We synthesize a series of Mn substituted （Li, Fe）OHFeSe superconductor single crystals via a modified ion-exchange method, with the Mn concentration z （the atomic ratio of Mn：Se） ranging from 0 to 0.07. The distr...We synthesize a series of Mn substituted （Li, Fe）OHFeSe superconductor single crystals via a modified ion-exchange method, with the Mn concentration z （the atomic ratio of Mn：Se） ranging from 0 to 0.07. The distribution homogeneity of the Mn element incorporated into the lattice of （Li, Fe）OHFeSe is checked by combined measurements of high-angle- annular-dark-field （HAADF） imaging and electron energy-loss spectroscopy （EELS）. Interestingly, we find that the superconducting transition temperature Tc and unit cell parameter c of the Mn-doped （Li, Fe）OHFeSe samples display similar V-shaped evolutions with the increasing dopant concentration z. We propose that, with increasing doping level, the Mn dopant first occupies the tetrahedral sites in the （Li, Fe）OH layers before starting to substitute the Fe element in the su- perconducting FeSe layers, which accounts for the V-shaped change in cell parameter c. The observed positive correlation between the Tc and lattice parameter c, regardless of the Mn doping level z, indicates that a larger interlayer separation, or a weaker interlayer coupling, is essential for the high-Tc superconductivity in （Li, Fe）OHFeSe. This agrees with our previous observations on powder, single crystal, and film samples of （Li, Fe）OHFeSe superconductors.展开更多
Lithium-sulfur(Li-S)batteries,although a promising candidate of next-generation energy storage devices,are hindered by some bottlenecks in their roadmap toward commercialization.The key challenges include solving the ...Lithium-sulfur(Li-S)batteries,although a promising candidate of next-generation energy storage devices,are hindered by some bottlenecks in their roadmap toward commercialization.The key challenges include solving the issues such as low utilization of active materials,poor cyclic stability,poor rate performance,and unsatisfactory Coulombic efficiency due to the inherent poor electrical and ionic conductivity of sulfur and its discharged products(e.g.,Li2S2 and Li_(2)S),dissolution and migration of polysulfide ions in the electrolyte,unstable solid electrolyte interphase and dendritic growth on an odes,and volume change in both cathodes and anodes.Owing to the high specific surface area,pore volume,low density,good chemical stability,and particularly multimodal pore sizes,hierarchical porous carbon(HPC)mate rials have received considerable attention for circumventing the above pro blems in Li-S batteries.Herein,recent progress made in the synthetic methods and deployment of HPC materials for various components including sulfur cathodes,separators and interlayers,and lithium anodes in Li-S batteries is presented and summarized.More importantly,the correlation between the structures(pore volume,specific surface area,degree of pores,and heteroatom-doping)of HPC and the electrochemical performances of Li-S batteries is elaborated.Finally,a discussion on the challenges and future perspectives associated with HPCs for Li-S batteries is provided.展开更多
Lithium-sulfur batteries(LSBs)have become promising next-generation energy storage technologies for electric vehicles and portable electronics,due to its excellent theoretical specific energy.However,the low conductiv...Lithium-sulfur batteries(LSBs)have become promising next-generation energy storage technologies for electric vehicles and portable electronics,due to its excellent theoretical specific energy.However,the low conductivity of sulfur species,notorious lithium dendrites,the severe"shuttle effect"of polysulfides(LiPSs)and the inferior kinetic reaction for LiPSs/Li_(2)S conversion during discharge-charge have seriously hindered their practical application,and also pose potential safety hazards.Owing to their superior porous architectures,high specific surface areas,excellent structural designability,functional modifiability,abundant active sites and flexibility of carbon-containing electrospun nanofibers(CENFs),they exhibited the superior characteristics that can simultaneously solve the above issues.In this review,we summarize the recent progress and application of CENFs in LSBs.First,we provide a brief introduction to the structure and composition controlled of carbon nanofibers by electrospinning.We then review progress in recent developments of CENFs for LSBs including cathodes,anodes,separators,and interlayers.We focus on how to solve practical issues that arise when the CENFs are applied to various parts of LSBs,and the relevant working mechanisms are described,from high sulfur loading and Li dendrites suppression to LiPSs’confinement and conversion.Finally,we summarize and propose the existing challenges and future prospects of CENFs,for the design and architecture of electrochemical components in Li-S energy storage systems.展开更多
