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Composite copper oxide-copper bromide films for the selective electroreduction of carbon dioxide

机译:用于选择性电还原二氧化碳的复合氧化铜-溴化铜薄膜

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摘要

Composite copper oxide-copper bromide films were electrodeposited on gas diffusion layer (GDL) supports under controlled potential from aqueous copper salt solutions in the presence of a complexing/surfactant agent such as lactate. The solution pH was adjusted to target simultaneous deposition of cubic nanostructures composed of copper, oxygen, and bromine elements. The film composition and morphology were carefully tuned for enhanced electrochemical conversion of CO_2 to hydrocarbons. Hydrocarbon products, predominantly ethylene and minor amounts of methane, ethane, and propylene were observed along with inevitable H_2 co-generation. Importantly, CO gas was not detected during CO_2 electrolyses. Low temperatures (3-5 °C) enhanced the conversion of CO intermediate to C_2H_4. The durability and electroactivity of these composite films were maintained for extended periods (up to 10 h) of CO_2 electrolysis by periodic in situ application of anodic pulses to regenerate the cathode surface.
机译:在络合/表面活性剂(如乳酸盐)的存在下,在可控电位下,将铜氧化铜-溴化铜复合膜电沉积在铜盐水溶液的控制电势下,沉积在气体扩散层(GDL)载体上。调节溶液的pH值以同时沉积由铜,氧和溴元素组成的立方纳米结构为目标。仔细调整了膜的组成和形态,以增强CO_2向碳氢化合物的电化学转化。观察到碳氢化合物产物,主要是乙烯,以及少量的甲烷,乙烷和丙烯,以及不可避免的H_2热电联产。重要的是,在CO_2电解过程中未检测到CO气体。低温(3-5°C)促进了CO中间体向C_2H_4的转化。通过定期在原位施加阳极脉冲以再生阴极表面,可以使这些复合膜的耐久性和电活性在延长的CO_2电解时间内(长达10小时)得以保持。

著录项

  • 来源
    《Journal of Materials Research》 |2017年第9期|1727-1734|共8页
  • 作者单位

    Department of Chemistry & Biochemistry, The University of Texas at Arlington, Arlington, Texas 76019-0065;

    Department of Mechanical & Aerospace Engineering, The University of Texas ai Arlington, Arlington, Texas 76019-0018;

    Department of Mechanical & Aerospace Engineering, The University of Texas ai Arlington, Arlington, Texas 76019-0018;

    Department of Chemistry & Biochemistry, The University of Texas at Arlington, Arlington, Texas 76019-0065;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
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