TY - JOUR
T1 - Electrochemical hydrogenation of non-aromatic carboxylic acid derivatives as a sustainable synthesis process
T2 - From catalyst design to device construction
AU - Sadakiyo, Masaaki
AU - Hata, Shinichi
AU - Fukushima, Takashi
AU - Juhász, Gergely
AU - Yamauchi, Miho
N1 - Funding Information:
This works is partly supported by Core Research for Evolutional Science and Technology (CREST), Japan Science and Technology Agency (JST). This work was supported by the International Institute for Carbon Neutral Energy Research (WPI-I2CNER), sponsored by the World Premier International Research Center Initiative (WPI). This work was supported by MEXT KAKENHI Grant Number JP12852953 and JP18H05517, and JST-CREST, Japan.
Publisher Copyright:
© 2019 the Owner Societies.
PY - 2019
Y1 - 2019
N2 - Electrochemical hydrogenation of a carboxylic acid using water as a hydrogen source is an environmentally friendly synthetic process for upgrading bio-based chemicals. We systematically studied electrochemical hydrogenation of non-aromatic carboxylic acid derivatives on anatase TiO2 by a combination of experimental analyses and density functional theory calculations, which for the first time shed light on mechanistic insights for the electrochemical hydrogenation of carboxylic acids. Development of a substrate permeable TiO2 cathode enabled construction of a flow-type electrolyser, i.e., a so-called polymer electrode alcohol synthesis cell (PEAEC) for the continuous synthesis of an alcoholic compound from a carboxylic acid. We demonstrated the highly efficient and selective conversion of oxalic acid to produce glycolic acid, which can be regarded as direct electric power storage into an easily treatable alcoholic compound.
AB - Electrochemical hydrogenation of a carboxylic acid using water as a hydrogen source is an environmentally friendly synthetic process for upgrading bio-based chemicals. We systematically studied electrochemical hydrogenation of non-aromatic carboxylic acid derivatives on anatase TiO2 by a combination of experimental analyses and density functional theory calculations, which for the first time shed light on mechanistic insights for the electrochemical hydrogenation of carboxylic acids. Development of a substrate permeable TiO2 cathode enabled construction of a flow-type electrolyser, i.e., a so-called polymer electrode alcohol synthesis cell (PEAEC) for the continuous synthesis of an alcoholic compound from a carboxylic acid. We demonstrated the highly efficient and selective conversion of oxalic acid to produce glycolic acid, which can be regarded as direct electric power storage into an easily treatable alcoholic compound.
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U2 - 10.1039/c8cp07445c
DO - 10.1039/c8cp07445c
M3 - Article
C2 - 30865734
AN - SCOPUS:85062846853
SN - 1463-9076
VL - 21
SP - 5882
EP - 5889
JO - Physical Chemistry Chemical Physics
JF - Physical Chemistry Chemical Physics
IS - 11
ER -