![]() |
个人信息Personal Information
硕士生导师
教师拼音名称:Liu Zheng
电子邮箱:
入职时间:2024-02-28
所在单位:化学化工学院
学历:博士研究生毕业
办公地点:瘦西湖校区老化馆213
性别:男
联系方式:18846135380
学位:工学博士学位
在职信息:在岗
毕业院校:哈尔滨工程大学
通过离子交换介导的3D交联ZIF-L超结构用于灵活的电化学能量存储
点击次数:
发表刊物:Angewandte Chemie International Edition
关键字:metal–organic frameworks · ZIF-L · superstructure · ion exchange · energy storage
摘要:Metal–organic frameworks (MOFs) are considered as a promising candidate for advancing energy storage owing to their intrinsic multi-channel architecture, high theoretical capacity, and precise adjustability. However, the low conductivity and poor structural stability lead to unsatisfactory rate and cycling performance, greatly hindering their practical application. Herein, we propose a sea urchin-like Co-ZIF-L superstructure using molecular template to induce self-assembly followed by ion exchange method, which shows improved conductivity, successive channels, and high stability. The ion exchange can gradually etch the superstructure, leading to the reconstruction of Co-ZIF-L with three-dimensional (3D) cross-linked ultrathin porous nanosheets. Moreover, the precise control of Co to Ni ratios can construct effective micro-electric field and synergistically enhance the rapid transfer of electrons and electrolyte ions, improving the conductivity and stability of CoNi-ZIF-L. The Co6.53Ni-ZIF-L electrode exhibits a high specific capacity (602 F g−1 at 1 A g−1) and long cycling stability (95.3 % retention after 4,000 cycles at 5 A g−1). The Co6.53Ni-ZIF-L//AC asymmetric flexible supercapacitor employing gel electrolyte also exhibits excellent cycling stability (93.3 % retention after 4000 cycles at 5 A g−1). This discovery provides valuable insights for electrode material selection and energy storage efficiency improvement.
合写作者:刘征
第一作者:丁弘业
论文类型:SCI一区TOP
通讯作者:庞欢
是否译文:否