Search Results (77)

Windows are a major contributor to energy loss in buildings, particularly in hot climates where solar radiation heat gain significantly increases cooling demand. An ideal energy-efficient window must maintain high visible light transmittance while effectively blocking ultraviolet and near-infrared radiation, presenting a significant challenge for material design. We propose a plasma silica aerogel window utilizing the local surface plasmon resonance effect of plasmonic nanoparticles. This design incorporates indium tin oxide (ITO) nanospheres (for broad-band UV/NIR blocking) and silver (Ag) nanocylinders (targeted blocking of the 0.78–0.9 μm NIR band) co-doped into the silica aerogel. This design achieves a visible light transmittance of 0.8, a haze value below 0.12, and a photothermal ratio of 0.91. Building simulations indicate that compared to traditional glass, this window can achieve annual energy savings of 20–40% and significantly reduce the economic losses associated with traditional glass, providing a feasible solution for sustainable buildings. Full article

In this article, Pt-Sn_xO_y hybrid nanoparticles encaged in porous silica nanospheres (Pt-Sn_xO_y@PSNs) were prepared by using 1-dodecanethiol (C₁₂-SH) as a coordination agent to confine Pt and Sn ions in a microemulsion system, which is formed by cetyltrimethylammonium bromide (CTAB) and C₁₂-SH as co-surfactants in water. Compared with Pt@PSNs, when different molar ratios of Sn_xO_y were introduced into Pt@PSNs to form Pt-Sn_xO_y@PSNs, the catalytic efficiency of 4-nitrophenol (4-NP) reduction with NaBH₄ can be significantly enhanced. At molar ratios of 4-NP/Pt of 150/1, the 4-NP conversion reached 100% over Pt-Sn_xO_y@PSNs with Pt/Sn molar ratios of 1/0.75 in 8 min. This catalytic performance showed a slight decrease after six reaction cycles. This enhanced catalytic efficiency can be ascribed to the synergistic effect between Pt and Sn_xO_y, and the protection of porous silica nanostructures can effectively improve the stability of the catalyst. Full article

Silica–zirconia nanoparticles were successfully synthesised using the precipitation process. The surface area and shape of the Si-ZrO₂ nanoparticles were investigated using BET, X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (HRTEM). The HRTEM results demonstrate that silica was successfully integrated into ZrO₂ nanoparticles with a mixture of nanorod and nanosphere shapes. The element analysis (EDX) reveals the presence of silica (14.61%) and zirconia (1.18%) nanoparticles, as well as oxygen (83.65) on the surface. The BET results demonstrate a larger surface area of 185 m²/g and pore volume (0.14 cm³/g). The XRD measurements confirmed the transition of amorphous silica into the monoclinic phase of the zirconia nanoparticles. The electrochemical characteristics of the silica–zirconia nanoparticles were tested in a potassium chloride solution. With a large specific surface area and an appropriate pore size distribution, a pair of broad and symmetric redox peaks were centred at −0.15 V and 0.6 V. Full article

(1) Background/Objectives: Primary and secondary brain tumours often hold devastating prognoses and low survival rates despite the application of maximal neurosurgical resection, and state-of-the-art radiotherapy and chemotherapy. One limiting factor in their management is that several antineoplastic agents are unable to cross the blood–brain barrier (BBB) to reach the tumour microenvironment. Nanomedicine could hold the potential to become an effective means of drug delivery to overcome previous hurdles towards effective neuro-oncological treatments. (2) Methods: A scoping review following the PRISMA-ScR guidelines and checklist was conducted using key terms input into PubMed to find articles that reflect emerging trends in the utilisation of nanomedicine in drug delivery for primary and secondary brain tumours. (3) Results: The review highlights various strategies by which different nanoparticles can be exploited to bypass the BBB; we provide a synthesis of the literature on the ongoing contributions to therapeutic protocols based on chemotherapy, immunotherapy, focused ultrasound, radiotherapy/radiosurgery, and radio-immunotherapy. (4) Conclusions: The emerging trends summarised in this scoping review indicate encouraging advantageous properties of nanoparticles as potential effective drug delivery mechanisms; however, there are still nanotoxicity issues that largely remain to be addressed before the translation of these innovations from laboratory to clinical practice. Full article

