Synergistic Engineering of Energy Band Alignment and Interfacial Electric Field Distribution over Bi-bismuth-Based Hetero-nanofibers for Boosting Visible-Light-Driven Photocatalytic Ammonia Synthesis and Antibiotic Removal.

Synergistic engineering of energy band alignment and interfacial electric field distribution is essential for photocatalyst design but is still challenging because of the limitation on refined regulation in the nanoscale. This study addresses the issue by employing surface modification and thermal-induced phase transformation in Bi2MoO6/BixOyIz hetero-nanofiber frameworks. The energy band alignment switches from a type-II interface to a Z-scheme contact with stronger redox potentials and inhibited electron traps, and the optimized built-in electric field distribution could be reached based on experimental and theoretical investigations. The engineered hetero-nanofibers exhibit outstanding visible-light-driven photocatalytic nitrogen reduction activity (605 µmol/g/h) and tetracycline hydrochloride removal rate (81.5% within 30 min), ranking them among the top-performing bismuth series materials. Furthermore, the photocatalysts show promise in activating advanced oxidants for efficient organic pollutant degradation. Moreover, the Bi2MoO6/Bi5O7I hetero-nanofibers possess good recycling stability owing to their three-dimensional network structure. This research offers valuable insights into heterojunction design for environmental remediation and industrial applications.

Photocatalytic CO2 Reduction to Ethanol by ZnCo2O4/ZnO Janus Hollow Nanofibers.

Photocatalytic carbon dioxide (CO2) reduction for high-value hydrocarbon fuel production is a promising strategy to tackle global energy demand and climate change. However, this technology faces formidable challenges, primarily stemming from low yield and poor selectivity of C2 products of the desired hydrocarbon fuels. This study reported ZnO/ZnCo2O4 Janus hollow nanofibers (ZnO/ZCO JHNFs) prepared by electrospinning and atomic layer deposition. Photocatalytic tests revealed an ethanol yield of 4.99 µmol g-1 h-1 for ZnO/ZnCo2O4 JHNFs, surpassing mixed ZnO/ZnCo2O4 nanofibers (ZnO/ZCO NFs) by 4.35 times and pure ZnO by 12.7 times. The selectivity of 58.8% is 2.38 and 4.49 times higher than those of ZnO/ZnCo2O4 NFs and ZnO, respectively. These enhancements are attributed to efficient carrier separation facilitated by the ordered internal electric field of the Z-scheme heterojunction interface, validated by the energy band evaluations from experimentation and density functional theory (DFT) simulations and charge separation characterizations of photocurrent, impedance, and photoluminescence spectra. The Janus structure also effectively exposes the surface of ZnCo2O4 to CO2 molecules, increasing the active site availability, as confirmed by BET nitrogen adsorption/desorption, temperature-programmed desorption tests, and DFT adsorption energy calculations. This study proposes a novel approach for efficient photocatalytic hydrocarbon fuel production, with potential applications in energy and climate crisis mitigation.

An Fc Binding Peptide-Based Facile and Versatile Build Platform for Multispecific Antibodies.

Multispecific antibodies (MsAbs) maintain the specificity of versatile antibodies while simultaneously addressing different epitopes for a cumulative, collaborative effect. They could be an alternative treatment to chimeric antigen receptor-T cell therapy by helping to redirect T cells to tumors in vivo. However, one major limitation of their development is their relatively complex production process, which involves performance of a massive screen with low yield, inconsistent quality, and nonnegligible impurities. Here, a poly(l-glutamic acid)-conjugated multiple Fc binding peptide-based synthesis nanoplatform was proposed, in which MsAbs were constructed by mixing the desired monoclonal antibodies (mAbs) with polymeric Fc binding peptides in aqueous solution without purification. To determine its efficacy, a dual immune checkpoint-based PD1/OX40 bispecific antibody and PDL1/CD3e/4-1BB trispecific antibody-based T cell engager were generated to trigger antitumor CD8+ T responses in mice, showing superior tumor suppression over free mixed mAbs. In this study, a facile, versatile build platform for MsAbs was established.

