Bridging the Synthesis Gap: Ionic Liquids Enable Solvent-Mediated Reaction in Vapor-Phase Deposition

被引:10
作者
Shi, Jingwei [1 ]
Bent, Stacey F. [1 ]
机构
[1] Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA
基金
美国国家科学基金会;
关键词
molecular layer deposition; atomic layer deposition; thin film; ionic liquid; vapor deposition; organic; MOLECULAR LAYER DEPOSITION; FRIEDEL-CRAFTS ACYLATION; ORGANIC FILMS; THIN-FILMS; NANOSCALE; CATALYSIS; KINETICS; KETONE); ISOCYANATE; ALUMINUM;
D O I
10.1021/acsnano.0c09329
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Molecular layer deposition (MLD) is an attractive, vapor-phase deposition method for applications requiring ultrathin organic materials, such as photolithography, lithium batteries, and microelectronics. By using sequential self-limiting surface reactions, MLD offers excellent control over thickness and conformality, but there are also challenges such as a limited range of possible film compositions and long deposition times. In this study, we introduce a modified technique, termed ionic liquid assisted MLD (IL-MLD), that can overcome these barriers. By performing the surface reactions inside of an ultrathin layer of a compatible ionic liquid (IL), solvent effects are replicated inside a vacuum system, broadening the possible reactions to a much wider suite of chemistries. Using this strategy, the MLD of polyetherketoneketone, an industrially and research-relevant, high-performance thermoplastic, is reported. With this proof-of-concept, we demonstrate that IL-MLD can enable the synthesis of polymers via solvent- or catalyst-mediated reactions and establish an approach that may allow solution chemistries to be accessed in other vapor deposition techniques as well.
引用
收藏
页码:3004 / 3014
页数:11
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