The present work describes the synthesis of zinc ferrite nanoparticles by a chemical coprecipitation method and its surface modification with poly(diallyldimethylammonium chloride) (PDDA), tetramethylammonium hydroxide (TMAOH) and poly(ethylene glycol) (PEG). The effect of coating on the colloidal stability of obtained systems as well as the effect of modification procedure on the final characteristics of particles were studied. The unmodified and modified nanoparticles were characterized by X-ray diffractometry (XRD), scanning electron microscopy (SEM) and Raman spectroscopy. The particle size distribution and stability of these systems were investigated by dynamic light scattering (DLS) and zeta potential measurements. The results have shown the profound effect of the used modification procedure on colloidal stability of the investigated particles.

The adsorptive potential has been evaluated for the aminopropyl functionalized mesoporous silica materials obtained by co-condensation and post grafting methods. Nitrogen sorption, small angle neutron and X-ray scattering (SANS and SAXS) demonstrated high surface area and well-ordered hexagonal pore structure suitable for applications as adsorbents of metals from waste waters. A comparison of Cr(VI) adsorption properties of the materials prepared by different functionalization methods has been performed. The obtained results demonstrated the adsorption capacity due to the affinity of the chromium ions to the amino groups, and showed that co-condensation of tetraethoxysilane (TEOS) and 3-aminopropyl triethoxysilane (APTES) resulted in higher metal sorption capacity of the materials compared to post-synthesis grafting of aminopropyl groups onto the mesoporous silica particles.

Solid state compounds exhibiting multiple and coupled macroscopic orders, named multiferroics, represent a challenge for both theoretical and experimental modern condensed-matter physics. Spins and the electric polarisation in conventional magnetic and ferroelectric materials can be manipulated on their fundamental timescales, by means of femtosecond laser pulses. In view of the resounding success and popularity of the all-optical approach, it is only natural to wonder about the application of this scheme to study the intrinsic coupling between spins and charges in multiferroics. Deeply fundamental questions arise: can ultrashort laser pulses deterministically activate, enhance or suppress the magnetoelectric coupling on the femtosecond timescale? Can these processes be triggered in a fully coherent fashion, thus being unrestrained by any thermal load? Which mechanism of spin-charge coupling is most favourable to overcome these overarching and daunting challenges? This problem is interdisciplinary in nature, requiring contributions from materials science and condensed matter physics from both theoretical and experimental perspectives. High-quality materials suitable for optical investigations have to be identified, synthetized and characterised. General and valid models offer then a guide to the plethora of possible light-induced processes, resulting in the desired ultrafast multiferroic manipulations. Finally, healthy experimental schemes, able to unambiguously track the ultrafast dynamics of either the ferroelectric or the magnetic order parameter have to be developed and implemented. Our motivation to write this review is to lay a broad and multidisciplinary foundation, which may be employed as a starting point for non-equilibrium approaches to the manipulation of the multiferroicity on the femtosecond timescale. This was also one of the main goals of the COST Action MAGNETOFON, whose network constitutes the core of the authors of this review. The present work thus represents a part of the scientific legacy of MAGNETOFON itself.

The increasing presence of various organics poses significant threats to aquatic ecosystems and living organisms. Conventional water treatment methods are often insufficient, necessitating the development of powerful and sustainable alternatives. This study addresses this challenge by exploring the synthesis of ZnO nanoparticles using green tea leaves extract—an eco-friendly approach—for the sunlight-activated removal of organics in agri-food wastewater. The research examined different conditions for the removal of clomazone (CLO), tembotrione (TEM), ciprofloxacin (CIP), and zearalenone (ZEA). Nitrate-derived ZnO synthesized in a water medium (N-gZnO_w) exhibited the highest photocatalytic activity, removing 98.2, 95.8, 96.2, and 96.6% of CLO, TEM, CIP, and ZEA. Characterization techniques (XRD, Raman spectroscopy, SEM, zeta potential measurements, UV–visible spectroscopy) confirmed the synthesis of N-gZnO_w, with an average particle size of 14.9 nm, an isoelectric point of 9.9, and a band gap energy of 2.92 eV. Photocatalytic experiments identified 0.5 mg/cm³ as an optimal catalyst loading, while a higher initial pollutant concentration reduced degradation efficiency. LC-ESI-MS/MS measurements confirmed the efficient pollutant degradation and the formation of degradation intermediates. Hence, this study demonstrates that green tea extract-synthesized ZnO nanoparticles offer a promising, sustainable solution for removing herbicides, pharmaceuticals, and mycotoxins from wastewater, paving the way for eco-friendly water purification technologies.

Titanate structures were synthesized in highly alkaline solution using hydrothermal procedure. As-prepared powders were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) and transmission electron microscopy (TEM). A specific surface area of the powders was measured by BET method. Results confirmed formation of layered trititanates, already after one hour of hydrothermal synthesis. To examine the photocatalytic activity of the as-prepared layered titanates, methylene blue (MB) was employed as a target compound in response to visible light at ambient temperature. It was observed that the specific surface area, size distribution and crystallinity are important factors to get high photocatalytic activity for the decomposition of MB. .