Source abstract
Abstract
Rechargeable sodium–chlorine (Na–Cl 2 ) batteries have attracted attention for next-generation energy storage. However, their application is hindered by poor cycling stability, primarily caused by sluggish reaction kinetics and uneven NaCl nucleation. Herein, we prepared a series of polarized metal organic frameworks (MOFs) and verified that polar groups anchored on the penetrated porous skeletons can act as confined nanoreactors, enhancing the Cl – /Na + adsorption capability and simultaneously repulsing the formed Cl 2, finally boosting the uniform deposition/exfoliation of NaCl nanocrystals and reversible reaction between NaCl and Cl 2 . The Na–Cl 2 @UiO-66-SO 3 H battery demonstrates a polarization of 0.27 V, along with cycling for 600 cycles at 10,000 mA g –1, and even operates at a current density of 20,000 mA g –1 . Moreover, this sodium–chlorine battery shows performance at low temperature, increased areal capacity, and capacity scaling in large-format pouch cells.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Thermal Expansion and Ionic Conductivity · Advancements in Battery Materials · Advanced battery technologies research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Chemistry and Materials, Yangzhou Key Laboratory of Smart Materials and Clean Energy, Interdisciplinary Research Center for Advanced Energy
Yangzhou University
Canadian Light Source Inc.
University of Saskatchewan
Zhejiang Key Laboratory for Industrial Solid Waste Thermal Hydrolysis Technology and Intelligent Equipment, Huzhou Key Laboratory of Environmental Functional Materials and Pollution Control, Department of Materials Engineering
Huzhou University
Funding
Basic Research Program of Jiangsu Province · National Natural Science Foundation of China · Yangzhou Innovation Capability Enhancement Fund/program
References (43)
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