Szunerits Sabine, Coffinier Yannick, Janel Sébastien, Boukherroub Rabah
Laboratoire d'Electrochimie et de Physicochimie des Matériaux et des Interfaces (LEPMI), CNRS-INPG-UJF, 1130 rue de la piscine, BP 75, 38402 St. Martin d'Hères Cedex, France.
Langmuir. 2006 Dec 5;22(25):10716-22. doi: 10.1021/la060793o.
This article reports chemical stability studies of a gold film electrode coated with thin silicon oxide (SiOx) layers using electrochemical, surface plasmon resonance (SPR) and atomic force microscopy (AFM) techniques. Silica films with different thicknesses (d = 6.4, 9.7, 14.5, and 18.5 nm) were deposited using a plasma-enhanced chemical vapor deposition technique (PECVD). For SiOx films with d >/= 18.5 nm, the electrochemical behavior is characteristic of a highly efficient barrier for a redox probe. SiOx films with thicknesses between 9.5 and 14.5 nm were found to be less efficient barriers for electron transfer. The Au/SiOx interface with 6.4 nm of SiOx, however, showed an enhanced steady-state current compared to that of the other films. The stability of this interface in solutions of different pH was investigated. Whereas a strongly basic solution led to a continuous dissolution of the SiOx interface, acidic treatment produced a more reticulated SiOx film and improved electrochemical behavior. The electrochemical results were corroborated by SPR measurements in real time and AFM studies.
本文报道了使用电化学、表面等离子体共振(SPR)和原子力显微镜(AFM)技术对涂有薄氧化硅(SiOx)层的金膜电极进行的化学稳定性研究。采用等离子体增强化学气相沉积技术(PECVD)沉积了不同厚度(d = 6.4、9.7、14.5和18.5 nm)的二氧化硅膜。对于d≥18.5 nm的SiOx膜,其电化学行为表现为对氧化还原探针具有高效阻挡作用的特征。发现厚度在9.5至14.5 nm之间的SiOx膜对电子转移的阻挡效率较低。然而,具有6.4 nm SiOx的Au/SiOx界面与其他膜相比显示出增强的稳态电流。研究了该界面在不同pH溶液中的稳定性。强碱性溶液会导致SiOx界面持续溶解,而酸性处理则产生更网状的SiOx膜并改善了电化学行为。实时SPR测量和AFM研究证实了电化学结果。