Development of ALD Coatings for Harsh Environment Applications

被引:26
作者
Singh, Ankit K. [1 ]
Adstedt, Katarina [1 ]
Brown, Billyde [2 ]
Singh, Preet M. [1 ]
Graham, Samuel [1 ,3 ]
机构
[1] Georgia Inst Technol, Dept Mat Sci & Engn, Atlanta, GA 30332 USA
[2] Georgia Inst Technol, Georgia Tech Mfg Inst, Atlanta, GA 30332 USA
[3] Georgia Inst Technol, George W Woodruff Sch Mech Engn, Atlanta, GA 30332 USA
关键词
atomic layer deposition; electrochemical impedance spectroscopy; ionic solutions; stability; photoluminescence; ATOMIC LAYER DEPOSITION; GAS-DIFFUSION BARRIERS; CORROSION-RESISTANCE; STAINLESS-STEEL; AL2O3; FILMS; TIO2; ENCAPSULATION; STABILITY; BEHAVIOR;
D O I
10.1021/acsami.8b11557
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Atomic layer deposition (ALD) is a well-known technique for the fabrication of ultrathin and highly conformal barrier coatings which have extensively been used for the protection of electronic devices in open atmospheric conditions. Here, we extend the scope for the application of low-temperature-deposited plasma-enhanced ALD barrier coatings for the protection of devices in a variety of chemical environments. The chemical stability tests were conducted in 3.5% NaCl, sea water, HCl (pH 4), and H2SO4 (pH 4) solutions for ALD Al2O3, HfO2, TiO2, and ZrO2, deposited at 100 degrees C on TiO2-coated Au and ALD ZnO (photoactive)-coated Si substrates. Using electrochemical impedance spectroscopy (EIS) and photoluminescence (PL) study, various aspects of the barrier properties and performance of ALD demonstrate that the combined approach involving EIS and PL provides films in harsh chemical environments were explored. We unique insights into the suitability of ALD films as barriers in harsh environments involving ionic solutions. The observations from EIS and PL tests are supported by the X-ray photoelectron spectroscopy analysis of ALD materials. Of the materials tested, ALD TiO2 and ZrO2 were found to be the most stable, chemically, in all four solutions, whereas TiO2 was a better permeation barrier.
引用
收藏
页码:7498 / 7509
页数:12
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