Herein, CuO/ZnO nanocomposites at different ratios were successfully synthesized through a green biosynthesis approach. This was performed by harnessing the fungal-secreted enzymes and proteins during the sol-gel process for nanocomposites seed growth. All fabricated nanoparticles/nanocomposites were characterized using Fourier Transform Infra-Red (FT-IR) Spectroscopy, X-Ray Diffraction (XRD), Transmission Electron Microscopy (TEM), Scanning Electron Microscopy (SEM-EDX) and X-ray Photoelectron Spectroscopy ( XPS) analyses. The photocatalytic degradation efficacy of the synthesized nanocomposites was evaluated using a cationic methylene blue (MB) dye as a model of reaction. Results obtained from the FT-IR and EDX analyses revealed that CuO-NPs, ZnO-NPs, CuO/ZnO 50/50 , CuO/ZnO 80/20, and CuO/ZnO 20/80 were successfully prepared by harnessing the biomass filtrate of Penicillium corylophilum As-1. Furthermore, XRD and TEM revealed the variation in the particle size of the nanocomposites (10–55 nm) with the ratio of the nanoparticles. Notably, the size of the nanocomposites was proportionally increased with an increasing ratio of ZnO-NPs. XPS analysis affirmed the presence of both Cu and Zn in the nanocomposites with varying binding energies compared with individual nanoparticles. Furthermore, a high photo-degradation efficacy was achieved by increasing the ratio of ZnO-NPs in the nanocomposite formulation, and 97% of organic MB dye was removed after 85 min of irradiation using the CuO/ZnO 20/80 nanocomposite.

New photochromic film was developed toward the preparation of anti‐counterfeiting documents utilizing inorganic/organic nanocomposite enclosing a photoluminescent inorganic pigment and a polyacrylic binder polymer. To generate a translucent film from pigment/polyacrylic nanocomposite, the phosphorescent strontium aluminum oxide pigment should be well‐dispersed in the solution of the polyacrylic‐based binder without agglomeration. The photochromic nanocomposite was applied efficiently onto commercial cellulose paper documents utilizing the effective and economical spray‐coating technology followed with thermofixation. A homogeneous photochromic film was immobilized onto cellulose paper surface to introduce a transparent film changing to greenish‐yellow upon exposure to ultraviolet light as depicted by CIE coloration measurements. The photochromic effect was monitored at lowest pigment concentration (0.25 wt%). The spray‐coated paper documents exhibit two absorbance bands at 256 and 358 nm, and two fluorescence peaks at 433 and 511 nm. The morphologies of the spray‐coated documents were explored. The spray‐coated paper sheets showed a reversible photochromic effect without fatigue under ultraviolet irradiation. The rheology of the produced photochromic composites as well as the mechanical properties and photostability of the spray‐coated documents were studied.

In this paper, a novel lanthanum metal–organic framework La‐MOF was prepared via hydrothermal and reflux methods. The La‐MOF was achieved through the reaction of a 5‐amino‐isophthalic acid with 1, 2‐phenylenediamine and lanthanum chloride. The prepared La‐MOF structure was confirmed by XRD, mass spectrometry, IR, UV–Vis and elemental analysis, whereas the size, and morphology was examined by FE‐SEM/EDX and HR‐TEM. The results indicated that the La‐MOF prepared via both methods have the same structure and composition. Meanwhile, the MOF yield, reaction time, morphology, physiochemical and sensing properties were highly depended on the used preparation method. The photoluminescence (PL) study was carried out for the La‐MOF, and the results showed that La‐MOF exhibits strong emission at 558 nm after excitation at 369 nm. Moreover, the PL data indicating that the La‐MOF has highly selective sensing properties for iron (III) competing with different metal ions. The Stern‐Völmer graph shows a linear calibration curve which achieved over a concentration range 1.0–500 μM of Fe3+ with a correlation coefficient, detection, and quantitation limits 0.998, 1.35 μM and 4.08 μM, respectively. According to the remarkable quenching of the PL intensity of La‐MOF using various concentrations of Fe3+, it was successfully used as a sensor for Fe3+detecting in different water resources (pure and waste) samples. The quenching mechanism was studied and it has a dynamic type and due to efficient energy transfer between the La‐MOF and Fe3+.

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