journal article·2025-12-20

A Large-Scalable Synthesis of Highly Efficient Pt–Ni Alloy Electrocatalyst for Proton Exchange Membrane Fuel Cells

Bolong Yang, Junfei Peng, Yunfei Shen, Zhansheng Wu

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Abstract

Large-scale preparation of ordered intermetallic PtM/C alloy catalysts is essential to advance the development of proton exchange membrane fuel cells (PEMFCs). Herein, ordered Pt 3 Ni-600J alloy catalysts were synthesized using impregnation reduction as well as secondary high-temperature pyrolytic reduction, and the effect of carbon with different specific surface areas and graphitization as support on oxygen reduction reaction (ORR) performance was compared. The ordered intermetallic compound Pt 3 Ni nanocatalyst not only exhibits stronger atomic interaction between Pt and Ni, resulting in high chemical and structural stability of the catalysts, but also can be tuned by adjusting the Ni/Pt component ratio in order to obtain higher ORR catalytic activity. The results show that the ordered Pt 3 Ni-600J alloy catalyst exhibits high ORR activity with half-wave potentials of 0.87 V compared to other catalysts obtained with different carbon carriers. In PEMFCs, the power density of Pt 3 Ni-600J exceeded 2 W cm –2 under H 2 –O 2 conditions. More significantly, we have achieved the synthesis of a single batch of catalysts larger than 100 g using an indigenously designed fluidized bed pyrolysis method with a half-wave potential only 25 mV different from that synthesized in a small scale, and also showed good durability.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Electrocatalysts for Energy Conversion · Fuel Cells and Related Materials · Hybrid Renewable Energy Systems

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

School of Environmental and Chemical Engineering, Xi’an Key Laboratory of Textile Chemical Engineering’ Auxiliaries

Xi’an Polytechnic University

Funding

National Natural Science Foundation of China

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