Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...
Abstract
The electroreduction of C
1
feedgas to high-energy-density fuels provides an attractive avenue to the storage of renewable electricity. Much progress has been made to improve selectivity to C
1
and C
2
products, however, the selectivity to desirable high-energy-density C
3
products remains relatively low. We reason that C
3
electrosynthesis relies on a higher-order reaction pathway that requires the formation of multiple carbon-carbon (C-C) bonds, and thus pursue a strategy explicitly designed to couple C
2
with C
1
intermediates. We develop an approach wherein neighboring copper atoms having distinct electronic structures interact with two adsorbates to catalyze an asymmetric reaction. We achieve a record
n
-propanol Faradaic efficiency (FE) of (33 ± 1)% with a conversion rate of (4.5 ± 0.1) mA cm
−2
, and a record
n
-propanol cathodic energy conversion efficiency (EE
cathodic half-cell
) of 21%. The FE and EE
cathodic half-cell
represent a 1.3× improvement relative to previously-published CO-to-
n
-propanol electroreduction reports.