材料科学
超级电容器
阳极
煅烧
阴极
电化学
介孔材料
功率密度
法拉第效率
化学工程
纳米颗粒
离子
电极
储能
纳米技术
催化作用
电气工程
物理
工程类
物理化学
量子力学
功率(物理)
化学
生物化学
作者
Yang Ma,Liuyang Zhang,Zhaoxiong Yan,Bei Cheng,Jiaguo Yu,Tao Liu
标识
DOI:10.1002/aenm.202103820
摘要
Abstract Sodium hybrid supercapacitors (Na‐HSCs) are regarded as one promising electrochemical energy storage device, because of the low price of sodium, prolonged life cycle, and high‐energy/power density. Nonetheless, the imparity between the fast capacitive reactions at cathode and the sluggish Faradaic reactions at the anode leads to an imbalance in the electrochemical reaction kinetics, limiting the development of Na‐HSCs. Therefore, it is urgent to develop suitable anode materials for performance‐enhanced Na‐HSCs. Herein, sandwich‐shell‐structured CoMn 2 O 4 /C hollow spheres are synthesized by a facile hydrothermal reaction and subsequent calcination, where mesoporous carbon hollow spheres (CHSs) serve as nonsacrificial hard templates. CHSs with numerous mesoporous channels are beneficial for the penetration of reactant ions. Therefore, CoMn 2 O 4 nanosheets are successfully deposited on the inner and outer surfaces of CHSs, generating sandwich‐shell‐structured CoMn 2 O 4 /C hollow spheres. Benefiting from the unique design, CoMn 2 O 4 /C HSs exhibit excellent sodium storage performance, including a high‐specific capacity of 290 mAh g –1 at 0.1 A g –1 and prolonged cycling durability. A Na‐HSC assembled by CoMn 2 O 4 /C HSs anode and activated carbon cathode exhibits a high‐energy density (265 Wh kg –1 ) and a wide‐operating voltage range (0.01–4.0 V).
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