Zhong Lin, Zhou Hu, Li Ruifeng, Cheng Hao, Wang Sheng, Chen Boyuan, Zhuang Yongyue, Chen Junfeng, Yuan Aihua
School of Materials Science and Engineering, Jiangsu University of Science and Technology, Zhenjiang 212003, China.
School of Materials Science and Engineering, Jiangsu University of Science and Technology, Zhenjiang 212003, China.
J Colloid Interface Sci. 2021 Oct;599:46-57. doi: 10.1016/j.jcis.2021.04.084. Epub 2021 Apr 20.
Developing highly efficient oxygen electrocatalysts is of vital importance for rechargeable Zn-air batteries (ZABs). Herein, Co/CoO nano-heterojunctions encapsulated into nitrogen-doped carbon sheets (NCS@Co/CoO) are fabricated via a dual-template-guided approach by using zeolitic imidazolate frameworks (ZIFs) as templates. The synergistic integration of structural and compositional advantages endows such catalyst with superior catalytic properties to benchmark noble-metal catalysts. To be specific, the hierarchical micro/mesopores affords massive mass transport channels and maximizes the exposure of accessible active sites, whereas the NCS matrix accelerates electron transfer and prevents the self-aggregation of active species during the electrocatalytic reaction. Moreover, abundant and synergistic Co-based active sites (CoO, CoO, Co-N) greatly promote the catalytic activity. As the cathode of both liquid and flexible solid-state ZABs, excellent device properties are achieved, outperforming those assembled with commercial Pt/C+RuO catalyst. This work presents a feasible and cost-effective strategy for developing oxygen electrocatalysts derived from ZIFs templates.
开发高效的氧电催化剂对于可充电锌空气电池(ZABs)至关重要。在此,通过使用沸石咪唑酯骨架(ZIFs)作为模板的双模板导向方法,制备了封装在氮掺杂碳片(NCS@Co/CoO)中的Co/CoO纳米异质结。结构和组成优势的协同整合赋予这种催化剂优于基准贵金属催化剂的催化性能。具体而言,分级微/介孔提供了大量的质量传输通道,并使可及活性位点的暴露最大化,而NCS基质加速电子转移并防止电催化反应过程中活性物种的自聚集。此外,丰富且协同的钴基活性位点(CoO、CoO、Co-N)极大地促进了催化活性。作为液体和柔性固态ZABs的阴极,实现了优异的器件性能,优于使用商业Pt/C+RuO催化剂组装的器件。这项工作为开发源自ZIFs模板的氧电催化剂提供了一种可行且具有成本效益的策略。