Morphology Of Nanospheres Research Articles

Non-cytotoxic, biocompatible pyrochlore Cerium Zirconium Oxide nanoparticles for asymmetric supercapacitor applications

A novel biocompatible and non-cytotoxic Ce2Zr2O7 (CZO) nano-sized particles were developed by a straightforward hydrothermal method. Cubic structure with Fd-3m space group (227) of prepared nanoparticles has been confirmed from X-ray diffraction (XRD) patterns. Nano-sphere like particle morphology was conspicuously noticed from the FE-SEM and TEM investigations thoroughly. Particle size, inter-planar distance, SAED pattern and elemental presence were affirmatively evaluated. The elemental presence in the sample and their ionic states were systematically investigated through X-ray photoelectron spectroscopy analysis. We have investigated the cytotoxicity of the Ce2Zr2O7 nanoparticles on C2C12 (mouse myoblast cell line) cells and observed to be non-cytotoxicity on C2C12 cells which supports the eco-friendly and biocompatible nanoparticles. We have investigated the electrochemical performance of Ce2Zr2O7 nanoparticles using various electrolytes such as Na2SO4, Li2SO4 and KOH. We have obtained the predominant electrochemical performance of 250 F g−1 at 0.05 A g−1 along with appreciable cycling durability from KOH electrolyte interestingly. In addition, we fabricated asymmetric supercapacitor device and evaluated its energy and power densities systematically. We have evaluated maximum energy and power densities are in the order of 13 Wh kg−1 and 3692 W kg−1, respectively. Therefore, eco-friendly and biocompatible Ce2Zr2O7 nanoparticles could be suggested as a contender for the electrode substance for supercapacitor applications. This investigation has also been an usher hope of further technological advancement in the field of nano-biomedical along with energy storage research fields.

Antimicrobial gelatin-based films with cinnamaldehyde and ZnO nanoparticles for sustainable food packaging

Cinnamaldehyde (CIN), a harmless bioactive chemical, is used in bio-based packaging films for its antibacterial and antioxidant properties. However, high amounts can change food flavor and odor. Thus, ZnO nanoparticles (NPs) as a supplementary antimicrobial agent are added to gelatin film with CIN. The CIN/ZnO interactions are the main topic of this investigation. FTIR-Attenuated Total Reflection (ATR), X-ray diffraction (XRD), and scanning electron microscopy (SEM) were utilized to investigate CIN/ZnO@gelatin films. Transmission electron microscope (TEM) images revealed nanospheres morphology of ZnO NPs, with particle sizes ranging from 12 to 22 nm. ZnO NPs integration increased the overall activation energy of CIN/ZnO@gelatin by 11.94%. The incorporation of ZnO NPs into the CIN@gelatin film significantly reduced water vapour permeability (WVP) of the CIN/ZnO@gelatin film by 12.07% and the oxygen permeability (OP) by 86.86%. The water sorption isotherms of CIN/ZnO@gelatin were described using Guggenheim-Anderson-de Boer (GAB) model. The incorporation of ZnO NPs into the CIN@gelatin film reduced monolayer moisture content (M0) by 35.79% and significantly decreased the solubility of CIN/ZnO@gelatin by 15.15%. The inclusion of ZnO into CIN@gelatin film significantly decreased tensile strength of CIN/ZnO@gelatin by 13.32% and Young`s modulus by 18.33% and enhanced elongation at break by 11.27%. The incorporation of ZnO NPs into the CIN@gelatin film caused a significant decrease of antioxidant activity of CIN/ZnO@gelatin film by 9.09%. The most susceptible organisms to the CIN/ZnO@gelatin film included Candida albicans, Helicobacter pylori, and Micrococcus leutus. The inhibition zone produced by the CIN/ZnO@gelatin film versus Micrococcus leutus was 25.0 mm, which was comparable to the inhibition zone created by antibacterial gentamicin (23.33 mm) and cell viability assessment revealed that ZnO/CIN@gelatin (96.8 ± 0.1%) showed great performance as potent biocompatible active packaging material.

