Surface Charge Carrier Research Articles

Heterophase homojunction construction by amorphous TiOx and N–TiO2 photoanode for oxygen evolution reaction kinetics and charge carriers’ transportation enhancement

Photoelectrochemical (PEC) water splitting by TiO2 photoanode for clean hydrogen production is limited by the poor charge separation and inert oxygen evolution reaction (OER) kinetics issues for now. In this work, a band-matched heterophase homojunction (TiOx/N–TiO2) by amorphous TiOx and N-doped TiO2 nanotube arrays is constructed by two-step anodic oxidation and impregnation. The photocurrent density of TiOx/N–TiO2 reaches 0.69 mA/cm2 at 1.23 V vs. RHE, which is 1.86 folds than bare TiO2. The enhanced charge carriers' injection/separation efficiency, smaller Tafel slope (37.79 mF dec−1) and larger electrochemical active surface area (ECSA) (1.98 mF cm−2) of TiOx/N–TiO2 indicate that N doping and heterophase homojunction with amorphous TiOx effectively facilitate the surface OER kinetics and charge carriers' transportation. TiOx/N–TiO2 is annealed with a transformation of the surface amorphous TiOx layer into anatase TiO2 (a-TiOx/N–TiO2) to study the role of amorphous TiO2 in PEC water splitting. The photocurrent density and applied bias photon-to-current efficiency (ABPE) for a-TiOx/N–TiO2 decrease, even lower than the pristine TiO2. This is due to the reduction of surface oxygen vacancies, which causes the slowdown of OER kinetics and the weakening of charge carrier transportation ability. That is favorable for a better understanding of the OER kinetics and charge carriers’ transportation enhancement mechanism by the surficial modification on the semiconductor during the PEC water splitting.

Evaluation of the effect of oxygen addition on charge carrier transport properties in single-crystal diamond growth

The effects of oxygen addition during single-crystal diamond growth by microwave plasma CVD method on crystal surface morphology and charge carrier transport properties were evaluated. Diamond single-crystals were homoepitaxially grown on (001) surface of high-pressure and high-temperature (HPHT) synthesized type IIa single-crystal diamond substrates with a fixed methane concentration of 1 % and oxygen concentrations of 0–0.8 %. Inverted pyramid-shaped pits were generated as the oxygen concentration increased. The free exciton recombination emission intensity in the cathodoluminescence spectrum reached a maximum at oxygen concentration of 0.5 %. The samples with oxygen concentrations of 0.5 % and 0.8 % showed excellent charge collection efficiency and energy resolution. On the other hand, the mobility-lifetime (μτ) product was only (7.1 ± 1.7) × 10−5 cm2/V, which is approximately 1/4 of that of the sample with 0.2 % methane and no oxygen addition.

Full-Space Electric Field in Mo-Decorated Zn2In2S5 Polarization Photocatalyst for Oriented Charge Flow and Efficient Hydrogen Production.

Integration of photocatalytic hydrogen (H2) evolution with oxidative organic synthesis presents a highly attractive strategy for the simultaneous production of clean H2 fuel and high-value chemicals. However, the sluggish dynamics of photogenerated charge carriers across the photocatalysts result in low photoconversion efficiency, hindering the wide applications of such a technology. Herein, this work overcomes this limitation by inducing the full-space electric field via charge polarization engineering on a Mo cluster-decorated Zn2In2S5 (Mo-Zn2In2S5) photocatalyst. Specifically, this full-space electric field arises from a cascade of the bulk electric field (BEF) and local surface electric field (LSEF), triggering the oriented migration of photogenerated electrons from [Zn-S] regions to [In-S] regions and eventually to Mo cluster sites, ensuring efficient separation of bulk and surface charge carriers. Moreover, the surface Mo clusters induce a tip enhancement effect to optimize charge transfer behavior by augmenting electrons and proton concentration around the active sites on the basal plane of Zn2In2S5. Notably, the optimized Mo1.5-Zn2In2S5 catalyst achieves exceptional H2 and benzaldehyde production rates of 34.35 and 45.31mmol gcat -1 h-1, respectively, outperforming pristine ZnIn2S4 by 3.83- and 4.15-fold. These findings mark a significant stride in steering charge flow for enhanced photocatalytic performance.

