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Efficient Electrosynthesis of Urea over Single-Atom Alloy with Electronic Metal Support Interaction.
Zhan, Peng; Zhuang, Jinjie; Yang, Shuai; Li, Xuechun; Chen, Xuehan; Wen, Tian; Lu, Lu; Qin, Peiyong; Han, Buxing.
Afiliação
  • Zhan P; National Energy R&D Center for Biorefinery, Beijing University of Chemical Technology, Beijing, 100029, China.
  • Zhuang J; Paris Curie Engineer School, Beijing University of Chemical Technology, Beijing, 100029, China.
  • Yang S; National Energy R&D Center for Biorefinery, Beijing University of Chemical Technology, Beijing, 100029, China.
  • Li X; College of Chemistry, Beijing University of Chemical Technology, Beijing, 100029, China.
  • Chen X; Paris Curie Engineer School, Beijing University of Chemical Technology, Beijing, 100029, China.
  • Wen T; Paris Curie Engineer School, Beijing University of Chemical Technology, Beijing, 100029, China.
  • Lu L; Paris Curie Engineer School, Beijing University of Chemical Technology, Beijing, 100029, China.
  • Qin P; National Energy R&D Center for Biorefinery, Beijing University of Chemical Technology, Beijing, 100029, China.
  • Han B; Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Colloid and Interface and Thermodynamics, CAS Research, Education Center for Excellence in Molecular Sciences, Center of Carbon Neutral Chemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100029, China.
Angew Chem Int Ed Engl ; : e202409019, 2024 May 24.
Article em En | MEDLINE | ID: mdl-38785222
ABSTRACT
Urea electrosynthesis from carbon dioxide (CO2) and nitrate (NO3 -) is an alternative approach to traditional energy-intensive urea synthesis technology. Herein, we report a CuAu single-atom alloy (SAA) with electronic metal support interaction (EMSI), achieving a high urea yield rate of 813.6 µg h-1 mgcat -1 at -0.94 V versus reversible hydrogen electrode (vs. RHE) and a Faradaic efficiency (FE) of 45.2 % at -0.74 V vs. RHE. In situ experiments and theoretical calculations demonstrated that single-atom Cu sites modulate the adsorption behavior of intermediate species. Bimetallic sites synergistically accelerate C-N bond formation through spontaneous coupling of *CO and *NO to form *ONCO as key intermediates. More importantly, electronic metal support interaction between CuAu SAA and CeO2 carrier further modulates electron structure and interfacial microenvironment, endowing electrocatalysts with superior activity and durability. This work constructs SAA electrocatalysts with EMSI effect to tailor C-N coupling at the atomic level, which can provide guidance for the development of C-N coupling systems.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article