TY - JOUR
T1 - Operando Characterization of Iron Phthalocyanine Deactivation during Oxygen Reduction Reaction Using Electrochemical Tip-Enhanced Raman Spectroscopy
AU - Chen, Zhu
AU - Jiang, Song
AU - Kang, Gyeongwon
AU - Nguyen, Duc
AU - Schatz, George C.
AU - Van Duyne, Richard P
N1 - Funding Information:
The authors acknowledge financial support from the Air Force Office of Scientific Research MURI (FA9550-14-1-0003). Z.C. acknowledges support from the National Science Foundation under grant no. CHE-1807278. G.K., D.N., G.C.S., and R.P.V.D. acknowledge support from the National Science Foundation Center for Chemical Innovation dedicated to Chemistry at the Space-Time Limit (CaSTL) Grant CHE-1414466. G.K. and G.C.S. acknowledge support from Northwestern University Information Technology (NUIT) team and the Center for Nanoscale Materials (CNM) at Argonne National Laboratory for the computational resources. The authors thank Dr. Allen J. Bard, Dr. Henry White, Dr. Martin Edwards, and Dr. Katherine A. Willets for helpful discussions.
Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/10/2
Y1 - 2019/10/2
N2 - Electrochemical tip-enhanced Raman spectroscopy (EC-TERS) has been implemented to investigate the structure and activity of iron(II) phthalocyanine (FePc) - a model catalyst for the oxygen reduction reaction (ORR). Using EC-TERS, both reversible change and irreversible degradation to FePc have been observed during ORR. The reversible change in the Raman spectrum of FePc can be related to the FePc molecules that adapt a nonplanar geometry during catalysis. In contrast, the irreversible degradation of FePc is a consequence of FePc demetalation, leading to the subsequent formation of free base phthalocyanine. This observation affirms that FePc demetalation during ORR proceeds via a direct loss of Fe2+ and that carbon corrosion is not the operative mechanism. Importantly, the FePc demetalation process can be correlated with a loss of ORR activity suggesting that Fe-containing sites are essential for FePc to achieve high catalytic activity. This study establishes EC-TERS as a promising technique for the operando characterization of electrocatalytic reactions at the molecular scale.
AB - Electrochemical tip-enhanced Raman spectroscopy (EC-TERS) has been implemented to investigate the structure and activity of iron(II) phthalocyanine (FePc) - a model catalyst for the oxygen reduction reaction (ORR). Using EC-TERS, both reversible change and irreversible degradation to FePc have been observed during ORR. The reversible change in the Raman spectrum of FePc can be related to the FePc molecules that adapt a nonplanar geometry during catalysis. In contrast, the irreversible degradation of FePc is a consequence of FePc demetalation, leading to the subsequent formation of free base phthalocyanine. This observation affirms that FePc demetalation during ORR proceeds via a direct loss of Fe2+ and that carbon corrosion is not the operative mechanism. Importantly, the FePc demetalation process can be correlated with a loss of ORR activity suggesting that Fe-containing sites are essential for FePc to achieve high catalytic activity. This study establishes EC-TERS as a promising technique for the operando characterization of electrocatalytic reactions at the molecular scale.
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U2 - 10.1021/jacs.9b07979
DO - 10.1021/jacs.9b07979
M3 - Article
C2 - 31503482
AN - SCOPUS:85072848527
SN - 0002-7863
VL - 141
SP - 15684
EP - 15692
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 39
ER -