Evidence of topological surface states with upward band bending in (Bi[formula omitted]Sb[formula omitted])[formula omitted]Te[formula omitted] topological insulator

Significant efforts have been put in the past to minimize the bulk conduction to probe the exotic surface states of topological insulators (TIs), nevertheless, the surface transport is usually hindered by the presence of bulk conduction. The identification and separation of the contribution of topological surface states (TSS) by electrical transport is important for understanding the unique properties of TIs and developing new electronic devices based on these materials. In this report we have studied Shubnikov-de Haas (SdH) oscillations, magneto-resistance (MR) and hall resistivity under high magnetic field in (Bi0.45Sb0.60)2Te3 single crystal grown by modified Bridgman method. Our results show the existence of SdH oscillations which arise from TSS. The obtained Fermi wave vector and Fermi velocity of surface charge carriers show a good agreement with those found by angle-resolved photoemission spectroscopy experiments. Two band model fit to hall resistivity confirms the high mobility of surface bands and low mobility of bulk bands. Band bending effect is investigated which exhibits a depletion of carriers from near by bulk towards the surface states resulting in an upward band bending. A large non-saturating MR (∼347)% is observed as a result of multichannel quantum coherent transport mechanism.

Accelerating Surface Reaction Kinetics and Enhancing Bulk as well as Surface Charge Carrier Dynamics in Al/ Al2O3‐Coated BiVO4 Photoanode

AbstractPhotoelectrochemical (PEC) hydrogen evolution from water splitting of semiconductor photoanodes is intricately linked to their light‐absorbing capacity, surface reaction kinetics, bulk charge carrier separation efficiency, and surface charge carrier injection efficiency. Harnessing the surface plasmon resonance effect of metals emerges as a promising approach to enhance PEC performance of semiconductor photoanodes. This work presents the first application of non‐noble metal Al nanoparticles to sensitize a BiVO4 nanoporous film (NPF) photoanode. This process significantly expedites the surface kinetics of water oxidation, and improves both bulk charge carrier separation and surface carrier injection efficiencies of BiVO4 NPF photoanode. Additionally, the surface‐formed Al2O3 film effectively preserves the stability of photoanode, leading to a substantial improvement in PEC hydrogen evolution of BiVO4 NPF photoanode in a three‐electrode PEC cell with sulfite scavenger. The constructed BiVO4/Al NPF heterojunction photoanode exhibits a hydrogen evolution rate of 73.9 µmol cm⁻2 h⁻¹ at 1.23 V versus reversible hydrogen electrode, 1.68 times of BiVO4 photoanode. Additionally, BiVO4/Al NPF photoanode exhibits excellent stability under long‐time light irradiation of 8 h. This study provides valuable insights into the design of nonnoble‐metal‐based plasmonic photoanodes for efficient hydrogen generation through PEC cell from the perspectives of surface reaction kinetics, charge carrier injection, and separation.

Surface charge manipulation for improved humidity sensing of TEMPO-oxidized cellulose nanofibrils

Cellulose-based humidity sensors have attracted great research interest due to their hydrophilicity, biodegradability, and low cost. However, they still suffer from relatively low humidity sensitivity. Due to the presence of negatively charged carboxylate groups, 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO)-oxidized cellulose nanofibril (CNF) exhibits enhanced hydrophilicity and ion conductivity, which is considered a promising candidate for humidity sensing. In this work, we developed a facile strategy to improve the humidity sensitivity of CNF films by regulating their surface charge density. With the increase in surface charge density, both water uptake and charge carrier densities of the CNF films can be improved, enabling a humidity sensitivity of up to 44.5 % (%RH)−1, higher than that of most polymer-based humidity sensors reported in the literature. Meanwhile, the sensor also showed good linearity (R2 = 0.998) over the 15–75 % RH at 1 kHz. With these features, the CNF film was further demonstrated for applications in noncontact sensing, such as human respiration, moisture on fingertips, and water leakage, indicating the great potential of CNF film in humidity monitoring.

