The best performing Mn-based catalysts have been synthesized from a Mn doped ZIF-8 structure, but due to the high oxophilicity of Mn and difficulty in incorporating Mn into the ZIF structure, a laborious Mn catalyst synthesis route has been adopted, which requires acid leaching, secondary doping, and multiple pyrolysis steps2. This causes problems in scaling up the synthesis and limits the active site density when compared to the Fe catalyst.
We aim to use highly reactive Mn metal precursors in an air-free environment to incorporate Mn into the metal sites of ZIF. High temperature pyrolysis (1100°C) leads to manganese catalyst synthesis in one step.
We show that using a highly active manganese borohydride precursor allows for the formation of a metal organic framework (MOF) when combined with 2-methylimidazole, which can subsequently be pyrolyzed to form the target catalyst. Using zinc borohydride as a secondary metal source we can also form bimetallic MOF structures with increased thermal stability and varied Mn loading. With this strategy Mn can be incorporated directly into the metal MOF sites with a wide range of Mn loading. The utilization of an air-free environment prevents metal oxide formation thus giving a facile one step synthesis of a manganese-based catalyst.
(1) Liu, K.; Qiao, Z.; Hwang, S.; Liu, Z.; Zhang, H.; Su, D.; Xu, H.; Wu, G.; Wang, G. Mn- and N- Doped Carbon as Promising Catalysts for Oxygen Reduction Reaction_ Theoretical Prediction and Experimental Validation. 2018.
(2) Li, J.; Chen, M.; Cullen, D. A.; Hwang, S.; Wang, M.; Li, B.; Liu, K.; Karakalos, S.; Lucero, M.; Zhang, H.; et al. Atomically Dispersed Manganese Catalysts for Oxygen Reduction in Proton-Exchange Membrane Fuel Cells. Nat. Catal. 2018, 1 (12), 935–945.
