Perovskite Nanoparticles Research Articles

Perovskite oxide nanoparticles: Dual role as supports for luminescent Eu(III) ions and photocatalysts for bisphenol degradation

Perovskite oxides, such as CaTiO3, SrTiO3, and BaTiO3, have gained significant recognition for their dual role as luminescence supports and photocatalytic materials. In this study, we synthesized perovskite oxide nanoparticles (NPs) using the thermal calcination method and employed them as photocatalysts for the degradation of bisphenol S (BPS) and bisphenol AF (BPAF) under UVC irradiation. The as-synthesized photocatalysts were thoroughly examined for the photocatalytic degradation process and identified secondary products were identified using liquid chromatography in conjunction with high-resolution mass spectrometry. Our observations highlighted the relatively faster photocatalytic degradation of BPS compared to BPAF. Notably, among the perovskite oxide materials, SrTiO3 exhibited the highest catalytic activity for BPS degradation, while BaTiO3 outperformed in the case of BPAF degradation. Perovskite oxide NPs were also utilized as supports for doping with Eu3+ ions to create phosphor supports. Luminescent emissions from the Eu3+ ions, characterized by the 5D0 → 7FJ = 0-4 transitions, were observed and varied depending on the support material. Notably, Eu3+ doped in CaTiO3 nanoparticles exhibited the highest luminescence efficiency. These results highlight the dual functionality of perovskite oxide-based materials in phosphor applications and photocatalysis, offering valuable insights into their potential for both enhancing luminescence efficiency and treating bisphenols.

Synthesis, characterization, and implementation of BaNiO3 perovskite nanoparticles as thin film supercapacitor electrode

AbstractThis work is the first attempt to explore the supercapacitor applications of Barium nickelate (BaNiO3) perovskite nanoparticles. The nanoparticles are synthesized using a simple combustion method and their morphology, elemental composition, and so forth are studied using standard characterization methods such as x‐ray diffraction spectroscopy (XRD), field emission scanning electron microscopy (FESEM), and so forth. The nanoparticles were found to be hexagonal in shape, with an average particle size of 16 nm, and the elemental analysis confirms the successful synthesis of the BaNiO3 perovskite nanoparticles. For electrochemical studies, the electrodes are fabricated over a wearable and flexible conductive fabric (CF) substrate. A slurry paste of the synthesized BaNiO3 nanoparticles is applied over CF and dried overnight, thereby forming a thin film electrode. The fabricated electrode acts as a positive electrode with a high specific capacitance of 508.64 F g−1 at 2.2 A g−1 current density. Upon increasing the current density, the electrode maintains 60% of its specific capacitance and displays 97% cyclic stability over 5000 cycles. The electrochemical impedance spectroscopy (EIS) study indicates excellent conductivity of the electrode, with a bulk resistance of 3.2 Ohms. The electrochemical performance of the fabricated electrode is also compared with various previously reported works and the electrode displays higher specific capacitance and better cyclic stability. These findings suggest that the BaNiO3 perovskite nanoparticles‐based electrode holds promise for utilization as an anode material in supercapacitor applications.

Synthesis and characterization of BaIrO3-doped YBCO superconducting thin films via TFA-MOD technique

High-temperature superconducting materials (HTS) are characterized by remarkably high critical current density (Jc) values when exposed to low temperatures and magnetic fields. In the realm of such investigations, various crystalline imperfections, including finely dispersed non-superconducting phases, dislocations, vacancies, grain boundaries, twin boundaries, antiphase boundaries, and insulating regions within grain boundaries, have been recognized as potential sources of pinning centers. However, it is essential to acknowledge that Jc values experience a rapid decline as the temperature rises in the presence of a magnetic field. The primary contributing factors to this decline are attributed to the intrinsic crystalline anisotropy of HTS materials and the thermal fluctuations that prevail at elevated temperatures. Nevertheless, a noteworthy factor in the diminishment of Jc values is the scarcity of efficacious pinning centers. In response to these challenges, a pioneering technology has emerged, revolving around nanostructure engineering for the deliberate creation of artificial pinning centers within HTS materials. In alignment with this approach, the present study endeavors to augment the critical current density and enhance the flux pinning properties of YBa2Cu3O6.56 (YBCO) superconducting films. This augmentation is achieved through the integration of BaIrO3 (BIO) perovskite nanodots, nanorods, or nanoparticles as strategically positioned pinning centers. The films are deposited on a SrTiO3 (STO) substrate employing the Trifluoroacetate Metal–Organic Deposition (TFA-MOD) technique. This research initiative seeks to contribute to the advancement of knowledge regarding the controlled manipulation of artificial pinning centers in HTS materials, particularly focusing on YBCO thin films, with the ultimate goal of enhancing their performance under the influence of elevated magnetic fields.