A Facile Approach to Develop Polyvinyl Alcohol‐Based Bio‐Triboelectric Nanogenerator Containing Graphene‐ Doped Zinc Oxide Quantum Dots

This article presents an environmentally friendly, low‐cost polymer nanocomposite, polyvinyl alcohol/sodium alginate‐graphene‐zinc oxide (PVA‐SA/G‐ZnO) based triboelectric nanogenerator by spin coating. ZnO quantum dots of average particle size <10 nm and the graphene oxide (GO)‐doped ZnO are synthesized by co‐precipitation following ageing. ZnO and G‐ZnO particles are filled into the PVA/SA blend system using the solution mixing method. Spin‐coated films of ≈1.2 μm and casted films of 120 μm thicknesses were used to prepare triboelectric nanogenerators (TENGs) to test the output voltage performances. Irrespective of the thickness values, the films gave similar voltage responses with contact electrification. This illustrates triboelectric power generation as a surface charge carrier phenomenon based on morphological analyses by scanning electron microscope (SEM) and atomic force microscopy (AFM). The maximum output voltage of 0.24 V was approximately 5 times higher for the PVA/SA composite containing 2 wt% G‐ZnO nanomaterials compared to the neat polymer are obtained. The nanocomposites also demonstrate excellent dielectric constant (22 times higher) values, suggesting the role of the biodegradable thin‐film TENGs in various self‐powering devices.

PH-Dependent photocatalytic performance of faceted BiOBr semiconductor particles in degradation of dyes

Bismuth oxyhalides, such as bismuth-oxy-bromide (BiOBr), show high performance in photocatalytic oxidation of water pollutants. Process conditions, and in particular the pH of the solution, largely affect the photocatalytic efficacy, which is fundamentally poorly understood. We prepared {001} faceted bismuth-oxy-bromide (BiOBr), and determined by advanced AFM analysis that the surface charge of the {001} facet of BiOBr is slightly positive at acidic pH (pH 3) and significantly negative and increasing in negative surface charge in the order pH 6 < pH 9. Decomposition of MB or RhB by illumination of BiOBr is strongly favored by basic conditions (pH 9-10), as evident from discoloration experiments, and determination of the TOC as a function of time of illumination. Reference experiments show the pH dependent degradation profiles cannot be explained by differences in quantities of adsorption of the dye, but rather by the lifetime and/or quantity of BiOBr related photoexcited (surface) charge carriers (holes and electrons) – correlating with surface charge. Using MeOH and other scavengers, we show oxidation of MB or RhB is mainly induced by superoxide anions (•O2− radicals) at low pH and by holes or hydroxyl radicals at high pH – in agreement with surface charge induced band bending. This study provides novel understanding of the pH dependence of the rates of photocatalytic degradation of dyes using BiOBr photocatalysts.

Room temperature persisting surface charge carriers driven by intense terahertz electric fields in a topological insulator Bi2Se3

Topologically protected surface current is highly promising for next-generation low-dissipation and disorder-tolerant quantum electronics and computing. Yet, electric transport from the co-existing bulk state dominates the responses of the Dirac surface state, especially at elevated temperatures relevant to technological applications. Here, we present an approach that convincingly showcases the generation, disentanglement, and precise control of enduring surface charge carriers on a topological insulator, Bi2Se3, with high bulk conductivity, all achieved at room temperature. By using pump–probe modulation spectroscopy under ultrabroadband driving tunable from 4 meV to 1.55 eV, we show the terahertz (THz) field-induced surface carriers by discovering their initial temporal responses dominant over high density trivial bulk carriers. Strikingly, the response of the induced surface carrier responses persists for more than ∼5 ps and is enhanced by reducing pump photon energy. The dynamics and lifetime of the distinct surface response manifest themselves as the enhanced THz pump-induced THz transmission, which directly correlates with the transient negative THz conductivity. Increasing the THz driving field reduces the induced surface carrier lifetime and identifies, particularly, an optimal pump field of Es ∼ 224 kV cm−1 for generating the dominant surface response relative to the bulk. This surface carrier dominant regime is suppressed by a joint effect of enhanced surface-bulk scattering and a more rapid saturation of surface excitation compared to the bulk that sets in above Es. The controllability of room temperature topologically surface carriers through pump photon energy offer compelling possibilities for extending this approach to other topological complex materials.

