TY - JOUR
T1 - Squaric acid adsorption and oxidation at gold and platinum electrodes
AU - Cheuquepán, William
AU - Martínez-Olivares, Jorge
AU - Rodes, Antonio
AU - Orts, José Manuel
N1 - Publisher Copyright:
© 2017 Elsevier B.V.
PY - 2018/6/15
Y1 - 2018/6/15
N2 - The adsorption and oxidation of squaric acid (3,4-dihydroxycyclobut-3-ene-1,2-dione, H2C4O4, SQA) at platinum and gold electrodes were studied spectroelectrochemically in perchloric acid solutions. Voltammetric experiments demonstrate that reversible adsorption takes place at gold electrodes in the double-layer region. As a difference with platinum electrodes, no dissociative adsorption processes leading to the blocking of the electrode surface are detected. ATR-SEIRAS experiments show potential-dependent adsorbate bands at potentials below 1.20 V vs RHE that, according to DFT calculations, can be assigned to adsorbed squarate. For platinum electrodes, the potential-dependent adsorption of squarate anions is coupled with the oxidative stripping of adsorbed carbon monoxide, which is formed upon dissociative SQA adsorption. Bonding of squarate species to the platinum and gold surfaces involves two oxygen atoms in a bidentate configuration, with the molecular plane perpendicular to the metal surface. The ATR-SEIRA spectra obtained for gold electrodes in the SQA oxidation region show bands for adsorbed bicarbonate anions formed from dissolved carbon dioxide molecules. In the case of platinum, distinct bands are observed for adsorbed oxidation products which probably are formed upon opening of the SQA ring.
AB - The adsorption and oxidation of squaric acid (3,4-dihydroxycyclobut-3-ene-1,2-dione, H2C4O4, SQA) at platinum and gold electrodes were studied spectroelectrochemically in perchloric acid solutions. Voltammetric experiments demonstrate that reversible adsorption takes place at gold electrodes in the double-layer region. As a difference with platinum electrodes, no dissociative adsorption processes leading to the blocking of the electrode surface are detected. ATR-SEIRAS experiments show potential-dependent adsorbate bands at potentials below 1.20 V vs RHE that, according to DFT calculations, can be assigned to adsorbed squarate. For platinum electrodes, the potential-dependent adsorption of squarate anions is coupled with the oxidative stripping of adsorbed carbon monoxide, which is formed upon dissociative SQA adsorption. Bonding of squarate species to the platinum and gold surfaces involves two oxygen atoms in a bidentate configuration, with the molecular plane perpendicular to the metal surface. The ATR-SEIRA spectra obtained for gold electrodes in the SQA oxidation region show bands for adsorbed bicarbonate anions formed from dissolved carbon dioxide molecules. In the case of platinum, distinct bands are observed for adsorbed oxidation products which probably are formed upon opening of the SQA ring.
KW - ATR-SEIRAS
KW - DFT
KW - Gold
KW - Platinum
KW - Squarate anions
KW - Squaric acid
KW - Thin film electrodes
UR - http://www.scopus.com/inward/record.url?scp=85032277171&partnerID=8YFLogxK
U2 - 10.1016/j.jelechem.2017.10.023
DO - 10.1016/j.jelechem.2017.10.023
M3 - Article
AN - SCOPUS:85032277171
SN - 1572-6657
VL - 819
SP - 178
EP - 186
JO - Journal of Electroanalytical Chemistry
JF - Journal of Electroanalytical Chemistry
ER -