Silicon oxide-coated lithium aluminum layered double hydroxide (Li Al -LDH@SiO ) nanocrystals (NCs) are investigated to selectively separate lithium cations in aqueous lithium resources. We directly synthesized Li Al -LDH NC arrays by oxidation of aluminum foil substrate under a urea and lithium solution. Various lithium salts, including Cl , CO , NO , and SO , were applied in aqueous solution to confirm the anion effect on the captured and released lithium quantity of the Li Al -LDH NCs. In a 5% solution of sulfate ions mix with lithium chloride, the Li Al -LDH NCs separated a larger quantity of lithium than in other anion conditions. To enhance regeneration stability and lithium selectivity, thin layers of SiO were coated onto the Li Al -LDH nanostructure arrays for inhibition of nanostructure destruction after desorption of lithium cations in hot water. The Li Al -LDH@SiO nanostructures showed enhanced properties for lithium adsorption, including increase of stable regeneration cycles from three to five cycles, and they showed high lithium selectivity in the Mg , Na , and K cation mixed aqueous resource. Our nanostructured LDH lithium adsorbents would provide a facile and efficient application for cost-efficient and large-scale lithium production.
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http://dx.doi.org/10.1002/asia.202100126 | DOI Listing |
Nanomicro Lett
January 2025
Department of Chemical and Biomolecular Engineering, Yonsei University, 50 Yonsei-Ro, Seodaemun-Gu, Seoul, 03722, Republic of Korea.
Amidst the ever-growing interest in high-mass-loading Li battery electrodes, a persistent challenge has been the insufficient continuity of their ion/electron conduction pathways. Here, we propose cellulose elementary fibrils (CEFs) as a class of deagglomerated binder for high-mass-loading electrodes. Derived from natural wood, CEF represents the most fundamental unit of cellulose with nanoscale diameter.
View Article and Find Full Text PDFNano Lett
January 2025
College of Chemistry and Materials Science, Hebei University, Baoding 071002, Hebei, P. R. China.
Ultrahigh nickel cathode materials are widely utilized due to their outstanding energy and power densities. However, the presence of cobalt can cause significant lattice distortion during charge and discharge cycles, leading to the loss of active lithium, the formation of lattice cracks, and the emergence of a rock salt phase that hinders lithium-ion transport. Herein, we developed a novel cobalt-free, aluminum-doped cathode material, LiNiMnAlO (NMA), which effectively delays the harmful H2-H3 phase transition, reduces lattice distortion, alleviates stress release, and significantly enhances structural stability.
View Article and Find Full Text PDFOncotarget
January 2025
Department of Orthopedics, The First Affiliated Hospital of Soochow University, Suzhou, China.
Nano Lett
January 2025
Frontiers Science Center for Transformative Molecules, School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240, China.
Lithium nitrate (LiNO) stands as an effective electrolyte additive, mitigating the degradation of Li metal anodes by forming a LiN-rich solid electrolyte interphase (SEI). However, its conversion kinetics are impeded by energy-consuming eight-electron transfer reactions. Herein, an isoreticular metal-organic framework-8-derived carbon is incorporated into the carbon cloth (RMCC) as a catalytic current collector to regulate the LiNO conversion kinetics and boost LiN generation inside the SEI.
View Article and Find Full Text PDFNanoscale
January 2025
Advanced Batteries Research Center, Korea Electronics Technology Institute, 25, Saenari-ro, Seongnam-si, 13509, Republic of Korea.
The SiO electrode interface is passivated with a SiO layer, which hinders the deposition of an inorganic solid electrolyte interphase (SEI) due to its high surface work function and low exchange current density of electrolyte decomposition. Consequently, a thermally vulnerable, organic-based SEI formed on the SiO electrode, leading to poor cycling performance at elevated temperatures. To address this issue, the SEI formation process is thermoelectrochemically activated.
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