Aqueous batteries have been considered as the most promising alternatives to the dominant lithium-based battery technologies because of their low cost, abundant resources and high safety. The output voltage of aqueous batteries is limited by the narrow stable voltage window of 1.23 V for water, which theoretically impedes further improvement of their energy density. However, the pH-decoupling electrolyte with an acidic catholyte and an alkaline anolyte has been verified to broaden the operating voltage window of the aqueous electrolyte to over 3 V, which goes beyond the voltage limitations of the aqueous batteries, making high-energy aqueous batteries possible. In this Review, we summarize the latest decoupled aqueous batteries based on pH-decoupling electrolytes from the perspective of ion-selective membranes, competitive redox couples and potential battery prototypes. The inherent defects and problems of these decoupled aqueous batteries are systematically analysed, and the critical scientific issues of this battery technology for future applications are discussed.
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http://dx.doi.org/10.1038/s41570-022-00397-3 | DOI Listing |
Green Chem
December 2024
KU Leuven, Department of Chemistry Celestijnenlaan 200F P.O. box 2404 B-3001 Leuven Belgium
In order to comply with the expected tightening of discharge limits for lithium to surface waters, the lithium-ion battery industry will need access to methods to reduce the concentration of lithium in wastewater down to ppm levels. In this Communication, we discuss the possibility of using sodium and choline soaps as precipitating agents for lithium, comparing the two soap classes and probing the influence of the carbon chain length. It was found that lithium concentrations down to 10 ppm can be reached with sodium stearate, and down to 1 ppm with choline stearate, using a slight excess of the precipitating agent.
View Article and Find Full Text PDFAdv Mater
January 2025
College of Energy, Key Laboratory of Core Technology of High Specific Energy Battery and Key Materials for Petroleum and Chemical Industry, Soochow University, Suzhou, 215006, China.
Coupling ion exclusion and interaction screening within sub-nanoconfinement channels in novel porous material membranes hold great potential to realize highly efficient ion sieving, particularly for high-performance lithium-ion extraction. Diverse kinds of advanced membranes have been previously reported to realize this goal but with moderate performance and complex operations gained. Herein, these issues are circumvented by preparing the consecutive and intact imine-linked three-dimensional covalent organic framework (i.
View Article and Find Full Text PDFSmall
January 2025
Research Institute for Sustainable Energy (RISE), TCG-CREST, Salt Lake, Kolkata, 700091, India.
Advancing next-generation battery technologies requires a thorough understanding of the intricate phenomena occurring at anodic interfaces. This focused review explores key interfacial processes, examining their thermodynamics and consequences in ion transport and charge transfer kinetics. It begins with a discussion on the formation of the electro chemical double layer, based on the GuoyChapman model, and explores how charge carriers achieve equilibrium at the interface.
View Article and Find Full Text PDFNature
January 2025
School of Environment and Energy, State Key Laboratory of Luminescent Materials and Devices, Guangdong Provincial Key Laboratory of Atmospheric Environment and Pollution Control, South China University of Technology, Guangzhou, China.
Lithium (Li) metal batteries (LMBs) are promising for high-energy-density rechargeable batteries. However, Li dendrites formed by the reaction between highly active Li and non-aqueous electrolytes lead to safety concerns and rapid capacity decay. Developing a reliable solid-electrolyte interphase is critical for realizing high-rate and long-life LMBs, but remains technically challenging.
View Article and Find Full Text PDFChem Asian J
January 2025
Indian Institute of Science, Inorganic and Physical Chemistry, INDIA.
The growing energy demands have led to an increased attention towards the development of efficient energy storage devices. In this direction, aqueous rechargeable batteries have attracted considerable attention due to their affordability, environmental friendliness and quite importantly, safety. In the present studies, a two-dimensional copolymer of benzoquinone and pyrrole that is insoluble in aqueous solutions is explored as an electrode for aqueous, rechargeable divalent ion storage.
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