Exploring a supramolecular gel to in‐situ crystal fabrication from the low molecular weight gelators: a crystal engineering approach towards microelectronic device application

超分子化学 材料科学 晶体工程 纳米技术 微电子 Crystal(编程语言) 结晶学 化学工程 晶体结构 化学 工程类 计算机科学 程序设计语言
作者
Subhendu Dhibar,Baishakhi Pal,Kripasindhu Karmakar,Sandip Kundu,Subham Bhattacharjee,Rupam Sahoo,Sk Mehebub Rahaman,Dhananjay Dey,Partha Pratim Ray,Bidyut Saha
出处
期刊:ChemistrySelect [Wiley]
卷期号:8 (12) 被引量:5
标识
DOI:10.1002/slct.202204214
摘要

Abstract A novel functional supramolecular gel (SA‐MEA) has been produced through the mixing of succinic acid and monoethanolamine directly in DMF medium under ambient conditions. The semi‐solid and viscoelastic nature of mechanically stable SA‐MEA gel has been established through the rheological analysis. The major chemical components of the gel are confirmed by EDX elemental mapping, while FESEM microstructural analysis investigates the morphological patterns of the gel. The gel gives rise to crystalline materials at room temperature and in the absence of external stimuli. Single‐crystal diffraction study of the in‐situ generated crystals shows the existence of different supramolecular synthons involving the hydrogen‐bonding interactions (N−H⋅⋅⋅O and O−H⋅⋅⋅O) leading to the formation of graph set motifs. These structural building blocks provide the stability to hold the overall molecular framework of SA‐MEA gel. Moreover, the contribution of O⋅⋅⋅H/H⋅⋅⋅O contacts plays a crucial role in this gel formation, which is established from the Hirshfeld surfaces along with linked 2D fingerprint patterns of the plot for both molecular components. Additionally, the SA‐MEA gel‘s supramolecular structure exhibits electrical conductivity, which was exploited to construct an electronic device with a metal‐semiconductor (MS) junction. Analyses of the gel‘s electrical properties were done in‐depth. Inclusive, this work demonstrates that the SA‐MEA gel may be used to create a semi‐conductive microelectronic device, such as a Schottky barrier diode.

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