Ultra-Flexible, Breathable, and Robust PAN/MWCNTs/PANI Nanofiber Networks for High-Performance Wearable Gas Sensor Application.

Wearable gas sensors have drawn great attention for potential applications in health monitoring, minienvironment detection, and advanced soft electronic noses. However, it still remains a great challenge to simultaneously achieve excellent flexibility, high sensitivity, robustness, and gas permeability, because of the inherent limitation of widely used traditional organic flexible substrates. Herein, an electrospinning polyacrylonitrile (PAN) nanofiber network was designed as a flexible substrate, on which an ultraflexible wearable gas sensor was prepared with in situ assembled polyaniline (PANI) and multiwalled carbon nanotubes (MWCNTs) as a sensitive layer. The unique nanofiber network and strong binding force between substrate and sensing materials endow the wearable gas sensor with excellent robustness, flexibility, and gas permeability. The wearable sensor can maintain stable NH3 sensing performance while sustaining extreme bending and stretching (50% of strain). The Young's modulus of wearable PAN/MWCNTs/PANI sensor is as low as 18.9 MPa, which is several orders of magnitude smaller than those of reported flexible sensors. The water vapor transmission rate of the sensor is 0.38 g/(cm2 24 h), which enables the wearing comfort of the sensor. Most importantly, due to the effective exposure of sensing sites as well as the heterostructure effect between MWCNTs and PANI, the sensor shows high sensitivity to NH3 at room temperature, and the theoretical limit of detection is as low as 300 ppb. This work provides a new avenue for the realization of reliable and high-performance wearable gas sensors.

Wearable Inorganic Oxide Chemiresistor Based on Flexible Al2O3-Stabilized ZrO2 Ceramic Sponge Substrate for NO2 Sensing.

Wearable gas sensors, possessing the advantages of high sensitivity, excellent flexibility, high permeability, low weight, and workability at ambient conditions, hold great promise for real-time health monitoring and early warnings of poisonous gases. However, obtaining high-performance wearable gas sensors utilizing the current well-developed inorganic semiconductor oxide sensing materials is still very limited due to their fragile and rigid nature. Herein, a newly designed wearable gas sensor based on an all-inorganic ASZ (Al2O3-stabilized ZrO2)/ZnO/SnO2 nanofibers is introduced for the first time. The flexible ASZ ceramic sponge substrate (with a Young's modulus of 4.15 MPa) and ultrathin ZnO/SnO2 sensing layer endow the wearable gas sensor with promising properties such as super flexibility (with a bending radius of 5 mm), high gas permeability, and low weight. Furthermore, driven by UV light irradiation, this all-inorganic wearable sensor also demonstrates a stable NO2 sensing response under different bending states at room temperature, which enables the gas sensor to be more compatible with wearable sensing applications. This work offers a general method to achieve a high-performance wearable gas sensor based on inorganic materials and provides new insights into their potential in wearable gas-sensing applications.

Photocatalytic process of simultaneous desulfurization and denitrification of flue gas by TiO2-polyacrylonitrile nanofibers.

TiO2 nanoparticles were successfully fabricated on electrospun polyacrylonitrile (PAN) nanofibers via the coupling of electrospinning and hydrothermal pathway. A straightforward photocatalysis oxidation process has been developed for simultaneous desulfurization and denitrification of flue gas using the TiO2-PAN photocatalyst. Also, the influences of some important operating parameters, such as titanium loading content of catalyst, flue gas humidity, flue gas flow, and inlet flue gas temperature on removal efficiencies of SO2 and NO were investigated. The results demonstrated that removal efficiencies of 99.3% for SO2 and 71.2% for NO were attained under the following optimal experiment conditions: titanium loading content, 6.78 At %; gas flow rate, 200 mL/min; flue gas humidity, 5%; inlet flue gas temperature, 40 °C. Furthermore, the presumed reaction mechanism of SO2 and NO removal using TiO2-PAN photocatalyst under UV light was proposed.

