Boosting the Durability of High‐Pt‐Content Fuel Cell Cathode Catalysts Through TaOx Decorating
Source abstract
Abstract
Abstract Enhancing the durability of carbon‐supported platinum catalysts (Pt/C) for the oxygen reduction reaction remains a significant challenge in the field of proton exchange membrane fuel cells (PEMFCs), especially for catalysts with high‐Pt contents. Herein, a TaOx decorating strategy that is capable of effectively boosting the durability of Pt/C catalysts even with a high‐Pt content of 50 wt.% is introduced. This strategy involves introducing reducible Ta2O5 nanoparticles into carbon supports, depositing Pt nanoparticles, and finally conducting high‐temperature H2 annealing to convert reducible Ta2O5 nanoparticles into amorphous TaOx decorating the Pt nanoparticles. The annealing temperature found in the Ta2O5 incorporation step is critical for the formation of reducible Ta2O5 nanoparticles, which, in turn, determines the continuity of the TaOx subsequently formed around the Pt nanoparticles. By controlling annealing temperature, the formation of a relatively continuous TaOx distribution on the Pt nanoparticle surface is achieved, thereby maximizing the interaction between Pt and TaOx and enhancing the electrochemical stability of Pt nanoparticles. Following the accelerated durability test, the resulting high‐Pt‐content catalyst demonstrates an array of exceptional durability metrics, including an electrochemical surface area loss of 30%, a mass activity loss of 35%, and a voltage loss of 22 mV at 0.8 A cm‒2.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Fuel Cells and Related Materials · Advanced battery technologies research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Hefei National Research Center for Physical Sciences at the Microscale Department of Chemistry University of Science and Technology of China Hefei 230026 China
National Engineering Research Center for Domestic and Building Ceramics Jingdezhen Ceramic University Jingdezhen 333403 China
Funding
National Natural Science Foundation of China
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