Oxygen crossover effect on palladium and platinum based electrocatalysts during formic acid oxidation studied by scanning electrochemical microscopy

The electrocatalytic activity towards formic acid oxidation reaction (FAOR) in the presence of simultaneous oxygen reduction reaction (ORR) displayed by 5 different metallic nanoparticles (NPs) (Pt100, Pt75Pd25, Pt50Pd50, Pt25Pd75 and Pd100) was studied and compared using chronoamperometry and the m...

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Veröffentlicht in:Journal of electroanalytical chemistry (Lausanne, Switzerland) Switzerland), 2017-05, Vol.793, p.218-225
Hauptverfasser: Perales-Rondón, Juan V., Herrero, Enrique, Solla-Gullón, José, Sánchez-Sánchez, Carlos M., Vivier, Vincent
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container_title Journal of electroanalytical chemistry (Lausanne, Switzerland)
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creator Perales-Rondón, Juan V.
Herrero, Enrique
Solla-Gullón, José
Sánchez-Sánchez, Carlos M.
Vivier, Vincent
description The electrocatalytic activity towards formic acid oxidation reaction (FAOR) in the presence of simultaneous oxygen reduction reaction (ORR) displayed by 5 different metallic nanoparticles (NPs) (Pt100, Pt75Pd25, Pt50Pd50, Pt25Pd75 and Pd100) was studied and compared using chronoamperometry and the micropipette delivery/substrate collection (MD/SC) mode of the scanning electrochemical microscopy (SECM). This is of special interest for understanding the O2 crossover effect in direct formic acid fuel cells (DFAFCs) and to search highly selective electrocatalysts useful in mixed-reactant fuel cells (MRFCs). A detailed analysis of the SECM results in comparison with chronoamperometry demonstrates, for the first time, the relevant role played by dissolved O2 in solution on the Pd100 NPs deactivation during FAOR, which cannot be explained neither by the specific adsorption of dichloroethane (DCE) on Pd nor by a simple addition of two opposed currents coming from simultaneous FAOR and ORR. Two main mechanistic factors are proposed for explaining the different sensitivity towards O2 presence in solution during FAOR when comparing Pd- and Pt-rich catalysts. On the one hand, the relevance of H2O2 production (ORR byproduct) and accumulation on Pd NPs, which alters its performance towards FAOR. On the other hand, the predominance of the poisoning pathway forming COads during FAOR on Pt NPs, whose oxidation is facilitated in the presence of traces of O2. Interestingly, the deactivation effect displayed on Pd100 NPs during FAOR due to the H2O2 generation and accumulation becomes negligible if a convective regime is applied in solution. SECM is proved as a fast and powerful technique for studying O2 crossover effect in different electrocatalysts and for identifying highly selective electrocatalysts candidates for MRFCs. In particular, among the samples evaluated, Pt75Pd25 NPs present the highest average performance for FAOR in 0.5M H2SO4 solution in the presence of O2 within the potential range under study (0.3–0.7V vs RHE). •SECM as a proper diagnostic tool to evaluate electrocatalysts in the presence of reactants crossover•Simultaneous FAOR and ORR on Pd, Pt and Pd-Pt alloyed nanoparticles imaged by SECM•Pd electrode deactivation during FAOR due to the role of O2 crossover•Pt75Pd25 nanoparticles display the highest performance for FAOR in the presence of O2.
