材料科学
电解质
电容器
电化学
离子
小型化
光电子学
聚合物电容器
放松(心理学)
水溶液
电解电容器
纳米技术
分析化学(期刊)
工作(物理)
时间常数
化学物理
石墨烯
离子运输机
电化学电位
储能
薄膜电容器
作者
Shuailong Zheng,Bin Chen,Zhaofeng Zhai,Chuyan Zhang,Jianing Gong,Guilin Shi,Tianwen Hu,Yuhua Yang,Lusheng Liu,Nan Huang
摘要
ABSTRACT Electrochemical capacitors (ECs) are expected to replace traditional aluminum electrolytic capacitors (AECs) in AC‐line filtering due to their advantages in miniaturization and circuit integration, yet their frequency response is severely limited by slow ion transport at low temperature. Herein, we demonstrated that the electrochemical interface integrating weakly hydrogen‐bonded electrolyte environment within vertical ion channels enables ECs to deliver millisecond‐level ultrafast response even at −50°C for AC‐line filtering. With aids of atomic calculation and spectroscopic characterizations, Mg(ClO 4 ) 2 aqueous electrolyte is shown to efficiently weaken hydrogen bonding and possess the lowest anion kinetic barrier (E a ), resulting in its superior low‐temperature performance over other aqueous electrolytes. By integrating this weakly hydrogen‐bonded electrolyte within vertical graphene electrode, the resulting EC unit delivers an ultra‐fast response with a relaxation time constant as low as 5.7 ms at −50°C, along with a high areal energy density of 1.49 mFV 2 /cm 2 at 120 Hz and stable 60‐Hz filtering capability at −50°C. This work bridges the gap between ultra‐fast response and low‐temperature adoptability in ECs and expands their applications in practical low‐temperature AC‐line filtering applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI