Anion Intercalation/De-Intercalation Mechanism Enabling High Energy and Power Densities of Lithium-Ion Capacitors

Author:

Zhang Yang1ORCID,Lao Junquan1ORCID,Xiao Ping1

Affiliation:

1. Department of Materials, Henry Royce Institute, University of Manchester, Manchester M13 9PL, UK

Abstract

The growing demands for electrochemical energy storage systems is driving the exploration of novel devices, with lithium-ion capacitors (LICs) emerging as a promising strategy to achieve both high energy density and fast charge capability. However, the low capacitance of commercial activated carbon (AC) cathode based on anion absorption/desorption limits LIC applications. Herein, commercial graphite is proposed as the cathode to construct an innovative AC (−)//graphite (+) system. The graphite cathode functions as anion hosting, allowing reversible intercalation/de-intercalation of anions into/from its interlayers. The as-designed AC (−)//graphite (+) full cell achieves stable cycling with 90.6% capacity retention after 200 cycles at 0.1 A g−1 and a prolonged lifespan with 87.5% capacity retention after 5000 cycles at 0.5 A g−1 with the upper cut-off voltage of 5.0 V, yielding a high average Coulombic efficiency (CE) of 99.3%. Moreover, the full cell exhibits a high energy density (>200 Wh kg−1) and power density of 7.7 kW kg−1 (calculated based on active mass in both electrodes). These performances exceed most LICs based on anions absorption/desorption on the surface of AC cathodes. This work explores an effective electrode revolution with the assistance of anion intercalation/de-intercalation chemistry for developing novel LICs with high energy and power densities.

Funder

China Scholarship Council/University of Manchester award

Royal Academy of Engineering and Rolls-Royce for appointment of the Rolls-Royce/Royal Academy of Engineering Research Chair in Advanced Coating Technology

Publisher

MDPI AG

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