首页> 外文期刊>Powder Technology: An International Journal on the Science and Technology of Wet and Dry Particulate Systems >Complex PtPdRh nanoparticles: Synthesis, characterization, and performance in the electrocatalytic oxidation of ammonia
【24h】

Complex PtPdRh nanoparticles: Synthesis, characterization, and performance in the electrocatalytic oxidation of ammonia

机译:复杂的PtPdRh纳米粒子:氨的电催化氧化反应的合成,表征和性能

获取原文
获取原文并翻译 | 示例
           

摘要

This study elucidates the electrocatalytic oxidation (ECO) of ammonia (NH3) over a complex PtPdRh nano-particle electrocatalytic material immersed in a 0.5-M H2SO4 solution, where the electrolyte was measured using a linear sweep voltammogram (LSV) technique. The complex PtPdRh nanoparticle electrode was synthesized from H2PtCl6, Pd(NO3)3 and Rh(NO3)3 and deposited on an alumina substrate to improve the NH3-ECO ability. The experimental data indicate that a high ECO activity was achieved during the catalytic oxidation over the PtPdRh electrocatalytic material when using a high potential sweep rate; the maximum current density reached for the NH3 oxidation was 0.4 mA in the voltage range of 0.1 V. Interesting, this LSV oxidation ability may explain the significant activity of the catalyst in an acidic environment. The catalyst structure was characterized by polarization curves, UV-vis, three-dimensional excitation-emission fluorescent matrix (EEFM) spectroscopy and TEM. EEFM was applied to evaluate the fresh catalyst yields for the fluorescent plots of 220/345 nm and 210/385 nm, and TEM determined the particle size of the nanoparticles and indicated a high dispersion phenomenon had occurred.
机译:这项研究阐明了浸在0.5M H2SO4溶液中的复杂PtPdRh纳米颗粒电催化材料上氨(NH3)的电催化氧化(ECO),其中使用线性扫描伏安法(LSV)技术测量了电解质。由H2PtCl6,Pd(NO3)3和Rh(NO3)3合成复合PtPdRh纳米粒子电极,并将其沉积在氧化铝基底上以提高NH3-ECO能力。实验数据表明,当使用高电位扫描速率时,在PtPdRh电催化材料上的催化氧化过程中实现了很高的ECO活性。在0.1 V的电压范围内,NH3氧化达到的最大电流密度为0.4 mA。有趣的是,这种LSV氧化能力可以解释催化剂在酸性环境中的显着活性。通过极化曲线,紫外可见光谱,三维激发-发射荧光矩阵(EEFM)光谱和TEM表征了催化剂的结构。应用EEFM评估220/345 nm和210/385 nm荧光图的新鲜催化剂收率,TEM分析确定了纳米颗粒的粒径并表明发生了高分散现象。

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