Capture Ability Research Articles

A comprehensive and single-use foot-and-mouth disease sero-surveillance prototype employing rationally designed multiple viral antigens

Foot-and-mouth disease (FMD) is a great havoc in agri-business-based countries like Bangladesh, for which existing detection system limits the identification and differentiation of serotypes. In this study, an engineered platform was introduced incorporating serotype-specific FMDV VP1 (structural), serotype-independent VP2 (structural) and 3AB (non-structural) proteins for holistic detection. VP1 sequences were engineered combining sequences of BAN/TA/Dh-301/2016 (serotype O), BAN/CH/Sa-304/2016 (serotype A) and BAN/DH/Sa-318/2016 (serotype Asia1). Consensus 3AB sequence was constructed from the selected prevalent viral genomes. Both VP1 and 3AB along with designed VP2 sequences were optimized for codon usage bias, stable mRNA, secondary and tertiary protein structure. Proteins were synthesized in pET-21a ( +) plasmid vector followed by transformation of Escherichia coli BL21(DE3) and IPTG-induced- expression. The western blot analysis of engineered proteins showed that purified VP1 prominently bound to anti-VP1 antibodies in vaccinated sera, whereas 3AB and VP2 bound anti-3AB and anti-VP2 antibodies, respectively from infected cattle sera, all previously collected during epidemiological investigation. Furthermore, dot blot hybridization confirmed efficient antibody capture ability of the membrane-immobilized proteins. This holistic diagnostic platform justifies a comprehensive prototype diagnostic kit that would be cost-effective and efficient for serotype specific and non-specific FMDV sero-surveillance.

Improved Gas Sensing Properties of Copper-Doped MoSe2 Monolayers: A First-Principles Study on CO2 and NO2 Adsorption

Abstract This paper investigates the impact of copper (Cu)-doped MoSe2 monolayer(ML) on gas sensing properties. The adsorption behaviour of CO2 and NO2 gas molecules on Cu-doped MoSe2 ML is reported and various sensing and electronic parameters such as adsorption energy, charge transfer and recovery time, are computed to delineate the adsorption characteristics and gas sensitivity. In our study, the doped Cu-atom in Se vacant MoSe2 ML shows the adsorption energies to be -1.32 eV (O-orient) and -1.72 eV (C-orient), for CO2 while for NO2, they are -0.879 eV (O-orient) and -1.06 eV (N-orient), respectively. The negative formation energy of -6.62 eV shows the electronic stability of Cu-doped MoSe2 ML and thermal stability is shown by the molecular dynamics study through the Nose-Vervlet Thermostat (NVT) algorithm. Also, significant changes are observed in electronic conductivity and work function upon adsorbed Cu-MoSe2 ML. Lastly, these outcomes illustrate that Cu doping amplifies the capture ability of MoSe2 ML towards gas molecules, fostering improved electron interaction between the substrate surface and gas molecules, consequently enhancing its gas sensing ability.

Medium and high temperature H2S removal via phosphazene polyoxometalate ionic liquids: Performance evaluation and mechanism exploration

The development of non-aqueous solvent desulfurizer is crucial to addressing the challenges associated with traditional liquid-phase wet desulfurization technologies. Based on this, we prepared a series of phosphazene polyoxometalate ionic liquids (PPILs) based of 1-butyl-3-methylimidazolium chloride using different kinds of phosphazenes (PNs) combined with polyoxometalate (POM), and used for hydrogen sulfide (H2S) dynamic absorption experiments. The effects of PN type and ratio, temperature and desulfurizer concentration on the desulfurization performance of different PPILs were explored. Among them, PPILs@IBuPN-9 as the optimal desulfurizer could keep almost 100 % desulfurization efficiency in the medium and high temperature range (100–200 °C). The results showed that the combination of PNs with POM significantly improved and widened the H2S removal performance and the operational temperature window of the desulfurizer. Besides, PPILs@IBuPN-9 required only air regeneration to maintain relatively stable cycle performance for at least four times and the sulfur capacity could be efficiently increased during multiple regenerations. It was found that the hydrogen bonding sites on IBuPN network formed significantly enhanced the H2S capture ability of PPILs and the sulfur capacity was substantially improved by S2− substitution of oxygen atoms in the POM according to the characterization results and density functional theory calculations. This study promotes the deep integration of polyoxometalate chemistry with ionic liquids in the field of gas purification and promotes the development of non-aqueous phase desulfurization process.

