A series of flexible and self-standing coal-derived carbon fibers(CCFs)were fabricated through electro-spinning coupled with carbonization using bituminous coal and polyacrylonitrile(PAN)as the carbon precursors.These...A series of flexible and self-standing coal-derived carbon fibers(CCFs)were fabricated through electro-spinning coupled with carbonization using bituminous coal and polyacrylonitrile(PAN)as the carbon precursors.These CCFs were utilized as free-standing lithium-ion battery(LIB)anodes.Optimizing car-bonization temperature reveals that the CCFs exhibit a one-dimensional solid linear structure with a uni-form distribution of graphite-like microcrystals.These fibers possess a dense structure and smooth surface,with averaging diameter from approximately 125.0 to 210.0 nm at carbonization temperatures ranging from 600 to 900℃.During electrospinning and carbonization,the aromatic rings enriched in bituminous coal crosslink with PAN chains,forming a robust three-dimensional(3D)framework.This 3D microstructure significantly enhances the flexibility and tensile strength of CCFs,while increasing the graphite-like sp^(2)microcrystalline carbon content,thus improving electrical conductivity.The CCFs carbonized at 700℃demonstrate an optimal balance of sp^(3)amorphous and sp^(2)graphite-like carbons.The average diameter of CCFs-700 is 177 nm and the specific surface area(SSA)is 7.2 m^(2)g^(-1).Additionally,the fibers contain oxygen-containing functional groups,as well as nitrogen-containing func-tional groups,including pyridinic nitrogen and pyrrolic nitrogen.Owing to its characteristics,the CCFs-700 showcases remarkable electrochemical performance,delivering a high reversible capacity of 631.4 mAh g^(-1).CCFs-700 also exhibit outstanding cycle stability,which retains approximately all of their first capacity(400.1 mAh g^(-1))after 120 cycles.This research offers an economical yet scalable approach for producing flexible and self-supporting anodes for LIBs that do not require current collectors,binders and conductive additives,thereby simplifying the electrode fabrication process.展开更多
As an emerging member of the two-dimensional(2D)material family,V_(2)CT_(X)MXene shows great potential in the application of lithium-ion capacitors(LICs)due to its unique structure and excellent electrical conductivit...As an emerging member of the two-dimensional(2D)material family,V_(2)CT_(X)MXene shows great potential in the application of lithium-ion capacitors(LICs)due to its unique structure and excellent electrical conductivity.However,severe nanosheets stacking and intra-layer transport barriers have limited the further development of V_(2)CT_(X)MXene-based materials.Herein,we prepared Kions and–O functional group co-modified V_(2)CT_(X)MXene(VCT-K)and further incorporated it with single-walled carbon nanotube(SWCNT),obtaining freestanding V_(2)CT_(X)composite films(VCT-K@C)with the 3D conductive network.Significantly,K+ions were introduced into V_(2)CT_(X)MXene to stabilize the interlayer structure and prevent the aggregation of nanosheets,the terminal group of–O was controllably modified on the surface of MXene to improve the Li+ions storage reversible capacities and the SWCNT acted as the bridge between MXene nanosheets to opens up the channels for ion/electron transportation in the longitudinal direction.Benefited from the synergistic effect of VCT-K and SWCNT,the VCT-K@C exhibits superior reversible specific capacities of 671.8 mA h g^(-1)at 0.1 A g^(-1)and 318 mA h g^(-1)at 1.0 A g^(-1).Furthermore,the assembled LICs with VCT-K@C anode coupling activated carbon(AC)cathode deliver an outstanding power density of 19.0 kW kg^(-1)at 67.4 Wh kg^(-1),a high energy density of 140.5 Wh kg^(-1)at 94.8 W kg^(-1)and a stable capacitance retention of 86%after 6000 cycles at 10 A g^(-1).Such unique structures and excellent electrochemical properties are expected to pave the way for the large-scale application in LICs of MXene-based materials.展开更多
基金supported by the National Natural Science Foundation of China(Nos.52474290,52274261,52074109,52304284)the Open Subjects of Henan Provincial Key Laboratory of Coal Green Conversion(No.CGCF202201)+1 种基金the Key Scientific and Technological Project of Henan Province(No.242102240008)the Key Scientific Research Projects of Colleges and Universities in Henan Province(No.24A440003).
