Singh Satya Pal, Singh Archana Kumari, Vishwakarma Suraj
Condensed Matter Physics & Nanoscience Research Laboratory, Department of Physics and Material Science, Madan Mohan Malaviya University of Technology, Gorakhpur, 273010, U.P, India.
Sci Rep. 2025 Jan 2;15(1):273. doi: 10.1038/s41598-024-80652-3.
We have blended MgO QDs with poly (methylmethacrylate) (PMMA) thin films using solution-casting method. MgO QDs were doped at 5 wt %, 10 wt %, and 15 wt % in PMMA film and annealed for 02, 04, 06, 08, 10, 12, 14, 20, 24, and 28 h at 130 degree Celsius. We have comprehensively investigated the molecular-scale restructuring and morphological evolution of the composite films and have accounted for the reasons based on the observations made on chemical bonding, crystallinity, bandgap, Urbach energy, and fluorescence and Raman spectra. We observe that the film loses its overall crystallinity in the initial stages of annealing, which improves slightly owing to the temperature-induced limited diffusion of MgO QDs (sizes in the range of 7.0603-9.5647 nm). MgO QDs undergo coarsening at temperatures as low as 130 C. The limited diffusion of MgO QDs allows for the formation of larger clusters, which in turn affects the local crystallinity of the composite films. We report local-scale re-crystallization driven by dispersion forces acting globally. As far as the quantum nature of forces is concerned, this work clearly demonstrates some unique energy dissipation mechanism of charge carriers in QDs via overlapping with long-range dispersion forces. The morphological evolution of the films is the outcome of the reconciliation of forces. We discuss the role of competing forces. The evolution of nano-micro scale structures inside films is governed by the reconciliation between inter- and intra-molecular forces. The temperature of the film plays an important role in facilitating the entire process. To obtain molecular-scale insights, we have estimated the crystallinity, bandgap, and Urbach energy of the pure and hybrid films. MgO QDs diffuse locally and coalesced to form larger spherical clusters. The anchoring of MgO QDs on the PMMA surface and vice-versa appears to provide thermal stability and mechanical strength to the nanocomposite films, as the MgO QDS-doped PMMA film form nanometer-sized particulates of PMMA. In contrast, the overall crystallinity of the hybrid film drastically decreases as the formation of boundaries, interfaces, and voids overwhelmed the entire process. The formation of larger nanoaggregates at later stages of annealing slightly improves the crystallinity of the films. The estimation of the bandgap and Urbach energy calculations confirm the same. The micro-level phenomenological understanding of the diffusion process of nanodots in a nearly solid film is technically important for ensuring the sustainability of such nanocomposites that undergo a heating process.
我们采用溶液浇铸法将氧化镁量子点与聚甲基丙烯酸甲酯(PMMA)薄膜混合。氧化镁量子点以5重量%、10重量%和15重量%的比例掺杂在PMMA薄膜中,并在130摄氏度下分别退火02、04、06、08、10、12、14、20、24和28小时。我们全面研究了复合薄膜的分子尺度结构重组和形态演变,并根据对化学键合、结晶度、带隙、乌尔巴赫能量以及荧光和拉曼光谱的观察结果说明了原因。我们观察到,在退火初期薄膜失去了整体结晶度,由于氧化镁量子点(尺寸在7.0603 - 9.5647纳米范围内)因温度诱导的有限扩散,结晶度略有改善。氧化镁量子点在低至130摄氏度的温度下会发生粗化。氧化镁量子点的有限扩散导致形成更大的团簇,进而影响复合薄膜的局部结晶度。我们报道了由全局作用的色散力驱动的局部尺度再结晶。就力的量子性质而言,这项工作清楚地展示了量子点中电荷载流子通过与长程色散力重叠而产生的一些独特能量耗散机制。薄膜的形态演变是各种力相互协调的结果。我们讨论了竞争作用力的作用。薄膜内部纳米 - 微观尺度结构的演变受分子间和分子内力之间协调的支配。薄膜的温度在促进整个过程中起着重要作用。为了获得分子尺度的见解,我们估算了纯薄膜和混合薄膜的结晶度、带隙和乌尔巴赫能量。氧化镁量子点局部扩散并聚结形成更大的球形团簇。氧化镁量子点在PMMA表面的锚定以及反之亦然,似乎为纳米复合薄膜提供了热稳定性和机械强度,因为掺杂氧化镁量子点的PMMA薄膜形成了PMMA的纳米级颗粒。相比之下,随着边界、界面和空隙的形成主导了整个过程,混合薄膜的整体结晶度急剧下降。在退火后期形成更大的纳米聚集体略微提高了薄膜的结晶度。带隙和乌尔巴赫能量计算的估算结果证实了这一点。从微观层面现象学地理解纳米点在近乎固态薄膜中的扩散过程,对于确保经历加热过程的此类纳米复合材料的可持续性在技术上具有重要意义。