An electron-rich free-standing carbon@Au core-shell nanofiber network as a highly active and recyclable catalyst for the reduction of 4-nitrophenol.

A three-dimensional (3D) free-standing network composed of cross-linked carbon@Au core-shell nanofibers was fabricated by combining the electrospinning technique and an in situ reduction approach. The results showed that a uniform Au layer of approximately 5 nm thickness was formed around the electrospun carbon nanofiber. What's more, it's interesting to note that the Au layer was composed of small Au nanoparticles. And, the as-prepared CNFs@Au network exhibited excellent catalytic activity for the reduction of 4-nitrophenol (4-NP) based on the electron-rich catalytic platform arising from the synergistic effect between carbon and Au. Notably, the free-standing 3D nanofibrous cross-linked network structure could improve the catalyst's performance in separation and reuse.

Highly dispersed g-C3N4 on well-designed three-dimensional porous nanostructured ZrO2 for high-performance photocatalytic degradation and H2 production.

A novel polymer-assisted freeze-drying method was adopted for preparing three-dimensional porous nanostructured ZrO2 (3DPZ) with macro self-supporting properties. Then, g-C3N4 was in-situ grown uniformly on the 3DPZ through a gas-solid reaction, forming 3D nanoporous ZrO2/g-C3N4 heterojunctions (3DP/ZC) with different g-C3N4 loadings that retained self-supporting characteristics. The kapp value of Rhodamine B (RhB) degradation and H2 evolution rate of the 3DP/ZC-2 under visible light reached 0.035 min-1 and 1013.1 µmol h-1 g-1, which were 19.6 and 6.6 times higher than pure g-C3N4, respectively. The ZrO2 nanoparticles (ZNps) prepared via freeze-drying, but without polymer precursor, were used as support to form ZrO2/g-C3N4 nanoparticles (ZCNps-2) for comparison study. The RhB degradation rate and H2 evolution rate of the 3DP/ZC-2 under visible light were about 3.7 and 5.3 times higher than ZCNps-2. Their enhanced photocatalytic activity could be attributed to their unique 3D heterointerface with matched energy bands for rapid charge separation and transfer and a hierarchical porous structure for mass transfer and surface reaction processes. The scavenger trapping and ESR measurements confirmed that the primary reactive radicals for degradation were superoxide radical ions (⋅O2-), hydroxyl radicals (⋅OH), and photogenerated holes (h+). The pH-dependent photocatalytic degradation activity originated from the H+-related ⋅OH conversion reaction. Besides, the macro self-supporting nature could provide excellent separability and recyclability, and self-supporting membranes were also constructed and demonstrated as stable and recyclable photocatalysts. This work provides a new routine for designing 3D-heterojunctions as new kinds of functional materials for applications in environmental remediation and green energy production.

Floating metal phthalocyanine@polyacrylonitrile nanofibers for peroxymonosulfate activation: Synergistic photothermal effects and highly efficient flowing wastewater treatment.

Highly efficient floating photocatalysis has potential applications in organic pollutant treatment but remains limited by low degradation efficiency in practical applications. By introducing the photothermal effect into a peroxymonosulfate (PMS) coupled photocatalysis system, tetracycline hydrochloride (TCH) degradation could be significantly enhanced using floating metal phthalocyanine@polyacrylonitrile (MPc@PAN) nanofiber mats. MPc@PAN nanofibers with different metal centers showed similar photothermal conversion performance but different activation energies for PMS activation, resulting in metal-center-dependent synergistic photothermal effects, i.e., light-enhanced dominated, thermal-enhanced dominated, and conjointly light-thermal dominated mechanisms. The porous structures and floating ability of the FePc@PAN nanofibers provided a fast mass transfer process, with higher solar energy utilization and superior photothermal conversion performance than the FePc nanopowders. Meanwhile, the FePc@PAN nanofibers showed excellent TCH removal stability within 10 cycles (>92%) and extremely low Fe ion leaching (<0.055 mg/L) in a dual-channel flowing wastewater treatment system. This work provides new insight into PMS activation via photothermal effects for environmental remediation.

