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胆碱氯化物和三苯甲基溴化膦基系统的能带隙能量。

Band-Gap Energies of Choline Chloride and Triphenylmethylphosphoniumbromide-Based Systems.

机构信息

Department of Chemistry, Materials and Chemical Engineering "G. Natta", Politecnico di Milano, Piazza L. da Vinci 32, 20133 Milano, Italy.

CNR-SCITEC Istituto di Scienze e Tecnologie Chimiche, Via Alfonso Corti 12, 20133 Milano, Italy.

出版信息

Molecules. 2020 Mar 25;25(7):1495. doi: 10.3390/molecules25071495.

DOI:10.3390/molecules25071495
PMID:32218347
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7180541/
Abstract

UV-VIS spectroscopy analysis of six mixtures containing choline chloride or triphenylmethylphosphonium bromide as the hydrogen bond acceptor (HBA) and different hydrogen bond donors (HBDs, nickel sulphate, imidazole, d-glucose, ethylene glycol, and glycerol) allowed to determine the indirect and direct band-gap energies through the Tauc plot method. Band-gap energies were compared to those relative to known choline chloride-containing deep band-gap systems. The measurements reported here confirmed the tendency of alcohols or Lewis acids to increment band-gap energy when employed as HBDs. Indirect band-gap energy of 3.74 eV was obtained in the case of the triphenylmethylphosphonium bromide/ethylene glycol system, which represents the smallest transition energy ever reported to date for such kind of systems.

摘要

使用 UV-VIS 光谱分析六种混合物,其中包含氯化胆碱或三苯甲基膦溴化物作为氢键受体(HBA)和不同的氢键供体(HBD,硫酸镍、咪唑、D-葡萄糖、乙二醇和甘油),通过 Tauc 图法确定间接和直接带隙能。将带隙能与已知的含氯化胆碱的深带隙系统进行比较。这里报道的测量结果证实了醇或路易斯酸作为 HBD 使用时增加带隙能的趋势。在三苯甲基膦溴化物/乙二醇体系中获得了 3.74eV 的间接带隙能,这是迄今为止此类体系报道的最小跃迁能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e78/7180541/186790a0c619/molecules-25-01495-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e78/7180541/5e94fa8c29b7/molecules-25-01495-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e78/7180541/476e23c6bd14/molecules-25-01495-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e78/7180541/6a1fb541249a/molecules-25-01495-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e78/7180541/3c532d5c28bd/molecules-25-01495-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e78/7180541/186790a0c619/molecules-25-01495-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e78/7180541/5e94fa8c29b7/molecules-25-01495-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e78/7180541/476e23c6bd14/molecules-25-01495-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e78/7180541/6a1fb541249a/molecules-25-01495-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e78/7180541/3c532d5c28bd/molecules-25-01495-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e78/7180541/186790a0c619/molecules-25-01495-g005.jpg

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