Harnessing ZnCr2O4/g-C3N4 nanosheet heterojunction for enhanced photocatalytic degradation of rhodamine B and ciprofloxacin.

Utilizing semiconductors for photocatalytic processes in water bodies as an approach to environmental remediation has gained considerable attention. Theoretical band position calculations revealed a type-II step-scheme charge flow mechanism for ZnCr2O4/g-C3N4 (ZCr/gCN), emphasizing effective heterojunction formation due to synergies between the materials. A composite of agglomerated nanoparticle ZnCr2O4 (Zinc chromium oxide - ZCr)/g-C3N4 (graphitic carbon nitride - gCN) nanosheets was synthesized using the ultrasonication and leveraging the heterojunction to enhance degradation efficiency and active sites participation. The synthesized sample was characterized by XRD, XPS, FTIR, BET, HRSEM, EDX, HRTEM, EIS PL, and UV-visible spectroscopy. XRD analysis confirmed the successful formation of pure ZnCr2O4, g-C3N4 (gCN), and their composite without any secondary phases. Optical investigations demonstrated a red shift (444-470 nm) in UV-visible spectra as ZnCr2O4 content increased. Morphological assessment via HRSEM unveiled agglomerated nanoparticle and nanosheet structures. FTIR analysis indicated the presence of gCN with the tri-s-triazine breathing mode at 807 cm-1, and the identification of octahedral Zn-O (598.11 cm-1) and tetrahedral Cr-O (447.01 cm-1) metal bonds within the spinel structure of ZnCr2O4. A Surface area of 134.162 m2/g was noticed with a microporous structure of pore radius 1.484 nm. Notably, the 15% ZCr/gCN composite achieved a remarkable 93.94 % (Rhodamine B-RhB) and 74.36 % (Ciprofloxacin - CIP) within 100 and 120 min, surpassing the performance of pure gCN. Improved degradation was attributed to higher charge separation (photo-excited electrons and holes), reducing charge recombination, as supported by photoluminescence and photoelectrochemical analyses. The presence of active species like superoxide during degradation was confirmed through a scavenger test. The stability analysis confirms the sample's stable nature (without secondary phase formation) after degradation. This work underscores the potential of ZnCr2O4 based metal-free compounds intended for effective environmental remediation.

Ultrasensitive and reversible NO2 gas sensor based on SnS2/TiO2 heterostructures for room temperature applications.

Nitrogen dioxide (NO2) is one of the toxic gases produced by chemical industries, power plants, and vehicles. In this work, we demonstrate an inexpensive sensing platform for NO2 detection at room temperature (RT-32 °C) based on a charge transfer mechanism. Three-dimensional hierarchical SnS2 and SnS2/mesoporous TiO2 nanocomposites were synthesized via the solvothermal method. SnS2/20 wt% mesoporous TiO2 nanocomposites sample showed 245.4% enhanced response compared to pristine SnS2. The fabricated device exhibits excellent selectivity among all other interfering gases with one-month stability. The rapid response and enhanced response achieved were obtained for the minimum concentration of 2 ppm NO2. The formation of heterojunction between SnS2 and mesoporous TiO2 has a synergetic effect, providing more active sites and porous structures for the detection of NO2 gas molecules.

Unleashing the room temperature boronization: Blooming of Ni-ZIF nanobuds for efficient photo/electro catalysis of water.

