4.8 Article

Breaking the Volcano-Shaped Relationship for Highly Efficient Electrocatalytic Nitrogen Reduction: A Computational Guideline

期刊

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.2c14134

关键词

first-principles calculations; Cu-based single-atom alloys; electrocatalytic nitrogen reduction reaction; volcano-shaped relationship; structure-activity relationship

资金

  1. National Natural Science Foundation of China [21905019, 91961125]
  2. Key Program for International Samp
  3. T Cooperation Projects of China from the Ministry of Science and Technology of China [2018YFE0124600]
  4. China Petrochemical Corporation [S20L00151]
  5. Science and Technology Project of Guangdong Province of China [2020B0101370001]

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In this study, a range of transition-metal-doped Cu-based single-atom alloys were investigated as catalysts for electrocatalytic nitrogen reduction reaction (e-NRR) using first-principles calculations. It was found that when the adsorption of N2 on the catalysts is strong enough, the inert N2 molecules can be effectively activated for the first hydrogenation step. Meanwhile, the last hydrogenation step is not affected by the scaling relationship and remains easy on all of the catalysts, which breaks the volcano-shaped relationship in e-NRR. Four promising catalysts with outstanding e-NRR activity and long-term stability were identified. This work provides a guideline for breaking the volcano-shaped relationship in e-NRR and designing highly efficient electrocatalysts.
The volcano-shaped relationship is very common in electrocatalytic nitrogen reduction reaction (e-NRR) and is usually caused by the competition between the first and last hydrogenation steps. How to break such a relationship to further improve the catalytic performance remains a great challenge. Herein, using first-principles calculations, we investigate a range of transition-metal (TM)-doped Cu-based single-atom alloys (TM1-Cu(111)) as catalysts for e-NRR. When the adsorption of N2 on the catalysts is strong enough, the inert N2 molecules can be effectively activated for the first hydrogenation step. Meanwhile, the last hydrogenation step is not affected by the scaling relationship and remains easy on all of the catalysts due to the unstable top-site adsorption of NH2, resulting in the break of the volcano-shaped relationship in e-NRR. Thus, only the first hydrogenation step is identified as the potential determining step. Four TM1-Cu(111) catalysts (TM = Re, W, Tc, and Mo) are selected as promising catalysts with limiting potential ranging from -0.38 to -0.56 V, showing outstanding e-NRR activity. Besides, the four catalysts also inhibit the competing hydrogen evolution reaction and long-term stability. Our work provides a guideline for breaking the volcano-shaped relationship in e-NRR and significant in the rational design of highly efficient electrocatalysts.

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