作为光电和非线性光学材料的 N-(1H-苯并[d]咪唑-2-基)-1-(3-取代苯基)甲亚胺:光谱和计算方法

IF 2.2 4区 化学 Q2 Engineering
Nathanael Damilare Ojo, Olaide Deborah Adekusibe, Nnenna Winifred Odozi, Nelson Okpako Obi-Egbedi
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引用次数: 0

摘要

化石燃料对环境造成的负面影响以及对可再生能源材料与日俱增的需求,使得人们有必要对光电材料进行深入研究。小斯托克斯位移导致的光子重吸收限制了许多光学材料的发光潜力。本研究通过一步缩合法合成了 3-(((1H-苯并[d]咪唑-2-基)亚氨基)甲基)苯酚 (1) 和 N-(1H-苯并[d]咪唑(-2-基)-1-(3-硝基苯基))甲亚胺 (2)这两种苯并咪唑席夫碱,并利用光谱(1H NMR、13C NMR、HRMS 和 FTIR)技术对其进行了表征。利用光谱、密度泛函理论(DFT)和蒙特卡洛(MC)模拟方法对 1 和 2 的光电、非线性光学(NLO)、吸附特性和天然键轨道(NBO)进行了分析。研究了溶液中的吸收、光收集效率(LHE)和荧光特性。使用随时间变化的 DFT/B3LYP/6-311++G(d,p) 方法计算了静态和动态第一和第二超极化率以及功率转换效率参数(Voc 和 ΔGinj)。超极化率与尿素(标准)的超极化率进行了比较。使用 MC 方法研究了 1 和 2 在 TiO2(锐钛型 101)上的结合特性。计算得出的电子特性与实验结果一致。这两种化合物显示出较大的斯托克斯位移(> 200 nm)、可观的量子产率和较低的带隙。染料 2 的 LHE 值高(87%),超极化率大。染料 2 显示出较高的 Voc,而染料 1 则显示出较负的ΔGinj。1-TiO2 (- 52.9 kJ/mol)和 2-TiO2 (- 57.1 kJ/mol)界面的负吸附能表明它们与锐钛矿有很强的结合相互作用。NBO 分析表明,共轭和超共轭是导致染料稳定的主要相互作用。这些染料具有光电和非线性光学应用的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

N-(1H-Benzo[d]imidazol-2-yl)-1-(3-substituted phenyl) methanimines as optoelectronic and nonlinear optical materials: spectroscopic and computational approaches

N-(1H-Benzo[d]imidazol-2-yl)-1-(3-substituted phenyl) methanimines as optoelectronic and nonlinear optical materials: spectroscopic and computational approaches

N-(1H-Benzo[d]imidazol-2-yl)-1-(3-substituted phenyl) methanimines as optoelectronic and nonlinear optical materials: spectroscopic and computational approaches

The negative environmental impact of fossil fuel and the ever-increasing need for renewable energy materials necessitate a rigorous search for optoelectronic materials. Photon reabsorption due to a small Stokes shift limits the light-emitting potentials of many optical materials. In this research, two benzimidazole Schiff bases, 3-(((1H-benzo[d]imidazol-2-yl)imino)methyl)phenol (1) and N-(1H-benzo[d]imidazole(-2-yl)-1-(3-nitrophenyl))methanimine (2), were synthesized via one-pot single-step condensation and characterized using spectrometric (1H NMR, 13C NMR, HRMS and FTIR) techniques. The optoelectronic, nonlinear optical (NLO), adsorption properties and natural bond orbital (NBO) analysis of 1 and 2 were explored using spectroscopic, density functional theory (DFT) and Monte Carlo (MC) simulation approaches. The absorption, light-harvesting efficiency (LHE) and fluorescence properties were studied in solution. Static and dynamic first and second hyperpolarizabilities and parameters for power conversion efficiency (Voc and ΔGinj) were computed using the time-dependent DFT/B3LYP/6–311++G(d,p) method. Hyperpolarizabilities were compared with those of urea (standard). The binding properties of 1 and 2 on TiO2 (anatase 101) were investigated using the MC method. The calculated electronic properties agree with the experimental results. The compounds display large Stokes shifts (> 200 nm), appreciable quantum yields and low band gaps. High LHE (87%) and large hyperpolarizabilities were obtained for 2. Dye 2 displayed a high Voc, while 1 exhibited a more negative ΔGinj. The negative adsorption energies of the 1-TiO2 (− 52.9 kJ/mol) and 2-TiO2 (– 57.1 kJ/mol) interfaces indicate their strong binding interactions with anatase. NBO analysis revealed that conjugation and hyperconjugation were the primary interactions responsible for the stabilization of the dyes. These dyes have the potential for use in optoelectronic and nonlinear optical applications.

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来源期刊
Chemical Papers
Chemical Papers Chemical Engineering-General Chemical Engineering
CiteScore
3.30
自引率
4.50%
发文量
590
期刊介绍: Chemical Papers is a peer-reviewed, international journal devoted to basic and applied chemical research. It has a broad scope covering the chemical sciences, but favors interdisciplinary research and studies that bring chemistry together with other disciplines.
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