阳极
甲酸
甲醇
材料科学
催化作用
原电池
化学工程
动力学
无机化学
化学
电极
物理化学
有机化学
冶金
物理
量子力学
工程类
作者
Yufei Wang,Shoulin Zhang,Yuxin Deng,Shi-Han Luan,Caikang Wang,Linfei Ding,Xian Jiang,Dongmei Sun,Yawen Tang
出处
期刊:Rare Metals
[Springer Science+Business Media]
日期:2024-07-29
卷期号:44 (1): 300-310
被引量:18
标识
DOI:10.1007/s12598-024-02921-4
摘要
Abstract To efficiently diminish the Pt consumption while concurrently enhancing the anodic reaction kinetics, a straightforward synthesis for PtPdAg nanotrees (NTs) with exceedingly low Pt content is presented, utilizing the galvanic replacement reaction between the initially prepared PdAg NTs and Pt ions. Due to the multilevel porous tree‐like structure and the incorporation of low amounts of Pt, the electrocatalytic activity and stability of PtPdAg NTs are markedly enhanced, achieving 1.65 and 1.69 A·mg −1 Pt + Pd for the anodic reactions of formic acid oxidation (FAOR) and methanol oxidation (MOR) within DLFCs, surpassing the performance of PdAg NTs, as well as that of commercial Pt and Pd black. Density functional theory (DFT) calculations reveal that the addition of low amounts of Pt leads to an increase in the d‐band center of PtPdAg NTs and lower the CO ads adsorption energy to −1.23 eV, enhancing the anti‐CO toxicity properties optimally. This approach offers an effective means for designing low Pt catalysts as exceptional anodic electrocatalysts for direct liquid fuel cells.
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