A comparative study of structural, optical, and magnetic properties of LaFeO3 and La2CuO4 perovskite nanoparticles

A comparative study of structural, optical, and magnetic properties of LaFeO3 and La2CuO4 perovskite nanoparticles

Flexible Wood‐Based X‐Ray Scintillator Film Using Lead‐Free Cs3Cu2I5 Perovskite Nanoparticles

The prevalent use of unsustainable polymers in current X‐ray scintillators poses a significant environmental concern. The advancement of biodegradable X‐ray scintillators holds promise in mitigating escalating environmental issues tied to electronic or medical waste and carbon footprints. Herein, a biodegradable and flexible X‐ray scintillation film is presented employing lead‐free 0D Cs3Cu2I5 perovskite nanoparticles integrated into densified‐delignified wood (Cs3Cu2I5@D‐Wood). The Cs3Cu2I5@D‐Wood film demonstrates precise and detailed X‐ray imaging capabilities, achieving a high spatial resolution of 10 line pairs per millimeter (lp·mm−1). To minimize the environmental impact associated with disposal, metal and halide ions (e.g., Cs+, Cu+, I−) from Cs3Cu2I5@D‐Wood can be easily retrieved by a simple solvent extraction process. The approach showcases the potential of biodegradable wood‐based X‐ray scintillation screens as alternatives to conventional, plastic‐based screens. This offers a significant contribution to environmental sustainability by reducing electronic or medical waste.

Exploring the structural, optical, and dielectric characteristics of polyacrylamide gel synthesized CeMnO3 nanoparticles with Co & Ni ion doping

Nanostructured perovskite materials doped with transition metal ions have attracted significant attention due to their unique electronic and dielectric properties. In this study, we present the synthesis and thorough characterization of cobalt (Co) and nickel (Ni) ion-doped CeMnO3 (CMO) perovskite nanoparticles using a modified polyacrylamide gel method. Our structural analysis suggests that the perovskite phase stabilizes with an orthorhombic phase (Pbnm space group). Morphological analysis conducted via field emission scanning electron microscopy (FESEM) unveils the formation of clustered nanospherical particles. X-ray photoelectron spectroscopy (XPS) reveals mixed oxidation states of Ce, Mn, and Ni ions. Furthermore, UV–Vis and photoluminescence spectra analyses demonstrate a distinctive reduction in band gap and suppressed charge carrier recombination upon doping. The substitution of Ni and Co ions also enhances the screening effect, reducing Coulombic interaction between photoexcited electrons and holes and subsequently increasing the dielectric constant. Analysis of the Cole-Cole plot demonstrates the augmentation of capacitance with Ni substitution. These findings collectively suggest that the decreased dielectric loss and enhanced dielectric constant support the feasibility of these materials for application in storage devices.

PEI-Mediated Assembly of Fe3O4 onto SiO2-Encapsulated CsPbBr3 for Highly Sensitive Fluorescent Lateral Flow Immunoassay.

The conventional lateral flow immunoassay (LFIA) method using colloidal gold nanoparticles (Au NPs) as labeling agents faces two inherent limitations, including restricted sensitivity and poor quantitative capability, which impede early viral infection detection. Herein, we designed and synthesized CsPbBr3 perovskite quantum dot-based composite nanoparticles, CsPbBr3@SiO2@Fe3O4 (CSF), which integrated fluorescence detection and magnetic enrichment properties into LFIA technology and achieved rapid, sensitive, and convenient quantitative detection of the SARS-CoV-2 virus N protein. In this study, CsPbBr3 served as a high-quantum-yield fluorescent signaling probe, while SiO2 significantly enhanced the stability and biomodifiability of CsPbBr3. Importantly, the SiO2 shell shows relatively low absorption or scattering toward fluorescence, maintaining a quantum yield of up to 74.4% in CsPbBr3@SiO2. Assembly of Fe3O4 nanoparticles mediated by PEI further enhanced the method's sensitivity and reduced matrix interference through magnetic enrichment. Consequently, the method achieved a fluorescent detection range of 1 × 102 to 5 × 106 pg·mL-1 after magnetic enrichment, with a limit of detection (LOD) of 58.8 pg·mL-1, representing a 13.3-fold improvement compared to nonenriched samples (7.58 × 102 pg·mL-1) and a 2-orders-of-magnitude improvement over commercial colloidal gold kits. Furthermore, the method exhibited 80% positive and 100% negative detection rates in clinical samples. This approach holds promise for on-site diagnosis, home-based quantitative tests, and disease procession evaluation.

