Selenium Impregnated Monolithic Carbons as Free-Standing Cathodes for High Volumetric Energy Lithium and Sodium Metal Batteries

被引:137
作者
Ding, Jia [1 ]
Zhou, Hui [1 ]
Zhang, Hanlei [1 ]
Tong, Linyue [1 ]
Mitlin, David [2 ]
机构
[1] SUNY Binghamton, Chem & Mat, Binghamton, NY 13902 USA
[2] Clarkson Univ, Chem & Biomol Engn & Mech Engn, Potsdam, NY 13699 USA
关键词
lithium selenium batteries; mesoporous carbon; polyselenide; sodium selenium batteries; volumetric energy; POLARIZED RAMAN; RATE CAPABILITY; COMPOSITE; SE; PERFORMANCE; SULFUR; STORAGE; CAPACITY; CHALLENGES; ORIGIN;
D O I
10.1002/aenm.201701918
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
Energy density (energy per volume) is a key consideration for portable, automotive, and stationary battery applications. Selenium (Se) lithium and sodium metal cathodes are created that are monolithic and free-standing, and with record Se loading of 70 wt%. The carbon host is derived from nanocellulose, an abundant and sustainable forestry product. The composite is extremely dense (2.37 g cm(-3)), enabling theoretical volumetric capacity of 1120 mA h cm(-3). Such architecture is fully distinct from previous Se-carbon nano- or micropowders, intrinsically offering up to 2x higher energy density. For Li storage, the cathode delivers reversible capacity of 1028 mA h cm(-3) (620 mA h g(-1)) and 82% retention over 300 cycles. For Na storage, 848 mA h cm(-3) (511 mA h g(-1)) is obtained with 98% retention after 150 cycles. The electrodes yield superb volumetric energy densities, being 1727 W h L-1 for Li-Se and 980 W h L-1 for Na-Se normalized by total composite mass and volume. Despite the low surface area, over 60% capacity is maintained as the current density is increased from 0.1 to 2 C (30 min charge) with Li or Na. Remarkably, the electrochemical kinetics with Li and Na are comparable, including the transition from interfacial to diffusional control.
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页数:10
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