This study investigated the coupling of sulfate radical generating oxidants, (persulfate, PS and peroxymonosulfate, PMS) with TiO2 photocatalysis for the degradation of microcystin-LR (MC-LR). Treatment efficiency was evaluated by estimating the electrical energy per order (EEO). Oxidant addition at 4 mg/L reduced the energy requirements of the treatment by 60% and 12% for PMS and PS, respectively compared with conventional photocatalysis. Quenching studies indicated that both sulfate and hydroxyl radicals contributed towards the degradation of MC-LR for both oxidants, while Electron Paramagnetic Resonance (EPR) studies confirmed that the oxidants prolonged that lifetime of both radicals (concentration maxima shifted from 10 to 20 min), allowing for bulk diffusion and enhancing cyanotoxin removal. Structural identification of transformation products (TPs) formed during all treatments, indicated that early stage degradation of MC-LR occurred mainly on the aromatic ring and conjugated carbon double bonds of the ADDA amino acid. In addition, simultaneous hydroxyl substitution of the aromatic ring and the conjugated double carbon bonds of ADDA (m/z = 1027.5) are reported for the first time. Oxidant addition also increased the rates of formation/degradation of TPs and affected the overall toxicity of the treated samples. The detoxification and degradation order of the treatments was UVA/TiO2/PMS > UVA/TiO2/PS>> UVA/TiO2.

Flame spray pyrolysis (FSP) is an industrially scalable technology that enables the engineering of a wide range of metal-based nanomaterials with tailored properties nanoparticles. In the present review, we discuss the recent state-of-the-art advances in FSP technology with regard to nanostructure engineering as well as the FSP reactor setup designs. The challenges of in situ incorporation of nanoparticles into complex functional arrays are reviewed, underscoring FSP’s transformative potential in next-generation nanodevice fabrication. Key areas of focus include the integration of FSP into the technology readiness level (TRL) for nanomaterials production, the FSP process design, and recent advancements in nanodevice development. With a comprehensive overview of engineering methodologies such as the oxygen-deficient process, double-nozzle configuration, and in situ coatings deposition, this review charts the trajectory of FSP from its foundational roots to its contemporary applications in intricate nanostructure and nanodevice synthesis.

H₂ production via dehydrogenation of formic acid (HCOOH, FA), sodium formate (HCOONa, SF), or their mixtures, at near-ambient conditions, T < 100 °C, P = 1 bar, is intensively pursued, in the context of the most economically and environmentally eligible technologies. Herein we discuss molecular catalysts (ML), consisting of a metal center (M, e.g., Ru, Ir, Fe, Co) and an appropriate ligand (L), which exemplify highly efficient Turnover Numbers (TONs) and Turnover Frequencies (TOFs) in H₂ production from FA/SF. Typically, many of these ML catalysts require the presence of a cofactor that promotes their optimal cycling. Thus, we distinguish the concept of such cofactors in additives vs. co-catalysts: When used at high concentrations, that is stoichiometric amounts vs. the substrate (HCOONa, SF), the cofactors are sacrificial additives. In contrast, co-catalysts are used at much lower concentrations, that is at stoichiometric amount vs. the catalyst. The first part of the present review article discusses the mechanistic key steps and key controversies in the literature, taking into account theoretical modeling data. Then, in the second part, the role of additives and co-catalysts as well as the role of the solvent and the eventual inhibitory role of H₂O are discussed in connection to the main mechanistic steps. For completeness, photons used as activators of ML catalysts are also discussed in the context of co-catalysts. In the third part, we discuss examples of promising hybrid nanocatalysts, consisting of a molecular catalyst ML attached on the surface of a nanoparticle. In the same context, we discuss nanoparticulate co-catalysts and hybrid co-catalysts, consisting of catalyst attached on the surface of a nanoparticle, and their role in the performance of molecular catalysts ML.

A flame spray pyrolysis (FSP) method has been developed, for controlled doping of BiVO₄ nanoparticles with W and Zr in tandem with the oxygen vacancies (Vo) of the BiVO₄ lattice. Based on XPS and Raman data, we show that the nanolattice of W-BiVO₄ and Zr-BiO₄ can be controlled to achieve optimal O₂ evolution from H₂O photocatalysis. A synergistic effect is found between the W- and Zr-doping level in correlation with the Vo-concentration. FSP- made W-BiVO₄ show optimal photocatalytic O₂-production from H₂O, up to 1020 μmol/(g × h) for 5%W-BiVO₄, while the best performing Zr-doped achieved 970 μmol/(g × h) for 5%Zr-BiVO₄. Higher W-or Zr-doping resulted in deterioration in photocatalytic O₂-production from H₂O. Thus, engineering of FSP-made BiVO₄ nanoparticles by precise control of the lattice and doping-level, allows significant enhancement of the photocatalytic O₂-evolution efficiency. Technology-wise, the present work demonstrates that flame spray pyrolysis as an inherently scalable technology, allows precise control of the BiVO₄ nanolattice, to achieve significant improvement of its photocatalytic efficiency.