Anchoring bismuth oxybromo-iodide solid solutions on flexible electrospun polyacrylonitrile nanofiber mats for floating photocatalysis.

Constructing floating photocatalysts with highly efficient visible-light utilization is a promising approach for practical photocatalytic wastewater treatment. In this study, we anchored bismuth oxybromo-iodide (BiOBrxI1-x (0 ≤ x ≤ 1)) on flexible electrospun polyacrylonitrile (PAN) nanofiber mats to create BiOBrxI1-x@PAN nanofibers with tunable light absorption properties as floating photocatalysts at room temperature. As x increased, the photocatalytic activity of the BiOBrxI1-x@PAN nanofibers with similar loading content initially increased, and then decreased, for the degradation of bisphenol A (BPA) and methyl orange (MO) under visible-light irradiation (λ > 420 nm) conditions. The BiOBrxI1-x@PAN (0 < x < 1) nanofibers exhibited better photocatalytic performance compared to the BiOBr@PAN and BiOI@PAN nanofibers. Under visible-light irradiation, the BPA degradation rate of the BiOBr0.5I0.5@PAN nanofibers was 1.9 times higher than that of the BiOI@PAN nanofibers, while the BiOBr@PAN nanofibers had no noticeable degradation performance. The MO degradation rate of the BiOBr0.5I0.5@PAN nanofibers was 2.5 and 3.2 times higher than that of the BiOBr@PAN and BiOI@PAN nanofibers, respectively. The enhanced performance possibly originated from a balance between the light absorption and redox capabilities, along with efficient separation of electron-hole pairs in the BiOBr0.5I0.5@PAN nanofibers, as determined by ultraviolet-visible diffuse reflectance spectroscopy, X-ray photoelectron spectra analysis of the valence bands, and photocurrent response characterization. Compared to the powder structures, the BiOBrxI1-x@PAN nanofibers showed enhanced performance due to the excellent dispersion and immobilization of the BiOBrxI1-x solid solution, which provided more active sites during photocatalytic degradation. In addition, their flexible self-supporting structures allowed for floating photocatalysis near the water surface. They could be reused directly without separation and maximized the absorption of visible light during the photocatalytic reaction. Therefore, these solid-solution-based floatable nanofiber photocatalysts are good potential candidates for wastewater treatment applications.

Oxidation of phthalate acid esters using hydrogen peroxide and polyoxometalate/graphene hybrids.

Phthalate acid esters (PAEs) have been adsorbed and oxidatively degraded into small molecules including lactic acid (LA), formic acid (FA), H2O and CO2 using polyoxometalates (POMs)/graphene hybrids. We demonstrated that super-lower concentrations of PAEs could be oxidized, which was due to their unique structure. POM molecules have been embedded onto graphene to form H5PMo10V2O40@surfactant(n)/Graphene(L wt%) (abbreviated as HPMoV@Surf(n)/GO(L wt%)) using surfactants with the carbon chain length n = 2, 4, 6 and 8 for the loading of HPMoV. The coexistence of the graphene and surfactant layer (on HPMoV@Surf(n)/GO(20 wt%)) adsorbed PAE molecules and transported them rapidly to HPMoV active sites. And n values determined the electron transfer ability between graphene and POMs that promoted PAEs oxidation. The loading of POMs on the surface of graphene permitted HPMoV@Surf(n)/GO(L wt%) act as interfacial catalyst which degraded various PAEs (i.e., diethyl phthalate (DEP), diallyl phthalate (DAP) and di (2-ethylhexyl) phthalate (DEHP)) while removed more than 70% of TOC and COD. The degradation of DEP achieved 93.0% with HPMoV@Surf(n)/GO(20 wt%) and H2O2, which followed first-order kinetics and the reaction activation energy (Ea) of 23.1 kJ/mol. Further, HPMoV@Surf(n)/GO(20 wt%) showed potential for the removal of PAEs in Wastewater Treatment Plant (WWTP), and the degradation efficiency for PAE (DEP) in secondary effluent achieved 55.0%. In addition, the loading method for POMs on graphene eliminated the leaching of POMs from graphene, and the degradation efficiency could still reach 88.1% after ten recycles.

