Atomically Dispersed Transition Metals on Carbon Nanotubes with Ultrahigh Loading for Selective Electrochemical Carbon Dioxide Reduction. 2018

Yi Cheng, and Shiyong Zhao, and Bernt Johannessen, and Jean-Pierre Veder, and Martin Saunders, and Matthew R Rowles, and Min Cheng, and Chang Liu, and Matthew F Chisholm, and Roland De Marco, and Hui-Ming Cheng, and Shi-Ze Yang, and San Ping Jiang
Fuels and Energy Technology Institute and Department of Chemical Engineering, Curtin University, Perth, Western Australia, 6102, Australia.

Single-atom catalysts (SACs) are the smallest entities for catalytic reactions with projected high atomic efficiency, superior activity, and selectivity; however, practical applications of SACs suffer from a very low metal loading of 1-2 wt%. Here, a class of SACs based on atomically dispersed transition metals on nitrogen-doped carbon nanotubes (MSA-N-CNTs, where M = Ni, Co, NiCo, CoFe, and NiPt) is synthesized with an extraordinarily high metal loading, e.g., 20 wt% in the case of NiSA-N-CNTs, using a new multistep pyrolysis process. Among these materials, NiSA-N-CNTs show an excellent selectivity and activity for the electrochemical reduction of CO2 to CO, achieving a turnover frequency (TOF) of 11.7 s-1 at -0.55 V (vs reversible hydrogen electrode (RHE)), two orders of magnitude higher than Ni nanoparticles supported on CNTs.

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