基金Project supported by the National Key Research and Development Program of China(Grant Nos.2017YFA0303003 and 2016YFA0300300)the National Natural Science Foundation of China(Grant No.11574370)the Strategic Priority Research Program and Key Research Program of Frontier Sciences of the Chinese Academy of Sciences(Grant Nos.QYZDY-SSW-SLH001,QYZDY-SSW-SLH008,and XDB07020100)
文摘We synthesize a series of Mn substituted （Li, Fe）OHFeSe superconductor single crystals via a modified ion-exchange method, with the Mn concentration z （the atomic ratio of Mn：Se） ranging from 0 to 0.07. The distribution homogeneity of the Mn element incorporated into the lattice of （Li, Fe）OHFeSe is checked by combined measurements of high-angle- annular-dark-field （HAADF） imaging and electron energy-loss spectroscopy （EELS）. Interestingly, we find that the superconducting transition temperature Tc and unit cell parameter c of the Mn-doped （Li, Fe）OHFeSe samples display similar V-shaped evolutions with the increasing dopant concentration z. We propose that, with increasing doping level, the Mn dopant first occupies the tetrahedral sites in the （Li, Fe）OH layers before starting to substitute the Fe element in the su- perconducting FeSe layers, which accounts for the V-shaped change in cell parameter c. The observed positive correlation between the Tc and lattice parameter c, regardless of the Mn doping level z, indicates that a larger interlayer separation, or a weaker interlayer coupling, is essential for the high-Tc superconductivity in （Li, Fe）OHFeSe. This agrees with our previous observations on powder, single crystal, and film samples of （Li, Fe）OHFeSe superconductors.
基金Yinyu Xiang is very grateful to the China Scholarship Council(CSC:No.201806950083)for his PhD scholarship。
文摘Lithium-sulfur(Li-S)batteries,although a promising candidate of next-generation energy storage devices,are hindered by some bottlenecks in their roadmap toward commercialization.The key challenges include solving the issues such as low utilization of active materials,poor cyclic stability,poor rate performance,and unsatisfactory Coulombic efficiency due to the inherent poor electrical and ionic conductivity of sulfur and its discharged products(e.g.,Li2S2 and Li_(2)S),dissolution and migration of polysulfide ions in the electrolyte,unstable solid electrolyte interphase and dendritic growth on an odes,and volume change in both cathodes and anodes.Owing to the high specific surface area,pore volume,low density,good chemical stability,and particularly multimodal pore sizes,hierarchical porous carbon(HPC)mate rials have received considerable attention for circumventing the above pro blems in Li-S batteries.Herein,recent progress made in the synthetic methods and deployment of HPC materials for various components including sulfur cathodes,separators and interlayers,and lithium anodes in Li-S batteries is presented and summarized.More importantly,the correlation between the structures(pore volume,specific surface area,degree of pores,and heteroatom-doping)of HPC and the electrochemical performances of Li-S batteries is elaborated.Finally,a discussion on the challenges and future perspectives associated with HPCs for Li-S batteries is provided.
基金financially supported by the National Natural Science Foundation of China(Grant No.51702241)Key Program of Natural Science Foundation of Hubei Province(Contract No.2017CFA004)+1 种基金the Special Project of Central Government for Local Science and Technology Development of Hubei Province(No.2019ZYYD076)Open Foundation of State Key Laboratory of Advanced Refractories(No.SKLAR202002)。
文摘Lithium-sulfur batteries(LSBs)have become promising next-generation energy storage technologies for electric vehicles and portable electronics,due to its excellent theoretical specific energy.However,the low conductivity of sulfur species,notorious lithium dendrites,the severe"shuttle effect"of polysulfides(LiPSs)and the inferior kinetic reaction for LiPSs/Li_(2)S conversion during discharge-charge have seriously hindered their practical application,and also pose potential safety hazards.Owing to their superior porous architectures,high specific surface areas,excellent structural designability,functional modifiability,abundant active sites and flexibility of carbon-containing electrospun nanofibers(CENFs),they exhibited the superior characteristics that can simultaneously solve the above issues.In this review,we summarize the recent progress and application of CENFs in LSBs.First,we provide a brief introduction to the structure and composition controlled of carbon nanofibers by electrospinning.We then review progress in recent developments of CENFs for LSBs including cathodes,anodes,separators,and interlayers.We focus on how to solve practical issues that arise when the CENFs are applied to various parts of LSBs,and the relevant working mechanisms are described,from high sulfur loading and Li dendrites suppression to LiPSs’confinement and conversion.Finally,we summarize and propose the existing challenges and future prospects of CENFs,for the design and architecture of electrochemical components in Li-S energy storage systems.