Water splitting provides an environmental-friendly and sustainable approach for generating hydrogen fuel. The inherent energetic barrier in two-core half reactions such as the Hydrogen Evolution Reaction (HER) and Oxygen Evolution Reaction (OER) leads to undesired increased overpotential and constrained reaction kinetics. These challenges pose significant challenges that demand innovative solutions to overcome. One of the efficient ways to address this issue is tailoring the morphology and crystal structure of metal-organic frameworks (MOF). Nickel Zeolite Imidazolate Framework (Ni-ZIF) is a popular MOF and it can be tailored using facile chemical methods to unleash a remarkable bifunctional electro/photo catalyst. This innovative solution holds the capability to address prevailing obstacles such as inadequate electrical conductivity and limited access to active metal centers due to the influence of organic ligands. Thereby, applying boronization to the Ni-ZIF under different duration, one can induce blooming of nanobuds under room temperature and modify oxygen vacancies in order to achieve higher reaction kinetics in electro/photo catalysis. It can be evidenced by the 24-h boronized Ni-ZIF (BNZ), exhibiting lower overpotentials as electrocatalyst (OER-396 mV & HER-174 mV @ 20 mA/cm2) in 1 M KOH electrolyte and augmented gas evolution rates when employed as a photocatalyst (Hydrogen-14.37 µmol g-1min-1 & Oxygen-7.40 µmol g-1min-1). The 24-h boronization is identified as the optimum stage of crystalline to amorphous transformation which provided crystalline/amorphous boundaries as portrayed by X-Ray diffraction (XRD) and High Resolution-Transmission Electron Microscopy (HR-TEM) analysis. The flower-like transformation of 24-BNZ, characterized by crystalline-amorphous boundaries initiates with partial disruption of Ni-N bonds and formation of Ni-B bonds as evident from X-ray Photoelectron Spectroscopy (XPS). Further, the 24-h BNZ exhibit bifunctional catalytic activities with pre-longed stability. Overall, this work presents a comprehensive study of the electrocatalytic and photocatalytic water splitting properties of the tailored Ni-ZIF material.

Interface engineering of heterogeneous NiMn layered double hydroxide/vertically aligned NiCo2S4 nanosheet as highly efficient hybrid electrocatalyst for overall seawater splitting.

We report the fabrication of a heterogeneous catalyst through vertically aligned NiCo2S4/Ni3S2 nanosheet with encapsulation of ultrathin NiMn layered double hydroxide over self-standing nickel foam (NM/NCS/NS/NF) via two-step hydrothermal processes. Benefiting from more adequate catalytic active centres and copious interfacial charge transfer channels, NM/NCS/NS/NF electrode demonstrates superior bifunctional activity for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) processes under alkaline fresh/simulated seawater electrolyte conditions. As a result, NM/NCS/NS/NF electrode requires the smallest overpotentials of 282 & 312 mV (OER) and 171 & 204 mV (HER) to attain current densities of 30 & 50 mA cm-2 respectively under alkaline simulated seawater electrolyte conditions. Besides, the presence of amorphous NiMn LDH layers over crystalline NiCo2S4/Ni3S2 catalyst stimulates surface adsorption of oxygen intermediate species, water dissociate ability on catalytic active centres, and mass transport with electron transfer at the interface. Further, the two-electrode configuration assisted electrolyser system delivers an efficient overall water splitting activity with minimum cell voltages of 1.54 V (in 1 M KOH) and 1.56 V (in 1 M KOH+0.5 M NaCl) at a current density of 10 mA cm-2. Besides, a fabricated electrolyser cell provides a more sustained water electrolysis process and robust durability for 20 h which displays NM/NCS/NS/NF electrode is a vibrant and potential candidate for realistic seawater electrolysis. Therefore, our proposed heterogeneous electrocatalyst could open up a new platform for developing efficient large-scale efficient seawater electrolysis.

Solvent-assisted synthesis of Ag2Se and Ag2S nanoparticles on carbon fabric for enhanced thermoelectric performance.

The challenge of developing low-cost, highly flexible, and high-performance thermoelectric (TE) materials persists due to the low thermoelectric efficiency of conducting polymers and the inflexibility of inorganic materials. In this study, we successfully integrated Ag2Se and Ag2S with highly conductive carbon fabric (CF) to produce a flexible thermoelectric material. A facile one-step solvothermal method was employed to synthesize the Ag2Se-CF and Ag2S-CF, which were then subjected to X-ray analysis to confine the phase formation of Ag2Se and Ag2S on the carbon fabric. The analysis revealed that Ag2Se and Ag2S nanoparticles were tightly packed on the surface of carbon fabric, and compositional analysis confirmed the interaction between the material and carbon fabric. The thermoelectric properties of Ag2Se-CF and Ag2S-CF were significantly altered due to carrier concentration and mobility variations, resulting in a low power factor of 6.7 µW/mK2 for Ag2Se-CF and a high-power factor of 24 µW/mK2 at 373 K for Ag2S-CF. The growth of Ag2Se-CF and Ag2S-CF on carbon fabric led to an enhancement in their thermoelectric properties. Further, TE legs were fabricated using the Ag2Se-CF (p-type) and Ag2S-CF (n-type), and the fabricated legs exhibited an output voltage of âˆ¼20 mV to âˆ¼86.65 mV at a temperature gradient (ΔT) of 3-8 K. This work represents a cutting-edge approach to the fabrication of high-performance, wearable thermoelectric devices.

