Composition and morphology are crucial factors in the design of Pt-based catalysts with high performance, particularly in direct methanol fuel cells (DMFCs). Herein, PtRu mesoporous nanospheres (PtRu MNs) with tunable compositions were synthesized a facile method and then deposited on a carbon support to act as electrocatalyst materials for the methanol oxidation reaction (MOR). Superior catalytic activity, better catalytic stability, and good tolerance to CO were achieved by the optimum PtRu (2 : 1) MNs/C catalyst compared with Pt MNs/C. The mass activity on PtRu (2 : 1) MNs/C reached 111.77 mA mg , which was approximately 6.45-fold higher than that of Pt MNs/C (17.33 mA mg ). Meanwhile, PtRu (2 : 1) MNs/C retained much more current density (84.7%) than Pt MNs/C (17.7%) after 500 cycles. The improved catalytic performance is due to several factors, including the formation of a mesoporous nanostructure with abundant active sites and the favorable effects of the Ru species. This work provides guidance toward designing and fabricating effective Pt-based electrocatalysts for DMFC applications.
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http://dx.doi.org/10.1039/d4na00210e | DOI Listing |
Membranes (Basel)
November 2024
Graduate Institute of Precision Engineering, National Chung Hsing University, Taichung City 402, Taiwan.
This work aims at the effects of anion-exchange membranes (AEMs) and ionomer binders on the catalyst electrodes for anion-exchange membrane fuel cells (AEMFCs). In the experiments, four metal catalysts (nano-grade Pt, PtRu, PdNi and Ag), four AEMs (aQAPS-S8, AT-1, X37-50T and X37-50RT) and two alkaline ionomers (aQAPS-S14 and XB-7) were used. They were verified through several technical parameters examination and cell performance comparison for the optimal selection of AMEs.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Xiamen University, College of Chemistry and Chemical Engineering, 402 Siming Road, 361005, Xiamen, CHINA.
PtRu-based catalysts toward hydrogen oxidation reaction (HOR) suffer from low efficiency, CO poisoning and over-oxidation at high potentials. In this work, an amorphization strategy is adopted for preparation of amorphous SrRuPtOxHy nanobelts (a-SrRuPtOxHy NBs). The a-SrRuPtOxHy NBs have optimized adsorption of intermediates (H and OH), increased number of active sites, highly weakened CO poisoning and enhanced anti-oxidation ability owing to the special amorphous structure.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
November 2024
State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, 361005, China.
As one of the best candidates for hydrogen oxidation reaction (HOR), ruthenium (Ru) has attracted significant attention for anion exchange membrane fuel cells (AEMFCs), although it suffers from sluggish kinetics under alkaline conditions due to its strong hydroxide affinity. In this work, we develop ternary hollow nanocages with Pt epitaxy on RuCu (Pt-RuCu NCs) as efficient HOR catalysts for application in AEMFCs. Experimental characterizations and theoretical calculations confirm that the synergy in optimized Pt-RuCu NCs significantly modifies the electronic structure and coordination environment of Ru, thereby balancing the binding strengths of H* and OH* species, which leads to a markedly enhanced HOR performance.
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
College of Mechanical and Electrical Engineering, Henan University of Technology, Zhengzhou 450052, China.
Volatile organic compounds (VOCs) constitute key pollutants in the environment, and exposure to them is associated with negative health impacts. The vigilant monitoring of these pernicious VOCs is imperative for their timely detection and for curtailing the likelihood of both immediate and prolonged exposure, thus safeguarding against the deterioration of environmental quality. In this study, porous PtRu nanoalloys are successfully synthesized via a hydrothermal method and innovatively integrated with SnO nanoparticles to significantly enhance the performance of gas sensors.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
October 2024
State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, Xiamen University, 422 Siming South Road, Xiamen, 361005, China.
Cation exchange (CE) reaction is a classical synthesis method for creating complex structures. A lock of study on intrinsic mechanism limits its understanding and practical application. Using X-ray absorption spectroscopy, we observed that the evolution from Ru-Cl to Ru-O/OH occurs during the CE between KRuCl and CoSn(OH) in aqueous solution, while CE between KPtCl and CoSn(OH) is inhibited due to the failure of structural evolution from Pt-Cl to Pt-O/OH.
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