4.6 Article

Unexpected electro-catalytic activity of the CO reduction reaction on Cr-embedded poly-phthalocyanine realized by strain engineering: a computational study

Journal

PHYSICAL CHEMISTRY CHEMICAL PHYSICS
Volume 25, Issue 18, Pages 12872-12881

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d3cp00861d

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In this study, the effect of strain engineering on the electrocatalysis of CO reduction reaction (CORR) by 2D transition metal embedded polyphthalocyanines (MPPcs) was computationally explored. It was found that only CrPPc under biaxial strain had the potential to significantly enhance the catalytic performance. The free energy diagrams showed that the optimal reaction pathway and rate-determining step were changed under specific biaxial strains, and applying 5% compressive strain on CrPPc resulted in unexpected electrocatalytic activity.
The electrochemical conversion of carbon monoxide (CO) into value-added products is highly promising for carbon utilization and CO removal. Based on previous theoretical studies, we computationally explored the effect of strain engineering on electrocatalysis of the CO reduction reaction (CORR) by two-dimensional (2D) transition metal embedded polyphthalocyanines (MPPcs). By calculating the adsorption energy of CO and the free energies of key intermediates on the MPPcs under uniaxial and biaxial strains, it was revealed that only CrPPc under biaxial strain has the potential to exhibit significant enhancement of the catalytic performance. The free energy diagrams of the CORR catalyzed by CrPPc were plotted under specific biaxial strains, where both the optimal reaction pathway and rate-determining step are found to be evidently changed. What's more, the 5% compressive strain imposed on CrPPc results in an ultra-low limiting potential (U-L = -0.09 V) with high selectivity on CH4 as the final product, indicating unexpected electro-catalytic activity. Our study clearly elucidates that moderate strain could greatly enhance the electrocatalytic performance of 2D materials in the CORR.

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