Polybenzimidazole (PBI) is a high-performance polymer known for its excellent thermal stability, mechanical strength, and chemical resistance, attributes that are derived from its unique structure comprising repeated benzene and imidazole rings. However, limitations such as relatively low thermal stability and moisture sensitivity restrict its application as a super engineering plastic. In this study, amide groups are incorporated into the PBI backbone to synthesize the copolymer poly(BI-co-A), effecting a structural modification at the molecular level. Additionally, silica nanospheres were composited into the poly(BI-co-A) film to further enhance its thermal performance. The resulting composite films exhibited remarkable thermal stability, with the temperature for 10% weight loss reaching as high as 761 °C. To address increased water absorption due to the high hydrophilicity of hydroxyl groups on the silica nanospheres’ surface, a dehydration treatment was applied in an electric furnace. This treatment produced a highly thermoresistant poly(BI-co-A) nanocomposite film with reduced wettability, making it suitable for applications in humid environments. Full article

With the development and improvement of analysis and detection systems, low-toxicity and harmless detection systems have received much attention, especially in the field of food detection. In this paper, a low-toxicity dual-emission molecularly imprinted fluorescence sensor (CdTe QDs@SiO₂/N-CDs@MIPs) was successfully designed for highly selective recognition and visual detection of tetracycline (TC) in food samples. Specifically, the non-toxic blue-emission N-doped carbon dots (N-CDs) with high luminous performance acted as the response signals to contact TC via the covalent bond between amino and carboxyl groups. The red-emission CdTe quantum dots (CdTe QDs) were coated in silica nanospheres as stable reference signals, which effectively avoided the direct contact of CdTe QDs. Under optimum conditions, CdTe QDs@SiO₂/N-CDs@MIPs had a rapid response within 1.0 min to TC, and the detection limit of CdTe QDs@SiO₂/N-CDs@MIPs was calculated at 0.846 μM in the linear range of 0–140 μM. In complex environments, the CdTe QDs@SiO₂/N-CDs@MIPs also exhibited excellent capabilities for the selective, rapid, and visual detection of TC. Furthermore, the accuracy of CdTe QDs@SiO₂/N-CDs@MIPs to detect TC was verified by the HPLC method, and satisfactory results were obtained. Moreover, CdTe QDs@SiO₂/N-CDs@MIPs showed a satisfactory recovery when measuring TC in milk and egg samples. This work provided an ideal approach for low-toxicity fluorescence sensor design and application. Full article

Constructing photonic crystals with core-shell structured nanoparticles is an important means for applications such as secure communication, anti-counterfeiting marking, and structural color camouflage. Nonetheless, the precise synthesis technology for core-shell structured nanoparticles at the hundred-nanometer scale faces significant challenges. This paper proposes a controlled synthesis method for core-shell structured nanoparticles using a template method. By using 100 nm diameter silica nanospheres as templates and coating them with a ferroferric oxide shell layer, SiO₂@Fe₃O₄ core-shell structured nanoparticles with regular morphology and good uniformity can be obtained. The study experimentally investigated the effects of feed amount, modifiers, temperature, and feed order on the coating effect, systematically optimizing the preparation process. Centrifugal driving technology was used to achieve structural colors in the visible wavelength range. Additionally, the method successfully created well-defined and uniform core-shell structured nanoparticles using 200 nm diameter silica nanospheres as templates, demonstrating that this controllable synthesis method can effectively produce core-shell structured nanoparticles over a wide range of particle sizes. The template method proposed in this paper can significantly improve morphological regularity and size uniformity while effectively reducing the preparation cost of core-shell structured nanoparticles. Full article

A series of nanospherical-shaped silicates containing heteroatoms (Al, Zr or Ti) were successfully synthesized using tetraethylorthosilicate (TEOS) or silica colloids as a silicon source. These metallosilicate nanospheres were used as silicon nutrients to obtain silicalite zeolites with micro-mesoporosity and improved textural properties. The results demonstrated that TEOS acted as a suitable silicon source to produce amorphous silicates and a spherical-type zeolite architecture with Zr and Ti heteroatoms included in their framework, with preferable particle size and crystallinity. The surface functionality of the mesostructured nanospheres and zeolite silicates provide active centers for the esterification of glycerol with acetic acid (EG) reaction. The dispersion of Cu entities on the surface of the zeolites achieved high glycerol conversions selectively producing triacetin in comparison with Fe counterparts. Full article

