Sodium decavanadate encapsulated Mn-BTC POM@MOF as high-capacity cathode material for aqueous sodium-ion batteries

被引:21
作者
Ullah, Irfan [1 ]
ul Haq, Tanveer [2 ,3 ]
Khan, Aqeel Aslam [1 ]
Inayat, Abid [4 ]
Shoaib, Muhammad [1 ,5 ]
Haider, Ali [4 ]
Saleem, Murtaza [1 ]
Abbas, Syed Mustansar [6 ]
Pope, Michael A. [7 ]
Hussain, Irshad [1 ]
机构
[1] Lahore Univ Management Sci, SBA Sch Sci & Engn, Dept Chem & Chem Engn, Lahore 54792, Pakistan
[2] Texas A&M Univ, Frank H Dotterweich Coll Engn, Sustainable Energy Engn, Kingsville, TX 78363 USA
[3] Univ Sharjah, Coll Sci, Dept Chem, POB 27272, Sharjah, U Arab Emirates
[4] Quaid I Azam Univ, Dept Chem, Islamabad 45320, Pakistan
[5] Univ Calgary, Dept Chem, 2500 Univ Dr NW, Calgary, AB T2N 1N4, Canada
[6] Natl Ctr Phys, Nanosci & Technol Dept, QAU Campus Islamabad, Islamabad, Pakistan
[7] Univ Waterloo, Quantum Nano Ctr, Dept Chem Engn, Waterloo, ON N2L 3G1, Canada
关键词
Polyoxometallates (POMs); Metal organic frameworks (MOFs); High capacity cathode materials; Aqueous sodium ion batteries; METAL-ORGANIC FRAMEWORK; HIGH-PERFORMANCE CATHODE; ANODE MATERIALS; POLYOXOMETALATE; INTERCALATION; NA3V2(PO4)(3); CLUSTER;
D O I
10.1016/j.jallcom.2022.167647
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Aqueous sodium-ion batteries are the promising candidates for large scale energy storage applications owing to their cost effectiveness and environmental safety. However, the development of a stable cathode material with high capacity is still a challenging task for the commercial viability of aqueous electrolyte -based sodium-ion batteries. This work demonstrates the development of a hierarchically nanostructured high-capacity cathode material by encapsulating sodium decavanadate Na6V10O28 (NaDV) in the scaffold of manganese-based metal-organic framework Mn-BTC (where BTC is 1,3,5-benzenetricarboxylic acid) by an in situ synthesis. The uniform distribution of NaDV in the pores of Mn-BTC enables the multielectron redox properties of NaDV whereas the diverse 3D diffusion channels, high surface area, and flexible architecture of Mn-BTC ensure high intercalation capacity by suppressing the agglomeration and providing faster ionic diffusion kinetics in the NaDV@Mn-BTC nano-hybrid cathode material. The Mn-BTC framework not only ensures the stabilization of NaDV but also enhances sodium storage capacity by the involvement of Mn in the redox process. The NaDV@Mn-BTC cathode material exhibits high reversible capacity of 137 mAh/g at 1 C rate. High capacity of this cathode material suggests that the development of these nano-hybrid materials is a feasible approach to design high energy cathode materials for aqueous batteries (C) 2022 Elsevier B.V. All rights reserved.
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页数:8
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