Ultra-high power factor of p-type Bi2Se3 for room-temperature thermoelectric applications.

Achieving high zT in n-type and p-type thermoelements in similar compounds is a great challenge for device construction. Herein, we report a high-power factor of 480 µW/mK2 in Ga and Mn co-doped Bi2Se3 along with a maximum zT of 0.25 at 303 K as a p-type thermoelement. The co-doped Ga and Mn play distinct roles in enhancing the hole concentration to 1.6 × 1019 cm-3 with a maximized effective mass. In addition, a drastic reduction in lattice thermal conductivity of 0.5 W/mK is attained due to point defects of mass and strain field fluctuation scattering in Bi2Se3.

Small polaron hopping conduction mechanism and enhanced thermoelectric power factor in the perovskite LaCoO3 ceramic.

Among the various thermoelectric oxide materials, perovskites offer more flexibility to adjust the interdependent thermoelectric parameters for an improved thermoelectric performance. In this work, we investigated the effect of A-site cation deficiency and Sr-substitution on the thermoelectric properties of the LaCoO3 ceramic synthesized via a solid-state reaction. A rhombohedral crystal structure with the R3̄c space group was revealed through Rietveld refinement of the XRD data. XPS analysis further confirmed the presence of multiple oxidation states of Co, and the mechanism of charge transport involving these multivalent cations was described using the small polaron hopping model. The La deficiency and Sr-substitution were found to increase the electrical conductivity in the LCO1 and LCO2 compositions, which resulted in a significant increase in the thermoelectric power factor. It was found that the increase in electrical conductivity of LCO1 and LCO2 was caused by a substantial reduction in the activation energy barrier for small polaron hopping conduction and an increase in fractional polaron concentration. The maximum power factor value of 78 µW m-1 K-2 was observed for the LCO2 composition at 403 K.

Realization of an ultra-low lattice thermal conductivity in Bi2AgxSe3 nanostructures for enhanced thermoelectric performance.

Bismuth Selenide is a Tellurium free topological insulator in V-VI compounds with an excellent thermoelectric performance from room temperature to mid-temperature region. Herein, hydrothermally prepared polycrystalline Bi2AgxSe3 nanostructures have been reported for thermoelectric application. The crystal structure identification and morphology with the elemental presence were analyzed by XRD (X-ray diffraction), HR-SEM with EDS (High resolution scanning electron microscope with energy dispersive X-ray), and HR-TEM (High-resolution transmission electron microscope) measurements. The reduced lattice thermal conductivity and enhanced electrical transport properties synergistically boost the thermoelectric properties through the highly-dense stacking faults with the presence of dislocations. The IFFT (Inverse Fast Fourier Transform) pattern reveals the existence of stacking faults and dislocations. These highly dense stacking faults and dislocations act as active phonon scattering centers, which can contribute to effective phonon scattering resultsin extremely low lattice thermal conduction of 0.3 W/mK at 543 K. On the other hand, the involvement of phonon-phonon scattering primarily reduced the lattice thermal conductivity at elevated temperatures. In addition, phonon-carrier scattering was less compared to phonon-phonon scattering at elevated temperature region. Moreover, the enhancement of electrical conductivity and controlled reduction of the Seebeck coefficient plays a vital role in achieving the maximum power factor of 335 µW/mK2 at 543 K due to the energy filtering effect. The synergistic combination of low thermal conduction and the maximum power factor helps to achieve the high peak zT of 0.3 at 543 K.

