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用于在碱性介质中电氧化小有机燃料的单异质结构和双异质结构M@聚-1,2-二氨基蒽醌(M = Pt、Pd和Pt-Pd)催化剂。

Mono and dual hetero-structured M@poly-1,2 diaminoanthraquinone (M = Pt, Pd and Pt-Pd) catalysts for the electrooxidation of small organic fuels in alkaline medium.

作者信息

Hathoot Abla Ahmed, Hassan Khalid Mahmoud, Ali Asmaa Galal, Shatla Ahmed Said, Baltruschat Helmut, Abdel-Azzem Magdi

机构信息

Electrochemistry Laboratory, Chemistry Department, Faculty of Science, Menoufia University Shibin El-Kom 32511 Egypt.

Electrochemistry Research Laboratory, Physics and Mathematics Engineering Department, Faculty of Electronic Engineering, Menoufia University Menouf 23952 Egypt

出版信息

RSC Adv. 2019 Jan 15;9(4):1849-1858. doi: 10.1039/c8ra09342c. eCollection 2019 Jan 14.

DOI:10.1039/c8ra09342c
PMID:35516099
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9059733/
Abstract

Oxidation of some small organic fuels such as methanol (MeOH), ethanol (EtOH) and ethylene glycol (EG) was carried out in an alkaline medium using palladium (Pd)-platinum (Pt) nanoparticles/poly1,2-diaminoanthraquinone/glassy carbon (p1,2-DAAQ/GC) catalyst electrodes. Pd and Pt were incorporated into the p1,2-DAAQ/GC electrode using the cyclic voltammetry (CV) technique. The obtained Pd/p1,2-DAAQ/GC, Pt/p1,2-DAAQ/GC, Pt/Pd/p1,2-DAAQ/GC and Pd/Pt/p1,2-DAAQ/GC nanocatalyst electrodes were characterized by scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX) and CV methods. Real active surface area ( ) achieved by carbon monoxide (CO) adsorption using differential electrochemical mass spectroscopy (DEMS) technique. The electrochemical activity was evaluated and normalized to per metal loading mass. The electrocatalytic oxidation of the small organic fuels at the prepared nanocatalyst electrodes was studied in 1.0 M NaOH solutions by CV and chronoamperometric (CA) techniques. Pt/Pd/p1,2-DAAQ/GC nanocatalyst electrode exhibited enhanced catalytic activity, better durability and higher tolerance to carbon monoxide generated in the oxidation reaction when compared with the other three studied nanocatalysts. The present investigation suggests that the studied nanocatalysts can be successfully applied in direct oxidation of small organic fuels, especially MeOH.

摘要

使用钯(Pd)-铂(Pt)纳米颗粒/聚1,2-二氨基蒽醌/玻碳(p1,2-DAAQ/GC)催化剂电极,在碱性介质中对甲醇(MeOH)、乙醇(EtOH)和乙二醇(EG)等一些小分子有机燃料进行了氧化反应。采用循环伏安法(CV)将Pd和Pt引入p1,2-DAAQ/GC电极中。通过扫描电子显微镜(SEM)、能量色散X射线光谱(EDX)和CV方法对所制备的Pd/p1,2-DAAQ/GC、Pt/p1,2-DAAQ/GC、Pt/Pd/p1,2-DAAQ/GC和Pd/Pt/p1,2-DAAQ/GC纳米催化剂电极进行了表征。利用差分电化学质谱(DEMS)技术通过一氧化碳(CO)吸附获得实际活性表面积( )。评估了电化学活性并将其归一化为每金属负载质量的 。通过CV和计时电流法(CA)技术研究了在1.0 M NaOH溶液中制备的纳米催化剂电极上小分子有机燃料的电催化氧化。与其他三种研究的纳米催化剂相比,Pt/Pd/p1,2-DAAQ/GC纳米催化剂电极在氧化反应中表现出增强的催化活性、更好的耐久性和对一氧化碳更高的耐受性。本研究表明,所研究的纳米催化剂可成功应用于小分子有机燃料的直接氧化,尤其是甲醇。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50cd/9059733/d41f18e428c1/c8ra09342c-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50cd/9059733/f43a7b2930ad/c8ra09342c-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50cd/9059733/6ec948636c68/c8ra09342c-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50cd/9059733/620c07f2f1f6/c8ra09342c-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50cd/9059733/56fa3e868fdb/c8ra09342c-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50cd/9059733/15ea8ef2eb03/c8ra09342c-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50cd/9059733/d41f18e428c1/c8ra09342c-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50cd/9059733/f43a7b2930ad/c8ra09342c-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50cd/9059733/6ec948636c68/c8ra09342c-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50cd/9059733/620c07f2f1f6/c8ra09342c-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50cd/9059733/56fa3e868fdb/c8ra09342c-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50cd/9059733/15ea8ef2eb03/c8ra09342c-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50cd/9059733/d41f18e428c1/c8ra09342c-f6.jpg

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