Enhanced Oxygen Reduction Activity of Platinum Micropore

Abstract The high overpotential of oxygen reduction reaction (ORR) prevents the wide commercialization of fuel cells and metal‐air batteries. To accelerate the reaction rate, porous electrocatalysts draw attention to obtain a higher specific surface area. However, the effect of micropores on ORR kin...

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Main Authors: Kota Nakahara, Dr. Atsunori Ikezawa, Dr. Takeyoshi Okajima, Prof. Dr. Hajime Arai
Format: Article
Language:English
Published: Wiley-VCH 2024-03-01
Series:ChemElectroChem
Subjects:
Online Access:https://doi.org/10.1002/celc.202300654
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author Kota Nakahara
Dr. Atsunori Ikezawa
Dr. Takeyoshi Okajima
Prof. Dr. Hajime Arai
author_facet Kota Nakahara
Dr. Atsunori Ikezawa
Dr. Takeyoshi Okajima
Prof. Dr. Hajime Arai
author_sort Kota Nakahara
collection DOAJ
description Abstract The high overpotential of oxygen reduction reaction (ORR) prevents the wide commercialization of fuel cells and metal‐air batteries. To accelerate the reaction rate, porous electrocatalysts draw attention to obtain a higher specific surface area. However, the effect of micropores on ORR kinetics has not been understood because of the non‐uniform pore sizes, length, and tortuosity of practical electrocatalysts. In this study, we evaluate ORR activity in a micropore using platinum model electrodes with arrays of cylindrical pores with a uniform pore diameter of 1.8 nm. The model electrodes having pore lengths of 45, 100, and 380 nm are fabricated, and their ORR performances are examined by electrochemical measurements and numerical simulations in 0.1 mol dm−3 KOH aqueous solution. The intrinsic ORR activity of the micropore is successfully obtained with the electrode having a pore length of 45 nm, where oxygen transport resistance in the micropore has little effect on ORR. It is found that the intrinsic ORR activity of the micropore is higher than that of a planar Pt surface. X‐ray photoelectron spectroscopy and CO stripping voltammetry indicate a downshift of the d‐band center, which can be the origin of the high intrinsic ORR activity.
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spelling doaj.art-c824dae633754134837f2eeb19833a172024-03-02T04:26:51ZengWiley-VCHChemElectroChem2196-02162024-03-01115n/an/a10.1002/celc.202300654Enhanced Oxygen Reduction Activity of Platinum MicroporeKota Nakahara0Dr. Atsunori Ikezawa1Dr. Takeyoshi Okajima2Prof. Dr. Hajime Arai3Department of Chemical Science and Engineering Tokyo Institute of Technology 4259 Nagatsuta-cho, Midori-ku, Yokohama Kanagawa 226–8501 JapanDepartment of Chemical Science and Engineering Tokyo Institute of Technology 4259 Nagatsuta-cho, Midori-ku, Yokohama Kanagawa 226–8501 JapanDepartment of Chemical Science and Engineering Tokyo Institute of Technology 4259 Nagatsuta-cho, Midori-ku, Yokohama Kanagawa 226–8501 JapanDepartment of Chemical Science and Engineering Tokyo Institute of Technology 4259 Nagatsuta-cho, Midori-ku, Yokohama Kanagawa 226–8501 JapanAbstract The high overpotential of oxygen reduction reaction (ORR) prevents the wide commercialization of fuel cells and metal‐air batteries. To accelerate the reaction rate, porous electrocatalysts draw attention to obtain a higher specific surface area. However, the effect of micropores on ORR kinetics has not been understood because of the non‐uniform pore sizes, length, and tortuosity of practical electrocatalysts. In this study, we evaluate ORR activity in a micropore using platinum model electrodes with arrays of cylindrical pores with a uniform pore diameter of 1.8 nm. The model electrodes having pore lengths of 45, 100, and 380 nm are fabricated, and their ORR performances are examined by electrochemical measurements and numerical simulations in 0.1 mol dm−3 KOH aqueous solution. The intrinsic ORR activity of the micropore is successfully obtained with the electrode having a pore length of 45 nm, where oxygen transport resistance in the micropore has little effect on ORR. It is found that the intrinsic ORR activity of the micropore is higher than that of a planar Pt surface. X‐ray photoelectron spectroscopy and CO stripping voltammetry indicate a downshift of the d‐band center, which can be the origin of the high intrinsic ORR activity.https://doi.org/10.1002/celc.202300654Microporous materialMicroporeNanostructuresOxygen reduction reactionPlatinum
spellingShingle Kota Nakahara
Dr. Atsunori Ikezawa
Dr. Takeyoshi Okajima
Prof. Dr. Hajime Arai
Enhanced Oxygen Reduction Activity of Platinum Micropore
ChemElectroChem
Microporous material
Micropore
Nanostructures
Oxygen reduction reaction
Platinum
title Enhanced Oxygen Reduction Activity of Platinum Micropore
title_full Enhanced Oxygen Reduction Activity of Platinum Micropore
title_fullStr Enhanced Oxygen Reduction Activity of Platinum Micropore
title_full_unstemmed Enhanced Oxygen Reduction Activity of Platinum Micropore
title_short Enhanced Oxygen Reduction Activity of Platinum Micropore
title_sort enhanced oxygen reduction activity of platinum micropore
topic Microporous material
Micropore
Nanostructures
Oxygen reduction reaction
Platinum
url https://doi.org/10.1002/celc.202300654
work_keys_str_mv AT kotanakahara enhancedoxygenreductionactivityofplatinummicropore
AT dratsunoriikezawa enhancedoxygenreductionactivityofplatinummicropore
AT drtakeyoshiokajima enhancedoxygenreductionactivityofplatinummicropore
AT profdrhajimearai enhancedoxygenreductionactivityofplatinummicropore