TY - JOUR
T1 - Why shouldn't double-layer capacitance (Cdl) be always trusted to justify Faradaic electrocatalytic activity differences?
AU - Anantharaj, Sengeni
AU - Sugime, Hisashi
AU - Noda, Suguru
N1 - Funding Information:
This work was supported by the Grant-in-Aid for researchers provided by the Waseda Research Institute for Science and Engineering, Waseda University. Authors also thank Mr. Shoei Yamaoka, Ms. Natsuho Akagi, and Mr. Bozhi Chen of Noda-Hanada lab, Waseda university for their help in characterizations.
Publisher Copyright:
© 2021 Elsevier B.V.
PY - 2021/12/15
Y1 - 2021/12/15
N2 - Electrocatalytic water splitting activity trend is mainly justified using two activity markers namely the electrochemical surface area measured in terms of double-layer capacitance (Cdl) and the charge transfer resistance (Rct). In general, a better active catalyst always tends to have higher Cdl and lower Rct. The non-Faradaic Cdl has so far been shown to match with the Faradaic catalytic activity trend. Nonetheless, emphasizing its non-Faradaic origin and the fact that all ion adsorption and desorption sites should not necessarily be electrocatalytically active sites, we show here a strong disagreement between non-Faradaic Cdl and Faradaic oxygen evolution reaction (OER) activity trend between stainless steel (SS) and bleached stainless steel (BSS). BSS apparently exhibited higher Cdl due to increased OER inactive iron oxide contents on the surface while significantly losing its OER activity. This study, therefore, questions the credibility of using non-Faradaic Cdl to justify the purely Faradaic electrocatalytic activity trend.
AB - Electrocatalytic water splitting activity trend is mainly justified using two activity markers namely the electrochemical surface area measured in terms of double-layer capacitance (Cdl) and the charge transfer resistance (Rct). In general, a better active catalyst always tends to have higher Cdl and lower Rct. The non-Faradaic Cdl has so far been shown to match with the Faradaic catalytic activity trend. Nonetheless, emphasizing its non-Faradaic origin and the fact that all ion adsorption and desorption sites should not necessarily be electrocatalytically active sites, we show here a strong disagreement between non-Faradaic Cdl and Faradaic oxygen evolution reaction (OER) activity trend between stainless steel (SS) and bleached stainless steel (BSS). BSS apparently exhibited higher Cdl due to increased OER inactive iron oxide contents on the surface while significantly losing its OER activity. This study, therefore, questions the credibility of using non-Faradaic Cdl to justify the purely Faradaic electrocatalytic activity trend.
KW - Double layer capacitance
KW - Electrocatalysis
KW - Intrinsic activity
KW - Oxygen evolution reaction
KW - Water splitting
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U2 - 10.1016/j.jelechem.2021.115842
DO - 10.1016/j.jelechem.2021.115842
M3 - Article
AN - SCOPUS:85118942705
SN - 0022-0728
VL - 903
JO - Journal of Electroanalytical Chemistry
JF - Journal of Electroanalytical Chemistry
M1 - 115842
ER -