TY - JOUR
T1 - Flow Electrolyzer Mass Spectrometry with a Gas-Diffusion Electrode Design
AU - Hasa, Bjorn
AU - Jouny, Matthew
AU - Ko, Byung Hee
AU - Xu, Bingjun
AU - Jiao, Feng
N1 - Publisher Copyright:
© 2020 Wiley-VCH GmbH
PY - 2021/2/8
Y1 - 2021/2/8
N2 - Operando mass spectrometry is a powerful technique to probe reaction intermediates near the surface of catalyst in electrochemical systems. For electrochemical reactions involving gas reactants, conventional operando mass spectrometry struggles in detecting reaction intermediates because the batch-type electrochemical reactor can only handle a very limited current density due to the low solubility of gas reactant(s). Herein, we developed a new technique, namely flow electrolyzer mass spectrometry (FEMS), by incorporating a gas-diffusion electrode design, which enables the detection of reactive volatile or gaseous species at high operating current densities (>100 mA cm−2). We investigated the electrochemical carbon monoxide reduction reaction (eCORR) on polycrystalline copper and elucidated the oxygen incorporation mechanism in the acetaldehyde formation. Combining FEMS and isotopic labelling, we showed that the oxygen in the as-formed acetaldehyde intermediate originates from the reactant CO, while ethanol and n-propanol contained mainly solvent oxygen. The observation provides direct experimental evidence of an isotopic scrambling mechanism.
AB - Operando mass spectrometry is a powerful technique to probe reaction intermediates near the surface of catalyst in electrochemical systems. For electrochemical reactions involving gas reactants, conventional operando mass spectrometry struggles in detecting reaction intermediates because the batch-type electrochemical reactor can only handle a very limited current density due to the low solubility of gas reactant(s). Herein, we developed a new technique, namely flow electrolyzer mass spectrometry (FEMS), by incorporating a gas-diffusion electrode design, which enables the detection of reactive volatile or gaseous species at high operating current densities (>100 mA cm−2). We investigated the electrochemical carbon monoxide reduction reaction (eCORR) on polycrystalline copper and elucidated the oxygen incorporation mechanism in the acetaldehyde formation. Combining FEMS and isotopic labelling, we showed that the oxygen in the as-formed acetaldehyde intermediate originates from the reactant CO, while ethanol and n-propanol contained mainly solvent oxygen. The observation provides direct experimental evidence of an isotopic scrambling mechanism.
KW - CO reduction
KW - CO utilization
KW - electrocatalysis
KW - operando mass spectrometry
UR - https://www.scopus.com/pages/publications/85096996219
U2 - 10.1002/anie.202013713
DO - 10.1002/anie.202013713
M3 - Article
C2 - 33090694
AN - SCOPUS:85096996219
SN - 1433-7851
VL - 60
SP - 3277
EP - 3282
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 6
ER -