A facile in situ hydrothermal method to SrTiO3/TiO2 nanofiber heterostructures with high photocatalytic activity.

Heterostructured SrTiO3/TiO2 nanofibers were fabricated by in situ hydrothermal method using TiO2 nanofibers as both template and reactant. The as-fabricated heterostructures composite included SrTiO3 nanocubes or nanoparticles assembled uniformly on the surface of TiO2 nanofibers. Compared with the pure TiO2 nanofibers, SrTiO3/TiO2 nanofibers exhibited enhanced photocatalytic activity in the decomposition of Rhodamine B (RB) under ultraviolet light. The enhanced photocatalytic activity of SrTiO3/TiO2 nanofibers could be attributed to the improvement of charge separation derived from the coupling effect of TiO2 and SrTiO3 nanocomposite.

A self-floating electrospun nanofiber mat for continuously high-efficiency solar desalination.

Solar desalination is an environment-friendly and sustainable technology to address the shortage of freshwater resources. However, it still faces huge challenges to develop a salt-rejection solar desalination system with continuous high efficiency. Herein, an electrospun nanofiber mat was fabricated for continuously high-efficiency solar desalination with carbon nanotube as a photothermal material, polyvinylidene fluoride as a floating support material and polyvinylpyrrolidone as a pore-forming agent. The porous structure and superhydrophilic surface provide significant water transport channels and thus avoid salt deposition, even in the high-salinity brine (20 wt% NaCl). The integration of strong broadband absorption property, excellent photothermal performance, floatability, durability and stability endows the solar desalination system with continuously high evaporation efficiency. The evaporation rate and solar conversion efficiency reached up to 1.372 kg m-2 h-1 and 86.1%, respectively, in simulated seawater under one sun irradiation and lasted for 11 h with little fluctuation. This work opens a new avenue for the rational design and fabrication of solar desalination systems to promote practical application.

Flexible All-Inorganic Room-Temperature Chemiresistors Based on Fibrous Ceramic Substrate and Visible-Light-Powered Semiconductor Sensing Layer.

As the most extensively used gas-sensing devices, inorganic semiconductor chemiresistors are facing great challenges in realizing mechanical flexibility and room-temperature gas detection for developing next-generation wearable sensing devices. Herein, for the first time, flexible all-inorganic yttria-stabilized zirconia (YSZ)/In2 O3 /graphitic carbon nitride (g-C3 N4 ) (ZIC) gas sensor is designed by employing YSZ nanofibers as substrate, and ultrathin In2 O3 /g-C3 N4 heterostructures as active sensing layer. The YSZ substrate possesses small nanofiber diameter (310 nm), ultrafine grain size (23.9 nm), and abundant dangling bonds, endowing it with striking mechanical flexibility and strong adhesion with In2 O3 /g-C3 N4 sensing layer. Meanwhile, the ultrathin thickness (≈7 nm) of In2 O3 /g-C3 N4 ensures that the inorganic sensing layer has tiny linear strain along with the deformation of flexible YSZ substrate, thereby enabling unusual bending capacity. To address the operating temperature issue, the gas sensor is operated by using a visible-light-powered strategy. Under visible-light illumination, the flexible ZIC sensor exhibits a perfectly reversible response/recovery dynamic process and ultralow detection limit of 50 ppb to toxic nitrogen dioxide at room temperature. This work not only provides an insight into the mechanical flexibility of inorganic materials, but also offers a valuable reference for developing other flexible inorganic-semiconductor-based room-temperature gas sensors.

Construction of In2O3/ZnO yolk-shell nanofibers for room-temperature NO2 detection under UV illumination.

