Student or educator? Sign up with your school email and get 6 months of Pro free.
Cited by 325

The DOI matches its Crossref record.

Ordered Porous Carbons with Tunable Pore Sizes as Catalyst Supports in Direct Methanol Fuel Cell

Chai, Geun Seok, Yoon, Suk Bon, Yu, Jong-Sung, Choi, Jong-Ho, Sung, Yung-Eun·2004·The Journal of Physical Chemistry B

Abstract

Ordered uniform porous carbon frameworks with pore sizes in the range of 10 to ∼1000 nm were synthesized against removable colloidal silica crystalline templates by carbonization of phenol and formaldehyde as a carbon precursor. The porous carbons were used as supports for a Pt(50)−Ru(50) alloy catalyst to study their supporting effect on the anodic performance of the catalyst in a direct methanol fuel cell (DMFC). The use of the ordered uniform porous carbons resulted in much improved catalytic activity for methanol oxidation in the fuel cell probably due to their high surface areas, large pore volumes, and three-dimensionally interconnected uniform pore structures, which allow a higher degree of dispersion of the catalysts and efficient diffusion of reagents. In general, the smaller the pore sizes in the porous carbons were, the better the catalytic activity for methanol oxidation was. In addition, as pore sizes are getting smaller, the structural integrity with good pore interconnection seems to be getting more important for the catalytic oxidation of methanol. Among the porous carbons studied in this work, the one with about 25 nm in pore diameter (PtRu−C-25) showed the highest performance with power densities of ∼58 and ∼167 mW/cm 2 at 30 and 70 °C, respectively. These values roughly correspond to ∼70 and ∼40% increase as compared to those of a commercially available Pt−Ru alloy catalyst (E-TEK), respectively.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1021/jp0370472

Cites

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cited by

Metadata

Authors
Chai, G. S., Yoon, S. B., Yu, J.-S., Choi, J.-H., & Sung, Y.-E.
Venue
The Journal of Physical Chemistry B
Published
2004-04-30
Volume
108
Issue
22
Pages
7074-7079
ISSN
  • 1520-5207 (ISSN-L)
  • 1520-6106
OpenAlex
W2033029508
Cited by
325
References
0
FWCI
17.66
Type
journal article
Language
en
Open access
closed

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.