Detail View

Low temperature synthesis of new highly graphitized N-doped carbon for Pt fuel cell supports, satisfying DOE 2025 durability standards for both catalyst and support
Citations

WEB OF SCIENCE

Citations

SCOPUS

Metadata Downloads

Title
Low temperature synthesis of new highly graphitized N-doped carbon for Pt fuel cell supports, satisfying DOE 2025 durability standards for both catalyst and support
Issued Date
2023-04
Citation
Lee, Ha-Young. (2023-04). Low temperature synthesis of new highly graphitized N-doped carbon for Pt fuel cell supports, satisfying DOE 2025 durability standards for both catalyst and support. Applied Catalysis B: Environmental, 323. doi: 10.1016/j.apcatb.2022.122179
Type
Article
Author Keywords
Real-time degradation analysisGrand canonical reaction kineticsPEMFCsGraphitized carbonPyrrolic-N
Keywords
NITROGENELECTROCATALYSTSPERFORMANCENITRIDEDEGRADATIONOPERATIONGRAPHENE
ISSN
0926-3373
Abstract
For polymer electrolyte membrane fuel cells (PEMFCs), the state-of-the-art electrocatalysts are based on carbon-supported Pt group metals. However, current carbon supports suffer from carbon corrosion during repeated start-stop operations, causing performance degradation. We report a new strategy to produce highly graphitized carbon with controllable N-doping that uses low-temperature synthesis (650 ℃) from g-C3N4 carbon-nitrogen precursor with pyrolysis using Mg. The high graphiticity is confirmed by high-intensity 2D Raman peak with low ID/IG (0.57), pronounced graphitic XRD planes, and excellent conductivity. Without further post-treatment, this highly graphitized N-doped carbon (HGNC) material combines high pyrrolic-N content with high porosity. Supporting Pt on HGNC exhibits excellent oxygen reduction activity for PEMFC with greatly improved durability as proved by real-time loss measurements of Pt and carbon, the first to surpass the DOE 2025 durability targets for both catalyst and support. The Pt/HGNC-65 shows 32% and 24% drop in mass activity after accelerated durability tests of both electrocatalyst and support, respectively, which are less than DOE target of 40% loss. The atomistic basis for this durability is explained via quantum mechanics-based molecular dynamics simulations. Interestingly, it is found that pyrrolic-N strongly interacts with Pt, making the Pt catalyst more stable during fuel cell reaction. © 2022 Elsevier B.V.
URI
http://hdl.handle.net/20.500.11750/17413
DOI
10.1016/j.apcatb.2022.122179
Publisher
Elsevier B.V.
Show Full Item Record

File Downloads

  • There are no files associated with this item.

공유

qrcode
공유하기

Related Researcher

유종성
Yu, Jong-Sung유종성

Department of Energy Science and Engineering

read more

Total Views & Downloads