Molecular Regulation on Carbonyl-Based Organic Cathodes: Toward High-Rate and Long-Lifespan Potassium–Organic Batteries
Source abstract
Abstract
Organic redox-active molecules have been identified as promising cathodes for practical usage of potassium-ion batteries (PIBs) but still struggle with serious dissolution problems and sluggish kinetic properties. Herein, we propose a pseudocapacitance-dominated novel insoluble carbonyl-based cathode, [2,6-di[1-(perylene-3,4,9,10-tetracarboxydiimide)]anthraquinone, AQ–diPTCDI], which possesses high reversible capacities of 150 mAh g–1, excellent cycle stability with capacity retention of 88% over 2000 cycles, and fast kinetic properties. The strong intermolecular interactions of AQ–diPTCDI and in situ formed cathode electrolyte interphase films support it against the dissolution problem. The high capacitive-like contribution in capacities and fast potassium-ion diffusion enhance its reaction kinetics. Moreover, a symmetric organic potassium-ion battery (OPIB) based on AQ–diPTCDI electrodes also exhibits outstanding K-storage capability. These results suggest that AQ–diPTCDI is a promising organic cathode for OPIBs and provide a practicable route to realize high-performance K storage.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Advanced battery technologies research · Advanced Battery Materials and Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Chemistry, Chemical Engineering and Life Science, Wuhan University of Technology, 122 Luoshi Road, Wuhan, Hubei 430070, People’s Republic of China
State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Center of Smart Materials and Devices, Wuhan University of Technology, 122 Luoshi Road, Wuhan, Hubei 430070, People’s Republic of China
Funding
China Postdoctoral Science Foundation · National Natural Science Foundation of China · Hubei Province
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