Construction of PtAg-on-Au Heterostructured Nanoplates for Improved Electrocatalytic Activity of Formic Acid Oxidation

IF 2.6 4区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY
ChemNanoMat Pub Date : 2024-10-21 DOI:10.1002/cnma.202400399
Quansen Wu, Yuanyuan Min, Yingying Wang, Yanyun Ma, Yiqun Zheng
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Abstract

Direct formic acid fuel cells have attracted significant attention due to their low fuel crossover, high safety, and high theoretical power density among all proton-exchange membrane fuel cells. Numerous efforts have been dedicated to studying formic acid oxidation, particularly in the fabrication of high-performance electrocatalysts with economical utilization of Pt metal. In this work, we report a synthetic strategy to create PtAg dots supported on plate-like Au nanoparticles and explore their applications in electrocatalytic formic acid oxidation. The highly dispersed nature of the catalytic Pt centers and the successful construction of PtAg−Au trimetallic interfaces makes the current nanostructure an ideal system to allow for a synergetic effect between Pt, Au, and Ag, leading to improved electrocatalysis. Compared with commercial Pt/C, our PtAg-on-Au heterogenous nanoplates exhibit superior mass activity, along with enhanced reaction kinetics and long-term durability for FAOR in an acidic medium. Density functional theory (DFT) simulation results indicate that AgPtAu(111) exhibits a relatively high activity for HCOOH oxidation into CO2 among the various Au-based catalysts. This work provides a viable strategy for constructing Pt-based electrocatalysts with controlled Pt ensembles, offering insights into the development of fuel cell catalysts that make highly efficient use of costly noble metals.

Abstract Image

构建 PtAg-on-Au 异质结构纳米板以提高甲酸氧化的电催化活性
在所有质子交换膜燃料电池中,直接甲酸燃料电池因其燃料交叉性低、安全性高和理论功率密度高而备受关注。人们一直致力于甲酸氧化的研究,尤其是在经济地利用铂金属制造高性能电催化剂方面。在这项工作中,我们报告了一种在板状金纳米粒子上支持铂钯点的合成策略,并探讨了它们在电催化甲酸氧化中的应用。催化铂中心的高度分散性和 PtAg-Au 三金属界面的成功构建,使当前的纳米结构成为铂、金和银之间产生协同效应的理想体系,从而改善了电催化性能。与商用 Pt/C 相比,我们的 PtAg-on-Au 异质纳米板具有更高的质量活性、更强的反应动力学和在酸性介质中的长期耐久性。密度泛函理论(DFT)模拟结果表明,在各种金基催化剂中,AgPtAu(111) 将 HCOOH 氧化成 CO2 的活性相对较高。这项工作为构建具有可控铂组合的铂基电催化剂提供了一种可行的策略,为高效利用昂贵贵金属的燃料电池催化剂的开发提供了启示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ChemNanoMat
ChemNanoMat Energy-Energy Engineering and Power Technology
CiteScore
6.10
自引率
2.60%
发文量
236
期刊介绍: ChemNanoMat is a new journal published in close cooperation with the teams of Angewandte Chemie and Advanced Materials, and is the new sister journal to Chemistry—An Asian Journal.
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