Room-temperature gas sensors have emerged as effective platforms for sensing explosive or toxic gases in ambient environment. However, room-temperature gas sensor usually suffers from extremely poor sensitivity and sluggish response/recovery characteristics due to the low reacting activity at low temperature. Herein, we present a room-temperature NO2 sensor with greatly enhanced sensitivity and rapid response/recovery speed under ultraviolet (UV) illumination. The sensor based on In2O3/ZnO yolk-shell nanofibers exhibits remarkable sensitivity (Rg/Ra = 6.0) to 1 ppm NO2 and rapid response/recovery time (≤36, 68 s) under UV illumination, obviously better than negligible sensing performance and inefficient response/recovery properties in dark condition. Such excellent gas sensing properties of the In2O3/ZnO yolk-shell nanofibers were not only attributed to the improved photo-generated charge separation efficiency derived from the effect of heterojunction, but also related to the enhanced receptor function towards NO2 endowed by increased reactive sites and gas adsorption. These proposed strategies will provide a reference for developing high-performance room-temperature gas sensors.

TiO2/SrTiO3/g-C3N4 ternary heterojunction nanofibers: gradient energy band, cascade charge transfer, enhanced photocatalytic hydrogen evolution, and nitrogen fixation.

TiO2/SrTiO3/g-C3N4 ternary heterojunction nanofibers with a cascade energy band alignment were designed and then fabricated by a combination of electrospinning technology and gas-solid reaction. Their photocurrent responses were 1.4 and 1.8 times higher while their transient photoluminescence lifetime were about 0.75 and 0.79 times shorter than those of TiO2/g-C3N4 nanofibers and SrTiO3/g-C3N4 nanofibers, respectively. The enhanced photocurrent response, decreased lifetime, and their dramatically decreased photoluminescence intensity clearly indicated that highly efficient cascade charge transfer and separation were achieved in the ternary nanofibers with the gradient energy band alignment compared with the corresponding traditional binary nanofibers noted above. When tested in photocatalytic reduction reactions of H2 evolution and nitrogen fixation, the corresponding reaction rates under simulated sunlight irradiation values of 1304 µmol g-1 h-1 and 2192 µmol g-1 h-1 L-1 were 2.1 and 1.9 times better than those of TiO2/g-C3N4 nanofibers and 4.2 and 3.3 times better than those of SrTiO3/g-C3N4 nanofibers, respectively. Furthermore, the photocatalytic activities of the TiO2/SrTiO3/g-C3N4 nanofibers had no significant decrease after several cycles, indicating that they possessed good structural stability properties. This work provides a new route to design and fabricate an efficient photocatalyst for photocatalytic reduction reactions.

Discrete heterojunction nanofibers of BiFeO3/Bi2WO6: Novel architecture for effective charge separation and enhanced photocatalytic performance.

Designing and constructing one-dimensional (1D) discrete heterojunctions comprise an ideal strategy to improve the charge-separation efficiency and enhance the photocatalytic activities of semiconductor materials. Here, a novel architecture of discrete heterojunction nanofibers (DH-NFs) was obtained by growing Bi2WO6 nanosheets (NSs) on electrospun BiFeO3 nanofibers (NFs) via solvothermal technology. The charge-separation efficiency of BiFeO3/Bi2WO6 DH-NFs was approximately 2 times higher than that of BiFeO3 NFs and Bi2WO6 NSs. As expected, the BiFeO3/Bi2WO6 DH-NFs exhibited enhanced photocatalytic activities for oxygen evolution and RhB degradation. The reaction rates of BiFeO3/Bi2WO6 DH-NFs for oxygen evolution and RhB degradation were 18.3 and 36.7 times higher, respectively, than those of BiFeO3 NFs, and 31.9 and 8.7 times higher than those of Bi2WO6 NSs, respectively. The improved charge-separation efficiency and enhanced photocatalytic activities of BiFeO3/Bi2WO6 DH-NFs could be attributed to the following three points. The 1D heterojunctions could realize the separation and axial transport of photogenerated charges. The discrete structure could facilitate the spatial separation of redox reaction sites as well as photogenerated charges. The high surface area of BiFeO3/Bi2WO6 DH-NFs might provide more active sites for photocatalytic reaction. Moreover, the BiFeO3/Bi2WO6 DH-NFs possessed good recycling performance owing to the magnetic-separable property derived from the ferromagnetic behavior of BiFeO3.