Recently, UVC LEDs, which emit deep ultraviolet light, have found extensive applications across various fields. This study demonstrates the design and implementation of thin films of three-dimensional photonic crystals (3D PhCs) as reflectors to enhance the light output power (LOP) of UVC LEDs. The 3D PhC reflectors were prepared using the self-assembly of silica nanospheres on a UVC LED lead frame substrate via the evaporation-induced method (side) and the gravitational sedimentation method (bottom), respectively. These PhCs with the (111) crystallographic plane were deposited on the side wall and bottom of the UVC LED lead frame, acting as functional materials to reflect UVC light. The LOP of UVC LEDs with 3D PhC reflectors at a driving current of 100 mA reached 19.6 mW. This represented a 30% enhancement compared to commercial UVC LEDs with Au-plated reflectors, due to the UVC light reflection by the photonic band gaps of 3D PhCs in the (111) crystallographic plane. Furthermore, after aging tests at 60 °C and 60% relative humidity for 1000 h, the relative LOP of UVC LEDs with 3D PhC reflectors decreased by 7%, which is better than that of commercial UVC LEDs. Thus, this study offers potential methods for enhancing the light output efficiency of commercial UVC light-emitting devices. Full article

SiO₂ has a much higher theoretical specific capacity (1965 mAh g⁻¹) than graphite, making it a promising anode material for lithium-ion batteries, but its low conductivity and volume expansion problems need to be improved urgently. In this work, pompon mum-like SiO₂/C nanospheres with the sandwich and porous nanostructure were obtained by using dendritic fibrous nano silica (DFNS) and glucose as matrix and carbon source, respectively, through hydrothermal, carbonization and etching operations. The influence of SiO₂ content and porous structure on its electrochemical performance was discussed in detail. The final results showed that the C/DFNS-6 with a SiO₂ content of 6 wt% exhibits the best electrochemical performance as a negative electrode material for lithium-ion batteries due to its optimal specific surface area, porosity, and appropriate SiO₂ content. C/DFNS-6 displays a high specific reversible capacity of 986 mAh g⁻¹ at 0.2 A g⁻¹ after 200 cycles, and 529 mAh g⁻¹ at a high current density (1.0 A g⁻¹) after 300 cycles. It also has excellent rate capability, with a reversible capacity that rises from 599 mAh g⁻¹ to 1066 mAh g⁻¹ when the current density drops from 4.0 A g⁻¹ to 0.2 A g⁻¹. These SiO₂/C specific pompon mum-like nanospheres with excellent electrochemical performance have great research significance in the field of lithium-ion batteries. Full article

Polyacrylamide, silica, and other nanoparticles have all been realized in the field of enhanced oil recovery. Researchers often explore the mechanisms of spreading behavior and simulated displacement to develop more efficient types of nanoparticles. In this study, copper quantum dots were introduced into a acrylamide copolymerization system to obtain composite nanospheres and its structure, topographic, and application performance were characterized. The results show that the composite nanospheres have a particle size of around 25 nm, are uniformly loaded with copper particles, and have good temperature resistance. The spreading ability on the quartz flake surfaces and displacement effect in microchannels of composite nanospheres, acrylamide copolymer nanospheres, and copper quantum dots were compared by nanofluid spreading experiments and microchannel chip oil displacement experiments. The results indicate that the composite nanospheres can effectively reduce the water contact angle, promote the spreading of aqueous phase, and accelerate the oil droplet removal process; the accelerating effect is stronger than other samples. Its oil displacement effect is also the strongest, and it is minimized by the influence of channel size, temperature, and dispersing medium, with better stratigraphic adaptability. This work supports the practical application of copper quantum dot/polyacrylamide composite nanospheres in the oilfield. Full article

Optimized sustainable procedures in both acidic and basic conditions are considered to meet some of the current environmental challenges of the scientific community. In this paper, the successful syntheses of two classes of indium-based silica nanomaterials are reported. Both procedures were conceived to enhance the sustainability of the synthesis methods and promote their preparations at room temperature while avoiding the hydrothermal treatment under static conditions at 100 °C. A fast, room-temperature synthesis of porous nanospheres was conceived together with an “acid-free” procedure for SBA-15-like materials. Moreover, the isomorphic substitution of silicon with indium was achieved. All the materials were deeply characterized to probe their structural, textural and morphological properties (e.g., transmission electron microscopy, N₂ physisorption, ss MAS NMR of ²⁹Si). The high specific surface area and the mesoporosity were always preserved even under the mild reaction conditions employed. The honeycomb structure and the spherical morphology of SBA-15-like materials and nanospheres, respectively, were also observed. The insertion of indium was confirmed via X-ray photoelectron spectroscopy (XPS) investigations. Full article

