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Atomically Dispersed Cu Catalysts on Sulfide-Derived Defective Ag Nanowires for Electrochemical CO2 Reduction.
Ma, Zhipeng; Wan, Tao; Zhang, Ding; Yuwono, Jodie A; Tsounis, Constantine; Jiang, Junjie; Chou, Yu-Hsiang; Lu, Xunyu; Kumar, Priyank V; Ng, Yun Hau; Chu, Dewei; Toe, Cui Ying; Han, Zhaojun; Amal, Rose.
Afiliação
  • Yuwono JA; College of Engineering and Computer Science, Australian National University, Canberra, Australian Capital Territory2601, Australia.
  • Ng YH; School of Energy and Environment, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong, 999077, China.
  • Toe CY; School of Engineering, The University of Newcastle, Callaghan, New South Wales2038, Australia.
ACS Nano ; 17(3): 2387-2398, 2023 Feb 14.
Article em En | MEDLINE | ID: mdl-36727675
ABSTRACT
Single-atom catalysts (SACs) have shown potential for achieving an efficient electrochemical CO2 reduction reaction (CO2RR) despite challenges in their synthesis. Here, Ag2S/Ag nanowires provide initial anchoring sites for Cu SACs (Cu/Ag2S/Ag), then Cu/Ag(S) was synthesized by an electrochemical treatment resulting in complete sulfur removal, i.e., Cu SACs on a defective Ag surface. The CO2RR Faradaic efficiency (FECO2RR) of Cu/Ag(S) reaches 93.0% at a CO2RR partial current density (jCO2RR) of 2.9 mA/cm2 under -1.0 V vs RHE, which outperforms sulfur-removed Ag2S/Ag without Cu SACs (Ag(S), 78.5% FECO2RR with 1.8 mA/cm2jCO2RR). At -1.4 V vs RHE, both FECO2RR and jCO2RR over Cu/Ag(S) reached 78.6% and 6.1 mA/cm2, which tripled those over Ag(S), respectively. As revealed by in situ and ex situ characterizations together with theoretical calculations, the interacted Cu SACs and their neighboring defective Ag surface increase microstrain and downshift the d-band center of Cu/Ag(S), thus lowering the energy barrier by ∼0.5 eV for *CO formation, which accounts for the improved CO2RR activity and selectivity toward related products such as CO and C2+ products.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article