...
首页> 外文期刊>Electrochimica Acta >Inhibitive effect of Pt on Pd-hydride formation of Pd@Pt core-shell electrocatalysts: An in situ EXAFS and XRD study
【24h】

Inhibitive effect of Pt on Pd-hydride formation of Pd@Pt core-shell electrocatalysts: An in situ EXAFS and XRD study

机译:PT对Pd核心壳电催化剂Pd-氢化物形成的抑制作用:原位外,XRD研究

获取原文
获取原文并翻译 | 示例
           

摘要

In situ EXAFS and XRD have been used to study the electrochemical formation of hydride phases, Habs, in 0.5 M H2SO4 for a Pd/C catalyst and a series of Pd@Pt core-shell catalysts with varying Pt shell thickness, from 0.5 to 4 monolayers. Based on the XRD data a 3% lattice expansion is observed for the Pd/C core catalyst upon hydride formation at 0.0 V. In contrast, the expansion was = 0.6% for all of the core-shell catalysts. The limited extent of the lattice expansion observed suggests that hydride formation, which may occur during periodic active surface area measurements conducting during accelerated aging tests or driven by H-2 crossover in PEM fuel cells, is unlikely to contribute significantly to the degradation of Pd@Pt core-shell electrocatalysts in contrast to the effects of oxide formation. (C) 2018 Elsevier Ltd. All rights reserved.
机译:原位EXAFS和XRD已被用于研究氢化物相,HAB,在0.5M H 2 SO 4中的电化学形成,以及具有不同PT壳厚度的Pd @ Pt核 - 壳催化剂,0.5至4 单层。 基于XRD数据,在0.0V的氢化物形成时观察到Pd / C核心催化剂的3%晶格膨胀。相反,对于所有核 - 壳催化剂,膨胀为0.6%。 所观察到的晶格膨胀的有限程度表明,在加速老化试验期间导通的氢化物形成,其可能发生在加速老化测试期间或由PEM燃料电池中的H-2交叉驱动,这不太可能导致PD @的降解显着贡献 与氧化物形成的影响相比,Pt核 - 壳电催化剂。 (c)2018年elestvier有限公司保留所有权利。

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