Defect engineering on BiFeO_(3) through Na and V codoping for aqueous Na-ion capacitors
作者机构:School of Physics and Physical EngineeringQufu Normal UniversityQufu 273165ShandongChina
出 版 物:《Journal of Energy Chemistry》 (能源化学(英文版))
年 卷 期:2024年第90卷第3期
页 面:453-463,I0011页
核心收录:
学科分类:0820[工学-石油与天然气工程] 080801[工学-电机与电器] 0808[工学-电气工程] 0817[工学-化学工程与技术] 08[工学] 080501[工学-材料物理与化学] 0805[工学-材料科学与工程(可授工学、理学学位)] 0703[理学-化学]
基 金:financial supports from National Natural Science Foundation of China(22005174 and 52271133)
主 题:BiFeO_(3) Na^(+) storage V doping Oxygen vacancy Capacitor
摘 要:Sodium with low cost and high abundance is considered as a substitute element of lithium for batteries and supercapacitors,which need the appropriate host materials to accommodate the relatively large Na^(+) *** to Li^(+) storage,Na^(+) storage makes higher demands on the structural optimization of perovskite bismuth ferrite(BiFeO_(3)).We propose a novel strategy of defect engineering on BiFeO_(3) through Na and V codoping for high-efficiency Na^(+) storage,to reveal the roles of oxygen vacancies and V ions played in the enhanced electrochemical energy storage performances of Na-ion *** formation of the oxygen vacancies in the Na and V codoped BiFeO_(3)(denoted as NV-BFO),is promoted by Na doping and suppressed by V doping,which can be demonstrated by XPS and EPR *** the first-principles calculations,the oxygen vacancies and V ions in NV-BFO are confirmed to substantially lower the Na^(+)migration energy barriers through the space and electric field effects,to effectively promote the Na^(+) transport in the *** kinetic analysis of the NV-BFO//NV-BFO capacitors indicates the dominant capacitive-controlled capacity,which depends on fast Na^(+) deintercalation-intercalation process in the NV-BFO *** NV-BFO//NV-BFO capacitors open up a new avenue for developing highperformance Na-ion capacitors.