Electrochemical nitrate reduction to ammonia (NORR) is promising to not only tackle environmental issues caused by nitrate but also produce ammonia at room temperatures. However, two critical challenges are the lack of effective electrocatalysts and the understanding of related reaction mechanisms. To overcome these challenges, we employed first-principles calculations to thoroughly study the performance and mechanisms of triple-atom catalysts (TACs) composed of transition metals (including 27 homonuclear TACs and 4 non-noble bimetallic TACs) anchored on N-doped carbon (NC). We found five promising candidates possessing not only thermodynamic and electrochemical stability, but also high activity and selectivity for ammonia production. Among them, non-noble homonuclear Ni@NC TAC show high activity with low theoretical limiting potential of -0.31 . Surprisingly, bimetallic CoNi@NC, CoCu@NC, and FeNi@NC TACs show ultrahigh activity with theoretical limiting potentials of 0.00 , without a potential determining step in the whole reaction pathways, representing the best theoretical activity been reported up to date. These promising candidates are facilitated by circumventing the limit of scaling relationships, a well-known obstacle for single-atom catalysts. This study indicates that designing suitable TACs can be a promising strategy for efficiently electro-catalyzing NORR and breaking the limit of the scaling relationship.
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http://dx.doi.org/10.1021/acsami.4c17726 | DOI Listing |
ACS Appl Mater Interfaces
January 2025
Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong SAR 999077, China.
Electrochemical nitrate reduction to ammonia (NORR) is promising to not only tackle environmental issues caused by nitrate but also produce ammonia at room temperatures. However, two critical challenges are the lack of effective electrocatalysts and the understanding of related reaction mechanisms. To overcome these challenges, we employed first-principles calculations to thoroughly study the performance and mechanisms of triple-atom catalysts (TACs) composed of transition metals (including 27 homonuclear TACs and 4 non-noble bimetallic TACs) anchored on N-doped carbon (NC).
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2024
Hong Kong Quantum AI Lab Limited, Pak Shek Kok, Hong Kong SAR 999077, China.
The carbon monoxide reduction reaction (CORR) toward C and C products such as propylene and cyclopropane can not only reduce anthropogenic emissions of CO and CO but also produce value-added organic chemicals for polymer and pharmaceutical industries. Here, we introduce the concept of triple atom catalysts (TACs) that have three intrinsically strained and active metal centers for reducing CO to C products. We applied grand canonical potential kinetics (GCP-K) to screen 12 transition metals (M) supported by nitrogen-doped graphene denoted as M3N7, where M stands for Mn, Fe, Co, Ni, Cu, Ru, Rh, Pd, Ag, Ir, Pt, and Au.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2024
School of Chemistry and Chemical Engineering, Anhui University of Technology, Maanshan, Anhui 243002, PR China. Electronic address:
Tremendous challenges remain to develop high-efficient catalysts for carbon dioxide reduction reaction (CORR) owing to the poor activity and low selectivity. However, the activity of catalyst with single active site is limited by the linear scaling relationship between the adsorption energy of intermediates. Motivated by the idea of multiple activity centers, triple metal clusters (M = Cr, Mn, Fe, Co, Ni, Cu, Pd, and Rh) doped PC monolayer (M@PC) were constructed in this study to investigate the CORR catalytic performance via density functional theory calculations.
View Article and Find Full Text PDFNanoscale
May 2024
School of Chemical Engineering, University of Science and Technology Liaoning, Anshan 114051, China.
In recent years, the development of highly active and selective electrocatalysts for the electrochemical reduction of CO to produce CO and formic acid has aroused great interest, and can reduce environmental pollution and greenhouse gas emissions. Due to the high utilization of atoms, atom-dispersed catalysts are widely used in CO reduction reactions (CORRs). Compared with single-atom catalysts (SACs), multi-atom catalysts have more flexible active sites, unique electronic structures and synergistic interatomic interactions, which have great potential in improving the catalytic performance.
View Article and Find Full Text PDFJ Phys Chem Lett
March 2024
Key Laboratory of Precision and Intelligent Chemistry, School of Chemistry and Material Sciences, CAS Key Laboratory of Materials for Energy Conversion, and Collaborative Innovation Center of Chemistry for Energy Materials (iChEM), University of Science and Technology of China, Hefei, Anhui 230026, China.
The sluggish kinetics of the sulfur reduction reaction (SRR) impedes the practical application of lithium-sulfur batteries (LSBs). Electrocatalysts are necessary to expedite the conversion of polysulfides. Here, we systematically investigate the chemical mechanisms and size dependence of catalytic activities toward the SRR from LiS to LiS on single-, double-, and triple-atom catalysts supported on CN (M@CN, where M is a 3d transitional metal and = 1-3) as model systems by using first-principles calculations and a comprehensive electrocatalytic model.
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