic barriers need to be overcome to access the entire structure. The reversible Mg intercalation involved concurrent V and Nb redox activity and changes in crystal structure, as confirmed by an array of complementary methods, including powder X-ray diffraction, X-ray absorption spectroscopy, and energy-dispersive X-ray spectroscopy. Consequently, it can be concluded that the tetragonal tungsten bronzes show promise as intercalation electrode materials for Mg batteries.

摘要

虽然商用锂离子电池在当前可充电电池技术中具有最高的能量密度,但其储能极限几乎已达到。因此,镁电池备受关注,如果能开发出一种高压电极材料,如过渡金属氧化物,镁电池相比锂离子电池可提供更高的能量密度。然而,目前很少有氧化物材料能在高电压下实现可逆且高效的镁嵌入和脱出;这被认为是由于镁在氧化物结构框架内的扩散动力学较差。在此,作者提供了镁电化学嵌入四方钨青铜VNbO的确凿证据,其最大可逆电化学容量为75 mA h g,对应于镁化组成MgVNbO。实验性的电化学镁化/脱镁化显示出充放电时较大的电压滞后(相对于Mg/Mg为1.12 V);当镁化限制在MgVNbO的组成时,这种滞后可降至仅0.5 V。杂化交换密度泛函理论(DFT)计算表明,通过低能量扩散路径可到达有限数量的镁位点,但要进入整个结构则需要克服更大的动力学障碍。一系列互补方法,包括粉末X射线衍射、X射线吸收光谱和能量色散X射线光谱证实,可逆的镁嵌入涉及V和Nb的同时氧化还原活性以及晶体结构的变化。因此,可以得出结论,四方钨青铜有望成为镁电池的嵌入电极材料。

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