Low Nickel-doped copper as the electrocatalyst for oxidation of formaldehyde and evolution of hydrogen. (10th February 2020)
- Record Type:
- Journal Article
- Title:
- Low Nickel-doped copper as the electrocatalyst for oxidation of formaldehyde and evolution of hydrogen. (10th February 2020)
- Main Title:
- Low Nickel-doped copper as the electrocatalyst for oxidation of formaldehyde and evolution of hydrogen
- Authors:
- Liao, Weicheng
Chen, Yi-wei
Liao, Yu-Chan
Lin, Xin-yi
Yau, Shuehlin
Shyue, Jing-Jong
Wu, Shiuan-Yau
Chen, Hsin-Tsung - Abstract:
- Abstract: As copper electrode can catalyze formaldehyde (HCHO) oxidation reaction (FOR) and oxygen reduction reaction in 0.1 M KOH, these redox systems can be utilized to assemble a HCHO fuel cell with an ideal rest potential of 0.8 V. As formaldehyde, a liquid at room temperature, can release hydrogen upon oxidation at a Cu electrode, this system can serve as a H2 portable source. This study employs home – made single crystal electrodes of Cu(111) and Cu100-x Nix (111) (x = 1.5 and 4.3) to highlight the surprising boosting effect of the Ni dopant (∼1.5% molar ratio) in a Cu electrode toward FOR in 0.1 M KOH. These ordered electrodes are made by an annealing and quenching method performed in the ambient air (without the involvement of vacuum). Their FOR activities in KOH are scrutinized by voltammetry and chronoamperometry, from which the Cu98·5 Ni1.5 (111) electrode is found to be 12 folds more active than the Cu(111) electrode. An increase of Ni content from 1.5 to 4.3% in the Cu crystal does not substantiate the FOR activity. The rate-determining steps of FOR at these electrodes are probed in media of KOH and KOD, revealing a 50% lower FOR peak current at the Cu98·5 Ni1.5 (111), but not the Cu(111), electrode in 0.1 M KOD + 0.1 M HCHO. The effect of Ni dopant on Cu(111) is considered theoretically by using density functional theory (DFT), showing that the adsorption of H2 COOH −, the main species of alkaline HCHO, is increased by the Ni dopant in the Cu matrix. A tinyAbstract: As copper electrode can catalyze formaldehyde (HCHO) oxidation reaction (FOR) and oxygen reduction reaction in 0.1 M KOH, these redox systems can be utilized to assemble a HCHO fuel cell with an ideal rest potential of 0.8 V. As formaldehyde, a liquid at room temperature, can release hydrogen upon oxidation at a Cu electrode, this system can serve as a H2 portable source. This study employs home – made single crystal electrodes of Cu(111) and Cu100-x Nix (111) (x = 1.5 and 4.3) to highlight the surprising boosting effect of the Ni dopant (∼1.5% molar ratio) in a Cu electrode toward FOR in 0.1 M KOH. These ordered electrodes are made by an annealing and quenching method performed in the ambient air (without the involvement of vacuum). Their FOR activities in KOH are scrutinized by voltammetry and chronoamperometry, from which the Cu98·5 Ni1.5 (111) electrode is found to be 12 folds more active than the Cu(111) electrode. An increase of Ni content from 1.5 to 4.3% in the Cu crystal does not substantiate the FOR activity. The rate-determining steps of FOR at these electrodes are probed in media of KOH and KOD, revealing a 50% lower FOR peak current at the Cu98·5 Ni1.5 (111), but not the Cu(111), electrode in 0.1 M KOD + 0.1 M HCHO. The effect of Ni dopant on Cu(111) is considered theoretically by using density functional theory (DFT), showing that the adsorption of H2 COOH −, the main species of alkaline HCHO, is increased by the Ni dopant in the Cu matrix. A tiny amount of Ni significantly modifies the electronic structure of the Cu substrate. Graphical abstract: Image 1 … (more)
- Is Part Of:
- Electrochimica acta. Volume 333(2020)
- Journal:
- Electrochimica acta
- Issue:
- Volume 333(2020)
- Issue Display:
- Volume 333, Issue 2020 (2020)
- Year:
- 2020
- Volume:
- 333
- Issue:
- 2020
- Issue Sort Value:
- 2020-0333-2020-0000
- Page Start:
- Page End:
- Publication Date:
- 2020-02-10
- Subjects:
- Ni-doped Cu(111) electrode -- Formaldehyde oxidation -- Organic hydrogen carrier
Electrochemistry -- Periodicals
Electrochemistry, Industrial -- Periodicals
541.37 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00134686 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.electacta.2019.135542 ↗
- Languages:
- English
- ISSNs:
- 0013-4686
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3698.950000
British Library DSC - BLDSS-3PM
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- 12576.xml