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一锅法可控合成具有增强的甲酸氧化和甘油氧化电催化性能的 AuPd@Pd 核壳纳米晶体。

One-pot controlled synthesis of AuPd@Pd core-shell nanocrystals with enhanced electrocatalytic performances for formic acid oxidation and glycerol oxidation.

机构信息

College of Chemistry and Life Science, College of Geography and Environmental Science, Zhejiang Normal University, Jinhua 321004, China.

School of Chemistry and Biological Engineering, Suzhou University of Science and Technology, Suzhou 215009, China.

出版信息

J Colloid Interface Sci. 2017 Dec 15;508:551-558. doi: 10.1016/j.jcis.2017.08.041. Epub 2017 Aug 16.

Abstract

In this work, AuPd@Pd core-shell nanocrystals (AuPd@Pd NCs) were fabricated by a one-pot co-reduction approach, where theophylline-7-acetic acid (TAA) acted asa new structure-directing agent. The crystal structure and composition were mainly characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM), X-ray diffraction (XRD), together with X-ray photoelectron spectroscopy (XPS). The growth mechanism of AuPd@Pd NCs was investigated in detail. The obtained AuPd@Pd NCs exhibited superior catalytic characters for formic acid oxidation reaction (FAOR) and glycerol oxidation reaction (GOR) in contrast with commercial Pd black in alkaline media.

摘要

在这项工作中,采用一锅共还原法制备了 AuPd@Pd 核壳纳米晶体(AuPd@Pd NCs),其中茶碱-7-乙酸(TAA)作为一种新的结构导向剂。通过扫描电子显微镜(SEM)、透射电子显微镜(TEM)、高角环形暗场扫描透射电子显微镜(HAADF-STEM)、X 射线衍射(XRD)和 X 射线光电子能谱(XPS)对晶体结构和组成进行了主要表征。详细研究了 AuPd@Pd NCs 的生长机制。与商业 Pd 黑相比,所获得的 AuPd@Pd NCs 在碱性介质中对甲酸氧化反应(FAOR)和甘油氧化反应(GOR)表现出优异的催化性能。

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