Defect-Engineered ZIF-Derived Non-Pt Cathode Catalyst at 1.5 mg cm -2 Loading for Proton Exchange Membrane Fuel Cells.
Weikang ZhuHaotian LiuYabiao PeiTao LiuJunfeng ZhangXin LiuLianqin WangYingjie FengYan YinMichael D GuiverPublished in: Small (Weinheim an der Bergstrasse, Germany) (2023)
Due to the sluggish kinetics of the oxygen reduction reaction (ORR) by non-Pt based catalyst, high loading of catalyst is required to achieve satisfactory fuel cell performance, which inevitably leads to the increase of the catalyst layer thickness with serious mass transport resistance. Herein, a defective zeolitic imidazolate framework (ZIF) derived Co/Fe-N-C catalyst with small mesopores (2-4 nm) and high density of CoFe atomic active sites are prepared by regulating the Fe dosage and pyrolysis temperature. Molecular dynamics simulation and electrochemical tests indicate that > 2 nm mesopores show insignificant influence on the diffusion process of O 2 and H 2 O molecules, leading to the high utilization of active sites and low mass transport resistance. The proton exchange membrane fuel cell (PEMFC) shows a high-power density of 755 mW cm -2 with only 1.5 mg cm -2 of non-Pt catalyst in the cathode. No apparent performance loss caused by concentration difference can be observed, in particular in the high current density region (1 A cm -2 ). This work emphasizes the importance of small mesopore design in the Co/Fe-N-C catalyst, which is anticipated to provide essential guidance for the application of non-Pt catalysts.
Keyphrases
- metal organic framework
- reduced graphene oxide
- ionic liquid
- highly efficient
- room temperature
- visible light
- carbon dioxide
- gold nanoparticles
- high density
- molecular dynamics simulations
- photodynamic therapy
- cell therapy
- stem cells
- molecular docking
- bone marrow
- mesenchymal stem cells
- cell death
- cell cycle arrest
- magnetic resonance
- risk assessment
- signaling pathway
- endoplasmic reticulum stress
- liquid chromatography
- electron transfer