Se-doped cobalt-nickel sulfide hollow nanospheres with heterostructure and engineered defects as high-performance electrode for supercapacitors

Porous structures with heterogeneous interfaces and defects are an important way to enhance electrochemically active sites and facilitate electron transfer, while also improving the permeability of the electrolyte and the rate of ion transport. In this study, Se-doped cobalt-nickel sulfide (Se-CoNi2S4) hollow nanospheres with heterostructure and defects were prepared from CoNi metal-organic framework (MOF) as substrate by sequential sulfidation and selenization treatments. Notably, the hollow structure not only offers additional ion transport channels to promote rapid transfer of ions in the electrolyte but also provides an increased number of electrochemically active sites. The morphology and electrochemical performance of Se-CoNi2S4 nanospheres with different levels of Se doping were compared. From the results, Se doping not only enhances the conductivity of CoNi2S4 but also increases its charge storage capacity. As an electrode material, the synthesized Se-CoNi2S4 composite that was synthesized demonstrated a notable specific capacitance of 1260 F g−1 at 1 A g−1. Additionally, when Se-CoNi2S4 was utilized as the anode and activated carbon served as the cathode in an asymmetric supercapacitor, it achieved an energy density of 44.6 Wh kg−1 at a power density of 827 W kg−1. After undergoing 10,000 cycles, this device demonstrated exceptional cycling stability, retaining 80.2 % of its initial capacitance. Therefore, the synthesized electrode material Se-CoNi2S4 has significant potential for energy storage applications.

Ppb-level H2 gas-sensor based on porous Ni-MOF derived NiO@CuO nanoflowers for superior sensing performance

Nickel oxide (NiO) is an optimal material for precise detection of hydrogen (H2) gas due to its high catalytic activity and low resistivity. However, the solid structure of NiO imposes limitations on the gas response kinetics of H2 gas molecules, resulting in a slower electron–hole transit and reduced gas response value. Herein, a unique NiO@CuO NFs with porous sharp-tip and nanospheres morphology was successfully synthesized by using a metal–organic framework (MOF) as a precursor. The fabricated porous 2 wt% NiO@CuO NFs describes outstanding selectivity towards H2 gas, including a high sensitivity of response value (170–20 ppm at 150 °C), is almost 28.3 % higher than that of porous Ni-MOF, low detection limit (300 ppb) with a notable response (21), short response and recovery times at (300 ppb, 40/63 s and 20 ppm, 100/167 s), exceptional long-term stability and repeatability. The study also explored the impact of relative humidity to evaluate the sensor performance under real-world conditions. The boosted hydrogen dioxide sensing properties may be attributed to synergistic effects of numerous factors including p-p heterojunction at the interface between NiO and CuO nanoflowers, especially a porous sharp-tip MOF structure and rough surface of nanospheres as well as the chemical sensitization effect of NiO. This research offers a viable method for creating unique MOS heterostructures from Ni-MOF and CuO that have unique morphologies and compositions that could be used for H2 gas sensing applications.

Microfluidic Continuous Synthesis of Size- and Facet-Controlled Porous Bi2O3 Nanospheres for Efficient CO2 to Formate Catalysis.

Bismuth-based catalysts are effective in converting carbon dioxide into formate via electrocatalysis. Precise control of the morphology, size, and facets of bismuth-based catalysts is crucial for achieving high selectivity and activity. In this work, an efficient, large-scale continuous production strategy is developed for achieving a porous nanospheres Bi2O3-FDCA material. First-principles simulations conducted in advance indicate that the Bi2O3 (111)/(200) facets help reduce the overpotential for formate production in electrocatalytic carbon dioxide reduction reaction (ECO2RR). Subsequently, using microfluidic technology and molecular control to precisely adjust the amount of 2, 5-furandicarboxylic acid, nanomaterials rich in (111)/(200) facets are successfully synthesized. Additionally, the morphology of the porous nanospheres significantly increases the adsorption capacity and active sites for carbon dioxide. These synergistic effects allow the porous Bi2O3-FDCA nanospheres to stably operate for 90h in a flow cell at a current density of ≈250mA cm- 2, with an average Faradaic efficiency for formate exceeding 90%. The approach of theoretically guided microfluidic technology for the large-scale synthesis of finely structured, efficient bismuth-based materials for ECO2RR may provide valuable references for the chemical engineering of intelligent nanocatalysts.

