Transition metal oxides as anode materials for high-performance lithium-ion batteries suffer from severe capacity decay,originating primarily from particle pulverization upon volume expansion/shrinkage and the intrins...Transition metal oxides as anode materials for high-performance lithium-ion batteries suffer from severe capacity decay,originating primarily from particle pulverization upon volume expansion/shrinkage and the intrinsically sluggish electron/ion transport.Herein,in-situ encapsulation ofα-Fe_(2)O_(3) nanoparticles into micro-sized ZnFe_(2)O_(4) capsules is facilely fulfilled through a co-precipitation process and followed by heat-treatment at optimal calcination temperature.The porous ZnFe_(2)O_(4) scaffold affords a synergistic confinement effect to suppress the grain growth ofα-Fe2 O3 nanocrystals during the calcination process and to accommodate the stress generated by volume expansion during the charge/discharge process,leading to an enhanced interfacial conductivity and inhibit electrode pulverization and mechanical failure in the active material.With these merits,the preparedα-Fe_(2)O_(3)/Fe_(2)O_(4) composite delivers prolonged cycling stability and improved rate capability with a higher specific capacity than soleα-Fe_(2)O_(3) and Fe_(2)O_(4).The discharge capacity is retained at 700 mAh g-1 after 500 cycles at 200 mA g^(-1) and 940 mAh g^(-1) after 50 cycles at 100 m A g^(-1).This work provides a new perspective in designing transition metal oxides for advanced lithium-ion batteries with superior electrochemical properties.展开更多
基金financially supported by the National Natural Science Foundation of China(No.51702217)the Shenzhen Government’s Plan of Science and Technology(No.JCYJ20190808121407676)+1 种基金the Natural Science Foundation of Guangdong(No.2020A1515011127)the Shenzhen University Initiative Research Program(No.2019005)。
文摘Transition metal oxides as anode materials for high-performance lithium-ion batteries suffer from severe capacity decay,originating primarily from particle pulverization upon volume expansion/shrinkage and the intrinsically sluggish electron/ion transport.Herein,in-situ encapsulation ofα-Fe_(2)O_(3) nanoparticles into micro-sized ZnFe_(2)O_(4) capsules is facilely fulfilled through a co-precipitation process and followed by heat-treatment at optimal calcination temperature.The porous ZnFe_(2)O_(4) scaffold affords a synergistic confinement effect to suppress the grain growth ofα-Fe2 O3 nanocrystals during the calcination process and to accommodate the stress generated by volume expansion during the charge/discharge process,leading to an enhanced interfacial conductivity and inhibit electrode pulverization and mechanical failure in the active material.With these merits,the preparedα-Fe_(2)O_(3)/Fe_(2)O_(4) composite delivers prolonged cycling stability and improved rate capability with a higher specific capacity than soleα-Fe_(2)O_(3) and Fe_(2)O_(4).The discharge capacity is retained at 700 mAh g-1 after 500 cycles at 200 mA g^(-1) and 940 mAh g^(-1) after 50 cycles at 100 m A g^(-1).This work provides a new perspective in designing transition metal oxides for advanced lithium-ion batteries with superior electrochemical properties.