Enhancement of thermoelectric power factor via electron energy filtering in Cu doped MoS2 on carbon fabric for wearable thermoelectric generator applications.

The design and construction of state-of-the-art wearable thermoelectric materials are important for the development of self-powered wearable thermoelectric generators (WTEGs). Molybdenum disulfide (MoS2) has been reported as a noteworthy thermoelectric (TE) material because of its large intrinsic bandgap and high carrier mobility. In this work, Cu-doped two-dimensional layered MoS2 nanosheets were grown on carbon fabric (CF) via a hydrothermal method. The electrical conductivity, Seebeck coefficient, and power factor for the Cu-doped MoS2 were found to increase with increasing temperature. The maximum Seebeck coefficient was obtained for a MoS2 sample doped with 4 at% of Cu (CM4) was ∼10 µV/K at 303 K and ∼13 µV/K at 373 K. The enhancement in the Seebeck coefficient was attributed to an energy-filtering effect caused by the interfacial barrier between MoS2 and Cu. In addition, a thermoelectric device was designed with four pairs of TE materials, where CM4 (4 at%) was used as a p-type material and Cu wire was used as an n-type material. These p- and n-type materials were connected electrically in series and thermally in parallel to generate a voltage of 190.7 µV at a temperature gradient of 8 K.

Investigation of non-covalent interactions in Polypyrrole/Polyaniline/Carbon black ternary complex for enhanced thermoelectric properties via interfacial carrier scattering and π-π stacking.

The thermoelectric (TE) performance of conducting polymers can be improved by the incorporation of carbon nanomaterials. In this work, the impact of carbon black (CB) on polypyrrole (PPy) and polypyrrole/polyaniline (PPy/PANI) binary composite have been investigated. Herein, PPy/PANI binary composite was initially prepared through chemical oxidative polymerization and then solution mixed with CB to form PPy/PANI/CB ternary nanocomposite. The structural and morphological analyses confirmed the formation of composites, and the strong interaction present between polymer matrix and CB. This was further confirmed by theoretical study, which showed strong noncovalent interaction and high complex stability between the materials. The thermoelectric results showed that both the electrical conductivity (σ) and Seebeck coefficient (S) has been increased with the increase in CB content (from 10 wt% to 30 wt%) and temperature (303 K to 373 K), while the thermal conductivity (κ) increase was low. The ternary nanocomposite involving 30 wt% of CB was found to be the most promising material which showed an enhanced power factor (PF) of 0.0251 µW/mK2 and high figure of merit (ZT) of 4.37x10-5 at 370 K. The enhancement in ZT for PPy/PANI/CB ternary composite is 2 times, 316 times, 17.3 times, 3.97 times, 11.7 times, and 6.8 times greater than other samples. The enhancement in power factor and ZT was due to energy filtering effect and strong non-covalent interactions between the homopolymers and CB.

Structural formation of multifunctional NiMoO4 nanorods for thermoelectric applications.

We report on the synthesis and characterization of NiMoO4 (NMO) nanorods via the hydrothermal method. The High-Resolution Scanning Electron Microscopy (HRSEM) image reveals the nanorod morphology of NMO. The formation of mixed phase α,ß-NMO is confirmed and the crystallite size of the nanorods is measured to be 40 nm from the XRD data. The structural formation of NMO is confirmed by Raman, FTIR, and XPS. The content of Ni, Mo and O was identified from XPS. NMO is optically active in the visible region with the band gap of 3.085 eV. The presence of four oxygen anions in the chemical formula gives the maximum electrical resistivity of 102 Ω m at 313 K and the material exhibits n-type semiconducting nature which is observed through Seebeck measurement and the Hall coefficient. The n-type semiconducting properties are observed due to the material being richer in Mo than Ni. The attained maximum Seebeck value of -159.723 µV K-1 at 513 K is comparable with that of other good thermoelectric materials at low temperatures. A decrease in the value of thermal conductivity was observed as a function of increasing temperature; NMO has the minimum thermal conductivity of 3.851 W m-1 K-1 at 513 K.

Boosting the energy density of supercapacitors by constructing hybrid molybdenum disulphide nanostructures as a highly durable novel electrode.