Supramolecular Self-Assembled Nanostructures Derived from Amplified Structural Isomerism of Zn(II)-Sn(IV)-Zn(II) Porphyrin Triads and Their Visible Light Photocatalytic Degradation of Pollutants.

Two structural isomeric porphyrin-based triads (Zn(II)porphyrin-Sn(IV)porphyrin-Zn(II)porphyrin) denoted as T1 and T2 were prepared from the reaction of meso-[5-(4-hydroxyphenyl)-10,15,20-tris(3,5-di-tert-butylphenyl)porphyrinato]zinc(II) (ZnL) with trans-dihydroxo-[5,10-bis(3-pyridyl)-15,20-bis(phenyl)porphyrinato]tin(IV) (SnP1) and trans-dihydroxo-[5,15-bis(3-pyridyl)-10,20-bis(phenyl)porphyrinato]tin(IV) (SnP2), respectively. All the compounds were characterized using UV-vis spectroscopy, emission spectroscopy, ESI-MS, 1H NMR spectroscopy, and FE-SEM. Most importantly, the two structurally isomeric porphyrin-based triads supramolecularly self-assembled into completely different nanostructures. T1 exhibits a nanosphere morphology, whereas T2 exhibits a nanofiber morphology. The amplified geometric feature in the structural isomeric porphyrin-based triads dictates the physical and chemical properties of the two triads. Both compounds showed the morphology-dependent visible light catalytic photodegradation of rhodamine B dye (74-97% within 90 min) and tetracycline antibiotic (44-71% within 45 min) in water. In both cases, the photodegradation efficiency of T2 was higher than that of T1. The present investigation can significantly contribute to the remediation of wastewater by tuning the conformational changes in porphyrin-based photocatalysts.

Direct Z-scheme heterojunction impregnated MoS2–NiO–CuO nanohybrid for efficient photocatalyst and dye-sensitized solar cell

In this present work, the preparation of ternary MoS2–NiO–CuO nanohybrid by a facile hydrothermal process for photocatalytic and photovoltaic performance is presented. The prepared nanomaterials were confirmed by physio-chemical characterization. The nanosphere morphology was confirmed by electron microscopy techniques for the MoS2–NiO–CuO nanohybrid. The MoS2–NiO–CuO nanohybrid demonstrated enhanced crystal violet (CV) dye photodegradation which increased from 50 to 95% at 80 min; The degradation of methyl orange (MO) dye increased from 56 to 93% at 100 min under UV–visible light irradiation. The trapping experiment was carried out using different solvents for active species and the Z-Scheme photocatalytic mechanism was discussed in detail. Additionally, a batch series of stability experiments were carried out to determine the photostability of materials, and the results suggest that the MoS2–NiO–CuO nanohybrid is more stable even after four continuous cycles of photocatalytic activity. The MoS2–NiO–CuO nanohybrid delivers photoconversion efficiency (4.92%) explored efficacy is 3.8 times higher than the bare MoS2 (1.27%). The overall results indicated that the MoS2–NiO–CuO nanohybrid nanostructure could be a potential candidate to be used to improve photocatalytic performance and DSSC solar cell applications as well.

Tuning the optical properties of transparent ZIF-8 thin films by adjusting the crystal morphology

