Feng Jing-Dong, Zhang Wen-Da, Liu Yong, Han Wang-Kang, Zhu Ruo-Meng, Gu Zhi-Guo
Key Laboratory of Synthetic and Biological Colloids, Ministry of Education, School of Chemical and Material Engineering, Jiangnan University, Wuxi, 214122, P. R. China.
Chemistry. 2023 Nov 8;29(62):e202302201. doi: 10.1002/chem.202302201. Epub 2023 Sep 28.
Non-platinum noble metals are highly desirable for the development of highly active, stable oxygen reduction reaction (ORR) electrocatalysts for fuel cells and metal-air batteries. However, how to improve the utilization of non-platinum noble metals is an urgent issue. Herein, a highly efficient catalyst for ORR was prepared through homogeneous loading of Pd precursors by a domain-limited method in a three-dimensional covalent organic framework (COF) followed by pyrolysis. The morphology of the Pd nanoparticles (Pd NPs) was well maintained after carbonization, which was attributed to the rigid structure of the 3D COF. Thanks to the uniform distribution of Pd NPs in the carbon, the catalyst exhibited a remarkable half-wave potential of 0.906 V and a Tafel slope of 70 mV dec in 0.1 M KOH, surpassing the commercial Pt/C catalyst (0.863 V and 75 mV dec ). Furthermore, a maximum power density of 144.0 mW cm was achieved at 252 mA cm , which was significantly higher than the control battery (105.1 mW cm ). This work not only provides a simple strategy for in-situ preparation of highly dispersible metal catalysts in COFs, but also offers new insights into the ORR electrocatalysis.
非铂族贵金属对于开发用于燃料电池和金属空气电池的高活性、稳定的氧还原反应(ORR)电催化剂非常理想。然而,如何提高非铂族贵金属的利用率是一个紧迫的问题。在此,通过在三维共价有机框架(COF)中采用域限制法均匀负载钯前驱体,随后进行热解,制备了一种用于ORR的高效催化剂。碳化后钯纳米颗粒(Pd NPs)的形态得到了很好的保持,这归因于三维COF的刚性结构。由于Pd NPs在碳中的均匀分布,该催化剂在0.1 M KOH中表现出显著的半波电位0.906 V和塔菲尔斜率70 mV dec,超过了商业Pt/C催化剂(0.863 V和75 mV dec)。此外,在252 mA cm时实现了144.0 mW cm的最大功率密度,这明显高于对照电池(105.1 mW cm)。这项工作不仅为在COF中原位制备高度分散的金属催化剂提供了一种简单策略,也为ORR电催化提供了新的见解。