Kiven Dinyuy Emmanuel, Bine Fritzgerald Kogge, Nkungli Nyiang Kennet, Tamafo Fouegue Aymard Dider, Tasheh Stanley Numbonui, Ghogomu Julius Numbonui
Department of Chemistry, Faculty of Science, The University of Bamenda P. O. Box 39, Bambili Bamenda Cameroon
Department of Fundamental and Cross-cutting Sciences, National Advanced School of Public Works P. O. Box 510 Yaounde Cameroon,
RSC Adv. 2024 Jun 11;14(26):18646-18662. doi: 10.1039/d4ra02250e. eCollection 2024 Jun 6.
Organic light emitting diode (OLED) and organic solar cell (OSC) properties of ethyl 4-[()-(2-hydroxy-4-methoxyphenyl)methyleneamino]benzoate (EMAB) and its Pt, Pd, Ni, Ir, Rh, and Zn complexes have been theoretically studied herein. Geometry optimizations have been performed the rSCAN-3c composite method while single-point calculations have been carried out at the PBE0-D3(BJ)/def2-TZVP level of theory. Results have shown that complexation with selected metal ions improves hole and electron transfer rates in Pt[EMAB] and Rh[EMAB] . Specifically, the hole transport rate of Pt[EMAB], ( (h) = 6.15 × 10 s), is found to be 44 times greater than that of [EMAB], ( (h) = 1.42 × 10 s), whereas electron transport rate of Pt[EMAB], ( (e) = 4.6 × 10 s) is 4 times that of EMAB ( (e) = 1.1 × 10 s). Charge mobility for holes and electrons are equal to 19.182 cm V s and 1.431 cm V s respectively for Pt[EMAB], and equal to 4.11 × 10 cm V s and 3.43 × 10 cm V s for EMAB respectively. These results show that, charge transport in EMAB can be tuned for better performance through complexation with transition metals such as Pt. OSC properties of the complexes were also studied by comparing their HOMO/LUMO energies with those of (6,6)-phenyl-C-butyric acid methyl ester (PCBM) and poly(3-hexylthiophene) (P3HT). It turned out that the energy gap of EMAB reduced significantly upon complexation from 2.904 eV to 0.56 eV in [Rh(EMAB)] and to a lesser extent in the other complexes. The energy values of the HOMOs remained higher than those of PCBM while those of the LUMOs were found to be greater than that of P3HT with the exception of [Rh(EMAB)]. These findings show that the aforementioned species are good electron donors to PCBM. The open circuit voltage, , of the compounds ranged between 0.705 × 10 V and 6.617 × 10 V, values that are good enough for practical usage in OSC applications. The UV-visible absorption spectra revealed absorption maxima well below 900 nm in all compounds, vital in the efficient functioning of solar cells. In general, this study has shown that platinoid complexation of EMAB can successfully modify both its OLED and OSC properties, making them better precursors in the electronic industry.
本文对4- [()-(2-羟基-4-甲氧基苯基)亚甲基氨基]苯甲酸乙酯(EMAB)及其铂、钯、镍、铱、铑和锌配合物的有机发光二极管(OLED)和有机太阳能电池(OSC)性能进行了理论研究。采用rSCAN-3c复合方法进行几何优化,同时在PBE0-D3(BJ)/def2-TZVP理论水平上进行单点计算。结果表明,与选定金属离子络合可提高Pt[EMAB]和Rh[EMAB]中的空穴和电子转移速率。具体而言,发现Pt[EMAB]的空穴传输速率((h) = 6.15 × 10 s)比[EMAB]的空穴传输速率((h) = 1.42 × 10 s)大44倍,而Pt[EMAB]的电子传输速率((e) = 4.6 × 10 s)是EMAB电子传输速率((e) = 1.1 × 10 s)的4倍。Pt[EMAB]的空穴和电子迁移率分别等于19.182 cm V s和1.431 cm V s,而EMAB的空穴和电子迁移率分别等于4.11 × 10 cm V s和3.43 × 10 cm V s。这些结果表明,通过与过渡金属如铂络合,可以调节EMAB中的电荷传输以获得更好的性能。还通过比较它们与(6,6)-苯基-C-丁酸甲酯(PCBM)和聚(3-己基噻吩)(P3HT)的HOMO/LUMO能量来研究配合物的OSC性能。结果表明,络合后EMAB的能隙从2.904 eV显著降低至[Rh(EMAB)]中的0.56 eV,在其他配合物中降低程度较小。除[Rh(EMAB)]外,HOMO的能量值仍高于PCBM,而LUMO的能量值大于P3HT。这些发现表明,上述物质是PCBM的良好电子供体。化合物的开路电压在0.705 × 10 V至6.617 × 10 V之间,这些值足以在OSC应用中实际使用。紫外可见吸收光谱显示所有化合物的吸收最大值远低于900 nm,这对太阳能电池的有效运行至关重要。总的来说,这项研究表明EMAB的铂类络合可以成功地改变其OLED和OSC性能,使其成为电子工业中更好的前体。