Optical properties are the most significant properties of optical thin films, which determine its application in optical and photoelectric devices. Designable optical properties are the most challenging goals in optical material engineering. Recently, Metal-organic framework (MOF)-based optical thin films have attracted increasing attention due to their novel optical properties, especially their modular design, which allows fine-tuning of the relevant properties. In this work, a strategy for tuning the optical properties of MOF-based thin films is developed, which is realized by adjusting MOF crystal morphology. A commonly used MOF, ZIF-8 (zeolitic imidazolate framework-8), is selected as the research model. The morphology of ZIF-8 nanocrystal is adjusted using a surfactant/end-capping agent modulation method. The surfactant/end-capping agents are absorbed onto different crystal planes of ZIF-8, slowing the growth of the crystal planes and causing the formation of ZIF-8 crystals with different morphologies. Six different morphologies of ZIF-8 crystals are successfully synthesized in the presence of different amounts of CTAB and/or TRIS: nano-spherical, rhombohedral dodecahedron, nano-cubic, rough octahedron, flake-shaped and hexapod-like morphology. Then, the corresponding ZIF-8 thin films with different crystal morphologies are prepared via spin-coating. The optical properties of the thin films are investigated using UV–vis spectroscopy and ellipsometry in detail. The results indicate that the film with rough octahedron morphology has the best transmittance, reaching 93.35 % at 581 nm. As a key optical parameter of the film, its refractive index can be adjusted between 1.27 and 1.54. The success of tuning of the optical properties of MOF optical thin films by adjusting the crystal morphology will make it meet the different required optical properties in various optical and photoelectric devices.

Smart gradient coating suitable for bone growth prepared on plasma-electrolytically oxidised Mg and its sequential degradation behaviour

A gradient coating containing collagen and inorganic strontium/calcium phosphate (Sr/CaP) was fabricated on plasma-electrolytically oxidised magnesium via one-step cathodic electrodeposition. First, Sr-doped dicalcium phosphate dihydrate and hydroxyapatite (DCPD and HA) was deposited, followed by a collagen/CaP layer. The morphological evolution, sequential degradation behaviour, and in vitro bio-properties of the coatings were investigated. The incorporation of collagen remarkably refined the morphology of the CaP, and a more aggregated nano-spherical morphology was observed with increasing collagen concentration. Sr could partially replace Ca in the CaP crystals. Collagen combined with CaP formed a relatively stable skeletal frame, which provided sufficient barrier properties and more sites for the re-precipitation of bone tissue, as well as a more promising proliferation and differentiation ability of osteoblasts. A gradient coating that matches the requirements of bone growth at various periods is suggested for implantation.

Effect of Ga doping on the structural, optical, and electrical properties of ZnO nanopowders elaborated by sol-gel method

Nanostructured ZnO has received a considerable amount of interest, owing to its unique physical and chemical characteristics, as well as its remarkable performance in the fields of electronics, optics, and photonics. This work aims to study the influence of Ga dopant on the structural, optical, and electrical properties of ZnO nanopowders. Undoped and Ga-doped ZnO (GZO) nanopowders were successfully synthesised with the soft chemical sol-gel method. The solution was prepared using zinc acetate dihydrate and gallium (III) nitrate hydrate as precursors. The ethylene glycol is used as solvent. The X-ray diffractometer, scanning electronic microscope (SEM), UV–Vis, FTIR, and four-point probe method are used to analyse the properties of the synthesised powders. XRD and FTIR measurements show the growth of pure and Ga-doped ZnO crystals, which have a hexagonal wurtzite structure, and the average crystallite size varies from 9.09 nm to 24.8 nm. The nanospherical morphology of the nanopowders synthesised can be seen in the SEM images. The UV–visible spectroscopy shows that the optical gap energy increases with Ga concentration, from 3.59 eV to 3.67 eV. The I-V electrical measurements indicate that the breakdown voltage and the non-linear coefficient increase with Ga doping. This study will open the way for the investigation of a relationship between the electrical and nanostructural features of ZnO-based varistors for future device applications.

The role of Ga and Y on binary Al2O3-Y2O3 and Al2O3-Ga2O3 mixed oxides nanoparticles towards potential Ni water-gas shift catalysts

This work focuses on the study of binary Al2O3-Y2O3-x and Al2O3-Ga2O3-x mixed oxides with varying Y2O3 or Ga2O3 nominal loading (x=25, 50) prepared by hydrothermal synthesis assisted by Triton X-100. The mixed oxides were used to prepare Ni-based (5 wt%) catalysts for the Water Gas Shift Reaction. The Al2O3 sample presented urchin-like hollow nanosphere morphology, which evolved to solid nanospheres with Y2O3 or Ga2O3 in the mixed oxides. The physicochemical characterization indicated good integration of the mixed oxides, especially on the low-content additive oxides. The theoretical results confirmed that Ga goes deeper into the alumina matrix than Y, partially explaining the XPS and HRTEM results in which the Ni dispersion was better in the Ni/AlGa-x samples. The FTIR in-situ measurements of the reaction allowed us to propose that the reaction occurs minimally through the carbonyl mechanism at low temperatures (<300 °C) and the formate mechanism at high temperatures (>300 °C).