Thermal and electrostatic tuning of surface phonon-polaritons in LaAlO3/SrTiO3 heterostructures

Phonon polaritons are promising for infrared applications due to a strong light-matter coupling and subwavelength energy confinement they offer. Yet, the spectral narrowness of the phonon bands and difficulty to tune the phonon polariton properties hinder further progress in this field. SrTiO3 – a prototype perovskite oxide - has recently attracted attention due to two prominent far-infrared phonon polaritons bands, albeit without any tuning reported so far. Here we show, using cryogenic infrared near-field microscopy, that long-propagating surface phonon polaritons are present both in bare SrTiO3 and in LaAlO3/SrTiO3 heterostructures hosting a two-dimensional electron gas. The presence of the two-dimensional electron gas increases dramatically the thermal variation of the upper limit of the surface phonon polariton band due to temperature dependent polaronic screening of the surface charge carriers. Furthermore, we demonstrate a tunability of the upper surface phonon polariton frequency in LaAlO3/SrTiO3 via electrostatic gating. Our results suggest that oxide interfaces are a new platform bridging unconventional electronics and long-wavelength nanophotonics.

Distinctive Electric Properties of Group 14 Oxides: SiO2, SiO, and SnO2

The oxides of group 14 have been widely used in numerous applications in glass, ceramics, optics, pharmaceuticals, and food industries and semiconductors, photovoltaics, thermoelectrics, sensors, and energy storage, namely, batteries. Herein, we simulate and experimentally determine by scanning kelvin probe (SKP) the work functions of three oxides, SiO2, SiO, and SnO2, which were found to be very similar. Electrical properties such as electronic band structure, electron localization function, and carrier mobility were also simulated for the three crystalline oxides, amorphous SiO, and surfaces. The most exciting results were obtained for SiO and seem to show Poole–Frankel emissions or trap-assisted tunneling and propagation of surface plasmon polariton (SPP) with nucleation of solitons on the surface of the Aluminum. These phenomena and proposed models may also describe other oxide-metal heterojunctions and plasmonic and metamaterials devices. The SiO2 was demonstrated to be a stable insulator interacting less with the metals composing the cell than SnO2 and much less than SiO, configuring a typical Cu/SiO2/Al cell potential well. Its surface charge carrier mobility is small, as expected for an insulator. The highest charge carrier mobility at the lowest conduction band energy is the SnO2’s and the most symmetrical the SiO’s with a similar number of electron holes at the conduction and valence bands, respectively. The SnO2 shows it may perform as an n-type semiconductor.

Simultaneous removal of Cr(Ⅵ) and tetracycline from wastewater by dielectric barrier discharge plasma coupled with TiO2/rGO/Cu2O composites: Performance and mechanism