Enhanced electrical, optical and magnetic properties of BiFeO3 perovskite nanoparticles co-doped with Y and Cu

The present work includes the fabrication of pure BiFeO3 and Bi0.9Y0.1Fe1−xCuxO3 (x = 0.05, 0.10, 0.15) nanoparticles by the usual sol-gel route. The characterization of structural, morphological, optical, electrical, and magnetic properties of the synthesized samples was achieved through x-ray diffraction spectroscopy, Raman spectroscopy, Fourier transform infrared spectroscopy, scanning electron microscopy, an impedance analyzer, and a vibrating sample magnetometer. The Fourier transform infrared study confirmed the presence of Bi–O and Fe–O bonds. The x-ray diffraction patterns confirmed the rhombohedral (R3c) structure as a major phase with the orthorhombic (Pnma) structure as a secondary phase in all samples, and few amount of impurity phase of Bi25FeO40 was also determined. The surface morphology analysis showed the variation of particle size from 63 to 174 nm. The Raman spectra of 13 optical phonon modes, including 4A1 and 9E symmetric phonons, are observed for all samples, and the positions of these modes are almost similar, except the intensities of A1 modes. The optical measurements show a reduction in bandgap from 2.17 to 2.03 eV with co-doping, revealing itself as a more promising applicant in photovoltaics. An enhanced value of the dielectric constant is observed for different doped samples at different frequency regions from 100 Hz to 10 MHz. Magnetic investigation demonstrates the improved ferromagnetism with co-doping of Y and Cu due to distortion in the FeO6 octahedron. A maximum saturation magnetization of 0.26 emu/gm and a coercivity of 2915 Oe were found for Y concentration of 10% and Cu concentration of 15%.

In situ temperature synthesis and characterization of ferroelectric PZN-4.5PT nanoparticles’ thin films using synchrotron light source

ABSTRACT Despite the excellent properties of Pb(Zn1/3Nb2/3)O3-4.5PbTiO3 (PZN-4.5PT) single crystals, the greatest difficulty for their application on electronic devices is to make them to thin layers related to the difficulty to make them as ceramic materials. In this paper, we use the combined USAXS/SAXS/WAXS instrument at 9ID beamline at APS-ANL for in situ characterization of PZN-4.5PT inorganic perovskite nanoparticles thin films deposited on nanotextured silicon to understand the phase transitions and determine the observed microcrystals' structure. The sample was annealed from ambient to 1000°C. The results revealed structure changes in the nanoparticles' thin films which could be explained by the new phase that can be assigned to the Pb3(PO4)2-based component. The peak at 31° indicates the presence of the rhombohedral phase perovskites assigned to the nanoparticles. WAXS characterization permitted to identification of many transitions during thermal annealing like dehydration or dihydroxylation of phosphorus gel –OH bonds and internal water.

Colloidal Synthesis of (PbBr2)2(AMTP)2PbBr4 a Periodic Perovskite "Heterostructured" Nanocrystal.

Heterostructures in nanoparticles challenge our common understanding of interfaces due to quantum confinement and size effects, giving rise to synergistic properties. An alternating heterostructure in which multiple and reoccurring interfaces appear in a single nanocrystal is hypothesized to accentuate such properties. We present a colloidal synthesis for perovskite layered heterostructure nanoparticles with a (PbBr2)2(AMTP)2PbBr4 composition. By varying the synthetic parameters, such as synthesis temperature, solvent, and selection of precursors, we control particle size, shape, and product priority. The structures are validated by X-ray and electron diffraction techniques. The heterostructure nanoparticles' main optical feature is a broad emission peak, showing the same range of wavelengths compared to the bulk sample.

