Nanoporous gold electrodes modified with self-assembled monolayers for electrochemical control of the surface charge

被引:6
作者
Hengge, Elisabeth [1 ]
Hirber, Markus [1 ]
Brunner, Philipp [1 ]
Steyskal, Eva-Maria [1 ]
Nidetzky, Bernd [2 ]
Wuerschum, Roland [1 ]
机构
[1] Graz Univ Technol, Inst Mat Phys, Petersgasse 16, A-8010 Graz, Austria
[2] Graz Univ Technol, Inst Biotechnol & Biochem Engn, Petersgasse 12, A-8010 Graz, Austria
关键词
TERMINATED ALKANETHIOL MONOLAYERS; IMPEDANCE SPECTROSCOPY; POLYCRYSTALLINE GOLD; POROUS-ELECTRODES; PROTON-TRANSFER; ZERO CHARGE; ACID; IMMOBILIZATION; VOLTAMMETRY; DESORPTION;
D O I
10.1039/d1cp01491a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The electrochemical behaviour of nanoporous gold modified with self-assembled monolayers is investigated with regard to its point of zero charge (pzc) and proton transfer reaction. Due to their high surface-to-volume ratio and conductivity, nanoporous electrodes represent promising materials for numerous applications, including the immobilization of biomolecules in biotechnology and biosensing. Therefore, the fundamental understanding and controllability of the surface state of the electrode is essential. To achieve a precise surface charge control, nanoporous gold (npAu) is modified with self-assembled monolayers (SAMs) of different lengths (3-mercaptopropionic acid (MPA) and 16-mercaptohexadecanoic acid (MHDA)). Cyclic voltammetry and impedance spectroscopy are used to determine the pzc. The most distinct pzc, and thus the most precise charge control, is found for the long-chain MHDA. Subsequently, the proton transfer reaction was investigated as a function of pH and scan rate. The observed protonation/deprotonation reaction was qualitatively well in line with the literature for planar gold electrodes, albeit the fraction of electrochemical controllable SAMs increased by a factor of 10 compared to planar electrodes indicating attractive application potential.
引用
收藏
页码:14457 / 14464
页数:8
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