Z-Scheme LaFeO3/Cd0.7Zn0.3S heterojunction based on 3DOM LaFeO3 perovskite for enhanced photocatalytic hydrogen activity

The narrow band gap semiconductor LaFeO3 with ABO3 perovskite structure has been deeply studied in the field of photocatalysis due to its good thermal stability, chemical stability, photoelectric properties and suitable band position. The inverse opal structure gives the material a large specific surface area and increases the adsorption area and active site of the catalyst. In this work, it is reported for the first time that perovskite LaFeO3 inverse opal was applied to photocatalytic hydrogen production. The Cd0.7Zn0.3S QDs were deposited on the skeleton wall of LaFeO3 inverse opal to construct LaFeO3/Cd0.7Zn0.3S binary heterojunction catalyst. The LaFeO3 3DOM can effectively increase the contact area with Cd0.7Zn0.3S QDs with an increase in specific surface area, and the multiple scattering effect improves the efficiency of light utilization. The introduction of Zn2+ ions regulate the band gap position of Cd0.7Zn0.3S QDs and increases the thermodynamic reduction ability of photo generated electrons. The Z-type heterojunction effect formed by LaFeO3 inverse opal and Cd0.7Zn0.3S QDs facilitates the separation and transmission of photo generated charges. The LaFeO3/Cd0.7Zn0.3S heterojunction catalysts achieved a hydrogen production performance of 277.48 μmol/g/h due to the large specific surface area of 3DOM, good light capture ability, band gap regulation of element doping, and efficient charge separation synergistic effect of heterojunction. This work provides new insights into the design and manufacture of perovskite-type 3DOM heterojunction photocatalysts.

Constructing CO2 capture nanotraps via tentacle-like covalent organic frameworks towards efficient CO2 separation in mixed matrix membrane

The structure and morphology of fillers are crucial factors in the process of CO2 separation within mixed matrix membranes (MMMs). In this study, the tentacle-like covalent organic framework (COF) as a filler was incorporated into the Pebax matrix for CO2/CH4 separation. The COF has abundant Lewis base sites (O atom and N atom) and porous pores, thereby constructing efficient CO2 capture nanotraps in the MMMs. The CO2 capture nanotraps facilitate the CO2 transport in the MMMs, and this can be verified by the Grand Canonical Monte Carlo (GCMC) simulation and density functional theory (DFT) calculation. Simultaneously, the CO2 capture nanotraps are distributed on the surface of tentacle-like COF, which is conducive to strengthening CO2 capture ability. Therefore, Pebax/COF MMMs exhibited superior CO2 gas separation performance compared to the pure Pebax membrane. Among them, the MMM with 3 wt% COF loading displayed the highest CO2 gas separation performance, exhibiting permeability and selectivity that were 73.4% and 32.9% higher than the pure Pebax membrane, respectively. Thus, CO2 capture nanotraps constructed in the MMMs via tentacle-like COF showed a promising potential for CO2 separation.

Phage-Modified Clear Hydrogel for Simultaneous Detection of Multiple Bacteria.

The proliferation speed of live foodborne pathogens is fast. A small number of pathogens will have a great impact on food and the environment if positive samples are not detected timely. In this study, transparent porous hydrogel stir bars, modified by two different phages (corresponding to two different bacteria (Escherichia coli and Hafnia sp)), have been developed for rapid detection of foodborne bacteria. A large number of samples can be analyzed simultaneously with a small animal live imager device to screen out the positive samples, while an adenosine triphosphate (ATP) bioluminescence sensor can be used to quantify the number of bacteria in the positive samples. The phage has good specificity and capture ability to bacteria, which makes the method highly sensitive. In addition, the use of multiple phages also enables the method to detect multiple bacteria simultaneously. The three-dimensional structure of the hydrogel allows it to modify more phages, and its transparent nature also allows the inside bioluminescence to be detected. Both can enhance the sensitivity of the detection. Finally, the reagents needed for bioluminescence, such as d-luciferin, can also be preencapsulated in the hydrogel, thus simplifying the detection step. Under the best conditions, the detection range of the method is 102-108 CFU·mL-1, and the limit of detection is 30 CFU·mL-1 within 11 min. The test results of actual samples show that there is no difference between using the method developed through this study and the traditional plate counting method, but the detection time is greatly shortened.

Modulation of p-Block Electron Orbits in Metal-Organic Frameworks for CO2 Capture and Electrochemical Reduction.

