Calcium-metal batteries (CMBs) provide a promising option for high-energy and cost-effective energy-storage technology beyond the current state-of-the-art lithium-ion batteries. Nevertheless, the development of room-temperature CMBs is significantly impeded by the poor reversibility and short lifespan of the calcium-metal anode. A solvation manipulation strategy is reported to improve the plating/stripping reversibility of calcium-metal anodes by enhancing the desolvation kinetics of calcium ions in the electrolyte. The introduction of lithium salt changes the electrolyte structure considerably by reducing coordination number of calcium ions in the first solvation shell. As a result, an unprecedented Coulombic efficiency of up to 99.1 % is achieved for galvanostatic plating/stripping of the calcium-metal anode, accompanied by a very stable long-term cycling performance over 200 cycles at room temperature. This work may open up new opportunities for development of practical CMBs.
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http://dx.doi.org/10.1002/anie.202002274 | DOI Listing |
ACS Appl Mater Interfaces
December 2024
Department of Chemistry and Materials Science, College of Science, Nanjing Forestry University, Nanjing 210037, P. R. China.
Covalent-organic-framework (COF) materials with a designable periodic framework have been expected as a kind of promising anode material for potassium ion batteries (PIBs). However, these materials suffer seriously from low capacity, poor rate performance, and slow reaction kinetics during the K-storage process, significantly limiting their widespread applications. Herein, a three-dimensional (3D) COF material denoted as CN-COF with a high N content and defined configuration as well as a graphite-like layer stacking structure was developed as a promising anode to realize efficient 3D K-storage performance with enhanced interfacial stability and reaction kinetics via an electrolyte chemistry compatibility strategy.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
State Key Laboratory of Reliability and Intelligence of Electrical Equipment, School of Materials Science and Engineering, Hebei University of Technology, Tianjin, 300401, China.
J Colloid Interface Sci
November 2024
State Key Laboratory of Powder Metallurgy, Central South University, Changsha 410083, PR China.
Angew Chem Int Ed Engl
November 2024
Guangdong Provincial Key Laboratory of Fuel Cell Technology, School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou, 510641, P.R. China.
Organic molecule in solutions is the energy storage unit in the organic redox flow batteries (ORFBs), of which the aggregation is acknowledged pivotal but has been rarely investigated. By establishing a pyridinium library, the manipulation over the aggregation in solutions is investigated at the molecular level. Both theoretical calculations and physiochemical methods are used to characterize the aggregate's structure, and salient findings are as follows.
View Article and Find Full Text PDFJ Colloid Interface Sci
February 2025
Jilin Provincial Key Laboratory of Organic Functional Molecular Design & Synthesis, Faculty of Chemistry, Northeast Normal University, Changchun 130024, PR China. Electronic address:
The practical application of aqueous Zn metal batteries (AZMBs) is impeded by inferior reversibility and stability of Zn metal anode (ZMA) originated from side reactions and dendrite growth. Herein, anion receptor l-Proline (LP) is selected to simultaneously manipulate solvation chemistry and electric double layer (EDL) for constructing dendrite-free and stable AZMBs with an ultra-high depth of discharge (DOD of 100 %) and low negative/positive capacity ratio (N/P of 1.1).
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