首页> 外文期刊>RSC Advances >Galvanic replacement of electrodeposited nickel by palladium and investigation of the electrocatalytic activity of synthesized Pd/(Ni) for hydrogen evolution and formic acid oxidation
【24h】

Galvanic replacement of electrodeposited nickel by palladium and investigation of the electrocatalytic activity of synthesized Pd/(Ni) for hydrogen evolution and formic acid oxidation

机译:通过钯更换电沉积镍的电沉积镍及其合成Pd /(Ni)电催化活性的氢气进化和甲酸氧化

获取原文
获取原文并翻译 | 示例
           

摘要

A series of controllable Pd/(Ni) catalysts were synthesized by the use of galvanic replacement between electrodeposited nickel and palladium in [PdCl4](2-) containing solution. The mechanisms of galvanic replacement were investigated by monitoring the potential variations versus time, field emission scanning electron microscopy (FESEM), and energy dispersive X-ray spectroscopy (EDS). The electrocatalytic activities of the prepared catalysts were evaluated by linear sweep voltammetry for the hydrogen evolution reaction (HER) in 0.5 M H2SO4 and formic acid oxidation in 0.5 M H2SO4 + 0.5 M HCOOH. In addition, the effect of the Ni loading amount on the final morphology, chemical composition and electrocatalytic activity of the galvanically replaced Pd/(Ni) catalysts was studied. The results indicated that the morphology of the Pd/(Ni) changes from thin film to nano/micro dendrite depending on the amounts of electrodeposited Ni loading. The sharp and relatively symmetric peaks that were observed in the voltammograms indicated the reversibility of electrochemical hydrogen absorption/extraction. The same Tafel slopes estimated for all Pd/(Ni) suggested the predomination of Volmer-Heyrovsky mechanisms in catalyzing the hydrogen evolution reaction. In addition, the Pd/(Ni) thin film catalyst exhibited superior electrocatalytic mass activity towards the oxidation of formic acid (1.39 A mg(-1) at the peak potential). Moreover, comparison of the Pd/(Ni) thin film activity with some other palladium-based catalysts in some recent studies with relatively good results showed that the galvanically replaced Pd/(Ni) thin film has great potential as a fast, easily prepared, and active electrocatalyst for formic acid oxidation.
机译:通过使用电沉积镍和钯在含溶液中的电沉积镍和钯之间的电催化替换来合成一系列可控的Pd /(Ni)催化剂。通过监测电位变化与时间,场发射扫描电子显微镜(FeSEM)和能量分散X射线光谱(EDS)来研究通过监测电致置换替换机制。通过线性扫描伏安法评价制备的催化剂的电催化活性在0.5M H 2 SO 4 + 0.5M HCOOH中的0.5M H 2 SO 4和甲酸氧化中的线性扫描伏安法评价。此外,研究了Ni加载量对电流替代的Pd /(Ni)催化剂的最终形态,化学成分和电催化活性的影响。结果表明,取决于电沉积Ni负荷的量,Pd /(Ni)的形态从薄膜到纳米/微生枝的变化。在伏安图中观察到的尖锐且相对称的峰表示电化学氢吸收/萃取的可逆性。所有PD /(NI)估计的相同的TAFEL斜率建议了Volmer-Heyrovsky机制在催化氢进化反应方面的追偏。另外,Pd /(Ni)薄膜催化剂表现出优异的电催化质量活性朝向甲酸的氧化(1.39A mg(-1)处的峰值电位)。此外,在一些近期基于钯的催化剂的Pd /(Ni)薄膜活性与较近的结果的比较显示,具有相对良好的结果表明,电镀层替换的Pd /(Ni)薄膜具有快速,容易准备的潜力很大,甲酸氧化的活性电催化剂。

著录项

  • 来源
    《RSC Advances》 |2016年第27期|共11页
  • 作者单位

    Amirkabir Univ Technol Tehran Polytech Dept Min &

    Met Engn Hafez Ave POB 15875-4413 Tehran Iran;

    Amirkabir Univ Technol Tehran Polytech Dept Min &

    Met Engn Hafez Ave POB 15875-4413 Tehran Iran;

    Amirkabir Univ Technol Tehran Polytech Dept Min &

    Met Engn Hafez Ave POB 15875-4413 Tehran Iran;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

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