Source abstract
Abstract
Rechargeable sodium batteries (RSBs) are pivotal for fulfilling the energy requirements of large-scale grid storage. Organic-ether-based electrolytes still suffer from poor antioxidation stability against the cathode materials. Here we introduce an “ionic diluent”, N -butyl- N -methyl-piperidinium bis(trifluoromethyl)imide (PP 14 TFSI), into the ether-based electrolyte to stimulate the formation of an “anion-enriched” Na + solvation sheath via creating an anion-rich ( c anion / c Na + > 1) environment. The tailored solvation structure endows the modified electrolyte with an improved oxidation potential (>4.8 V vs Na + /Na) while maintaining an ionic conductivity of 4.12 mS cm –1 at 30 °C. Both Na 3 V 2 (PO 4 ) 2 F 3 (NVPF)-based and NaNi 1/3 Fe 1/3 Mn 1/3 O 2 (NFM)-based RSBs demonstrate enhanced interfacial stability, achieving 94.4% capacity retention after 1000 cycles (4.3 V) and 83.5 mAh g –1 after 250 cycles at 1C (4.2 V), respectively. The impressive performances of NVPF||Hard carbon full cell further indicate the practical applicability of the designed electrolyte and provides insights into the rational design of RSBs via electrolyte engineering.
Source: openalex_inverted_index · Quality: baseline
Affiliations
School of Chemical Engineering, Ocean and Life Science
Dalian University of Technology
CAS Key Laboratory of Molecular Nanostructure and Nanotechnology, CAS Research/Education Center for Excellence in Molecular Sciences, Beijing National Laboratory for Molecular Sciences (BNLMS)
Institute of Chemistry, Chinese Academy of Sciences (CAS)
State Key Laboratory of Integrated Optoelectronics, MOE Key Laboratory for UV Light-Emitting Materials and Technology
Northeast Normal University
Funding
National Natural Science Foundation of China