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Green synthesis of bifunctional phthalocyanine-porphyrin cofs in water for efficient electrocatalytic CO2 reduction coupled with methanol oxidation.
Zhang, Mi; Liao, Jia-Peng; Li, Run-Han; Sun, Sheng-Nan; Lu, Meng; Dong, Long-Zhang; Huang, Pei; Li, Shun-Li; Cai, Yue-Peng; Lan, Ya-Qian.
Afiliación
  • Zhang M; School of Chemistry, South China Normal University, Guangzhou510006, China.
  • Liao JP; School of Chemistry, South China Normal University, Guangzhou510006, China.
  • Li RH; School of Chemistry, South China Normal University, Guangzhou510006, China.
  • Sun SN; School of Chemistry, South China Normal University, Guangzhou510006, China.
  • Lu M; School of Chemistry, South China Normal University, Guangzhou510006, China.
  • Dong LZ; School of Chemistry, South China Normal University, Guangzhou510006, China.
  • Huang P; School of Chemistry, South China Normal University, Guangzhou510006, China.
  • Li SL; School of Chemistry, South China Normal University, Guangzhou510006, China.
  • Cai YP; School of Chemistry, South China Normal University, Guangzhou510006, China.
  • Lan YQ; School of Chemistry, South China Normal University, Guangzhou510006, China.
Natl Sci Rev ; 10(11): nwad226, 2023 Nov.
Article en En | MEDLINE | ID: mdl-37818117
ABSTRACT
Electrocatalytic CO2 reduction (ECR) coupled with organic oxidation is a promising strategy to produce high value-added chemicals and improve energy efficiency. However, achieving the efficient redox coupling reaction is still challenging due to the lack of suitable electrocatalysts. Herein, we designed two bifunctional polyimides-linked covalent organic frameworks (PI-COFs) through assembling phthalocyanine (Pc) and porphyrin (Por) by non-toxic hydrothermal methods in pure water to realize the above catalytic reactions. Due to the high conductivity and well-defined active sites with different chemical environments, NiPc-NiPor COF performs efficient ECR coupled with methanol oxidation reaction (MOR) (Faradaic efficiency of CO (FECO) = 98.12%, partial current densities of CO (jCO) = 6.14 mA cm-2 for ECR, FEHCOOH = 93.75%, jHCOOH = 5.81 mA cm-2 for MOR at low cell voltage (2.1 V) and remarkable long-term stability). Furthermore, experimental evidences and density functional theory (DFT) calculations demonstrate that the ECR process mainly conducts on NiPc unit with the assistance of NiPor, meanwhile, the MOR prefers NiPor conjugating with NiPc. The two units of NiPc-NiPor COF collaboratively promote the coupled oxidation-reduction reaction. For the first time, this work achieves the rational design of bifunctional COFs for coupled heterogeneous catalysis, which opens a new area for crystalline material catalysts.
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