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Record W2597704047 · doi:10.1149/ma2017-01/31/1465

Effect of Carbon Support and Synthesis Method on Pt NP Utilization and Activity

2017· article· en· W2597704047 on OpenAlexaff
Sanaz Ketabi, Ehab N. El Sawy, Viola Birss

Bibliographic record

VenueECS Meeting Abstracts · 2017
Typearticle
Languageen
FieldEnergy
TopicElectrocatalysts for Energy Conversion
Canadian institutionsUniversity of Calgary
Fundersnot available
KeywordsCatalysisSolventCarbon fibersAqueous solutionProton exchange membrane fuel cellChemical engineeringPlatinumColloidMaterials scienceTransmission electron microscopyCarbon blackButanolNanoparticleChemistryNuclear chemistryEthanolInorganic chemistryNanotechnologyOrganic chemistryComposite material

Abstract

fetched live from OpenAlex

A key requirement for the large-scale commercialization of proton exchange membrane (PEM) fuel cells is to produce highly active, durable catalysts, while minimizing the use of precious noble metals, especially platinum (Pt). Higher utilization of Pt catalyst can be realized by understanding the effect of the carbon support microstructure on the distribution and formation of Pt nanoparticles (NPs) and by optimizing the synthesis method. In this work, Pt NPs were fabricated using a simple alcohol reduction method and then varying the carbon support pore structure and surface properties. The catalysts were then tested for their activity in 1 M C2H5OH + 0.5 M H2SO4 solutions. For Pt NP preparation, either ethanol or butanol were used as the solvent and reductant. The ethanolic or butanolic solution containing H2PtCl6 was then added to the carbon support dispersed in the same solvent at room temperature, and the mixture was heated at the boiling point for 2 hrs. In the case of the ethanol solvent, an aqueous alkaline solution was added to ensure the completion of Pt reduction [1]. However, this step was not used during synthesis when using butanol, due to its higher reducing power. Three types of carbon supports were investigated, Vulcan carbon (VC), Ketjenblack (KB), and colloid-imprinted carbon powders (CICs). The structure and distribution of the Pt NPs were confirmed by X-ray powder diffraction (XRD) and transmission electron microscopy (TEM). Figure 1 shows the cyclic voltammograms of JM Pt/VC and Pt/CIC85 (i.e., 85 nm pore size), prepared by both the ethanol and butanol synthesis methods, in 0.5 M H2SO4. Even though the theoretical specific surface areas were 70-80 m2/gPt (particle size of 3-3.5 nm), the electrochemical active surface area (ECSA) was found to depend on the synthesis method and the carbon support. The ethanol oxidation activity of catalysts per Pt area for the three carbon supports is shown in Figure 2. A strong dependence on the carbon microstructure was observed, with Pt/CIC and Pt/KB, showing a higher activity than Pt/VC, likely due to their higher content of mesopores in the catalyst layer [2]. The correlation between catalyst activity and the carbon microstructure for each synthesis method will be discussed in detail. References: 1. J. Xie, Q. Zhang, L. Gu, S. Xu, P. Wang, J. Liu, Y. Ding, Y.F. Yao, C. Nan, M. Zhao, Y. You, Z. Zou, Nano Energy (2016) 21, 247–257. 2. T. Soboleva, X. Zhao, K. Malek, Z. Xie, T. Navessin, S. Holdcroft, ACS applied materials and interfaces (2010) 2, 2, 375–384. Figure 1

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.001
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.002
Threshold uncertainty score0.005

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.001
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0010.000
Insufficient payload (model declined to judge)0.0020.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.018
GPT teacher head0.288
Teacher spread0.270 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2017
Admission routes1
Has abstractyes

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