Engineering Mn-Doped CdS Thin Films Through Chemical Bath Deposition for High-Performance Photoelectrochemical Water Splitting.

Doping conventional materials with a second element is an exciting strategy for enhancing catalytic performance via electronic structure modifications. Herein, Mn-doped CdS thin films were successfully synthesized with the aid of the chemical bath deposition (CBD) by varying the pH value (8, 10, and 12) and the surfactant amount (20, 40, 60 mg). Different morphologies like nano-cubes, nanoflakes, nano-worms, and nanosheets were obtained under different deposition conditions. The optimized Mn-doped CdS synthesized at pH=8 exhibited better photoelectrochemical (PEC) performance for oxygen evolution reaction (OER) than pure CdS films, with a maximum photocurrent density of 300 μA/cm2 at an external potential of 0.5 V, under sunlight illumination. The observed performance is attributed to the successful Mn doping, porosity, high surface area, and nanosphere morphology.

Synthesis of SiO2@Ag Nanocomposite for Investigating Metal-Enhanced Fluorescence and Surface-Enhanced Raman Spectroscopy.

SiO2@Ag nanocomposite (NC) has been synthesized by the chemical reduction and Stӧber method for Metal-enhanced fluorescence (MEF) of Rhodmine 6G (R6G) and Surface-enhanced Raman spectroscopy (SERS) of Malachite green (MG). As-synthesized SiO2@Ag NC indicated SiO2 nanosphere (NS) and Ag nanoparticle (NP) morphologies. The SiO2@Ag NC was high quality with a well-defined crystallite phase with average sizes of 24nm and 132nm for Ag NP and SiO2 NC, respectively. By using SiO2@Ag NC, the photoluminescence (PL) intensity of the R6G (at 59.17ppm) was increased approximately 133 times. The SERS of the MG (at 1.0ppm) with SiO2@Ag NC as substrate clearly observed vibrational modes in MG dye at 798, 916, 1172, 1394, and 1616cm-1. As a result, the SERS enhancement factor (EFSERS) at 1172cm-1 obtained 6.3 × 106. This initial study points to the potential of SiO2@Ag NC as a promising material for MEF and SERS substrates to detect dyes at low concentrations.

Lignin-xylan nanospheres prepared by green and quick method from lignocellulose and used as additive in PVA films

Lignin, as an amorphous three-dimensional aromatic polymer, was able to self-assemble into lignin nanoparticles (LNPs) to realize valorization of lignin. Here, lignin-xylan extractives were extracted from grape seed (GS) and poplar by acidic THF at room temperature, and effectively produced lignin-xylan nanospheres via spin evaporation. The morphology and chemical properties of nanospheres were determined by its natural origins, consequently influencing its application. For the lignin-xylan extractive from grape seed, the lignin was composed of guaiacyl (G) and p-hydroxylphenyl (H) units and the hollowed nanospheres (GS-LNPs) with 362.72 nm diameter was produced. The extractive from poplar was composed of G-syringyl (S) typed lignin (80.30 %) and xylan (12.33 %), that can assemble into LNPs with smaller size (229.87 nm), better PDI (0.1), and light color. The hybrid particles showed the qualities of lignin and xylan, that properties led to the LNPs@PVA composite films with UV-blocking capability, strong mechanical strength and hydrophobicity, and transparency ability of visible light. P-LNPs showed better performance as the film additives, due to its lower particles size and high content of unconjugated -OH from xylan. Xylan was significant in the composite films, and lowering the xylan content resulted in the decrease of the composite film's mechanical properties and hydrophobicity.