文摘A series of flexible and self-standing coal-derived carbon fibers(CCFs)were fabricated through electro-spinning coupled with carbonization using bituminous coal and polyacrylonitrile(PAN)as the carbon precursors.These CCFs were utilized as free-standing lithium-ion battery(LIB)anodes.Optimizing car-bonization temperature reveals that the CCFs exhibit a one-dimensional solid linear structure with a uni-form distribution of graphite-like microcrystals.These fibers possess a dense structure and smooth surface,with averaging diameter from approximately 125.0 to 210.0 nm at carbonization temperatures ranging from 600 to 900℃.During electrospinning and carbonization,the aromatic rings enriched in bituminous coal crosslink with PAN chains,forming a robust three-dimensional(3D)framework.This 3D microstructure significantly enhances the flexibility and tensile strength of CCFs,while increasing the graphite-like sp^(2)microcrystalline carbon content,thus improving electrical conductivity.The CCFs carbonized at 700℃demonstrate an optimal balance of sp^(3)amorphous and sp^(2)graphite-like carbons.The average diameter of CCFs-700 is 177 nm and the specific surface area(SSA)is 7.2 m^(2)g^(-1).Additionally,the fibers contain oxygen-containing functional groups,as well as nitrogen-containing func-tional groups,including pyridinic nitrogen and pyrrolic nitrogen.Owing to its characteristics,the CCFs-700 showcases remarkable electrochemical performance,delivering a high reversible capacity of 631.4 mAh g^(-1).CCFs-700 also exhibit outstanding cycle stability,which retains approximately all of their first capacity(400.1 mAh g^(-1))after 120 cycles.This research offers an economical yet scalable approach for producing flexible and self-supporting anodes for LIBs that do not require current collectors,binders and conductive additives,thereby simplifying the electrode fabrication process.
基金funded by the National Natural Science Foundation of China(Grant Nos.22005167 and 21905152)the Shandong Provincial Natural Science Foundation of China(Grant Nos.ZR2020QB125 and ZR2020MB045)+1 种基金the China Postdoctoral Science Foundation(Grant Nos.2021M693256,2021T140687 and 2022M713249)the Qingdao Postdoctoral Applied Research Project and the Youth Innovation Team Project for Talent Introduction and Cultivation in Universities of Shandong Province。
文摘As an emerging member of the two-dimensional(2D)material family,V_(2)CT_(X)MXene shows great potential in the application of lithium-ion capacitors(LICs)due to its unique structure and excellent electrical conductivity.However,severe nanosheets stacking and intra-layer transport barriers have limited the further development of V_(2)CT_(X)MXene-based materials.Herein,we prepared Kions and–O functional group co-modified V_(2)CT_(X)MXene(VCT-K)and further incorporated it with single-walled carbon nanotube(SWCNT),obtaining freestanding V_(2)CT_(X)composite films(VCT-K@C)with the 3D conductive network.Significantly,K+ions were introduced into V_(2)CT_(X)MXene to stabilize the interlayer structure and prevent the aggregation of nanosheets,the terminal group of–O was controllably modified on the surface of MXene to improve the Li+ions storage reversible capacities and the SWCNT acted as the bridge between MXene nanosheets to opens up the channels for ion/electron transportation in the longitudinal direction.Benefited from the synergistic effect of VCT-K and SWCNT,the VCT-K@C exhibits superior reversible specific capacities of 671.8 mA h g^(-1)at 0.1 A g^(-1)and 318 mA h g^(-1)at 1.0 A g^(-1).Furthermore,the assembled LICs with VCT-K@C anode coupling activated carbon(AC)cathode deliver an outstanding power density of 19.0 kW kg^(-1)at 67.4 Wh kg^(-1),a high energy density of 140.5 Wh kg^(-1)at 94.8 W kg^(-1)and a stable capacitance retention of 86%after 6000 cycles at 10 A g^(-1).Such unique structures and excellent electrochemical properties are expected to pave the way for the large-scale application in LICs of MXene-based materials.