Rational designing of TiO2-X@Cs3Bi2X9 nanocomposite for boosted hydrogen evolution

Halide perovskites are known as compounds possessing interesting properties, including visible light-induced photoactivity, however, they suffer from instability. Herein, a novel technique for reducing the decomposition rate of halide bismuth-based perovskites Cs3Bi2X9 (X=I, Br, Cl) in the aqueous environment by combining with different types of TiO2 (anatase TiO2-I, anatase/rutile TiO2-B, and rutile TiO2-C synthesized using HI, HBr, and HCl acids, respectively) has been described. The specific type of HX has a notable impact on the crystallinity, morphology, and photocatalytic abilities of TiO2-X and they constitute a reaction environment that allows perovskites to survive the synthesis of TiO2. Studies reveal that TiO2-I is the optimal support material for immobilizing perovskite nanoparticles, owing to its extensive surface area and the synergistic effect it has with Cs3Bi2I9. Adding a small amount of Cs3Bi2I9 to iodine-doped TiO2-I improved the photocatalytic performance in the aqueous environment. As a result, 24.3, 22.5, 22.0, and 13.5-fold improvement in H2 production has been realized with decreasing amounts of Cs3Bi2I9 perovskite (10, 50, 100, and 300 mg). Upon detailed characterization and analysis of photocatalytic properties, it has been suggested that when Cs3Bi2I9 nanoparticles are dispersed within the TiO2-I structure, they can establish a close connection which allows the photogenerated electrons of TiO2-I to be extracted to Cs3Bi2I9, effectively preventing the charge recombination. This study provides a feasible possibility for the photocatalytic application of perovskite-based nanocomposites in the aqueous environment.

Synthesis and Exploring structural, magnetic, morphology and optical properties of La2−xAlxCuO4 (0 ≤ x ≤ 0.25) perovskite nanoparticles by microwave-assisted combustion method

La2CuO4 perovskite nanoparticles doped with aluminum were synthesized through the microwave-assisted combustion technique. Comprehensive studies on the structural, magnetic optical, functional and morphological properties were conducted using various techniques, including XRD, EDX, VSM, DRS-UV, FT-IR and FESEM respectively, .The XRD patterns of pristine La2CuO4 and Al-doped La2CuO4 unequivocally validated the exclusive development of a perovskite structure, devoid of any impurities. Nevertheless, the augmentation in Al3+ content (x = 0–0.25) induced a noteworthy phase shift from orthorhombic to cubic configuration. The average crystallite dimensions spanned from 54 to 41 nm. Distinct FT-IR bands at approximately 687 and 434 cm-1 were intricately linked to the La-O and Cu-O stretching modes inherent to the orthorhombic La2CuO4 phase. The energy gap determined through the Kubelka–Munk (K–M) methodology, experienced an elevation concomitant with the heightened Al3+ content (1.67–1.72 eV), attributable to quantum confinement phenomena. Within the La2-xAlxCuO4 (x = 0 to 0.25) system, the genesis of nanoscaled crystallized grains, interspersed with pores resulting from the amalgamation of grains, was evident. Analysis of hysteresis curves unveiled the emergence of soft ferromagnetic behavior at ambient temperature.

Antimony-Based Halide Perovskite Nanoparticles as Lead-Free Photocatalysts for Controlled Radical Polymerization.

Metal halide perovskites have emerged as versatile photocatalysts to convert solar energy for chemical processes. Perovskite photocatalyzed polymerization draws special attention due to its straightforward synthesis process and the ability to create advanced perovskite-polymer nanocomposites. Herein, this work employs Cs3Sb2Br9 perovskite nanoparticles (NPs) as a lead-free photocatalyst for light-controlled atom transfer radical polymerization (ATRP). Cs3Sb2Br9 NPs exhibit high reduction potential and interact with electronegative bromide initiator with Lewis acid Sb sites, enabling efficient photoinduced reduction of initiators and controlled polymerization under blue light irradiation. Methacrylate monomers with various functional groups are successfully polymerized, and the resulting polymer showcased a dispersity (Đ) as small as 1.27. The living nature of polymerization is confirmed by high chain end fidelity and kinetic studies. Moreover, Cs3Sb2Br9 NPs serve as heterogeneous photocatalysts, demonstrating recyclability and reusability for up to four cycles. This work presents a promising approach to overcome the limitations of lead-based perovskites in photoinduced controlled radical polymerization, offering a sustainable and efficient alternative for the synthesis of well-defined polymeric materials.