The sensitivity of fluorescent lateral flow immunoassay (LFIA) test strips is compromised by the low fluorescence intensity of the signaling molecules. In this study, we synthesized novel phosphorus-doped carbon-dot-based dendritic mesoporous silica nanoparticles (DMSNs-BCDs) with a quantum yield as high as 93.7% to break this bottleneck. Meanwhile, the in situ growth method increased the loading capacity of carbon dots on dendritic mesoporous silica, effectively enhancing the fluorescence intensity of the composite nanospheres. Applied DMSNs-BCDs in LFIA can not only semi-quantitatively detect a single component in a short time frame (procalcitonin (PCT), within 15 min) but also detect the dual components with a low limit of detection (LOD) (carbohydrate antigen 199 (CA199) LOD: 1 U/mL; alpha-fetoprotein (AFP) LOD: 0.01 ng/mL). And the LOD of PCT detection (0.01 ng/mL) is lower by 1.7 orders of magnitude compared to conventional colloidal gold strips. For CA199, the LOD is reduced by a factor of four compared to LFIA using gold nanoparticles as substrates, and for AFP, the LOD is lowered by two orders of magnitude compared to colloidal gold LFIA. Furthermore, the coefficients of variation (CV) for intra-assay and inter-assay measurements are both less than 11%. Full article

In this study, we aim to minimize light loss and achieve high power conversion efficiencies (PCE) in perovskite solar cells (PSCs) by employing a spectral conversion film component with antireflection properties. In our scheme, NaYF₄:Tm, Yb, and Gd luminescent nanorod/silica nanosphere-based thin films are applied on CH₃NH₃PbI₃ PSCs to improve the device efficiency. The film was fabricated by spin coating an aged silica sol containing NaYF₄:Tm, Yb, and Gd luminescent nanorods. The size and the spectral conversion properties of the NaYF₄:Tm, Yb, and Gd luminescent nanorods were controlled by tuning the Gd³⁺ ion concentration. The microstructure and the transmittance properties of the thin film were controlled by changing the concentration of NaYF₄:Tm, Yb, and Gd luminescent nanorod in silica sol. The thin films have excellent spectral conversion properties while exhibiting a maximum transmittance. The photovoltaic performance of PSCs with NaYF₄:Tm, Yb, and Gd luminescent nanorod/silica nanosphere-based thin films was systematically investigated. The light transmittance was optimized to 95.1% on a cleaned glass substrate, which resulted in an average increase of about 3.0% across the broadband range of 400–800 nm. The optimized films widen the spectrum of light absorbed by conventional PSC cells and reduce reflections across a broad range, enhancing the photovoltaic performance of PSCs. As a result, the PCE of the PSC increased from 14.51% for the reference device without a thin film to 15.67% for the PSC device with an optimized thin film. This study presents a comprehensive solution to the problem of Fresnel reflection and spectral response mismatch of the PSCs, which provides new ideas for the light management of PSCs. Full article

The viability of spin-coating methods for the self-assembly of 150 nm diameter silica nanocolloids into large crystal structures on mica was investigated using different colloidal concentrations, accelerations, and rotational speeds. The samples were imaged by atomic force microscopy (AFM) in intermittent contact mode. Low colloidal concentration led to a size-dependent ordering configuration. The largest nanocolloidal particles formed crystalline close-packed structures that were surrounded by increasingly smaller nanocolloids configured into more polycrystalline or amorphous formations. This phenomenon became increasingly suppressed by increasing colloidal concentration. Two dimensional-fast Fourier transform (2D-FFT) radially averaged profiles of the topography images revealed increasing interparticle spacing with increasing rotational acceleration, from close-packed structuring at low accelerations to increasingly spaced packing at high acceleration (>800 rpm/s). This behaviour is attributed to rapid liquid shedding from the increased acceleration. Analysis with radial distribution functions quantified the extent of ordering and revealed an optimum spin speed that caused the formation of large, highly crystalline structures. This optimum spin speed is governed by the relationship between the rotational speed and the liquid film thickness that affect the uniformity of the film and the magnitude of the capillary forces generated. Full article