Lithium-oxygen(Li-O_(2))battery is favored among“beyond lithiumion”technologies for sustainability because of its exceptional energy density.Major impediments are the poor cycle stability and grievous capacity degra...Lithium-oxygen(Li-O_(2))battery is favored among“beyond lithiumion”technologies for sustainability because of its exceptional energy density.Major impediments are the poor cycle stability and grievous capacity degradation at high current densities.We address these issues by a“killing two birds with one stone”O_(2)-pressure protocol.It first resolves efficient O_(2) mass transport at high rates..The accelerated reaction kinetics optimizes the composition and growth pathway of discharge products.This protocol secondly achieves protection of Li anodes via densifying corrosion layers on them.Consequently,the battery delivers both ultrahigh discharge capacity(>9,000 mAh g^(-1))at 3,000 mA g^(-1) and excellent cycling stability.Under a dual-strategy effect of high-pressure O_(2) and artificial protection layers,the battery actualizes over 11-fold increase in cycle life of 5,170 h(2,585 cycles).The strategy opens avenues for advancing Li-O_(2) batteries towards practical application and confers the extension to other gas-based batteries.展开更多
Pore structure of hard carbon has a fundamental influence on the electrochemical properties in sodium-ion batteries(SIBs).Ultra-micropores(<0.5 nm)of hard carbon can function as ionic sieves to reduce the diffusion...Pore structure of hard carbon has a fundamental influence on the electrochemical properties in sodium-ion batteries(SIBs).Ultra-micropores(<0.5 nm)of hard carbon can function as ionic sieves to reduce the diffusion of slovated Na+but allow the entrance of naked Na^(+) into the pores,which can reduce the interficial contact between the electrolyte and the inner pores without sacrificing the fast diffusion kinetics.Herein,a molten diffusion-carbonization method is proposed to transform the micropores(>1 nm)inside carbon into ultra-micropores(<0.5 nm).Consequently,the designed carbon anode displays an enhanced capacity of 346 mAh g^(−1) at 30 mA g^(−1) with a high ICE value of~80.6%and most of the capacity(~90%)is below 1 V.Moreover,the high-loading electrode(~19 mg cm^(−2))exhibits a good temperature endurance with a high areal capacity of 6.14 mAh cm^(−2) at 25℃ and 5.32 mAh cm^(−2) at −20℃.Based on the in situ X-ray diffraction and ex situ solid-state nuclear magnetic resonance results,the designed ultra-micropores provide the extra Na+storage sites,which mainly contributes to the enhanced capacity.This proposed strategy shows a good potential for the development of high-performance SIBs.展开更多
基金support from the Major basic research project of Natural Science Foundation of Shandong Province(No.ZR2023ZD12)Singapore National Research Foundation Investigatorship(No.NRFNRFI08-2022-0009)NUS R&G Postdoc Fellowship Program.
文摘Lithium-oxygen(Li-O_(2))battery is favored among“beyond lithiumion”technologies for sustainability because of its exceptional energy density.Major impediments are the poor cycle stability and grievous capacity degradation at high current densities.We address these issues by a“killing two birds with one stone”O_(2)-pressure protocol.It first resolves efficient O_(2) mass transport at high rates..The accelerated reaction kinetics optimizes the composition and growth pathway of discharge products.This protocol secondly achieves protection of Li anodes via densifying corrosion layers on them.Consequently,the battery delivers both ultrahigh discharge capacity(>9,000 mAh g^(-1))at 3,000 mA g^(-1) and excellent cycling stability.Under a dual-strategy effect of high-pressure O_(2) and artificial protection layers,the battery actualizes over 11-fold increase in cycle life of 5,170 h(2,585 cycles).The strategy opens avenues for advancing Li-O_(2) batteries towards practical application and confers the extension to other gas-based batteries.
基金Singapore MOE Tier Ⅱ grant R143-000-A29-112the National Research Foundation under the Grant of NRF2017NRF-NSFC001-007.
文摘Pore structure of hard carbon has a fundamental influence on the electrochemical properties in sodium-ion batteries(SIBs).Ultra-micropores(<0.5 nm)of hard carbon can function as ionic sieves to reduce the diffusion of slovated Na+but allow the entrance of naked Na^(+) into the pores,which can reduce the interficial contact between the electrolyte and the inner pores without sacrificing the fast diffusion kinetics.Herein,a molten diffusion-carbonization method is proposed to transform the micropores(>1 nm)inside carbon into ultra-micropores(<0.5 nm).Consequently,the designed carbon anode displays an enhanced capacity of 346 mAh g^(−1) at 30 mA g^(−1) with a high ICE value of~80.6%and most of the capacity(~90%)is below 1 V.Moreover,the high-loading electrode(~19 mg cm^(−2))exhibits a good temperature endurance with a high areal capacity of 6.14 mAh cm^(−2) at 25℃ and 5.32 mAh cm^(−2) at −20℃.Based on the in situ X-ray diffraction and ex situ solid-state nuclear magnetic resonance results,the designed ultra-micropores provide the extra Na+storage sites,which mainly contributes to the enhanced capacity.This proposed strategy shows a good potential for the development of high-performance SIBs.
