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@ARTICLE{Schatz:907985,
author = {Schatz, Michael and Jovanovic, Sven and Eichel, Rüdiger-A.
and Granwehr, Josef},
title = {{Q}uantifying local p{H} changes in carbonate electrolyte
during copper-catalysed $\hbox{{CO}}_2$ electroreduction
using in operando $^{13}\hbox{{C}}$ {NMR}},
journal = {Scientific reports},
volume = {12},
number = {1},
issn = {2045-2322},
address = {[London]},
publisher = {Macmillan Publishers Limited, part of Springer Nature},
reportid = {FZJ-2022-02309},
pages = {8274},
year = {2022},
abstract = {The electrochemical carbon dioxide reduction on copper
attracted considerable attention within the last decade,
since Cu is the only elemental transition metal that
catalyses the formation of short‑chain hydrocarbons and
alcohols. Research in this field is mainly focused on
understanding the reaction mechanism in terms of adsorbates
and intermediates. Furthermore, dynamic changes in the
micro‑environment of the catalyst, i.e. local pH and
$\hbox{CO}_2$ concentration values, play an equivalently
important role in the selectivity of product formation. In
this study, we present an in operando $^{13}\hbox{C}$
nuclear magnetic resonance technique that enables the
simultaneous measurement of pH and $\hbox{CO}_2$
concentration in electrode vicinity during electroreduction.
The influence of applied potential and buffer capacity of
the electrolyte on the formation of formate is demonstrated.
Theoretical considerations are confirmed experimentally and
the importance of the interplay between catalyst and
electrolyte is emphasised.},
cin = {IEK-9},
ddc = {600},
cid = {I:(DE-Juel1)IEK-9-20110218},
pnm = {1232 - Power-based Fuels and Chemicals (POF4-123) / EXC
2186: The Fuel Science Center – Adaptive Conversion
Systems for Renewable Energy and Carbon Sources (390919832)},
pid = {G:(DE-HGF)POF4-1232 / G:(GEPRIS)390919832},
typ = {PUB:(DE-HGF)16},
pubmed = {35585102},
UT = {WOS:000797636300042},
doi = {10.1038/s41598-022-12264-8},
url = {https://juser.fz-juelich.de/record/907985},
}