无定形固体
材料科学
化学工程
介孔材料
析氧
水溶液
阴极
热液循环
锰
电极
扩散
储能
氧气
碳纤维
电化学
纳米技术
无机化学
电池(电)
钙钛矿(结构)
无定形碳
钠离子电池
离子
复合数
钠
多孔性
水热合成
功率密度
晶体结构
离子交换
Crystal(编程语言)
电导率
作者
Zubang Liu,Cheng Yang,Haining You,Yongkang Liu,Yongkang Liu,Xiaolei Sun,Song Guo,Zuocai Zhang,Yaxiong Tian,Yuanli Liu,Yuanli Liu
标识
DOI:10.1016/j.est.2025.118689
摘要
Manganese dioxide (MnO 2 ) materials have recently garnered attention as promising cathode materials for aqueous calcium-ion batteries, owing to their low cost, environmental friendliness, and high-capacity characteristics. However, the low electrical conductivity and slow diffusion kinetics of MnO 2 severely limit its application. Herein, a carboxymethylcellulose sodium (CMC)/MnO 2 (CMO) were synthesized through a simply hydrothermal method for Ca 2+ storage for the first time. CMC was employed to induce the structure of MnO 2 from crystal to amorphous transition, which was investigated by morphological evolution characterization. Notably, the CMO composite has an amorphous structure with numerous mesopores and oxygen vacancies, and this greatly facilitates the migration of Ca 2+ and results in high pseudocapacitive behavior. As a result, the CMO cathode achieved a specific capacity of 83 mAh g −1 at 1 A g −1 and retained 73 % after 2000 cycles. Importantly, used active carbon as anode, the full coin battery CMO//AC achieved up to 4000 cycles with an energy density of 126 Wh kg −1 and power density of 434.8 W kg −1 . This work provides a potential alternative and development for aqueous calcium-ion batteries. The CMO with abundant oxygen vacancies, mesoporous structure, and amorphous nature was synthesized via a facile hydrothermal method, achieving superior Ca 2+ storage performance. • 5-CMO possesses an amorphous, mesoporous structure along with abundant oxygen vacancies • Unveiling a CMC-induced amorphization evolution mechanism in MnO 2 • The 5-CMO electrode demonstrated rapid ion diffusion and a dominant pseudocapacitive charge storage behavior • The CMO//AC full cell delivered a remarkable capacity retention of 54 % after 4000 cycles at 1 A g −1
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