Stable and Highly Efficient Electrochemical Production of Formic Acid from Carbon Dioxide Using Diamond Electrodes

2018 ◽  
Vol 57 (10) ◽  
pp. 2639-2643 ◽  
Author(s):  
Keisuke Natsui ◽  
Hitomi Iwakawa ◽  
Norihito Ikemiya ◽  
Kazuya Nakata ◽  
Yasuaki Einaga
2018 ◽  
Vol 130 (10) ◽  
pp. 2669-2673 ◽  
Author(s):  
Keisuke Natsui ◽  
Hitomi Iwakawa ◽  
Norihito Ikemiya ◽  
Kazuya Nakata ◽  
Yasuaki Einaga

2015 ◽  
Vol 280 ◽  
pp. 215-221 ◽  
Author(s):  
Heng Zhong ◽  
Ying Gao ◽  
Guodong Yao ◽  
Xu Zeng ◽  
Qiuju Li ◽  
...  

2020 ◽  
Vol 385 ◽  
pp. 1-9 ◽  
Author(s):  
Andreas Weilhard ◽  
Kevin Salzmann ◽  
Miquel Navarro ◽  
Jairton Dupont ◽  
Martin Albrecht ◽  
...  

2020 ◽  
Vol 4 (8) ◽  
pp. 4030-4038 ◽  
Author(s):  
Kayode Adesina Adegoke ◽  
Shankara Gayathri Radhakrishnan ◽  
Clarissa L. Gray ◽  
Barbara Sowa ◽  
Claudia Morais ◽  
...  

Co-electrolysis of formic acid and water using an indium oxide cathode catalyst yields a mixture of methanol, ethanol and iso-propanol with a Faraday efficiency up to 82.4%. The reaction of aqueous carbon dioxide occurs via a competing pathway.


2019 ◽  
Author(s):  
Andreas Weilhard ◽  
Stephen Argent ◽  
Victor Sans

We present a highly efficient catalytic system to transform carbon dioxide to formic acid under base-free conditions. Our system employs a vbasic ionic liquid as a buffer for the producty. Our results show an exceptionally active catalyst with unprecedentedly high turnover numbers and frequency.


2019 ◽  
Author(s):  
Andreas Weilhard ◽  
Stephen Argent ◽  
Victor Sans

We present a highly efficient catalytic system to transform carbon dioxide to formic acid under base-free conditions. Our system employs a vbasic ionic liquid as a buffer for the producty. Our results show an exceptionally active catalyst with unprecedentedly high turnover numbers and frequency.


RSC Advances ◽  
2017 ◽  
Vol 7 (36) ◽  
pp. 22510-22514 ◽  
Author(s):  
Norihito Ikemiya ◽  
Keisuke Natsui ◽  
Kazuya Nakata ◽  
Yasuaki Einaga

Rb+ cations provide a greater effect on the electrochemical conversion of CO2 to formic acid using BDD electrodes.


2018 ◽  
Author(s):  
Chandan Dey ◽  
Ronny Neumann

<p>A manganese substituted Anderson type polyoxometalate, [MnMo<sub>6</sub>O<sub>24</sub>]<sup>9-</sup>, tethered with an anthracene photosensitizer was prepared and used as catalyst for CO<sub>2</sub> reduction. The polyoxometalate-photosensitizer hybrid complex, obtained by covalent attachment of the sensitizer to only one face of the planar polyoxometalate, was characterized by NMR, IR and mass spectroscopy. Cyclic voltammetry measurements show a catalytic response for the reduction of carbon dioxide, thereby suggesting catalysis at the manganese site on the open face of the polyoxometalate. Controlled potentiometric electrolysis showed the reduction of CO<sub>2</sub> to CO with a TOF of ~15 sec<sup>-1</sup>. Further photochemical reactions showed that the polyoxometalate-anthracene hybrid complex was active for the reduction of CO<sub>2</sub> to yield formic acid and/or CO in varying amounts dependent on the reducing agent used. Control experiments showed that the attachment of the photosensitizer to [MnMo<sub>6</sub>O<sub>24</sub>]<sup>9-</sup> is necessary for photocatalysis.</p><div><br></div>


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