Distinct changes of Debye relaxation in primary and secondary monoalcohols by carbon nano-dots

Distinct changes of Debye relaxation in primary and secondary monoalcohols by carbon nano-dots
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碳纳米点对伯和仲一元醇德拜弛豫的明显变化

DOI:
10.1016/j.molliq.2019.111738
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发表时间:
2020
影响因子:
6
通讯作者:
Wang Li-Min
Wang Li-Min
中科院分区:
化学2区
文献类型:
--
作者:
Guo Yuxing;Jin Xiao;Kang Zhenhui;Wang Li-Min

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The origin of the dielectric Debye relaxation in monoalcohols has kept interests for decades. In this work, we explored the Debye relaxation in a primary alcohol, 2-ethyl-1-hexanol, and a secondary one, 4-methyl-3-heptanol, by doping with carbon nano-dots. Dielectric and infrared spectra of the pure and doped samples were measured. We found that doping in 2-ethyl-1-hexanol decreases slightly the Debye relaxation strength together with a subtle decrease in the relaxation time, while, strikingly, the Debye relaxation strength in 4-methyl-3-heptanol is enhanced significantly, accompanied by increased relaxation time. Differently, the relaxation strength of the structural α-relaxation is both enhanced in the two monoalcohols. The infrared measurements reveal an evident increase in the fraction of associated hydrogen bonds for the doped 4-methyl-3-heptanol when compared to the pure sample. In contrast, only trivial difference is exhibited for the case of 2-ethyl-1-hexanol and its doped one. The remarkable effects of the carbon nano-dots on the Debye relaxation in the tested 4-methyl-3-heptanol sample could suggest the preferential transition from H-bond rings to chains.
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