Bimetallic Pt,Ir-containing coatings formed by MOCVD for medical applications

被引:0
作者
Svetlana I. Dorovskikh
Evgeniia S. Vikulova
Danila B. Kal’nyi
Yury V. Shubin
Igor. P. Asanov
Evgeniy A. Maximovskiy
Anton K. Gutakovskii
Natalya B. Morozova
Tamara V. Basova
机构
[1] Nikolaev Institute of Inorganic Chemistry SB RAS,
[2] Novosibirsk State University,undefined
[3] Rzhanov Institute of Semiconductor Physics SB RAS,undefined
来源
Journal of Materials Science: Materials in Medicine | 2019年 / 30卷
关键词
Bimetallic coating; MOCVD; Electrode; Pacemaker; Charge storage capacity;
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摘要
Biocompatible PtxIr(1−x) layers combining high mechanical strength of the iridium component and outstanding corrosion resistance of the platinum component providing reversible charge transfer reactions in the living tissue are one of the important materials required for implantable medical electrodes. The modern trend to complicate the shape and reduce the electrode dimensions includes the challenge to develop precise methods to obtain such bimetallic coatings with enhanced surface area and advanced electrochemical characteristics. Herein, PtxIr(1−x) coatings were firstly obtained on cathode and anode pole tips of endocardial electrodes for pacemakers using chemical vapor deposition technique. To deposit PtxIr(1−x) coatings with a wide range of metal ratios (x = 0.5–0.9) the combination of acetylacetonate-based volatile precursors with compatible thermal characteristics was used for the first time. The expected metal ratio in the coatings was regulated by a partial pressure of the precursor vapors in the reaction zone and was in the good agreement with its real value measured by various methods, including energy-dispersive and wavelength dispersive spectroscopy, X-ray photoelectron spectroscopy. According to the X-ray powder diffraction analysis, PtxIr(1−x) coatings consisted of fcc-PtxIr(1−x) solid solution phases. The microscopy data confirmed the formation of PtxIr1−x coatings with the enhanced surface areas. The effect of electrochemical activation on the surface composition and morphology of the samples was studied. The electrochemical characteristics of samples were estimated from cyclic voltammetry and electrochemical impedance spectroscopy data. The charge storage capacity (CSC) values of activated samples were in the range of 19–108 mCcm−2 (phosphate buffer saline solution, 100 mV/s).
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