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@ARTICLE{Bertelsen:640326,
author = {Bertelsen, Andreas Dueholm and Klemmt, Rebekka and Kolding,
Kirstine Nygaard and Bøjesen, Espen Drath and Iversen, Bo
Brummerstedt},
title = {{C}opper-{R}ich {P}d$_x${C}u$_{1–x}$ {A}lloy
{N}anoparticles as {C}atalyst for {E}lectrochemical
{R}eduction of {CO}$_2$},
journal = {Chemistry of materials},
volume = {37},
number = {17},
issn = {0897-4756},
address = {Washington, DC},
publisher = {American Chemical Society},
reportid = {PUBDB-2025-04777},
pages = {6619 - 6628},
year = {2025},
abstract = {Copper is uniquely able to catalyze the formation of
hydrocarbon-derived molecules through the electrochemical
carbon dioxide reduction reaction (CO2RR) in aqueous media.
Here, we investigate the change of selectivity and/or
activity in CO2RR by alloying Cu with palladium by using
PdxCu1–x nanoparticles as electrocatalysts. In situ powder
X-ray diffraction reveals a much lowered reduction
temperature of the Cu-precursor upon alloying and
establishes the importance of high heating rates during
synthesis to ensure homogeneous Pd alloying into copper-rich
PdxCu1–x nanoparticles. Two different synthetic approaches
were used to obtain PdxCu1–x nanoparticles with a
composition range of x = 0.025–0.20, and the complex
nanostructures of the particles were highlighted using
four-dimensional Scanning Transmission Electron Microscopy
(4D-STEM). The activity and selectivity toward
electrochemical CO2RR in 0.1 M KHCO3 were assessed for
increasing Pd contents, and a systematic decrease in
faradaic efficiency toward hydrocarbon products was found
coupled with an increase in faradaic efficiency toward
primarily H2. The results do not support PdxCu1–x alloying
as a viable method for increasing selectivity toward
specific hydrocarbon products in electrochemical CO2RR.},
cin = {DOOR ; HAS-User},
ddc = {540},
cid = {I:(DE-H253)HAS-User-20120731},
pnm = {6G3 - PETRA III (DESY) (POF4-6G3) / FS-Proposal: I-20220506
EC (I-20220506-EC)},
pid = {G:(DE-HGF)POF4-6G3 / G:(DE-H253)I-20220506-EC},
experiment = {EXP:(DE-H253)P-P21.1-20150101},
typ = {PUB:(DE-HGF)16},
doi = {10.1021/acs.chemmater.5c01148},
url = {https://bib-pubdb1.desy.de/record/640326},
}