| Literature DB >> 30098083 |
Zhi Cao1,2,3, Samson B Zacate4, Xiaodong Sun1,2, Jinjia Liu1,2, Elizabeth M Hale4, William P Carson4, Sam B Tyndall4, Jun Xu3, Xingwu Liu1,2, Xingchen Liu1,2, Chang Song1,2, Jheng-Hua Luo5, Mu-Jeng Cheng5, Xiaodong Wen1,2, Wei Liu4.
Abstract
Capped chelating organic molecules are presented as a design principle for tuning heterogeneous nanoparticles for electrochemical catalysis. Gold nanoparticles (AuNPs) functionalized with a chelating tetradentate porphyrin ligand show a 110-fold enhancement compared to the oleylamine-coated AuNP in current density for electrochemical reduction of CO2 to CO in water at an overpotential of 340 mV with Faradaic efficiencies (FEs) of 93 %. These catalysts also show excellent stability without deactivation (<5 % productivity loss) within 72 hours of electrolysis. DFT calculation results further confirm the chelation effect in stabilizing molecule/NP interface and tailoring catalytic activity. This general approach is thus anticipated to be complementary to current NP catalyst design approaches.Entities:
Keywords: CO2 reduction; chelate effect; electrocatalysis; gold nanoparticles; porphyrins
Year: 2018 PMID: 30098083 DOI: 10.1002/anie.201805696
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336