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Lithium metal is an ideal anode material due to its high specific capacity and low redox potential. However, issues such as dendritic growth and low Coulombic efficiency prevent its application in secondary lithium batteries. The use of three-dimensional (3D) porous current collector is an effective strategy to solve these problems. Herein, commercial carbon nanotube (CNT) sponge is used as a 3D current collector for dendrite-free lithium metal deposition to improve the Coulombic efficiency and the cycle stability of the lithium metal batteries. The high specific surface area of the CNT increases the density of the lithium nucleation sites and ensures the uniform lithium deposition while the "pre-lithiation" behavior of the porous CNT enhances its affinity with the deposited lithium. Meanwhile, the lithium plating/stripping on the sponge maintains high Coulombic efficiency and high cycling stability due to the robust structure of graphitic-amorphous carbon composite in the ether-based electrolyte. Our findings exhibit the feasibility of using CNT sponge as a 3D porous current collector for lithium deposition. They shed light on designing and developing advanced current collectors for the lithium metal electrode and will promote the commercialization of the secondary lithium batteries.
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http://dx.doi.org/10.1021/acs.nanolett.8b04376 | DOI Listing |
Angew Chem Int Ed Engl
March 2025
Wuhan University of Technology, State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, 122 Luoshi Road, 430070, Wuhan, CHINA.
Solid-state polymer electrolytes (SPEs) with high ionic conductivity, a wide voltage window, and an ultra-stability electrolyte/electrode interface are essential for practical applications of solid lithium-metal batteries but particularly challenging. The key to overcoming these long-term obstacles lies in the rational design of the Li+ solvation-desolvation behavior in SPEs. Herein, we propose an electric-dipole coupling ion-dipole strategy to modulate the Li+ solvation structure and enhance Li+ desolvation kinetics.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
March 2025
Xiamen University, College of Materials, CHINA.
The continuous rupture and rebuilding of unstable solid electrolyte interphase layer during cycling would block Na+ diffusion and induce Na dendrite formation, ultimately limiting the practical application of high-energy-density sodium metal batteries. Herein, a hybrid SEI layer containing Li-species is dexterously constructed on the surface of sodium metal anode. Li-containing inorganic components (Li3N, LiF and Li2CO3) are introduced to stabilize the Na/electrolyte interface and enhance the mechanical and diffusion kinetic properties of the SEI layer, which can reduce the side reactions and gas generation, regulate Na+ flux during cycling and promote rapid Na+ migration for uniform dendrite-free Na deposition.
View Article and Find Full Text PDFJ Colloid Interface Sci
March 2025
State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing 100029, China. Electronic address:
Leveraging abundant natural reserves and lower cost profiles, sodium-ion batteries (SIBs) are poised to supersede lithium-ion batteries (LIBs) within the domain of large-scale energy storage systems. Many achievements have been made in improving the properties of anodes in SIBs from the aspects of nanostructure and surface modification. Recently, the incorporation of anionic species into metal sulfides via defect engineering has emerged as an innovative strategy to boost sodium storage capabilities.
View Article and Find Full Text PDFJ Colloid Interface Sci
March 2025
Guangxi Key Laboratory of Low Carbon Energy Materials, Guangxi New Energy Ship Battery Engineering Technology Research Center, Guangxi Scientific and Technological Achievements Transformation Pilot Research Base of Electrochemical Energy Materials and Devices, School of Chemistry and Pharmaceutical Sciences, Guangxi Normal University, Guilin 541004 Guangxi, China. Electronic address:
Lithium metal batteries (LMBs) employing high-voltage cathode present a promising pathway toward high-energy-density energy storage systems. However, critical challenges have hindered their practical application, including lithium dendrite proliferation, unstable solid-electrolyte interphase (SEI), and limited oxidative stability of conventional 1,2-dimethoxyethane (DME)-based electrolytes. Herein, we rationally design a siloxane-based electrolyte system featuring enhanced oxidative stability through solvent molecular engineering.
View Article and Find Full Text PDFACS Nano
March 2025
State Key Laboratory of Precision Welding & Joining of Materials and Structures, School of Materials Science and Engineering, Harbin Institute of Technology (Shenzhen), Shenzhen 518055, China.
Lithium-oxygen batteries (LOBs), with an extremely high theoretical energy density (3500 Wh kg), have been regarded as potential candidates for future large-scale energy storage facilities. However, the unique semiopen system puts a hurdle on the long-lasting operation of LOBs with critical issues like the severe volatilization of the aprotic electrolyte, surface passivation or dendrite growth of the lithium metal anode, and the sluggish oxygen redox reactions. Herein, we propose a strategy to tackle the above issues with a solvation structure regulated deep eutectic electrolyte (DEE) for LOBs.
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