Hierarchical MoO3@MoS2/rGO nanocomposites with highly active sites deliver high power density and energy density are fabricated here by using a simple two-step process, the first one is a direct anion-exchange reaction of the inorganic MoO3 nanorods (NRs) for growth of few-layered MoS2 nanosheets in a perpendicular direction and other is the composition of rGO sheets with core-shell MoO3@MoS2. Interestingly, how the modification of hybrid solvent in the anion-exchange mechanism and the concentration of thiourea impact on the morphologies of core-shell MoO3@MoS2 at quantum level have been inspected. A fruitful synergistic effect between MoO3/MoS2 core-shell nanostructures and rGO nanosheets led to a high surface area and transporting properties are inspected obviously through fundamental studies. Therefore, in eventual, this novel and more active sites MoO3@MoS2/rGO hierarchical structures material has delivered an outstanding specific capacitance of 525.06F/g at 4 A/g when used as an electrode in supercapacitor and more importantly good stability (80.6% at 10 A/g) even after 1000 successive cycles has been procured in an electrode in which MoS2 shell layer prepared at 5 mmol thiourea ratio.

Synergistic effect of grain boundaries and phonon engineering in Sb substituted Bi2Se3 nanostructures for thermoelectric applications.

Phonon scattering by intrinsic defects and nanostructures has been the primary strategy for minimizing the thermal conductivity in thermoelectric materials. In this work, we present the effect of Isovalent substitution as a method to decouple the Seebeck coefficient and the thermal conductivity of antimony (Sb) substituted bismuth selenide (Bi2Se3). Transmission electron microscopy studies present the nanostructured Bi2-xSbxSe3 thermoelectric system represents the coexistence of hierarchical defect structure and dislocations. The observed giant reduction in thermal conductivity is due to the multi-scale phonon scattering caused by a combination of stacking faults, lattice dislocations and grain boundary scattering. This study reveals that a large number of dislocations about ∼1.09 × 1016 m-2 are particularly effective at lowering thermal conductivity. We achieved one of the ultra-low thermal conductivity values (∼0.26 W/m K) for the maximized dislocation concentration. Moreover, Isovalent substitution provides a new avenue for the reduction in thermal conductivity and significant enhancement in the Seebeck coefficient of thermoelectric materials.

Suppression of intrinsic thermal conductivity in Sr1-x Gd x TiO3 ceramics via phonon-point defect scattering for enhanced thermoelectric application.

A substantial reduction in the thermal conductivity for strontium titanate (ABO3) perovskite structure was realized for the A-site substitution of gadolinium (rare earth element) in SrTiO3 ceramics. The effect of Gd3+ substitution on the structure, composition, and thermoelectric properties of SrTiO3 was investigated. The substitution of Gd3+ in the SrTiO3 matrix resulted in the minimalization of thermal conductivity. The thermal conductivity followed a similar trend as that of thermal diffusivity, but specific heat capacity exhibited a non-monotonic trend. The thermal conductivity is reduced to 1.05 W m-1 K-1 for the minimal substitutional composition (Sr0.99Gd0.01TiO3) which is 30% less than that of SrTiO3 at 303 K. The variation in the ionic radii and atomic mass of the heavier rare earth Gd3+ substituted over Sr2+ resulted in the reduction of thermal conductivity of SGTO ceramics caused by the corresponding boundary scattering at low temperatures and temperature-independent phonon-impurity scattering at high temperatures.

Fabrication of novel hybrid Z-Scheme WO3@g-C3N4@MWCNT nanostructure for photocatalytic degradation of tetracycline and the evaluation of antimicrobial activity.

