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Electrochemical Reduction of Carbon Dioxide in an MFC-MEC System with a Layer-by-Layer Self-Assembly Carbon Nanotube/ Cobalt Phthalocyanine Modified Electrode

机译:具有层状自组装碳纳米管/酞菁钴修饰电极的MFC-MEC系统中二氧化碳的电化学还原

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摘要

Electrochemical reduction of carbon dioxide (CO_2) to useful chemical materials is of great significance to the virtuous cycle of CO_2. However, some problems such as high overpotential, high applied voltage, and high energy consumption exist in the course of the conventional electrochemical reduction process. This study presents a new CO_2 reduction technique for targeted production of formic acid in a microbial electrolysis cell (MEC) driven by a microbial fuel cell (MFC). The multiwalled carbon nanotubes (MWCNT) and cobalt tetra-amino phthalocyanine (CoTAPc) composite modified electrode was fabricated by the layer-by-layer (LBL) self-assembly technique. The new electrodes significantly decreased the overpotential of CO_2 reduction, and as cathode successfully reduced CO_2 to formic acid (production rate of up to 21.0 ± 0.2 mgL·h~(-1)) in an MEC driven by a single MFC. Compared with the electrode modified by CoTAPc alone, the MWCNT/CoTAPc composite modified electrode could increase the current and formic acid production rate by approximately 20% and 100%, respectively. The Faraday efficiency for formic acid production depended on the cathode potential. The MWCNT/CoTAPc composite electrode reached the maximum Faraday efficiency at the cathode potential of ca. -0.5 V vs Ag/AgCl Increasing the number of electrode modification layers favored the current and formic acid production rate. The production of formic acid was stable in the MFC-MEC system after multiple batches of CO_2 electrolysis, and no significant change was observed on the performances of the modified electrode. The coupling of the catalytic electrode and the bioelectrochemical system realized the targeted reduction of CO_2 in the absence of external energy input, providing a new way for CO_2 capture and conversion.
机译:将二氧化碳(CO_2)电化学还原成有用的化学物质对于CO_2的良性循环具有重要意义。然而,在常规的电化学还原过程中存在一些问题,例如高过电势,高施加电压和高能耗。这项研究提出了一种新的CO_2还原技术,用于在由微生物燃料电池(MFC)驱动的微生物电解池(MEC)中有针对性地生产甲酸。采用层层自组装技术制备了多壁碳纳米管(MWCNT)和四氨基钴酞菁钴(CoTAPc)复合修饰电极。新的电极显着降低了CO_2还原的过电位,并且在单个MFC驱动的MEC中,阴极成功地将CO_2还原为甲酸(生产率高达21.0±0.2 mgL·h〜(-1))。与单独用CoTAPc修饰的电极相比,MWCNT / CoTAPc复合修饰电极可以分别将电流和甲酸的产率提高约20%和100%。法拉第生产甲酸的效率取决于阴极电势。 MWCNT / CoTAPc复合电极的阴极电势达到约法拉第效率。 -0.5 V vs. Ag / AgCl增加电极修饰层的数量有利于电流和甲酸的产生速率。经过多批次的CO_2电解,在MFC-MEC系统中甲酸的生成是稳定的,并且修饰电极的性能未见明显变化。催化电极与生物电化学系统的耦合在没有外部能量输入的情况下实现了有针对性的CO_2还原,为CO_2的捕获和转化提供了新途径。

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  • 来源
    《Environmental Science & Technology》 |2012年第9期|p.5198-5204|共7页
  • 作者单位

    Department of Environmental Engineering, Peking University, Beijing 100871, People's Republic of China,The Key Laboratory of Water and Sediment Sciences, Ministry of Education, Beijing 100871, People's Republic of China;

    Department of Environmental Engineering, Peking University, Beijing 100871, People's Republic of China,The Key Laboratory of Water and Sediment Sciences, Ministry of Education, Beijing 100871, People's Republic of China;

    School of Environmental and Chemical Engineering, Tianjin Polytechnic University, Tianjin 300160, People's Republic of China,State Key Laboratory of Hollow Fiber Membrane Materials and Processes, Tianjin 300160, People's Republic of China;

    Department of Environmental Engineering, Peking University, Beijing 100871, People's Republic of China,The Key Laboratory of Water and Sediment Sciences, Ministry of Education, Beijing 100871, People's Republic of China;

    Department of Environmental Engineering, Peking University, Beijing 100871, People's Republic of China,The Key Laboratory of Water and Sediment Sciences, Ministry of Education, Beijing 100871, People's Republic of China;

  • 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);美国《化学文摘》(CA);
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  • 正文语种 eng
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