In this study, dielectric barrier discharge (DBD) plasma combined with titanium dioxide/reduced graphene oxide/copper oxide (TiO2/rGO/Cu2O) composites for simultaneous removal of hexavalent chromium (Cr(Ⅵ)) and tetracycline (TC) from wastewater were explored systematically. The TiO2/rGO/Cu2O composites were successfully prepared to improve the specific surface area and charge carrier separation rate. When Cr(Ⅵ) and TC coexist, the two pollutants have better removal efficiency without changing the initial pH. Moreover, the removal efficiency of Cr(Ⅵ) and TC could be further improved in the DBD-TiO2/rGO/Cu2O system, indicating that the TiO2/rGO/Cu2O composites also exhibited good synergistic effects with the DBD plasma. The mechanism exploration showed that the TiO2/rGO/Cu2O composite catalyst could be activated in DBD system to produce various active species by photocatalytic reaction, among which photo-generated electrons and •O2− could significantly enhance Cr(Ⅵ) reduction, while photo-generated holes and •OH could improve TC degradation. More importantly, the intermediate products obtained from TC degradation can be oxidized to •CO2− by photo-generated holes, which can also facilitate the reduction of Cr(Ⅵ). This study shows that DBD combined with TiO2/rGO/Cu2O composites are capable of simultaneous Cr(Ⅵ) reduction and TC degradation, which would provide novel ideas for practical wastewater remediation.

Revealing ppb order NO2 adsorption capability of 2D/0D p-p heterojunctions based on Sb/SnS nanocomposite

Highly sensitive p-p heterojunction-based gas sensors have a lot of promise in the field of trace gas detection. The ability to detect ppb-order NO2 reliably is critical for environmental monitoring, yet it is still a difficulty. In this work, we demonstrate the ultrasensitive p-p heterostructures based on Sb/SnS novel architect to detect the ppb order of NO2 gas at room temperature. The incorporation of 0D SnS QDs in Sb sheet enhanced the gas-capturing capability of nanomaterial. SnS-doped Sb outperformed state-of-art Sb-based NO2 sensor with a huge response of 0.13 at 75 ppb of NO2 and a limit of detection (LOD) of 15.2 ppb with an average power consumption of 1.49 nW. In comparison to other gases, the selectivity results show that Sb/SnS have the highest sensor response (1.73 ppm−1) to NO2. The enhanced NO2 gas sensing mechanism of Sb/SnS QDs is explained briefly, which is due to the enrichment of its surface charge carrier on the surface of the Sb/SnS sample as confirmed by the DFT simulations results. Our findings might be used to develop alternative p-p heterojunction-based novel architects for gas sensors and other applications.

Regulating Charge Carrier Dynamics in Stable Perovskite Nanorods for Photo-Induced Atom Transfer Radical Polymerization.

Semiconducting nanocrystals have attracted world-wide research interest in artificial photosynthesis due to their appealing properties and enticing potentials in converting solar energy into valuable chemicals. Compared to 0D nanoparticles, 1D nanorods afford long-distance charge carriers separation and extended charge carriers lifetime due to the release of quantum confinement in axial direction. Herein, stable CsPbBr3 nanorods of distinctive dimensions are crafted without altering their properties and morphology via grafting hydrophobic polystyrene (PS) chains through a post-synthesis ligand exchange process. The resulting PS-capped CsPbBr3 nanorods exhibit a series of enhanced stabilities against UV irradiation, elevated temperature, and polar solvent, making them promising candidates for photo-induced atom transfer radical polymerization (ATRP). Tailoring the surface chemistry and dimension of the PS-capped CsPbBr3 nanorods endows stable, but variable reaction kinetics in the photo-induced ATRP of methyl methacrylate. The trapping-detrapping process of photogenerated charge carriers lead to extended lifetime of charge carriers in lengthened CsPbBr3 nanorods, contributing to a facilitated reaction kinetics of photo-induced ATRP. Therefore, by leveraging such stable PS-capped CsPbBr3 nanorods, the effects of surface chemistry and charge carriers dynamics on its photocatalytic performance are scrutinized, providing fundamental understandings for designing next-generation efficient nanostructured photocatalyst in artificial photosynthesis and solar energy conversion.

Single-Atom Pt Doping Induced p-Type to n-Type Transition in NiO Nanosheets toward Self-Gating Modulated Electrocatalytic Hydrogen Evolution Reaction.

