Integrating Hydrogenated TiO<sub>2</sub>-Modified Carbon-Supported PtRu Anodes and Fe–N–C Cathodes for High-Performance Direct Methanol Fuel Cells

Direct methanol fuel cells (DMFCs) have attracted significant interest owing to their high energy density and ease of handling methanol. However, commercialization is challenged by the sluggish methanol oxidation kinetics of the PtRu anode and methanol crossover to the cathode. Although platinum group metal-free (PGM-free) cathode catalysts exhibit promising methanol tolerance, their performance is limited by cathode flooding due to methanol crossover. This study investigates various anode carbon support architectures modified with hydrogenated TiO2 to address methanol crossover issues in PGM-free cathodes and to improve the activity and durability of PtRu electrocatalysts. Systematic three-electrode studies and accelerated stress tests reveal the significant effect of different anode carbon supports on the activity and durability of PtRu electrocatalysts toward methanol and CO oxidation. DMFCs integrated with a PGM-free Fe-N-C cathode and a PtRu anode catalyst on the TiO2-modified carbon nanotube demonstrate peak power densities of 216.6 and 178.6 mW/cm2 in oxygen and air feed at 100 °C, respectively, among the highest reported. The performance remains unchanged with up to 4.0 M methanol feed for the carbon nanotube-supported anode, unlike conventional carbon support causing cathode flooding. This study reveals the importance of the anode carbon support architecture in mitigating methanol crossover, which is crucial for addressing cathode flooding in PGM-free cathodes, and improving the PtRu catalyst activity and durability.

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Publication Details

Journal
ACS Catalysis
Published
2024-10-03
DOI
https://doi.org/10.1021/acscatal.4c03089
Citations
6
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
0.61

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article

Integrating Hydrogenated TiO2-Modified Carbon-Supported PtRu Anodes and Fe–N–C Cathodes for High-Performance Direct Methanol Fuel Cells

Yachao Zeng, Archana Sekar, Nathaniel Metzger, Sabari Rajendran et al.
6 citations
ACS Catalysis
Electrocatalysts for Energy Conversion
0.61
article

Integrating Hydrogenated TiO2-Modified Carbon-Supported PtRu Anodes and Fe–N–C Cathodes for High-Performance Direct Methanol Fuel Cells

Yachao Zeng, Archana Sekar, Nathaniel Metzger, Sabari Rajendran, Jun Li, Gang Wu, Xianglin Li
article en
6 citations

Abstract

Direct methanol fuel cells (DMFCs) have attracted significant interest owing to their high energy density and ease of handling methanol. However, commercialization is challenged by the sluggish methanol oxidation kinetics of the PtRu anode and methanol crossover to the cathode. Although platinum group metal-free (PGM-free) cathode catalysts exhibit promising methanol tolerance, their performance is limited by cathode flooding due to methanol crossover. This study investigates various anode carbon support architectures modified with hydrogenated TiO2 to address methanol crossover issues in PGM-free cathodes and to improve the activity and durability of PtRu electrocatalysts. Systematic three-electrode studies and accelerated stress tests reveal the significant effect of different anode carbon supports on the activity and durability of PtRu electrocatalysts toward methanol and CO oxidation. DMFCs integrated with a PGM-free Fe-N-C cathode and a PtRu anode catalyst on the TiO2-modified carbon nanotube demonstrate peak power densities of 216.6 and 178.6 mW/cm2 in oxygen and air feed at 100 °C, respectively, among the highest reported. The performance remains unchanged with up to 4.0 M methanol feed for the carbon nanotube-supported anode, unlike conventional carbon support causing cathode flooding. This study reveals the importance of the anode carbon support architecture in mitigating methanol crossover, which is crucial for addressing cathode flooding in PGM-free cathodes, and improving the PtRu catalyst activity and durability.

ACS CatalysisVol. 14(20)
University of Kansas (US), Kansas State University (US), Washington University in St. Louis (US), University at Buffalo, State University of New York (US)
Office of Energy Efficiency and Renewable Energy
Openalex Percentile: Top 39%
Electrocatalysts for Energy Conversion
0.61
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