Improvement of product selectivity in bicarbonate reduction into formic acid on a tin-based catalyst by integrating nano-diamond particles
In this study, the efficiency of electrochemical reduction of bicarbonate into formic acid was improved by using a composite electrode made up of tin (Sn), nanodiamond (ND) and carbon nanotube (CNT). In the absence of ND, a compositional ratio of 10/90 (Sn/CNT) demonstrated the highest current densi...
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| Main Authors: | , , , , , |
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| Format: | Article |
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Institution of Chemical Engineers
2018
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| Subjects: | |
| Online Access: | http://eprints.um.edu.my/21864/ https://doi.org/10.1016/j.psep.2018.03.005 |
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| Summary: | In this study, the efficiency of electrochemical reduction of bicarbonate into formic acid was improved by using a composite electrode made up of tin (Sn), nanodiamond (ND) and carbon nanotube (CNT). In the absence of ND, a compositional ratio of 10/90 (Sn/CNT) demonstrated the highest current density. However, by adding ND in a compositional ratio of 10/90/100 (Sn/CNT/ND) the highest efficiency towards formate/formic acid was achieved. It was observed that the presence of ND enhanced the selectivity of product for formic acid. The effects of bicarbonate concentration and scan rate have also been studied to understand the reduction mechanism. The peak potential shifted towards larger negative values of applied potential with an increase in the scan rate from 0.01 to 0.1 V/s, confirming the irreversible nature of the reduction process. The linear relationship between the current and the square root of the scan rate (with a slope value of 0.519) suggested that the reaction process is fully diffusion-controlled. Formic acid was produced using both electrodes; however, the electrode containing nano-diamond successfully improved the process yield for formic acid. Electrochemical impedance study revealed a significant difference between Warburg coefficient for oxidation and reduction processes with values of 29.63 × 1012 and 67.4 Ω. S−0.5 for the applied potentials of 0.5 V and −0.4 V, respectively. This difference confirmed a low resistance at the electrode/electrolyte interface for the reduction potentials. |
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