SnO2 nanostructures-TiO2 nanofibers heterostructures: controlled fabrication and high photocatalytic properties.

Combining the versatility of the electrospinning technique and hydrothermal growth of nanostructures enabled the fabrication of hierarchical SnO(2)/TiO(2) composite nanostructures. The results revealed that not only were secondary SnO(2) nanostructures successfully grown on primary TiO(2) nanofiber substrates but also the SnO(2) nanostructures were uniformly distributed without aggregation on TiO(2) nanofibers. By adjusting fabrication parameters, the morphology as well as coverage density of secondary SnO(2) nanostructures could be further controlled, and then SnO(2)/TiO(2) heterostructures with SnO(2) nanoparticles or nanorods were facilely fabricated. The photocatalytic studies suggested that the SnO(2)/TiO(2) heterostructures showed enhanced photocatalytic efficiency of photodegradation of Rhodamine B (RB) compared with the bare TiO(2) nanofibers under UV light irradiation.

Water-dichloromethane interface controlled synthesis of hierarchical rutile TiO2 superstructures and their photocatalytic properties.

A water-dichloromethane interface is used for synthesis and assembly of rutile TiO(2) nanorods. By hydrothermal treatment of a dichloromethane solution of TiCl(4) at the interface of water-dichloromethane, turning to no surfactant or template, hierarchical rutile TiO(2) superstructures are developed. By tuning the molar ratio of reactants r(w) (H(2)O/TiCl(4)), the size and shape of the samples significantly change. At a low value of r(w), highly extended, robust, porous, and thick titania film with ordered rutile nanorod bundles are deposited at the interface. At a high value of r(w), powders consisting of hierarchical rutile nanorod spheres together with disordered nanorods are obtained. A rational formation mechanism is proposed on the basis of a range of experiments. The main factors influencing the morphologies of the samples may be attributed to the acidity of the reaction system and the adsorption ability of the precursor nanoparticles to the water-dichloromethane interface. The as-obtained rutile TiO(2) hierarchical superstructures show higher photocatalytic property to decompose methylene blue (MB) dye compared with that of commercial P25, which can be ascribed to the contribution of high surface area and high crystallinity. Other applications, such as solar energy conversion, environmental remediation, and advanced optical/electric nanodevices may also benefit from the unique properties of the hierarchically rutile TiO(2) superstructures.

Direct Z-scheme heterostructure of p-CuAl2O4/n-Bi2WO6 composite nanofibers for efficient overall water splitting and photodegradation.

Constructing heterostructures can facilitate photoinduced charge separation, leading to enhanced photocatalytic performance. However, spatial separation of charge carriers in traditional type II heterojunctions is at the expense of their redox ability. In this paper, well-designed direct Z-scheme systems (ZSS) of p-CuAl2O4/n-Bi2WO6 composite nanofibers with uniform non-woven web nanostructure was built by electrospinning technique and solvothermal reactions. The formation mechanism of the ZSS and the charge migration pathway is investigated in detail. Results show that as-prepared composite nanofibers exhibit desirable photocatalytic performance for overall water splitting due to its stronger redox power and efficient charge separation. Meantime, it shows great activity for photodegradation of various organic pollutant models (RhB, MO, 4-NP), which is 1 order of magnitude higher than the single-component CuAl2O4 and Bi2WO6. Furthermore, the composite nanofibers exhibit well separable properties by natural sedimentation because of its ultra-long and non-woven web nanostructure. The paper explores CuAl2O4 and its Z-scheme heterostructures in water splitting for the first time, which may highlight its new applications.