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Record W4307344422 · doi:10.1021/jacs.2c08305

Fe–N–C Boosts the Stability of Supported Platinum Nanoparticles for Fuel Cells

2022· article· en· W4307344422 on OpenAlexfundno aff
Fei Xiao, Yian Wang, Gui‐Liang Xu, Fei Yang, Shangqian Zhu, Cheng‐Jun Sun, Yingdan Cui, Zhiwen Xu, Qinglan Zhao, Juhee Jang, Xiaoyi Qiu, Ershuai Liu, Walter S. Drisdell, Zidong Wei, Meng Gu, Khalil Amine, Minhua Shao

Bibliographic record

VenueJournal of the American Chemical Society · 2022
Typearticle
Languageen
FieldEnergy
TopicElectrocatalysts for Energy Conversion
Canadian institutionsnot available
FundersOffice of ScienceShenzhen Fundamental Research ProgramShenzhen Municipal Science and Technology Innovation CouncilLawrence Berkeley National LaboratorySouthern Marine Science and Engineering Guangdong Laboratory (Guangzhou)Southern University of Science and TechnologyFoshan Science and Technology BureauScience, Technology and Innovation Commission of Shenzhen MunicipalityInnovation and Technology CommissionChongqing UniversityCanada Excellence Research Chairs, Government of CanadaNatural Science Foundation of Shenzhen CityResearch Grants Council, University Grants CommitteeHong Kong University of Science and TechnologyUniversité Mohammed VI PolytechniqueMinistry of Science and Technology of the People's Republic of ChinaBrookhaven National LaboratoryArgonne National LaboratoryU.S. Department of EnergyCanadian Light Source
KeywordsChemistryDissolutionPlatinumElectrocatalystElectrochemistryElectrolyteCarbon fibersNanoparticleOxideCarbon blackChemical engineeringSubstrate (aquarium)MetalPlatinum nanoparticlesInorganic chemistryCatalysisElectrodePhysical chemistryMaterials scienceOrganic chemistryComposite materialComposite number

Abstract

fetched live from OpenAlex

The poor durability of Pt-based nanoparticles dispersed on carbon black is the challenge for the application of long-life polymer electrolyte fuel cells. Recent work suggests that Fe- and N-codoped carbon (Fe–N–C) might be a better support than conventional high-surface-area carbon. In this work, we find that the electrochemical surface area retention of Pt/Fe–N–C is much better than that of commercial Pt/C during potential cycling in both acidic and basic media. In situ inductively coupled plasma mass spectrometry studies indicate that the Pt dissolution rate of Pt/Fe–N–C is 3 times smaller than that of Pt/C during cycling. Density functional theory calculations further illustrate that the Fe–N–C substrate can provide strong and stable support to the Pt nanoparticles and alleviate the oxide formation by adjusting the electronic structure. The strong metal–substrate interaction, together with a lower metal dissolution rate and highly stable support, may be the reason for the significantly enhanced stability of Pt/Fe–N–C. This finding highlights the importance of carbon support selection to achieve a more durable Pt-based electrocatalyst for fuel cells.

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)0.000
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 score0.001
Threshold uncertainty score0.004

Distilled classifier scores by category (both heads)

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

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 head0.011
GPT teacher head0.229
Teacher spread0.219 · 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".

Quick stats

Citations178
Published2022
Admission routes1
Has abstractyes

Explore more

Same venueJournal of the American Chemical SocietySame topicElectrocatalysts for Energy ConversionFrench-language works237,207