Zhang Zhengping, Sun Junting, Wang Feng, Dai Liming
State Key Laboratory of Chemical Resource Engineering, Beijing Key Laboratory of Electrochemical Process and Technology for Materials, Beijing University of Chemical Technology, Beijing, 100029, China.
Center of Advanced Science and Engineering for Carbon (Case4carbon), Department of Macromolecular Science and Engineering, Case Western Reserve University, Cleveland, OH, 44106, USA.
Angew Chem Int Ed Engl. 2018 Jul 16;57(29):9038-9043. doi: 10.1002/anie.201804958. Epub 2018 Jun 19.
Single Fe atoms dispersed on hierarchically structured porous carbon (SA-Fe-HPC) frameworks are prepared by pyrolysis of unsubstituted phthalocyanine/iron phthalocyanine complexes confined within micropores of the porous carbon support. The single-atom Fe catalysts have a well-defined atomic dispersion of Fe atoms coordinated by N ligands on the 3D hierarchically porous carbon support. These SA-Fe-HPC catalysts are comparable to the commercial Pt/C electrode even in acidic electrolytes for oxygen reduction reaction (ORR) in terms of the ORR activity (E =0.81 V), but have better long-term electrochemical stability (7 mV negative shift after 3000 potential cycles) and fuel selectivity. In alkaline media, the SA-Fe-HPC catalysts outperform the commercial Pt/C electrode in ORR activity (E =0.89 V), fuel selectivity, and long-term stability (1 mV negative shift after 3000 potential cycles). Thus, these nSA-Fe-HPCs are promising non-platinum-group metal ORR catalysts for fuel-cell technologies.
通过对限制在多孔碳载体微孔内的未取代酞菁/铁酞菁配合物进行热解,制备出分散在分级结构多孔碳(SA-Fe-HPC)框架上的单铁原子。单原子铁催化剂在三维分级多孔碳载体上具有由氮配体配位的铁原子明确的原子分散状态。这些SA-Fe-HPC催化剂在氧还原反应(ORR)的ORR活性(E = 0.81 V)方面,即使在酸性电解质中也与商业Pt/C电极相当,但具有更好的长期电化学稳定性(3000次电位循环后负移7 mV)和燃料选择性。在碱性介质中,SA-Fe-HPC催化剂在ORR活性(E = 0.89 V)、燃料选择性和长期稳定性(3000次电位循环后负移1 mV)方面优于商业Pt/C电极。因此,这些nSA-Fe-HPC是用于燃料电池技术的有前景的非铂族金属ORR催化剂。