TY - JOUR
T1 - Carbon-neutral energy cycles using alcohols
AU - Fukushima, Takashi
AU - Kitano, Sho
AU - Hata, Shinichi
AU - Yamauchi, Miho
N1 - Funding Information:
This work was supported by Japan Science and Technology Agency – CREST.
Publisher Copyright:
© 2018 The Author(s). Published by National Institute for Materials Science in partnership with Taylor & Francis.
PY - 2018/12/31
Y1 - 2018/12/31
N2 - We demonstrated carbon-neutral (CN) energy circulation using glycolic acid (GC)/oxalic acid (OX) redox couple. Here, we report fundamental studies on both catalyst search for power generation process, i.e. GC oxidation, and elemental steps for fuel generation process, i.e. OX reduction, in CN cycle. The catalytic activity test on various transition metals revealed that Rh, Pd, Ir, and Pt have preferable features as a catalyst for electrochemical oxidation of GC. A carbon-supported Pt catalyst in alkaline conditions exhibited higher activity, durability, and product selectivity for electrooxidation of GC rather than those in acidic media. The kinetic study on OX reduction clearly indicated that OX reduction undergoes successive two-electron reductions to form GC. Furthermore, application of TiO2 catalysts with large specific area for electrochemical reduction of OX facilitates the selective formation of GC.
AB - We demonstrated carbon-neutral (CN) energy circulation using glycolic acid (GC)/oxalic acid (OX) redox couple. Here, we report fundamental studies on both catalyst search for power generation process, i.e. GC oxidation, and elemental steps for fuel generation process, i.e. OX reduction, in CN cycle. The catalytic activity test on various transition metals revealed that Rh, Pd, Ir, and Pt have preferable features as a catalyst for electrochemical oxidation of GC. A carbon-supported Pt catalyst in alkaline conditions exhibited higher activity, durability, and product selectivity for electrooxidation of GC rather than those in acidic media. The kinetic study on OX reduction clearly indicated that OX reduction undergoes successive two-electron reductions to form GC. Furthermore, application of TiO2 catalysts with large specific area for electrochemical reduction of OX facilitates the selective formation of GC.
KW - Selective electrooxidation of alcohol
KW - TiO
KW - electrolyzer
KW - fuel cell
KW - hydrogenation of carboxylic acid
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U2 - 10.1080/14686996.2018.1426340
DO - 10.1080/14686996.2018.1426340
M3 - Article
AN - SCOPUS:85042293852
VL - 19
SP - 142
EP - 152
JO - Science and Technology of Advanced Materials
JF - Science and Technology of Advanced Materials
SN - 1468-6996
IS - 1
ER -