| Literature DB >> 31433551 |
Dan Ren1, Jing Gao1, Linfeng Pan2, Zaiwei Wang2, Jingshan Luo1,3, Shaik M Zakeeruddin1, Anders Hagfeldt2, Michael Grätzel1.
Abstract
Electrochemical reduction of carbon dioxide, if powered by renewable electricity, could serve as a sustainable technology for carbon recycling and energy storage. Among all the products, ethanol is an attractive liquid fuel. However, the maximum faradaic efficiency of ethanol is only ≈10 % on polycrystalline Cu. Here, CuZn bimetallic catalysts were synthesized by in situ electrochemical reduction of ZnO-shell/CuO-core bi-metal-oxide. Dynamic evolution of catalyst was revealed by STEM-EDS mapping, showing the migration of Zn atom and blending between Cu and Zn. CuZn bimetallic catalysts showed preference towards ethanol formation, with the ratio of ethanol/ethylene increasing over five times regardless of applied potential. We achieved 41 % faradaic efficiency for C2+ liquids with this catalyst. Transitioning from H-cell to an electrochemical flow cell, we achieved 48.6 % faradaic efficiency and -97 mA cm-2 partial current density for C2+ liquids at only -0.68 V versus reversible hydrogen electrode in 1 m KOH. Operando Raman spectroscopy showed that CO binding on Cu sites was modified by Zn. Free CO and adsorbed *CH3 are believed to combine and form *COCH3 intermediate, which is exclusively reduced to ethanol.Entities:
Keywords: carbon dioxide; electrocatalysis; ethanol; flow cell; operando Raman spectroscopy
Year: 2019 PMID: 31433551 DOI: 10.1002/anie.201909610
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336