Journal
NANO RESEARCH
Volume 15, Issue 5, Pages 4039-4047Publisher
TSINGHUA UNIV PRESS
DOI: 10.1007/s12274-021-4009-4
Keywords
electrocatalytic nitrogen reduction reaction; two-dimensional (2D) extended metalloporphyrin (MPP) monolayer; single-atom catalyst; two-dimensional materials; high-throughput screening; first-principles calculations
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Funding
- National Natural Science Foundation of China [22073033, 21873032, 21673087, 21903032]
- Huazhong University of Science and Technology [2006013118, 3004013105]
- Fundamental Research Funds for the Central Universities [2019kfyRCPY116]
- Innovation and Talent Recruitment Base of New Energy Chemistry and Device [B21003]
- Guangdong Basic and Applied Basic Research Foundation [2021A1515010382]
- Public Service Platform of High Performance Computing by Network and Computing Center of HUST
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In this study, we systematically investigated the catalytic performance of transition metals anchored onto two-dimensional porphyrin substrates for nitrogen reduction reaction. Through computational calculations and screening, we identified four novel metalloporphyrin single-atom catalysts with excellent catalytic performance. The high catalytic activity of these catalysts is attributed to significant orbital hybridization and charge transfer between N-2 and the catalysts.
We systematically investigated the catalytic performance of 3d, 4d, and 5d transition metals anchored onto two-dimensional extended porphyrin (PP) substrates as nitrogen reduction reaction (NRR) electrocatalysts, employing density functional theory (DFT) calculations and four-step high-throughput screening. Four novel metalloporphyrin (MPP, M = Zr, Nb, Hf, and Re) single-atom catalyst candidates have been identified due to their excellent catalytic performance (low onset potential, high stability, and selectivity). Through comprehensive reaction path search, the maximum Gibbs free energy changes for NRR on the ZrPP (enzymatic-consecutive hybrid path), NbPP (consecutive path), HfPP (enzymatic-consecutive hybrid path), and RePP (distal path) catalysts are 0.38, 0.41, 0.53, and 0.53 eV, respectively. Band structures, projected density of states, and charge/spin distributions show that the high catalytic activity is due to significant orbital hybridizations and charge transfer between N-2 and MPP catalysts. We hope our work will promote experimental synthesis of these NRR electrocatalysts and provide new opportunities to the electrochemical conversion of N-2 to NH3 under ambient conditions.
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