Exploring highly efficient visible-light-driven photocatalyst for the elimination organic pollutants is a great concern for constructing sustainable green energy systems. In the current work, a novel hybrid ternary WO3@g-C3N4@MWCNT nanocomposites have been fabricated for visible-light-driven photocatalyst by self-assembly method. The as-prepared photocatalyst was examined by XRD, Raman, FESEM, HRTEM, XPS EDS, EIS, UV-visible DRS, and PL analysis. The experimental results revealed that the photocatalytic activity of WO3@g-C3N4@MWCNT nanocomposites on the degradation of Tetracycline (TC) is 79.54% at 120 min, which is higher than the binary WO3@g-C3N4 composite and pristine WO3. The improved degradation performance towards TC is recognized for its higher surface area, intense light absorption towards the visible region, and enhanced charge separation efficiency. Consequently, the fabricated catalyst endows a promising application for antibiotic degradation.

Enhanced photocatalytic activity of ZnO hexagonal tube/r-GO composite on degradation of organic aqueous pollutant and study of charge transport properties.

ZnO hexagonal tube and ZnO/r-GO nanocomposites were synthesized by hydrothermal method and the nanostructures were characterized by XRD, UV-DRS, PL, FTIR, FESEM, and TEM techniques. The main violet emission peak of the synthesized nanostructures is due to the transition between interstitial zinc and hole (valence band) of ZnO. The potential of ZnO/r-GO nanocomposite was evaluated using methyl orange (MO) and rhodamine-B (RhB), and the results were compared with the activity of synthesized ZnO nanostructures. More than 95% of MO and RhB were by ZnO/r-GO nanocomposite and it was found to be higher than that of ZnO hexagonal tube. The degradation MO and RhB were found to follow first-order kinetics and it has a rate constant of 7.68 × 10-2and 7.83 × 10-2 min-1, respectively. These results are mainly due to the enhanced charge transport property. Trapping experiments show that superoxide radical anion and hydroxide radicals are chief species responsible for the degradation of MO and RhB. The chemical stability of the nanocomposite was evaluated by cycle test experiments and it reveals that the catalyst can be reused up to few cycles without considerable loss of photocatalytic activity. This work affords a simple stratagem to integrate ZnO hexagonal tubes and r-GO nanosheets to construct effective catalysts for the degradation of organic compounds.

Hierarchically ordered macroporous TiO2 architecture via self-assembled strategy for environmental remediation.

Hierarchical orderd macroporous TiO2 architecture (HOMTA) was prepared with aid of ethylenediamine (EDA) and investigated the impact of amine molecules on the properties of TiO2 architecture. The different variation of amine molecules (EDA) leads to tunning the morphology under hydrothermal approach which is confirmed by FESEM and TEM analysis. The XRD and Raman studies confirms the crystal structure of anatase and brookite phase of TiO2. The surface of the architecture strongly depended on the concentration of EDA which plays a vital role in surface area which is revealed by Brunauer Emmett-Teller (BET) analysis. The obtained HOMTA was employed as photocatalyst and active photoanode in the dye sensitized solar cells (DSSC). The DSSC device exhibits excellent efficiency (η) of 5.27% for the EDA capped TiO2 (S5) which had high surface area (167.11 m2/g) for better dye loading, whereas the lower concentration of EDA capped TiO2 (S1, S2, S3 and S4) resulted the efficiency of 2.14, 3.90, 3.25 and 4.37%, respectively. The efficiency of photocatlysis degradation of the prepared samples (S1, S2, S3, S4 and S5) was 94.8, 90.47, 91.41, 91.32 and 93.75% under light source. The excellent photocatalysis property was achieved by S5 within 6 min due to high surface area which inducing more active site.

Recoverable and reusable visible-light photocatalytic performance of CVD grown atomically thin MoS2 films.

The decomposition of water pollutants including industrial dyes and chemicals via photocatalytic decontamination is one of the major investigated problems in recent years. Two-dimensional molybdenum disulfide (MoS2) layers have shown great promise as an efficient visible-light photocatalyst owing to its numerous active sites and large surface area. In this study, atomically thin MoS2 films of different thicknesses from monolayer to five-layer and ten layers were fabricated on sapphire substrates using chemical vapor deposition (CVD). We demonstrate that these MoS2 thin films can be used as a photocatalyst to degrade Methylene Blue (MB) dye and can be recovered completely with utmost structural and chemical stability. Under visible-light irradiation, the MB absorption peak completely disappears with ∼95.6% of degradation after 120 min. We also demonstrate the reusability of the MoS2 thin films without significantly losing the photocatalytic activity even after 5-cycles of degradation studies. The chemical and structural stability of the MoS2 films after 5-cycles of degradation studies were affirmed using various spectroscopic studies. Our findings suggest that the MB degradation efficiency increases from 19.01% to 98.46% with an increase in pH from 4 to 14. Our approach may facilitate a further design of other transition metal dichalcogenides-based recoverable photocatalysts for industrial applications.

