Thorum Matthew S, Anderson Cyrus A, Hatch Jeremy J, Campbell Andrew S, Marshall Nicholas M, Zimmerman Steven C, Lu Yi, Gewirth Andrew A
Department of Chemistry, University of Illinois at Urbana-Champaign, Urbana, Illinois, 61801.
J Phys Chem Lett. 2010 Aug;1(15):2251-2254. doi: 10.1021/jz100745s.
Laccase, a multicopper oxidase, catalyses the four electron reduction of oxygen to water. Upon adsorption to an electrode surface, laccase is known to reduce oxygen at overpotentials lower than the best noble metal electrocatalysts usually employed. While the electrocatalytic activity of laccase is well established on carbon electrodes, laccase does not typically adsorb to better defined noble metal surfaces in an orientation that allows for efficient electrocatalysis. In this work, we utilized anthracene-2-methanethiol (AMT) to modify the surface of Au electrodes and examined the electrocatalytic activity of adsorbed laccase. AMT facilitated the adsorption of laccase, and the onset of electrocatalytic oxygen reduction was observed as high as 1.13 V(RHE). We observed linear Tafel behavior with a 144 mV/dec slope, consistent with an outer sphere single electron transfer from the electrode to a Cu site in the enzyme as the rate determining step of the oxygen reduction mechanism.
漆酶是一种多铜氧化酶,可催化氧气的四电子还原反应生成水。已知漆酶吸附到电极表面后,能够在比通常使用的最佳贵金属电催化剂更低的过电位下还原氧气。虽然漆酶在碳电极上的电催化活性已得到充分证实,但漆酶通常不会以允许有效电催化的取向吸附到更明确的贵金属表面上。在这项工作中,我们利用蒽-2-甲硫醇(AMT)修饰金电极表面,并研究了吸附的漆酶的电催化活性。AMT促进了漆酶的吸附,并且观察到电催化氧还原的起始电位高达1.13 V(相对于可逆氢电极)。我们观察到具有144 mV/dec斜率的线性塔菲尔行为,这与从电极到酶中铜位点的外层单电子转移作为氧还原机制的速率决定步骤一致。