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High‐Energy Density Li‐Ion Capacitor with Layered SnS 2 /Reduced Graphene Oxide Anode and BCN Nanosheet Cathode
Author(s) -
Hao Yizhan,
Wang Shouzhi,
Shao Yongliang,
Wu Yongzhong,
Miao Shiding
Publication year - 2020
Publication title -
advanced energy materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.08
H-Index - 220
eISSN - 1614-6840
pISSN - 1614-6832
DOI - 10.1002/aenm.201902836
Subject(s) - materials science , nanosheet , anode , graphene , electrode , cathode , oxide , capacitor , power density , chemical engineering , nanotechnology , optoelectronics , voltage , electrical engineering , power (physics) , metallurgy , chemistry , physics , engineering , quantum mechanics
Abstract Lithium‐ion capacitors (LICs) with capacitor‐type cathodes and battery‐type anodes are considered a promising next‐generation advanced energy storages system that meet the requirements of high energy density and power density. However, the mismatch of charge‐storage capacity and electrode kinetics between positive and negative electrodes remains a challenge. Herein, layered SnS 2 /reduced graphene oxide (RGO) nanocomposites are developed for negative electrodes and a 2D B/N codoped carbon (BCN) nanosheet is designed for the positive electrode. The SnS 2 /RGO derived from SnS 2 ‐bonded RGO of high conductivity exhibits a capacity of 1198 mA h g −1 at 100 mA g −1 . Boron and nitrogen atoms in BCN are found to promote adsorption of anions, which enhance the pseudocapacitive contribution as well as expanding the voltage of LICs. A quantitative kinetics analysis indicates that the SnS 2 /RGO electrodes with a dominating capacitive mechanism and a diminished intercalation process, benefit the kinetic balance between the two electrodes. With this particular structure, the LIC is able to operate at the highest operating voltage for these devices recorded to date (4.5 V), exhibiting an energy density of 149.5 W h kg −1 , a power density of 35 kW kg −1 , and a capacity retention ratio of 90% after 10 000 cycles.