首页> 外文期刊>Journal of Colloid and Interface Science >Facile synthesis of prickly platinum-palladium core-shell nanocrystals and their boosted electrocatalytic activity towards polyhydric alcohols oxidation and hydrogen evolution
【24h】

Facile synthesis of prickly platinum-palladium core-shell nanocrystals and their boosted electrocatalytic activity towards polyhydric alcohols oxidation and hydrogen evolution

机译:用刺铂 - 钯核 - 壳纳米晶体的容易合成及其促进多元醇氧化和氢气进化的升压电催化活性

获取原文
获取原文并翻译 | 示例
           

摘要

Herein, prickly platinum-palladium core-shell nanocrystals (Pt@Pd NCs) were prepared by a facile one pot aqueous method, only taking sodium pyrrolidone carboxylate (PCA-Na) as the structure director and stabilizing agent. The products were mainly characterized by microscopic analysis, X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS), followed by discussing the formation mechanism in details. The electrochemical characterizations were examined by cyclic voltammetry (CV), linear sweep voltammetry (LSV) and chronoamperometry (CA). The results revealed that the prepared architectures had the biggest current density (58.4 mA cm(-2)) for ethylene glycol oxidation, which is 3.5-fold, 1.2-fold, 2.3-fold and 2.4-flod enhancement relative to those of home-made single Pt nanoparticles (NPs) and Pd NPs, commercial Pt black and Pd black catalysts, respectively. Also, the obtained Pt@Pd NCs showed improved catalytic activity and stability towards glycerol oxidation and hydrogen evolution reactions compared to the references. (C) 2018 Elsevier Inc. All rights reserved.
机译:在此,刺铂 - 钯的核 - 壳纳米晶体(铂@钯NCS)通过一个浅显一锅水溶液的方法制备,只是以吡咯烷酮羧酸钠(PCA钠)作为结构导演和稳定剂。该产品主要特点是显微分析,X射线衍射(XRD)和X射线光电子能谱(XPS)中,随后在详细讨论的形成机理。电化学表征通过循环伏安法(CV),线性扫描伏安法(LSV)和计时(CA)检测。结果表明所制备的体系结构不得不为乙二醇氧化的最大电流密度(58.4毫安厘米(-2)),这是3.5倍,1.2倍,2.3倍,并且相对于这些的2.4弗洛德增强主页 - 制成单一的Pt纳米颗粒(NP)和Pd纳米颗粒,商业铂黑和钯黑催化剂,分别。另外,得到的Pt的Pd @的NC显示出改善的对甘油的氧化和相对于参考析氢反应的催化活性和稳定性。 (c)2018 Elsevier Inc.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号