N-Heterocyclic carbene-based gold etchants

被引:0
|
作者
Chevalier R.B. [1 ]
Pantano J. [1 ]
Kiesewetter M.K. [1 ]
Dwyer J.R. [1 ]
机构
[1] Department of Chemistry, University of Rhode Island, 140 Flagg Road, Kingston, 02881, RI
基金
美国国家科学基金会;
关键词
gold etchant; microfabrication; N-heterocyclic carbenes; self-assembled monolayer (SAM); thin films;
D O I
10.3762/BJNANO.14.71
中图分类号
学科分类号
摘要
N-Heterocyclic carbenes (NHCs) are an emerging alternative to thiols for the formation of stable self-assembled monolayers (SAMs) on gold. We examined several different species that have been used to produce NHC-based monolayers on gold, namely 1,3-diisopropyl-5-nitrobenzimidazolium iodide, 1,3-diisopropyl-5-nitrobenzimidazolium hydrogen carbonate, bis(1,3-diisopropyl-5-nitrobenzimidazolium)gold(I) iodide, and 1,3-diisopropyl-5-nitrobenzimidazole-2-ylidene. Contrary to expectation, solutions containing the first two species in tetrahydrofuran and dichloromethane caused visible loss of gold from thin-film-coated glass slides. The use of toluene solutions of all species resulted in no apparent dissolution of gold. We present scanning electron micrographs and elemental imaging analyses by energy dispersive X-ray spectroscopy to examine the effect of solutions of each species on the gold film. This work highlights the risk of unwanted etching during some routes to NHC-based surface functionalization but also the potential for deliberate etching, with the outcome determined by choice of chemically synthesized organic species and solvent. © 2023 Chevalier et al.; licensee Beilstein-Institut.
引用
收藏
页码:865 / 871
页数:6
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