Sharper, Stronger, Smarter: CuNi@Pt-Cu Nano-Octahedra Unlock New Potential for Formic Acid Fuel Cells

Published in Catal

Published in Chemistry and Materials

Sharper, Stronger, Smarter: CuNi@Pt-Cu Nano-Octahedra Unlock New Potential for Formic Acid Fuel Cells
Like

Share this post

Choose a social network to share with, or copy the URL to share elsewhere

This is a representation of how your post may appear on social media. The actual post will vary between social networks

Explore the Research

SpringerLink
SpringerLink SpringerLink

Shape-directed CuNi@Pt-Cu nano-octahedra for enhanced formic acid electrooxidation - Catal

Shape-controlled core@shell nanoparticles have attracted considerable interest for their potential to minimize the use of precious metals in the shell while enhancing catalytic performance through lattice strain and shape effects. However, challenges such as core dissolution and morphological degradation during shell growth remain major obstacles to their broader applications. In this study, we successfully demonstrated core@shell CuNi@Pt-Cu nano-octahedra by leveraging a previously developed protocol based on CuNi nano-octahedra templates. Precise control of key reaction parameters, including a high reaction temperature (240 °C), a rapid heating ramp (~ 12 °C/min), and slow injection of the Pt precursor, enabled the retention of sharp-edged morphology during shell formation. The resulting nanocrystals feature (111)-facet-dominated surfaces and exhibit lattice strain at the CuNi/Pt-Cu interface, both of which contribute to their enhanced electrocatalytic performance. In the formic acid oxidation reaction, the CuNi@Pt-Cu nano-octahedra demonstrated a high specific activity of ~ 25.2 $$mA{/cm}_{Pt}^{2}$$ m A / c m Pt 2 , significantly outperforming CuNi@Pt-Cu nanopolyhedra/C (15.7 $$mA{/cm}_{Pt}^{2}$$ m A / c m Pt 2 ) and commercial Pt/C catalysts (4.36 $$mA{/cm}_{Pt}^{2}$$ m A / c m Pt 2 ). They also exhibited enhanced stability, with only a 17% loss in activity after a 1-h chronoamperometry test, compared to a ~ 44% loss observed for both the polyhedral counterpart and Pt/C. These results underscore the effectiveness of integrating shape control, interfacial strain, and multimetallic synergy within Pt-based nanostructures to improve both electrocatalytic activity and durability. Graphical Abstract

In our recent publication in Catal, we report the design and synthesis of shape-controlled CuNi@Pt-Cu core–shell nano-octahedra that deliver a significant advancement in the electrochemical oxidation of formic acid (FAOR)—a key reaction in direct formic acid fuel cells (DFAFCs), which are increasingly recognized as promising candidates for portable and sustainable energy technologies.

Through precise control of synthesis conditions—including elevated temperature (240 °C), rapid thermal ramping (12 °C/min), and gradual Pt precursor injection—we achieved sharp-edged nano-octahedra with (111)-facet-dominated surfaces and a Pt-Cu alloy shell. These structural features synergistically enhance both catalytic activity and long-term durability.

Synthesis highlights:

  • Seed-mediated colloidal synthesis (two-pot method) with morphology control
  • Sharp-edged core@shell nano-octahedra with narrow size-distribution
  • Controlled deposition of uniform layers with sub-nanometer precision

Performance highlights:

  • ~5.75× higher specific activity than commercial Pt/C
  • ~2.09× higher mass activity
  • Only ~17% activity loss after 1-hour durability testing

Industry impact:

These results demonstrate that the nano-octahedra not only outperform conventional catalysts but also offer a platinum-efficient and scalable solution for DFAFCs. By reducing noble metal consumption while maintaining high performance, this work contributes to the development of cost-effective, durable fuel cell systems suitable for real-world applications in clean energy, backup power, and mobile electronics.

Authors:

Can Li, Xiaobo Chen, Lihua Zhang, Bo Zhao, Coby Woodver-Frost, Prabhu Bharathan, Anna Dennett, Guangwen Zhou, and Jiye Fang

Affiliations:

State University of New York at Binghamton, Brookhaven National Laboratory, and Texas Tech University
*Corresponding author: Jiye Fang (jfang@binghamton.edu )

Please sign in or register for FREE

If you are a registered user on Research Communities by Springer Nature, please sign in

Follow the Topic

Materials for Energy and Catalysis
Physical Sciences > Materials Science > Materials for Energy and Catalysis
Catalysis
Physical Sciences > Chemistry > Industrial Chemistry > Catalysis
Catalysis
Physical Sciences > Chemistry > Inorganic Chemistry > Catalysis
Catalysis
Physical Sciences > Chemistry > Physical Chemistry > Catalysis
Catalyst Synthesis
Physical Sciences > Chemistry > Chemical Synthesis > Catalyst Synthesis
  • Catal Catal

    Catal is an open access journal covering full spectrum of catalysis critical advances. From biocatalysts to heterogeneous catalysts, it integrates fundamental and applied sciences. Catal offers a primary platform for researchers and practitioners in the field.

Related Collections

With Collections, you can get published faster and increase your visibility.

Bio-Catalysis in Circular Bioeconomy and Green Chemistry

This collection emphasizes the role of bio-catalysis in advancing the circular bioeconomy, focusing on enzymatic transformations and eco-friendly processes that valorize renewable feedstocks. Contributions should highlight innovative applications of bio-catalysis in waste-to-value systems, biorefineries, and green chemical synthesis.

Catal invites research articles, reviews and reports on the topic of the development of enzymes, metabolic engineering, and integration of bio-catalysis into industrial processes, aiming to reduce dependency on fossil-based resources and promote sustainable practices.

Publishing Model: Open Access

Deadline: Dec 31, 2025

Nanocatalysis and Thermocatalysis in Precision Chemical Synthesis

This collection, hosted by Catal, highlights the intersection of nanocatalysis and thermocatalysis in precision chemical synthesis. It aims to disseminate cutting-edge research that drives innovation in catalytic materials, selective processes, and reaction pathways, fostering advancements in the production of fine chemicals and specialty compounds. Aligned with Catal's mission to prioritize impactful catalytic applications, this collection welcomes contributions from established and early-career researchers that advance both theoretical and applied catalysis.

The collection embraces the breadth of Catal’s coverage, including topics such as nanostructured catalysts, thermocatalytic processes, and advanced synthesis strategies. Contributions may explore catalytic mechanisms, computational modeling, or experimental breakthroughs, offering insights into scalable industrial applications and fundamental research. Articles types—original research, reviews, perspectives, and analyses—are all encouraged, ensuring a diverse platform for sharing high-impact advancements in catalysis.

Publishing Model: Open Access

Deadline: Dec 31, 2025