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Highly Efficient Ammonia Synthesis Electrocatalyst: Single Ru Atom on Naturally Nanoporous Carbon Materials
Author(s) -
Cao Yongyong,
Gao Yijing,
Zhou Hu,
Chen Xianlang,
Hu Hui,
Deng Shengwei,
Zhong Xing,
Zhuang Guilin,
Wang Jianguo
Publication year - 2018
Publication title -
advanced theory and simulations
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.068
H-Index - 17
ISSN - 2513-0390
DOI - 10.1002/adts.201800018
Subject(s) - electrocatalyst , overpotential , catalysis , carbon fibers , electrochemistry , graphene , density functional theory , nanoporous , materials science , gibbs free energy , adsorption , inorganic chemistry , chemistry , chemical engineering , nanotechnology , computational chemistry , electrode , organic chemistry , thermodynamics , physics , composite material , composite number , engineering
Stabilizing single‐atom metal catalysts with carbon materials and utilizing their synergistic effect remains challenging due to weak interactions between carbon‐based supports and metals. Density functional theory (DFT) calculations indicate that a single Ru atom was supported on a wide range of natural nanoporous carbon materials, including C 2 N, triazine‐C 3 N 4 (T‐C 3 N 4 ), and γ‐graphene. These carbon materials belong to a new generation of highly efficient electrocatalysts for the N 2 reduction reaction (NRR) and are named Ru 1 @C 2 N, Ru 1 @T‐C 3 N 4 , and Ru 1 @γ‐graphyne, respectively. Ab initio molecular dynamic (AIMD) simulations show that a single Ru atom can be stably anchored in the nanopores of these carbon materials with strong cohesive energy. Compared with parallel adsorption configuration, the vertical adsorption configuration of N 2 exhibits higher adsorption energy. The calculated Gibbs free energy reveals N 2 reduction on the three catalysts via associative mechanisms. Despite the similar limiting potentials (−0.96, −0.94, and −0.98 V on Ru 1 @C 2 N, Ru 1 @T‐C 3 N 4 , and Ru 1 @γ‐graphynes, respectively), the limiting step differs, indicating the significant effects of carbon material substrates on electrochemical NRR. However, the competitive and efficient hydrogen evolution reaction (HER) changes the potential determining step and increases the overpotential for the electrochemical nitrogen reduction (NRR). This study provides insights for experimental synthesis of electrocatalysts for N 2 reduction.