Hydrogen peroxide (H₂O₂) detection in both liquid and gas phases has garnered significant attention due to its importance in various biological and industrial processes. Monitoring H₂O₂ levels is essential for understanding its effects on biology, industry, and the environment. Significant advancements in the physical dimensions and performance of biosensors for H₂O₂ detection have been made, mainly through the integration of fluorescence techniques and nanotechnology. These advancements have resulted in more sensitive, selective, and versatile detection systems, enhancing our ability to monitor H₂O₂ in both liquid and gas phases effectively. However, limited comprehensive reviews exist on the detection of vaporized H₂O₂, which is used in disinfection and the production of explosive agents, making its detection vital. This review provides an overview of recent progress in nanostructured fluorescence sensors for H₂O₂ detection, covering both liquid and gas phases. It examines various fluorescence-based detection methods and focuses on emerging nanomaterials for sensor development. Additionally, it discusses the dual applications of H₂O₂ detection in biomedical and non-biomedical fields, offering insights into the current state of the field and future directions. Finally, the challenges and perspectives for developing novel nanostructured fluorescence sensors are presented to guide future research in this rapidly evolving area.

Tin-(IV) oxide nanocrystals (SnO₂ NCs) have significant potential in various applications, with their performance closely related to their band gap. The band gap is influenced by the size and shape of the NCs, which can be precisely controlled by adjusting reaction conditions. In this study, we present deliberately designed synthesis protocols to produce high-quality SnO₂ NCs with tunable band gaps using different methods. Key factors affecting the synthesis include control of the oxidizing agent, reaction temperature, solvent selection, and reaction time optimization. The resulting NCs were characterized by using TEM, XRD, XPS, and optical spectroscopy. Notably, SnO₂ NCs synthesized by controlling the oxidizing agent (air injection) in a hot organic solution were smaller in size and exhibited abundant oxygen vacancies. In contrast, extending the reaction time or using ethanol as a solvent in hydrothermal systems facilitated larger spherical or rod-like SnO₂ NCs with fewer oxygen vacancies. Further analysis of the band gap and valence band maximum energy revealed that the abundant vacancies in SnO₂ NCs synthesized with the air-controlled hot organic solution method resulted in a narrower band gap and an upshifted valence band. These synthetic strategies illustrate the potential for deliberately designing SnO₂ NCs with optimized electronic structures for various applications.

We present a one‐pot colloidal synthesis method for producing monodisperse multi‐metal (Co, Mn, and Fe) spinel nanocrystals (NCs), including nanocubes, nano‐octahedra, and concave nanocubes. This study explores the mechanism of morphology control, showcasing the pivotal roles of metal precursors and capping ligands in determining the exposed crystal planes on the NC surface. The cubic spinel NCs, terminated with exclusive {100}‐facets, demonstrate superior electrocatalytic activity for the oxygen reduction reaction (ORR) in alkaline media compared to their octahedral and concave cubic counterparts. Specifically, at 0.85 V, (CoMn)Fe₂O₄ spinel oxide nanocubes achieve a high mass activity of 23.9 A/g and exhibit excellent stability, highlighting the promising ORR performance associated with {100}‐facets of multi‐metal spinel oxides over other low‐index and high‐index facets. Motivated by exploring the correlation between ORR performance and surface atom arrangement (active sites), surface element composition, as well as other factors, this study introduces a prospective approach for shape‐controlled synthesis of advanced spinel oxide NCs. It underscores the significance of catalyst shape control and suggests potential applications as nonprecious metal ORR electrocatalysts.

Low-Pd PdO–CeO ₂ –carbon catalysts enable efficient H ₂ O ₂ electrosynthesis with high yield and activity. Synergistic interactions boost performance, though long-term stability remains a challenge due to Pd cluster agglomeration and coarsening.

Morphology-controlled nanostructures provide an effective strategy to modulate both oxygen evolution reaction (OER) activity and photovoltaic performance in perovskite solar cells (PSCs).