doi_str_mv 10.1016/j.jelechem.2016.12.049
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This is of special interest for understanding the O2 crossover effect in direct formic acid fuel cells (DFAFCs) and to search highly selective electrocatalysts useful in mixed-reactant fuel cells (MRFCs). A detailed analysis of the SECM results in comparison with chronoamperometry demonstrates, for the first time, the relevant role played by dissolved O2 in solution on the Pd100 NPs deactivation during FAOR, which cannot be explained neither by the specific adsorption of dichloroethane (DCE) on Pd nor by a simple addition of two opposed currents coming from simultaneous FAOR and ORR. Two main mechanistic factors are proposed for explaining the different sensitivity towards O2 presence in solution during FAOR when comparing Pd- and Pt-rich catalysts. On the one hand, the relevance of H2O2 production (ORR byproduct) and accumulation on Pd NPs, which alters its performance towards FAOR. On the other hand, the predominance of the poisoning pathway forming COads during FAOR on Pt NPs, whose oxidation is facilitated in the presence of traces of O2. Interestingly, the deactivation effect displayed on Pd100 NPs during FAOR due to the H2O2 generation and accumulation becomes negligible if a convective regime is applied in solution. SECM is proved as a fast and powerful technique for studying O2 crossover effect in different electrocatalysts and for identifying highly selective electrocatalysts candidates for MRFCs. 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This is of special interest for understanding the O2 crossover effect in direct formic acid fuel cells (DFAFCs) and to search highly selective electrocatalysts useful in mixed-reactant fuel cells (MRFCs). A detailed analysis of the SECM results in comparison with chronoamperometry demonstrates, for the first time, the relevant role played by dissolved O2 in solution on the Pd100 NPs deactivation during FAOR, which cannot be explained neither by the specific adsorption of dichloroethane (DCE) on Pd nor by a simple addition of two opposed currents coming from simultaneous FAOR and ORR. Two main mechanistic factors are proposed for explaining the different sensitivity towards O2 presence in solution during FAOR when comparing Pd- and Pt-rich catalysts. On the one hand, the relevance of H2O2 production (ORR byproduct) and accumulation on Pd NPs, which alters its performance towards FAOR. On the other hand, the predominance of the poisoning pathway forming COads during FAOR on Pt NPs, whose oxidation is facilitated in the presence of traces of O2. Interestingly, the deactivation effect displayed on Pd100 NPs during FAOR due to the H2O2 generation and accumulation becomes negligible if a convective regime is applied in solution. SECM is proved as a fast and powerful technique for studying O2 crossover effect in different electrocatalysts and for identifying highly selective electrocatalysts candidates for MRFCs. 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This is of special interest for understanding the O2 crossover effect in direct formic acid fuel cells (DFAFCs) and to search highly selective electrocatalysts useful in mixed-reactant fuel cells (MRFCs). A detailed analysis of the SECM results in comparison with chronoamperometry demonstrates, for the first time, the relevant role played by dissolved O2 in solution on the Pd100 NPs deactivation during FAOR, which cannot be explained neither by the specific adsorption of dichloroethane (DCE) on Pd nor by a simple addition of two opposed currents coming from simultaneous FAOR and ORR. Two main mechanistic factors are proposed for explaining the different sensitivity towards O2 presence in solution during FAOR when comparing Pd- and Pt-rich catalysts. On the one hand, the relevance of H2O2 production (ORR byproduct) and accumulation on Pd NPs, which alters its performance towards FAOR. On the other hand, the predominance of the poisoning pathway forming COads during FAOR on Pt NPs, whose oxidation is facilitated in the presence of traces of O2. Interestingly, the deactivation effect displayed on Pd100 NPs during FAOR due to the H2O2 generation and accumulation becomes negligible if a convective regime is applied in solution. SECM is proved as a fast and powerful technique for studying O2 crossover effect in different electrocatalysts and for identifying highly selective electrocatalysts candidates for MRFCs. In particular, among the samples evaluated, Pt75Pd25 NPs present the highest average performance for FAOR in 0.5M H2SO4 solution in the presence of O2 within the potential range under study (0.3–0.7V vs RHE). •SECM as a proper diagnostic tool to evaluate electrocatalysts in the presence of reactants crossover•Simultaneous FAOR and ORR on Pd, Pt and Pd-Pt alloyed nanoparticles imaged by SECM•Pd electrode deactivation during FAOR due to the role of O2 crossover•Pt75Pd25 nanoparticles display the highest performance for FAOR in the presence of O2.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/j.jelechem.2016.12.049</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-4285-4648</orcidid><orcidid>https://orcid.org/0000-0001-5424-0083</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1572-6657
ispartof Journal of electroanalytical chemistry (Lausanne, Switzerland), 2017-05, Vol.793, p.218-225
issn 1572-6657
1873-2569
language eng
recordid cdi_hal_primary_oai_HAL_hal_01552820v1
source Elsevier ScienceDirect Journals
subjects Accumulation
Chemical Sciences
Crossover
Deactivation
Dichloroethane
Electrocatalysis
Electrocatalysts
FAOR
Formic acid
Fuel cells
Hydrogen peroxide
Microscopy
Nanoparticles
ORR
Other
Oxidation
Oxygen
Oxygen reduction reactions
Palladium
Platinum
Scanning electron microscopy
SECM
Substrates
Sulfuric acid
title Oxygen crossover effect on palladium and platinum based electrocatalysts during formic acid oxidation studied by scanning electrochemical microscopy
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