Interfacial engineering in 3D/2D and 1D/2D bismuth ferrite (BiFeO3)/Graphene oxide nanocomposites for the enhanced photocatalytic activities under sunlight.

3D-particulate and 1D-fiber structures of multiferroic bismuth ferrite (BiFeO3/BFO) and their composites with 2D-graphene oxide (GO) have been developed to exploit the different scheme of interfacial engineering as 3D/2D and 1D/2D systems. Particulates and fibers of BFO were developed via sol-gel and electrospinning fabrication approaches respectively and their integration with GO was performed via the ultrasonic-assisted chemical reduction process. The crystalline and phase formation of BiFeO3 and GO was confirmed from the XRD patterns obtained. The electron microscopic images revealed the characteristic integration of 3D particulates (with average size of 100 nm) and 1D fibers (with diameter of ~150 nm and few µm length) onto the 2D GO layers (thickness of ~27 nm). XPS analysis revealed that the BFO nanostructures have been integrated onto the GO through chemisorptions process, where it indicated that the ultrasonic process engineers the interface through the chemical modification of the surface of these 3D/2D and 1D/2D nanostructures. The photophysical studies such as the impedance and photocurrent measurements showed that the charge separation and recombination resistance is significantly enhanced in the system, which can directly be attributed to the effective interfacial engineering in the developed hetero-morphological composites. The degradation studies against a model pollutant Rhodamine B revealed that the developed nanocomposites exhibit superior photocatalytic activity via the effective generation of OH radicals as confirmed by the radical analysis studies (100% degradation in 150 and 90 min for 15% GO/BFO particulate and fiber composites, respectively). The developed system also demonstrated excellent photocatalytic recyclability, indicated their enhanced stability.

The construction of a dual direct Z-scheme NiAl LDH/g-C3N4/Ag3PO4 nanocomposite for enhanced photocatalytic oxygen and hydrogen evolution.

Dual direct Z-scheme photocatalysts for overall water decomposition have demonstrated strong redox abilities and the efficient separation of photogenerated electron-hole pairs. Overall water splitting utilizing NiAl-LDH-based binary and ternary nanocomposites has been extensively investigated. The synthesized binary and ternary nanocomposites were characterized via XRD, FTIR, SEM, HRTEM, XPS, UV-DRS, and photoelectrochemical measurements. The surface wettability properties of the prepared nanocomposites were measured via contact angle measurements. The application of the NiAl-LDH/g-C3N4/Ag3PO4 ternary nanocomposite was investigated for photocatalytic overall water splitting under light irradiation. In this work, we found that in the presence of Ag3PO4, the evolution of H2 and O2 is high over LCN30, and 2.8- fold (O2) and 1.4-fold (H2) activity increases can be obtained compared with the use of LCN30 alone. It is proposed that Ag3PO4 is involved in the O2 evolution reaction during water oxidation and g-C3N4 is involved in overall water splitting. Our work not only reports overall water splitting using NiAl-LDH-based nanocomposites but it also provides experimental evidence for understanding the possible reaction process and the mechanism of photocatalytic water splitting. Photoelectrochemical measurements confirmed the better H2 and O2 evolution abilities of NiAl-LDH/g-C3N4/Ag3PO4 in comparison with NiAl LDH, g-C3N4, Ag3PO4, and LCN30. The observed improvement in the gas evolution properties of NiAl LDH in the presence of Ag3PO4 is due to the formation of a dual direct Z-scheme, which allows for the easier and faster separation of charge carriers. More importantly, the LCNAP5 heterostructure shows high levels of H2 and O2 evolution, which are significantly enhanced compared with LCN30 and pure NiAl LDH.