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Co-electrolysis of CO2 and H2O in high-temperature solid oxide electrolysis cells: Recent advance in cathodes

机译:高温固体氧化物电解槽中CO2和H2O的共电解:阴极的最新进展

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摘要

Co-electrolysis of CO2 and H2O using high-temperature solid oxide electrolysis cells (SOECs) into valuable chemicals has attracted great attentions recently due to the high conversion and energy efficiency,which provides opportunities of reducing CO2 emission,mitigating global warming and storing intermittent renewable energies.A single SOEC typically consists of an ion conducting electrolyte,an anode and a cathode where the co-electrolysis reaction takes place.The high operating temperature and dicult activated carbon-oxygen double-bond of CO2 put forward strict requirements for SOEC cathode.Great efforts are being devoted to develop suitable cathode materials with high catalytic activity and excellent long-term stability for CO2/H2O electro-reduction.The so far cathode material development is the key point of this review and alternative strategies of high-performance cathode material preparation is proposed.Understanding the mechanism of CO2/H2O electro-reduction is beneficial to highly active cathode design and optimization.Thus the possible reaction mechanism is also discussed.Especially,a method in combination with electrochemical impedance spectroscopy (EIS) measurement,distribution functions of relaxation times (DRT) calculation,complex nonlinear least square (CNLS) fitting and operando ambient pressure X-ray photoelectron spectroscopy (APXPS) characterization is introduced to correctly disclose the reaction mechanism of CO2/H2O co-electrolysis.Finally,different reaction modes of the CO2/H2O coelectrolysis in SOECs are summarized to offer new strategies to enhance the CO2 conversion.Otherwise,developing SOECs operating at 300-600℃ can integrate the electrochemical reduction and the FischerTropsch reaction to convert the CO2/H2O into more valuable chemicals,which will be a new research direction in the future.
机译:使用高温固体氧化物电解槽(SOEC)将CO2和H2O共电解成有价值的化学物质,由于其高转化率和高能效,近年来备受关注,这为减少CO2排放,缓解全球变暖和存储间歇性可再生能源提供了机会单一的SOEC通常由离子导电电解质,发生共电解反应的阳极和阴极组成。CO2的高工作温度和难燃的活性碳-氧双键对SOEC阴极提出了严格的要求。致力于开发合适的具有高催化活性和优异的长期稳定性的阴极材料,以用于CO2 / H2O电解还原。迄今为止,阴极材料的开发是本综述的重点,也是高性能阴极材料的替代策略。提出了制备方法。了解CO2 / H2O的电还原机理有利于Hig特别是结合电化学阻抗谱(EIS)测量,弛豫时间分布函数(DRT)计算,复杂非线性最小二乘(CNLS)拟合和电离的方法,探讨了可能的反应机理。引入操作环境压力X射线光电子能谱(APXPS)表征以正确揭示CO2 / H2O共电解的反应机理。最后,总结了SOEC中CO2 / H2O共电解的不同反应方式,为增强CO2 / H2O共电解提供了新的策略。 CO2转化。否则,在300-600℃下运行的SOEC可以整合电化学还原和FischerTropsch反应,将CO2 / H2O转化为更有价值的化学物质,这将是未来的新研究方向。

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  • 来源
    《天然气化学(英文版)》 |2017年第5期|839-853|共15页
  • 作者单位

    State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, Liaoning, China;

    State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, Liaoning, China;

    University of Chinese Academy of Sciences, Beijing 100039, China;

    State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, Liaoning, China;

    State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, Liaoning, China;

  • 收录信息 中国科学引文数据库(CSCD);中国科技论文与引文数据库(CSTPCD);
  • 原文格式 PDF
  • 正文语种 eng
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