材料科学
电容
超级电容器
电极
3D打印
纳米技术
电化学
储能
协调数
格子(音乐)
氧化还原
配位复合体
合理设计
光电子学
构造(python库)
想象
体积热力学
电荷(物理)
转印
螯合作用
材料设计
电化学储能
软质材料
传输(计算)
作者
Shunyu Gu,Huijie Zhou,Yichun Su,Mengyao Zhang,Chenfei Zhou,Yifan Sun,Jiming Xu,Qian Li,Yanfei Zhang,Hanchuan Liu,Yihao Kang,Huan Pang
摘要
ABSTRACT The rapid development of micro supercapacitors requires electrode materials that possess both high redox activity and structural robustness. Nickel‐based coordination compounds are promising candidate materials, but their practical applications are hindered by the intense volume fluctuations and lattice strain during repeated redox reactions. The 1D coordination structure has inherent characteristics such as providing directional mechanical buffering and continuous charge transfer channels, which can effectively alleviate the above problems. However, the disordered arrangement of 1D structures in traditional electrode structures weakens their inherent advantages. Therefore, we successfully synthesized a series of printable 1D fibrous nickel‐based coordination compounds of different lengths using 4‐chlorosalicylate ligands that can transition from chelation dominant to carboxyl/hydroxyl bridged coordination mode. Utilizing 3D printing technology, we have fabricated NCS3@CNT@GO//MXene micro‐devices with an ordered layered structure. The specific capacitance of this device reached 381.36 mF cm −2 , and the energy density was 52.97 µWh cm −2 . Compared with the disordered NCS2@CNT@GO//MXene (273.84 mF cm −2 ) and NCS4@CNT@GO//MXene (337.44 mF cm −2 ), its specific capacitance increased by 39.2% and 13%, respectively, indicating that the ordered structure has an advantage in improving electrochemical performance. This work provides a universal approach for designing structured programmable electrodes suitable for micro energy storage.
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