Electrochemical NADH regeneration and electroenzymatic CO2 reduction on Cu nanorods/glassy carbon electrode prepared by cyclic deposition

Authors
Kim, Seung-HanChung, Gui-YungKim, Seong-HoonVinothkumar, G.Yoon, Sung-HoJung, Kwang-Deog
Issue Date
2016-08-20
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Citation
ELECTROCHIMICA ACTA, v.210, pp.837 - 845
Abstract
Mimicking photosynthesis using NADH is a sustainable method to convert CO2 and mitigate global warming. Here, Cu nanorods with twin crystal structure on glassy carbon (GC) were prepared by a cyclic electrodeposition method with voltage from -0.2 V to -1.0. The prepared CuGC electrodes were used for the electrochemical NADH regeneration and electroenzymatic CO2 reduction at -1.0 V using formate dehydrogenase from Candida boidinii. The selective activation of NADH (1,4-NADH) approached 67% as the deposition cycle number increased. The electron mediator [Cp*Rh(bpy)Cl]Cl complex (Rh(III)) was used to obtain nearly 100% active NADH on the CuGC electrode. The electron transfer rate to Rh(III) is crucial for optimal NADH regeneration: Rh(III) should be reduced to RhH quickly as it has the capability to decompose NADH catalytically. This allows sufficiently high NAD(+) conversion and NADH regeneration reaction rates for the electroenzymatic CO2 reduction to formate. The optimum concentrations of Rh(III) and NAD(+) were estimated to be 0.25 and 1.00 mM, respectively. For the CuGC electrode prepared with 300 deposition cycles, the formate formation rate was estimated to be (6.28 +/- 0.02) x 10(-3) mu mol/mg(CbsFDH)/min, a three-fold increase compared to previously reported results on Cu foil electrode. (C) 2016 Elsevier Ltd. All rights reserved.
Keywords
FORMATE DEHYDROGENASE; FORMIC-ACID; NAD(+); EFFICIENT; CONVERSION; SURFACE; INTERCONVERSION; OXIDATION; HYDROGEN; COPPER; FORMATE DEHYDROGENASE; FORMIC-ACID; NAD(+); EFFICIENT; CONVERSION; SURFACE; INTERCONVERSION; OXIDATION; HYDROGEN; COPPER; Cu nanorods/GC electrode; NADH regeneration; formate dehydrogenase; electroenzymatic CO2 reduction; formate formation
ISSN
0013-4686
URI
https://pubs.kist.re.kr/handle/201004/123779
DOI
10.1016/j.electacta.2016.06.007
Appears in Collections:
KIST Article > 2016
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