Developing catalysts with excellent CO2 capture capability and electrochemical CO2 reduction reaction (CO2RR) at a wide potential range simultaneously is significant but remains a formidable challenge. Here, two novel InMg defective trinuclear cluster-based MOFs (SNNU-41 and SNNU-42) with abundant p-block unsaturated coordinated sites were reported and exhibited good CO2 capture and CO2RR performance simultaneously. Due to the suitable micropores, SNNU-41 showed higher CO2 capture ability at different adsorption pressure conditions. On account of the rigid framework and the closer p band center to Fermi level, SNNU-42 accelerated the conversion of CO2 molecule to C1 efficiency. Notably, via adjusting the ratio of p-block metal (In) in the SNNU-42 framework, the performance of the CO2RR was promoted drastically. SNNU-42 with the InMg (1:1.8) mixed cluster delivered an excellent Faradaic efficiency of 91.3% for C1 products and high selectivity of 72.0% for HCOOH at -2.5 V (vs Ag/Ag+) with a total current density of 77.2 mA cm-2. This work provides a possibility for efficient CO2 capture and CO2RR electrocatalysts through the modulation of electronic structures and composition in MOFs.

SparseMorph: A weakly-supervised lightweight sparse transformer for mono- and multi-modal deformable image registration

PurposeDeformable image registration (DIR) is crucial for improving the precision of clinical diagnosis. Recent Transformer-based DIR methods have shown promising performance by capturing long-range dependencies. Nevertheless, these methods still grapple with high computational complexity. This work aims to enhance the performance of DIR in both computational efficiency and registration accuracy. MethodsWe proposed a weakly-supervised lightweight Transformer model, named SparseMorph. To reduce computational complexity without compromising the representative feature capture ability, we designed a sparse multi-head self-attention (SMHA) mechanism. To accumulate representative features while preserving high computational efficiency, we constructed a multi-branch multi-layer perception (MMLP) module. Additionally, we developed an anatomically-constrained weakly-supervised strategy to guide the alignment of regions-of-interest in mono- and multi-modal images. ResultsWe assessed SparseMorph in terms of registration accuracy and computational complexity.Within the mono-modal brain datasets IXI and OASIS, our SparseMorph outperforms the state-of-the-art method TransMatch with improvements of 3.2 % and 2.9 % in DSC scores for MRI-to-CT registration tasks, respectively. Moreover, in the multi-modal cardiac dataset MMWHS, our SparseMorph shows DSC score improvements of 9.7 % and 11.4 % compared to TransMatch in MRI-to-CT and CT-to-MRI registration tasks, respectively. Notably, SparseMorph attains these performance advantages while utilizing 33.33 % of the parameters of TransMatch. ConclusionsThe proposed weakly-supervised deformable image registration model, SparseMorph, demonstrates efficiency in both mono- and multi-modal registration tasks, exhibiting superior performance compared to state-of-the-art algorithms, and establishing an effective DIR method for clinical applications.

Construction of aptamers-modified plasmonic GO/urchin-like Au nanoparticles with enhanced photothermal performance and their efficient capture and elimination of Staphylococcus aureus

Here, aptamers-modified graphene oxide/urchin-like Au nanoparticles (Apt-GUANPs) were developed for efficient capture and photothermal therapy (PTT) of Staphylococcus aureus (S. aureus). Specifically, anisotropic UANPs were first prepared, and the excellent photothermal property was related to the localized surface plasmon resonance (LSPR) in the near infrared (NIR) region caused by sharp branching. Then GO, which was used to enhance the photothermal effect, was added and assembled into GUANPs by electrostatic action. Infrared images showed that GUANPs exhibited a stronger photothermal effect than UANPs. Under the irradiation of 808 nm laser, the photothermal conversion efficiency (η) of GUANPs was as high as 40.5 %, which was attributed to the enhanced optical response of GUANPs at 808 nm and the strong plasmonic coupling effect between tightly packed UANPs loaded on GO surfaces. Aptamers were modified on the surfaces of GUANPs for specific capture of S. aureus, with the capture efficiency of up to 72 %. Utilizing the specific capture ability of aptamers and the excellent photothermal property of GUANPs, Apt-GUANPs exhibited the strong photothermal killing ability against S. aureus. Therefore, Apt-GUANPs will be a promising and efficient photothermal agent, and will have a great application prospect in the treatment of bacterial infections in the future.