Exploring highly efficient single atom catalysts with defined active centers and tunable electronic structures is highly desirable. Herein, we developed an efficient hydrogen evolution reaction (HER) electrocatalyst through a self-gating phenomenon induced by Pt single atoms (SAs) supported on ultrathin NiO nanosheets (PtSA-NiO). The Ni atoms in NiO are partially replaced by the atomically dispersed Pt atoms, leading to a transition from p-type NiO into n-type PtSA-NiO. When the n-type PtSA-NiO serves as HER electrocatalyst, the self-gating phenomenon occurs in the ultrathin nanosheets, resulting in a mixture of leakage ("active") and metal-insulator-semiconductor ("inert") regions. The "inert" region induced by the ionic gating and reverse potential is capable of accumulating relatively high surface charge carrier concentration with an ultrahigh electric field, making the PtSA-NiO highly conductive; meanwhile, the HER process occurs at the Pt SAs sites (active region) in the PtSA-NiO nanosheets. As a result, the PtSA-NiO requires only 55 mV to deliver 10 mA/cm2 in an alkaline solution with good stability.

Bias-voltage photoconductance and photoluminescence for the determination of silicon-dielectric interface properties in SiO2/Al2O3 stacks

This paper presents an advanced measurement method for controlling the surface charge carrier density of passivated silicon wafers during photoconductance and photoluminescence measurements, by employing semitransparent poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) electrodes with an applied bias voltage. This is employed to study and analyze charge carrier dynamics in dielectric layers by measuring their direct influence on effective lifetime. With this method, the carrier population at the surface and the effective carrier lifetimes of n- and p-type samples can be investigated, from which the fixed charge carrier density Qf of the passivation can be extracted. Additionally, the defect density Dit can also be derived from the minimum lifetime values at flatband voltage. In SiO2/Al2O3 stacks with varying SiO2 interlayer thickness, it was shown that by changing the SiO2 thickness, the carrier density Qf can be tuned to a wide range of values, which corresponds to the results obtained in other studies. An increase in interlayer thickness resulted in a decrease in Qf. Varying the SiO2 thickness, the behavior of the respective effective lifetime under bias voltage also changes, exhibiting hysteresis-like effects, which are attributed to additional charges getting trapped at the surface during bias-voltage application. This effect is much more pronounced for samples with a thinner SiO2 layer as well as for the n-type samples. Additionally, the doping type also influences the magnitude of Qf, with p-type samples generally reaching lower absolute values. It was also shown that aging of the samples had a significant effect on the measured Qf, which was increased compared to the initial Qf of the passivation. This effect was more pronounced for the n-type samples. The measurements were realized by a cost-effective and easy-to-use microcontroller-based potentiostat, which can be used as a simple add-on to existing photoconductance or photoluminescence measurement setups.

Surface conductivity in SmB6

We present a study of low temperature electron transport (resistivity, magnetoresistance and Hall coefficient) in SmB6 single crystals having different polar (100) and nonpolar (110) and (111) surfaces after mechanical polishing and chemical etching. The estimation of effective parameters for surface and bulk charge carriers allows us to conclude that surface conductivity is very sensitive to the method of surface treatment. The most pronounced change is observed for the polar (100) surface, for which the related Hall concentration of charge carriers at 2 K decreases more than by 2 orders of magnitude and the Hall mobility increases by a factor of 15 after etching these faces in diluted nitric acid. We suggest that the strong dependence of surface properties on the type of treatment may result from both topological protection, which is influenced by intrinsic defects or surface reconstruction, and band bending effects, which modulate the properties of the surface conduction layer in case of polar faces.

Promoting the BiVO4 Photoanode Solar Water Oxidation Performance by Coating Hole-Blocking and Oxygen Evolution Layers

Bismuth vanadate (BiVO4)-based photoelectrochemical (PEC) water-splitting is a propitious technique for green fuel production, while the high surface charge carrier recombination and sluggish oxygen production kinetics limits its practical applications. Herein, we discuss the favorable impacts of grafting a hole-blocking SnO2 layer as an inner layer onto the fluorine-doped tin oxide and an oxygen evolution N-FeCoOx layer on BiVO4 photoanodes. Interestingly, the optimized SnO2@BiVO4/N-FeCoOx photoanode demonstrates an exceptional photocurrent density of 4.6 mA cm–2 at 1.23 V versus reversible hydrogen electrode under AM 1.5 G illumination, accompanied by the long-term stability up to 10 h. More specifically, the synergistic effect of both hole-blocking as well as oxygen evolution layers promotes the interfacial charge separation, transport, and PEC stability. Altogether, this work offers a simple and effective approach for constructing highly efficient photoanodes for PEC water splitting.

