Open AccessMo 2 P Monolayer as a Superior Electrocatalyst for Urea Synthesis from Nitrogen and Carbon Dioxide Fixation: A Computational Study
Author(s) -
Jiao Dongxu,
Wang Zhongxu,
Liu Yuejie,
Cai Qinghai,
Zhao Jingxiang,
Cabrera Carlos R.,
Chen Zhongfang
Publication year - 2024
Publication title -
energy and environmental materials
Language(s) - English
Resource type - Journals
ISSN - 2575-0356
DOI - 10.1002/eem2.12496
Subject(s) - monolayer , electrocatalyst , phosphide , catalysis , chemisorption , adsorption , transition metal , electrochemistry , chemistry , materials science , inorganic chemistry , urea , chemical engineering , nanotechnology , organic chemistry , electrode , engineering
Urea synthesis through the simultaneous electrocatalytic reduction of N 2 and CO 2 molecules under ambient conditions holds great promises as a sustainable alternative to its industrial production, in which the development of stable, highly efficient, and highly selective catalysts to boost the chemisorption, activation, and coupling of inert N 2 and CO 2 molecules remains rather challenging. Herein, by means of density functional theory computations, we proposed a new class of two‐dimensional nanomaterials, namely, transition‐metal phosphide monolayers (TM 2 P, TM = Ti, Fe, Zr, Mo, and W), as the potential electrocatalysts for urea production. Our results showed that these TM 2 P materials exhibit outstanding stability and excellent metallic properties. Interestingly, the Mo 2 P monolayer was screened out as the best catalyst for urea synthesis due to its small kinetic energy barrier (0.35 eV) for C–N coupling, low limiting potential (−0.39 V), and significant suppressing effects on the competing side reactions. The outstanding catalytic activity of the Mo 2 P monolayer can be ascribed to its optimal adsorption strength with the key *NCON species due to its moderate positive charges on the Mo active sites. Our findings not only propose a novel catalyst with high‐efficiency and high‐selectivity for urea production but also further widen the potential applications of metal phosphides in electrocatalysis.