Leveraging Bromine-Induced Large Stokes Shift in Pyrrolidinium Perovskite Nanoparticles for Improved Organic Photovoltaic Performance

Leveraging Bromine-Induced Large Stokes Shift in Pyrrolidinium Perovskite Nanoparticles for Improved Organic Photovoltaic Performance

Ultrafast nanomanufacturing via high-temperature shock of La0.6Sr0.4CoO3 catalysts for overall water splitting

Electrochemical water splitting, as an effective sustainable and eco-friendly energy conversion strategy, can produce high-purity hydrogen (H2) and oxygen (O2) via hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), respectively, altering the nonrenewable fossil fuels. Here, La0.6Sr0.4CoO3 perovskite oxide nanoparticles with an orthorhombic phase were synthesized within 2 min in a one-step reaction, using a rapid and efficient high-temperature shock (HTS) method. Impressively, the as-prepared La0.6Sr0.4CoO3 with orthorhombic phase (HTS-2) exhibited better OER and HER performance than the hexagonal phase counterpart prepared using the traditional muffle furnace calcination method. The electrocatalytic performance enhancement of orthorhombic La0.6Sr0.4CoO3 can be attributed to the novel orthorhombic structure, such as confined strontium segregation, a higher percentage of highly oxidative oxygen species, and more active sites on the surface. This facile and rapid synthesis technique shows great potential for the rational design and crystal phase engineering of nanocatalysts.

Perovskite oxide-based nanoparticles embedded MXene composites for supercapacitors and oxygen evolution reactions

In this report, perovskite oxide-MnFeO3 nanoparticles embedded MXene sheets were prepared by hydrothermal approach for the effective water splitting and energy stowage uses. The prepared MXene@MnFeO3 hybrid nanocomposites exhibited outstanding 1077 F/g specific capacitance at a current density of 1 A g−1 and excellent cycling solidity (capacitance retention after the 3000 cycle is 96.5 %). In addition, an asymmetric capacitor delivered a ultimate specific energy of 114 Wh/kg at a specific power of 2117 W/kg. MXene@MnFeO3 hybrid catalyst required a credible overpotential of 235 mV to achieve the 10 mA cm−2 current density, along with the small Tafel slope of 41 mV dec−1 for OER in 1 M KOH and long-span 24 h stability. Our proposed strategy of perovskite oxide nanoparticles hybridized highly conductive MXene sheets would be suitable alternative as the potential electrode materials for the efficient energy storage/conversion application.

Electron-donating functional groups strengthen ligand-induced chiral imprinting on CsPbBr3 quantum dots

Chiral perovskite nanoparticles and films are promising for integration in emerging spintronic and optoelectronic technologies, yet few design rules exist to guide the development of chiral material properties. The chemical space of potential building blocks for these nanostructures is vast, and the mechanisms through which organic ligands can impart chirality to the inorganic perovskite lattice are not well understood. In this work, we investigate how the properties of chiral ammonium ligands, the most common organic ligand type used with perovskites, affect the circular dichroism of strongly quantum confined CsPbBr3 nanocrystals. We show that aromatic ammonium ligands with stronger electron-donating groups lead to higher-intensity circular dichroism associated with the lowest-energy excitonic transition of the perovskite nanocrystal. We argue that this behavior is best explained by a modulation of the exciton wavefunction overlap between the nanocrystal and the organic ligand, as the functional groups on the ligand can shift electron density toward the organic species-perovskite lattice interface to increase the imprinting.

High-entropy perovskite fluoride ultrasmall nanoparticles embedded in carbon nanofibers enable accelerated redox kinetic for K storage

Ultrasmall high-entropy perovskite fluoride nanoparticles impregnated in carbon nanofibers are prepared by electrospinning and pyrolysis. The unique structure prevents the fluoride conversion reaction and shows a low-strain intercalation mechanism.

Halide exchange mediated cation exchange facilitates room temperature co-doping of d-and f-block elements in cesium lead halide perovskite nanoparticles.

This study presents a halide exchange mediated cation exchange reaction to co-dope d- and f-block elements in CsPbX3 NPs at room temperature. Addition of MnCl2 and YbCl3 to CsPbBr3 NPs induces ion exchange reactions generating the corresponding CsPbBr3/MnCl2YbCl3 NPs. In addition to the perovskite emission, the NPs display sensitized Mn2+ and Yb3+ emissions in concert spanning the UV, visible, and NIR spectral region. Structural and spectroscopic characterizations indicate a substitutional displacement of Pb2+ by the Mn2+ and Yb3+. The identity of the host halide in modulating the ion exchange reactions was also tested. An effective perovskite host NP is presented that can be used to incorporate d-f or f-f dopant combinations to realize a gamut of dopant emission lines. A charge trapping based photophysical model is developed that focuses on rational energy alignments to predict dopant emissions semi-empirically and aids the design of optimal perovskite host-multi-dopant combinations.

Antimicrobial activity of ABO3 perovskite nanoparticles (BNN, SNN, and BSNN) against Bacillus subtilis

Antimicrobial activity of ABO3 perovskite nanoparticles (BNN, SNN, and BSNN) against Bacillus subtilis