Owing to excellent conductivity and abundant surface terminals,MXene-based heterostructures have been intensively investigated as energy storage materials.However,elaborate design of the structure and composition of M...Owing to excellent conductivity and abundant surface terminals,MXene-based heterostructures have been intensively investigated as energy storage materials.However,elaborate design of the structure and composition of MXene-based hybrids towards superior electrochemical performance is still challenging.Herein,we present an ingenious leaf-inspired design for preparing a unique Sb_(2)S_(3)/nitrogen-doped Ti_(3)C_(2)T_(x)MXene(L-Sb_(2)S_(3)/Ti_(3)C_(2))hybrid.In-situ TEM observations reveal that the leaflike Sb_(2)S_(3)nanoparticles with numerous mesopores can well relieve the large volume changes via an inward pore filling mechanism with only 20%outward expansion,whereas highly conductive N-doped Ti_(3)C_(2)T_(x)nanosheets can serve as the robust mechanical support to reinforce the structural integrity of the hybrid.Benefiting from the structural and constituent merits,the L-Sb_(2)S_(3)/Ti_(3)C_(2)anode fabricated exhibits a fast sodium storage behavior in terms of outstanding rate capability(339.5 mA h g^(-1)at 2,000 mA g^(-1))and high reversible capacity at high current density(358.2 mA h g^(-1)at 1,000 mA g^(-1)after 100 cycles).Electrochemical kinetic tests and theoretical simulation further manifest that the boosted electrochemical performance mainly arises from such a unique leaf-like Sb_(2)S_(3)mesoporous nanostructure with abundant active sites,and enhanced Na^(+)adsorption energy on the heterojunction formed between Sb_(2)S_(3)nanoparticles and Ti_(3)C_2)matrix.展开更多
Layered structure MoS_(2) nanosheets have shown great potential for energy storage applications.However,the methodology for elaborately controllable growth of MoS_(2) onto carbonaceous matrix for promoting the electro...Layered structure MoS_(2) nanosheets have shown great potential for energy storage applications.However,the methodology for elaborately controllable growth of MoS_(2) onto carbonaceous matrix for promoting the electrochemical performance is highly desirable.Herein,a high-effective,all-in-one in-situ conversion growth strategy has been proposed to construct a stable sandwich-type nanostructure.The formation of the optimized C-MoS_(2)/NCNTs product undergoes a dissolution-recrystallization process,in which ultra-thin carbon layer-coated MoS_(2) nanosheets densely assembled onto the surface of polyimide(PI)derived N-doped carbon nanotubes(CNTs).Theoretical simulation reveals that MoS_(2) nanosheets possessing an expanded interlayer spacing of 0.92 nm can greatly reduce the barrier energy of Na ions mitigation.Ac-cordingly,the as-made C-MoS_(2)/NCNTs anode delivers superior cycling stability(82%capacity retention after 400 cycles at 1 A g^(−1))and rate performance(348 mAh g^(−1) at 2 A g^(−1)).The results demonstrate that the expanded MoS_(2) interlayer distance,ultrathin outer carbon coating,and N-doped CNTs matrix together accounts for the outstanding sodium storage capability for the C-MoS_(2)/NCNTs electrode.展开更多
基金This work was supported by the Shuguang Program from Shanghai Education Development Foundation and Shanghai Municipal Education Commission(18SG035)State Key Laboratory for Modification of Chemical Fibers and Polymer Materials,Donghua University(KF2015).Dr.Q.Zhang thanks the support by the National Natural Science Foundation of China(52072323,51872098).
文摘Owing to excellent conductivity and abundant surface terminals,MXene-based heterostructures have been intensively investigated as energy storage materials.However,elaborate design of the structure and composition of MXene-based hybrids towards superior electrochemical performance is still challenging.Herein,we present an ingenious leaf-inspired design for preparing a unique Sb_(2)S_(3)/nitrogen-doped Ti_(3)C_(2)T_(x)MXene(L-Sb_(2)S_(3)/Ti_(3)C_(2))hybrid.In-situ TEM observations reveal that the leaflike Sb_(2)S_(3)nanoparticles with numerous mesopores can well relieve the large volume changes via an inward pore filling mechanism with only 20%outward expansion,whereas highly conductive N-doped Ti_(3)C_(2)T_(x)nanosheets can serve as the robust mechanical support to reinforce the structural integrity of the hybrid.Benefiting from the structural and constituent merits,the L-Sb_(2)S_(3)/Ti_(3)C_(2)anode fabricated exhibits a fast sodium storage behavior in terms of outstanding rate capability(339.5 mA h g^(-1)at 2,000 mA g^(-1))and high reversible capacity at high current density(358.2 mA h g^(-1)at 1,000 mA g^(-1)after 100 cycles).Electrochemical kinetic tests and theoretical simulation further manifest that the boosted electrochemical performance mainly arises from such a unique leaf-like Sb_(2)S_(3)mesoporous nanostructure with abundant active sites,and enhanced Na^(+)adsorption energy on the heterojunction formed between Sb_(2)S_(3)nanoparticles and Ti_(3)C_2)matrix.
基金financially supported by the Shuguang Program from Shanghai Education Development Foundation and Shanghai Municipal Education Commission (18SG035)State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, Donghua University (KF2015)。
文摘Layered structure MoS_(2) nanosheets have shown great potential for energy storage applications.However,the methodology for elaborately controllable growth of MoS_(2) onto carbonaceous matrix for promoting the electrochemical performance is highly desirable.Herein,a high-effective,all-in-one in-situ conversion growth strategy has been proposed to construct a stable sandwich-type nanostructure.The formation of the optimized C-MoS_(2)/NCNTs product undergoes a dissolution-recrystallization process,in which ultra-thin carbon layer-coated MoS_(2) nanosheets densely assembled onto the surface of polyimide(PI)derived N-doped carbon nanotubes(CNTs).Theoretical simulation reveals that MoS_(2) nanosheets possessing an expanded interlayer spacing of 0.92 nm can greatly reduce the barrier energy of Na ions mitigation.Ac-cordingly,the as-made C-MoS_(2)/NCNTs anode delivers superior cycling stability(82%capacity retention after 400 cycles at 1 A g^(−1))and rate performance(348 mAh g^(−1) at 2 A g^(−1)).The results demonstrate that the expanded MoS_(2) interlayer distance,ultrathin outer carbon coating,and N-doped CNTs matrix together accounts for the outstanding sodium storage capability for the C-MoS_(2)/NCNTs electrode.