Transition metal modified Al2O3 mesoporous nanospheres for catalysis of organic reactions

The performance of metal oxide-based catalysts are usually determined by their characteristics such as material composition, morphology, and surface/interface properties. Therefore, rational design of metal oxide-based catalysts with special surface/interface characteristics and porous microstructure still needs further research. In this work, a facile two-step solvothermal-annealing method is developed for the synthesis of transition metal (TM) modified Al2O3 (TM-Al2O3, TM = Cu, Fe, Ni, Co) nanospheres. The influences of different ratios of solvents (e.g., water and glycerol) on the morphology and particle size of the nanocatalysts are explored. Benefitting from the nano-spherical morphology and unique mesoporous structure, the representative catalyst (i.e., Cu-Al2O3) exhibits favorable catalytic performance in 4-nitrophenol reduction and benzyl alcohol oxidization reactions. The turnover frequency of Cu-Al2O3 is high up to 35.9 min−1 for the reduction of 4-nitrophenol, which is higher than that of its counterparts (i.e., Fe-Al2O3, Ni-Al2O3, and Ni-Al2O3) and many recently reported Al2O3-based catalysts. Moreover, the pH of the reaction system is regulated to enhance the catalytic efficiency in selective oxidization of benzyl alcohol by an additive addition strategy. These results suggest that the nano-spherical and mesoporous morphology is indeed effective for the activity enhancement of TM-Al2O3 catalysts. The same catalyst designing concept and performance regulation strategy may be extended to other TM-modified metal oxide systems, making it possible to tune the catalytic behavior for various chemical reactions.

Size-Dependent Response of Hydrothermally Grown SnO2 for a High-Performance NO2 Sensor and the Impact of Oxygen.

A NO2 sensor with a detection limit down to the ppb level based on pristine SnO2 has been developed through a facile poly(acrylic acid)-mediated hydrothermal method. SnO2 particles of solid microsphere, hollow microsphere, and nanosphere morphologies were synthesized, with respective constitutional crystallite of size ∼2 μm in length and 10-20 nm and ∼7 nm in diameter. All sensors show great selectivity to NO2. The hollow microsphere sensor exhibits the best performance, with medium specific surface area (SSA), followed by the nanosphere sensor with the largest SSA. This is attributed to the superposition of two opposite effects on sensor response with increased SSA: more adsorption sites and fewer electrons to be taken out with overly small crystallite that may reach complete depletion. O2 is found to speed up the response and recovery times but reduce the response because O adsorbates facilitate the adsorption/desorption of NO2 thermodynamically, and the two oxidizing gases compete in harvesting electrons from SnO2. The adverse effect of humidity can be minimized by operating the sensor at 110 °C. The response of the hollow microsphere sensor to 50 ppb of NO2 is 8.8 (Rg/Ra) at room temperature, and it increases to 15.1 at 110 °C. These findings are useful for developing other oxidizing gas semiconductor sensors.

Enhancing or Quenching of a Mitochondria-Targeted AIEgens-Floxuridine Sensor by the Regulation of pH-Dependent Self-assembly, Efficient Recognition of Hg2+, and Stimulated Response of GSH.

Biocompatible fluorescent probes have emerged as essential tools in life sciences for visualizing subcellular structures and detecting specific analytes. Herein, we report the synthesis and characterization of a novel fluorescent probe (TPE-FdU), incorporated with hydrophilic 2'-fluoro-substituted deoxyuridine and hydrophobic ethynyl tetraphenylethene moieties, which possessed typical aggregation-induced emission (AIE) behavior. In comparison to the TPE-FdU (pKa 7.68) treated in neutral conditions, it performed well at pH 4, exhibiting an enhanced 450 nm emission signal of approximately four times stronger. As the pH value was increased to 10, the fluorescence intensity was completely quenched. The TEM images of TPE-FdU in an acidic environment (nanospherical morphology, AIE enhance, pH = 4) and in a basic environment (microrods, fluorescence quenching, pH = 9) revealed that it was a pH-dependent self-assembled probe, which was also illustrated by the interpretation of the NMR spectrum. Furthermore, the TPE-FdU probe exhibited a specific response to trace Hg2+ ions. Interestingly, the quenched fluorescence of the TPE-FdU probe caused by Hg2+ can be recovered by the addition of GSH due to the formation of the Hg-S bond being released away. MTT assay and CLSM images demonstrated that TPE-FdU was nontoxic and selectively visualized in the intracellular mitochondria. These results contributed to the development of advanced fluorescent probes with diverse applications in cell imaging, environment protection, and biomedical research.

