2021
DOI: 10.3390/catal11121517
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Influence of Cathode Catalyst Layer with SiO2-Coated Pt/Ketjen Black Catalysts on Performance for Polymer Electrolyte Fuel Cells

Abstract: In this study, we investigated the effect of silica (SiO2) layer included in a cathode catalyst layer (CL) on the performance for polymer electrolyte fuel cells (PEFCs). Porous carbons such as Ketjen black (KB) have been widely used as a support for Pt catalysts in PEFCs. Such KB-supported Pt catalyst (Pt/KB) was used as a cathode CL with low ionomer content (a condition of low proton conductivity). The Pt/KB was then coated with SiO2. In addition, the Pt/KB and SiO2-coated Pt/KB (SiO2-Pt/KB) were measured and… Show more

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Cited by 4 publications
(8 citation statements)
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References 27 publications
(44 reference statements)
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“…Distinct from the transition-metal oxides stated above, silica (typical-metal oxide) is neither oxidized by ·OH radicals nor reduced by H 2 . It has been reported that the incorporation of SiO 2 –NPs in a Nafion membrane increased the σ H , specifically at low relative humidity (RH), due to its hygroscopic property. , Recently, Inoue et al added silica NPs to the anode and cathode CLs of gas diffusion electrodes (GDE) to increase the effective utilization of Pt catalysts under low RH conditions, , while Park et al reported an increase in the cell performance by coating an SiO 2 layer on Pt/C cathode catalysts . On the basis of these results, it is envisioned that the addition of hygroscopic silica NPs leads to a longer residence time of H 2 O 2 molecules within the anode CL, leading to a longer lifetime of the Nafion membrane, as well as an increase in the effective utilization of the Pt catalyst.…”
Section: Introductionmentioning
confidence: 99%
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“…Distinct from the transition-metal oxides stated above, silica (typical-metal oxide) is neither oxidized by ·OH radicals nor reduced by H 2 . It has been reported that the incorporation of SiO 2 –NPs in a Nafion membrane increased the σ H , specifically at low relative humidity (RH), due to its hygroscopic property. , Recently, Inoue et al added silica NPs to the anode and cathode CLs of gas diffusion electrodes (GDE) to increase the effective utilization of Pt catalysts under low RH conditions, , while Park et al reported an increase in the cell performance by coating an SiO 2 layer on Pt/C cathode catalysts . On the basis of these results, it is envisioned that the addition of hygroscopic silica NPs leads to a longer residence time of H 2 O 2 molecules within the anode CL, leading to a longer lifetime of the Nafion membrane, as well as an increase in the effective utilization of the Pt catalyst.…”
Section: Introductionmentioning
confidence: 99%
“…14,15 Recently, Inoue et al added silica NPs to the anode and cathode CLs of gas diffusion electrodes (GDE) to increase the effective utilization of Pt catalysts under low RH conditions, 16,17 while Park et al reported an increase in the cell performance by coating an SiO 2 layer on Pt/C cathode catalysts. 18 On the basis of these results, it is envisioned that the addition of hygroscopic silica NPs leads to a longer residence time of H 2 O 2 molecules within the anode CL, leading to a longer lifetime of the Nafion membrane, as well as an increase in the effective utilization of the Pt catalyst.…”
Section: Introductionmentioning
confidence: 99%
“…At lower concentrations and adjusted ionomer contents in the cathode electrode, SiO 2 ‐containing MEAs can provide better performances at low RH conditions, but also limited mass transport at high RH values and current densities. [ 23,24 ] In the present work, the effect on water retention appears to excel effect of the SiO 2 on electronic or reactant diffusion resistances visible in the slightly better performance in neat H 2 .…”
Section: Resultsmentioning
confidence: 54%
“…The measured Si loading of %0.6 wt% is low as compared to values ranging from 0.3 to 40 wt% reported in other studies on similar types of SiO 2 coatings. [18,19,[21][22][23][24]26] The comparably low concentration is assumed to either stem from adsorption of APTES and TEOS on container surfaces during the coating process or from unreacted reagent removed during the washing procedure at the end of the hydrolysis step. Whether the electrocatalyst stability and performance are enhanced, likely depends on the thickness, pore structure, and hydrophilicity of the SiO 2 coating, being a function of the precursor types, their amount and on the settings during the fabrication process.…”
Section: Resultsmentioning
confidence: 99%
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