TY - JOUR
T1 - A mechanism of adsorption of β-nicotinamide adenine dinucleotide on graphene sheets
T2 - Experiment and theory
AU - Pumera, Martin
AU - Scipioni, Roberto
AU - Iwai, Hideo
AU - Ohno, Takahisa
AU - Miyahara, Yuji
AU - Boero, Mauro
PY - 2009/10/19
Y1 - 2009/10/19
N2 - β-Nicotinamide adenine dinucleotide (NAD+) and its reduced form (NADH) play major roles in the development of electrochemical enzyme biosensors and biofuel cells. Unfortunately, the oxidation of NADH at carbon electrodes suffers from passivation of the electrodes and a decrease in passing currents. Here, we investigate experimentally and theoretically the reasons for such passivation. Highresolution X-ray photoelectron spectroscopy (HR-XPS), voltammetry, and amperometry show that adsorption occurs on the edges and "edge-like" defects of graphene sheets. HR-XPS and ab initio molecular dynamics show that the adsorption of NAD+ molecules on the edges of graphene happens due to interaction with oxygencontaining groups such as carboxylic groups, while graphene edges substituted only with hydrogen are prone to passivation.
AB - β-Nicotinamide adenine dinucleotide (NAD+) and its reduced form (NADH) play major roles in the development of electrochemical enzyme biosensors and biofuel cells. Unfortunately, the oxidation of NADH at carbon electrodes suffers from passivation of the electrodes and a decrease in passing currents. Here, we investigate experimentally and theoretically the reasons for such passivation. Highresolution X-ray photoelectron spectroscopy (HR-XPS), voltammetry, and amperometry show that adsorption occurs on the edges and "edge-like" defects of graphene sheets. HR-XPS and ab initio molecular dynamics show that the adsorption of NAD+ molecules on the edges of graphene happens due to interaction with oxygencontaining groups such as carboxylic groups, while graphene edges substituted only with hydrogen are prone to passivation.
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U2 - 10.1002/chem.200900399
DO - 10.1002/chem.200900399
M3 - Article
C2 - 19746361
AN - SCOPUS:70350238301
SN - 0947-6539
VL - 15
SP - 10851
EP - 10856
JO - Chemistry - A European Journal
JF - Chemistry - A European Journal
IS - 41
ER -