MétaCan
Menu
← Back to cohort
Record W2260813982 · doi:10.1149/ma2014-01/14/647

Sulfur-Doped Graphene Supported Platinum Electrocatalysts for Oxygen Reduction Reaction in PEM Fuel Cells

2014· article· en· W2260813982 on OpenAlexaff
Zhongwei Chen, Drew Higgins, Min Ho Seo

Bibliographic record

VenueECS Meeting Abstracts · 2014
Typearticle
Languageen
FieldEngineering
TopicFuel Cells and Related Materials
Canadian institutionsUniversity of Waterloo
Fundersnot available
KeywordsCatalysisMaterials scienceGrapheneProton exchange membrane fuel cellPlatinumElectrolytePlatinum nanoparticlesChemical engineeringNanoparticleCatalyst supportCarbon fibersNanotechnologyElectrodeChemistryComposite materialComposite numberOrganic chemistry

Abstract

fetched live from OpenAlex

Polymer electrolyte membrane (PEM) fuel cells have been viewed as promising power source candidates for transport, stationary, and portable applications due to their high efficiency and low emissions. The platinum is the most commonly used catalyst material for the oxygen reduction reaction (ORR) at the cathode of PEM fuel cells; however, despite ample investigations being done on this type of catalyst, the performance and durability of platinum still need to be improved in order to meet the commercial target. The material on which the catalyst is supported is important for the high dispersion and narrow distribution of Pt nanoparticles, and these characteristics are closely related to electrocatalytic activity of the catalysts. The support materials can influence the catalytic activity by interplaying with catalytic metals, and the durability of the catalyst is also greatly dependent on its supports. Graphene has recently emerged as a highly promising catalyst support material for PEMFC applications owing to its immense surface areas, along with excellent conductivity and electron transfer capabilities that are important criteria pertaining to electro-catalysis. Graphene is theoretically composed of only graphitic carbon atoms which can provide added resilience against carbon corrosion during PEMFC operation, although the relatively inert and hydrophobic nature of its surface does not culminate in facile Pt deposition, requiring functionalization procedures to obtain well dispersed nanoparticles and overcome stability limitations. To this end, nitrogen doped graphene and other graphitic carbons have been extensively developed and investigated for fuel cell catalyst applications, either as stand-alone ORR electrocatalysts in alkaline media as Pt nanoparticle supports under acidic (i.e. PEMFC) conditions. The presence of nitrogen dopants has been reported to exert a “tethering” effect on Pt nanoparticles, providing both beneficial catalyst activity and stability enhancements. While density functional theory simulations exist in the literature investigating the adsorption and binding interactions between Pt and either nitrogen and boron doped graphene or carbon nanotubes (CNTs), there exists an overall lack of fundamental understanding regarding the Pt-heteroatom doped graphene catalyst-support interactions and their associated impact on ORR performance and operational stability. Furthermore, the impact of graphene doped with various other heteroatoms (i.e. sulfur) remains largely unexplored despite their high potential for applications as ORR catalysts or catalyst support materials. Elucidation of these important considerations can be provided by effectively linking fundamental computational simulations with detailed experimental investigations. In the present work, we report the development of sulfur-doped graphene (SG) by thermal shock/quench annealing a mixture of graphene oxide (GO) and phenyl disulfide (PDS). These materials were used as Pt nanoparticle support materials, whereby after Pt deposition onto SG (Pt/SG) by a modified ethylene glycol (EG) method, uniformly sized nanoparticles well dispersed across the entirety of the SG surface were successfully obtained. Improved ORR activity was found for Pt/SG in comparison to Pt supported on un-doped graphene (Pt/G) along with commercial state of the art Pt/C (Figure 1). Furthermore and most notably, we also observed significantly enhanced stability of Pt/SG (Figure 1). On the basis of these observations, we performed ab initio density functional theory calculations to investigate the interactions occurring between SG and Pt and elucidate the root causes of ORR performance and stability enhancements. We found that the strengthened interaction and binding energies between Pt and SG arose, and could exclusively be linked to sulfur incorporation based on comparative investigations with un-doped G. Specifically, sulfur doping led to stronger adsorptive and cohesive binding energies with Pt, leading to the aforementioned catalyst-support tethering effect, along with negatively shifting the d-band center of the Pt atoms. These findings were used to explain the dramatically enhanced stability and improved activity of Pt/SG, respectively, in comparison to both Pt/G and Pt/C. This work represents the first comprehensive report of fundamental ab initio simulations linked to rigorous experimental investigations for sulfur doped graphene, and furthermore Pt/SG is presented for the first time as a highly active ORR catalyst with exemplary stability for PEMFC applications.

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 score0.003

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 integrity0.0000.001
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 head0.009
GPT teacher head0.206
Teacher spread0.197 · 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

Citations0
Published2014
Admission routes1
Has abstractyes

Explore more

Same venueECS Meeting Abstracts→Same topicFuel Cells and Related Materials→French-language works237,207→