Abstract

It continues to be challenging to develop low-cost, high-efficiency electrocatalysts for CO2 electrochemical reduction reaction (CRR). In this work, the electrocatalytic performance of several transition metal (TM = Ti, V, Cr, Mn, and Fe) anchored boron co-doped graphyne (GY) is systematically examined by first-principle calculations. Among them, MnB1@GY exhibits the most excellent CRR performance with low limit potential of −0.21 V and high selectivity for the generation of CH4. A deep investigation into the high-performance origin by comparative analysis of single atom doped Mn@GY and MB1@GY reveals that due to the synergistic effect of co-doped B and TM atoms which can break the linear-scaling relation of single atom catalyst, the selectivity is significantly improved. B in MnB1@GY regulates the charge transfer of the reaction, and the strong binding of *CHO with both B and Mn atom lower the energy required for the protonation step of *CO→*CHO, reducing the energy barrier of the rate determining steps and leading to the high performance of MnB1@GY. This work suggests that the synergistic effect of co-doped B and metal atoms can effectively enhance the catalytic activity, which can hopefully provide a potential strategy for the rational design of efficient CRR electrocatalysts.

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