Amorphous 1-D nanowires of calcium phosphate/pyrophosphate: A demonstration of oriented self-growth of amorphous minerals

Amorphous inorganic solids are traditionally isotropic, thus, it is believed that they only grow in a non-preferential way without the assistance of regulators, leading to the morphologies of nanospheres or irregular aggregates of nanoparticles. However, in the presence of (ortho)phosphate (Pi) and pyrophosphate ions (PPi) which have synergistic roles in biomineralization, the highly elongated amorphous nanowires (denoted ACPPNs) form in a regulator-free aqueous solution (without templates, additives, organics, etc). Based on thorough characterization and tracking of the formation process (e.g., Cryo-TEM, spherical aberration correction high resolution TEM, solid state NMR, high energy resolution monochromated STEM-EELS), the microstructure and its preferential growth behavior are elucidated. In ACPPNs, amorphous calcium orthophosphate and amorphous calcium pyrophosphate are distributed at separated but close sites. The ACPPNs grow via either the preferential attachment of ∼2 nm nanoclusters in a 1-dimension way, or the transformation of bigger nanoparticles, indicating an inherent driving force-governed process. We propose that the anisotropy of ACPPNs microstructure, which is corroborated experimentally, causes their oriented growth. This study proves that, unlike the conventional view, amorphous minerals can form via oriented growth without external regulation, demonstrating a novel insight into the structures and growth behaviors of amorphous minerals.

NiS2 @MWCNTs as a promising anode material for lithium and sodium-ion batteries with superior cycling stability

The NiS2 @MWCNTs materials were synthesized using a straightforward hydrothermal one-step process, forming a 3D conductive network structure with stable and uniformly distributed nanosphere morphology. Electrochemical tests yielded a sodium storage capacity of 463.99 mAh g−1 after 400 cycles with 0.2 A g−1, and a coulomb efficiency of 83.3% at the first cycle, followed by excellent long-cycle stability with a capacity retention rate of 96.7% after 600 cycles at a high current of 1 A g−1. It's interesting to note that Na+ storage mechanism is provided by a pseudocapacitor. The 3D conductive network was credited with enhanced electrochemical performance and structural stability. The incorporation of multi-walled carbon nanotubes (MWCNTs) also improves the material conductivity and accelerated the ion transport efficiency, while modulation of the nano microsphere structure increases the reactive active sites and reduce the capacity loss. These findings highlight the great potential NiS2 @MWCNTs composites as a perfect anode material for sodium-ion batteries (SIBs), opening up new possibilities for sustainable energy storage solutions.

A TiN-based nanophotosensitizer for enhanced photothermal therapy with the aid of ultrasound

Background and purposeTargeting and uptake are the most important strategies for enhancing the efficacy of cancer photothermal therapy (PTT) and reducing damage to surrounding normal tissues. In this study, a kind of nanophotosensitizer based on nanobubbles and TiN was prepared for synergetic therapy for hepatocellular carcinoma. MethodsThe photothermal agent titanium nitride (TiN) was wrapped in nanobubbles by membrane hydration method and verified in cells and animals. CCK-8, cell death staining, and JC-1 were used to verify the pernicious effect of photothermal combined with Ultrasound Targeted Nanobubble Destruction (UTND) and then injected into animals through the tail vein to observe its photothermal effect and in vivo inhibitory effect. A hemolysis test and body weight change verified its safety. ResultsThe average diameter of the novel nanophotosensitizer was 300.3 ± 12.7 nm, with a consistent nanospheres morphology. The UTND technology was utilized to improve the penetration of TiN into tumor cells through the physical energy of ultrasound irradiation. The therapeutic effects of the synergistic therapy of UTND and PTT were verified in vitro and in vivo. ConclusionThe research has established NBs@C3F8–TiN as a suitable ultrasound photothermal agent due to its appropriate size and efficient photothermal efficacy for visual photothermal therapy for HCC.