Photocatalytic Organic Contaminant Degradation of Green Synthesized ZrO2 NPs and Their Antibacterial Activities

The green synthesis of metal oxide nanoparticles is an efficient, simple, and chemical-free method of producing nanoparticles. The present work reports the synthesis of Murraya koenigii-mediated ZrO2 nanoparticles (ZrO2 NPs) and their applications as a photocatalyst and antibacterial agent. Capping and stabilization of metal oxide nanoparticles were achieved by using Murraya koenigii leaf extract. The optical, structural, and morphological valance of the ZrO2 NPs were characterized using UV-DRS, FTIR, XRD, and FESEM with EDX, TEM, and XPS. An XRD analysis determined that ZrO2 NPs have a monoclinic structure and a crystallite size of 24 nm. TEM and FESEM morphological images confirm the spherical nature of ZrO2 NPs, and their distributions on surfaces show lower agglomerations. ZrO2 NPs showed high optical absorbance in the UV region and a wide bandgap indicating surface oxygen vacancies and charge carriers. The presence of Zr and O elements and their O=Zr=O bonds was categorized using EDX and FTIR spectroscopy. The plant molecules’ interface, bonding, binding energy, and their existence on the surface of ZrO2 NPs were established from XPS analysis. The photocatalytic degradation of methylene blue using ZrO2 NPs was examined under visible light irradiation. The 94% degradation of toxic MB dye was achieved within 20 min. The antibacterial inhibition of ZrO2 NPs was tested against S. aureus and E. coli pathogens. Applications of bio-synthesized ZrO2 NPs including organic substance removal, pathogenic inhibitor development, catalysis, optical, and biomedical development were explored.

Microstructure and photocatalytic activity of SnO2:Bi3+ nanoparticles

SnO2:Bi3+ nanoparticles were synthesized by a one-step hydrothermal method. The influence of Bi3+ impurity concentrations on SnO2:Bi3+ samples was deeply investigated by studying the changes in size, morphology, and band gap width of SnO2:Bi3+ materials. In addition, the interaction between the SnO2 crystalline host and Bi3+ was studied in detail by several characterization techniques, such as SEM, XRD, UV–Vis, PL, and EPR. We also investigated the photocatalytic activity of the SnO2:Bi3+ nanoparticles by photodegrading methylene blue (MB), rhodamine B (RhB), and phenol under visible light. The photocatalytic efficiency of the SnO2:Bi3+ nanoparticles was higher than that of pure SnO2 nanoparticles. The photocatalytic degradation efficiency of SnO2:Bi3+-2% for MB was up to 52% and 15%–20% for the other samples. The photocatalytic degradation efficiency of SnO2:Bi3+-2% for RhB is up to 65% and that of the remaining samples is 25%–46%. The high degradation efficiency of the SnO2:Bi3+-2% sample was due to its small crystal size, which increased the specific surface area, resulting in higher photocatalytic efficiency. In addition, the high photocatalytic efficiency of the SnO2:Bi3+-2% sample is related to the defect states, increasing the surface charge carrier transfer rate and reducing the electron–hole recombination rate. Meanwhile, the photocatalytic efficiency of the SnO2:Bi3+ nanoparticles for phenol is 41% and 43% with SnO2:Bi3+-6% and −8% samples, respectively, and that of the remaining samples is 32%–34%. This finding is explained by the interaction between Bi3+ ions and phenol molecules, increasing the photocatalytic efficiency. This work increases the feasibility of degrading environmental pollutants using SnO2:Bi3+ photocatalysts with high efficiency.