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Confining Li^(+)Solvation in Core-Shell Metal-Organic Frameworks for Stable Lithium Metal Batteries at 100℃
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作者 Minh Hai Nguyen Jeongmin Shin +3 位作者 mee-ree kim Quan Van Nguyen JinHyeok Cha Sangbaek Park 《Nano-Micro Letters》 2026年第4期718-734,共17页
The practical deployment of lithium metal batteries remains severely constrained,especially under elevated temperatures.Although metal-organic frameworks(MOFs)improve the thermal stability of liquid electrolytes by ca... The practical deployment of lithium metal batteries remains severely constrained,especially under elevated temperatures.Although metal-organic frameworks(MOFs)improve the thermal stability of liquid electrolytes by capturing them in well-ordered sub-nanopores,interparticle voids between MOF particles readily absorb liquid electrolyte,obscuring our understanding of the intrinsic role of nanopores in directing Li^(+)transport.To address this challenge,we introduce a one-dimensional(1D)MOF model architecture that eliminates interparticle effects and enables direct observation of Li^(+)solvation and de-solvation dynamics.Comparative studies of 1D HKUST-1 and ZIF-8 uncover distinct transport behaviors,supported by both experimental measurements and neural network potential-based molecular dynamics simulations.Building on these insights,we construct a hierarchical core-shell MOF architecture by integrating ZIF-8(core)and HKUST-1(shell)onto a hybrid fiber scaffold.This design harnesses the complementary strengths of both MOFs to achieve continuous ion pathways,directional Li^(+)conduction,and improved thermal and electrochemical resilience. 展开更多
关键词 Quasi-solid-state electrolyte Metal-organic frameworks Li metal batteries Thermal stability Lithium-ion solvation/de-solvation
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