Deciphering heterojunction layered double hydroxide-polyaniline-carbon nanotubes for phosphorus capture in capacitive deionization

The capacitive deionization (CDI) has emerged as a robust technology due to its effective performance in removing and recovering phosphate in wastewater. However, there are still challenges in achieving fast charge transfer and high capacity phosphorus storage simultaneously. In this study, a layered double hydroxide-polyaniline-carbon nanotubes composite material (ZnFe-PANI/CNT) with heterojunction and pseudocapacitive characteristics was fabricated via a simple and effective precipitation strategy. The existence of heterojunction and pseudocapacitance of ZnFe-PANI/CNT was confirmed through material performance testing Moreover, with its fast charge transfer and high ion storage performance, it was achieved high phosphate adsorption efficiency (94 %) and sustainable electrode regeneration in low concentration phosphate wastewater. Ultraviolet photoelectron spectroscopy (UPS) and density functional theory revealed the ability to accelerate charge transfer, which was contributed by the heterojunction ZnFe-PANI/CNT. In addition, it was found that the synergies of electrostatic attraction, ligand exchange and surface complexation contributed to the high phosphate capture ability in the acidic environments. The binuclear bidentate or mononuclear bidentate structures dominated the surface configuration of phosphate adsorption at pH 4–9.

Toward Enhanced Biomimetic Artificial Visual Systems Based on Organic Heterojunction Optoelectronic Synaptic Transistors

AbstractArtificial visual systems, inspired by the human eye, hold significant potential in artificial intelligence. Optoelectronic synapses, integrating image perception, processing, and memory in a single device, offer promising solutions. The human eye exhibits different recognition accuracies for objects under varying light conditions. Therefore, a more biomimetic visual system is needed to better fit actual application scenarios. Here, an organic heterojunction‐based optoelectronic synaptic transistor (OHOST) is proposed to enhance biomimetic artificial visual systems. By utilizing the excellent carrier capture ability of core‐multi‐shell quantum dots (QDs) and the high exciton dissociation efficiency of heterojunction interfaces, the device achieves a recognition capability under different light intensities closely resembling that of the human eye. Under optimal light intensity, the recognition accuracy for the modified national institute of standards and technology (MNIST) dataset can reach 91.52%. Nevertheless, under both low and high light intensities, the accuracy drops to a low level. This work pushes the development of artificial visual systems toward higher levels of biomimicry.

NiFe2O4 magnetic nanoparticles supported on MIL-101(Fe) as bimetallic adsorbent for boosted capture ability toward levofloxacin

Levofloxacin (LVX) capture with microcrystalline particles of monometallic metal-organic frameworks (MOFs) is definitely restricted and challenged by its difficulties in solid-liquid separation and enhanced of adsorption capacity issues. Meanwhile, the development of magnetic MOFs with excellent adsorption capabilities and outstanding recyclability is crucial. Herein, a novel magnetic Fe/Ni bimetal MOFs composite (MIL-101(Fe)@NiFe2O4, MNFO) for LVX capture has been effectively fabricated for LVX capture, utilizing MIL-101(Fe) as the primary adsorbent and NiFe2O4 nanoparticles as the magnetic element. Attributed to the synergistic ability of bimetal ions (Fe2+ and Ni2+), MNFO exhibits a significant adsorption capacity (335 mg/g) and rapid adsorption rate (10 min) towards LVX. The adsorption capacity indicates an increasing-then-decreasing trend with an increase of the pH values. Additionally, the adsorption data are well fitted by the Freundlich and pseudo-second-order kinetic models. Thermodynamic studies indicated that the adsorption process was spontaneous and endothermic. In addition, the adsorbent demonstrated excellent reusability, as it could be readily recovered from the liquid phase through the magnetic properties of NiFe2O4. Remarkably, it retained approximately 90 % of its adsorption capacity of the uptakes after 5 cycles. This study offers a innovative approach to the development of highly efficient adsorbents for capturing LVX from water.

Optimized Porous Carbon Particles from Sucrose and Their Polyethyleneimine Modifications for Enhanced CO2 Capture

Carbon dioxide (CO2), one of the primary greenhouse gases, plays a key role in global warming and is one of the culprits in the climate change crisis. Therefore, the use of appropriate CO2 capture and storage technologies is of significant importance for the future of planet Earth due to atmospheric, climate, and environmental concerns. A cleaner and more sustainable approach to CO2 capture and storage using porous materials, membranes, and amine-based sorbents could offer excellent possibilities. Here, sucrose-derived porous carbon particles (PCPs) were synthesized as adsorbents for CO2 capture. Next, these PCPs were modified with branched- and linear-polyethyleneimine (B-PEI and L-PEI) as B-PEI-PCP and L-PEI-PCP, respectively. These PCPs and their PEI-modified forms were then used to prepare metal nanoparticles such as Co, Cu, and Ni in situ as M@PCP and M@L/B-PEI-PCP (M: Ni, Co, and Cu). The presence of PEI on the PCP surface enables new amine functional groups, known for high CO2 capture ability. The presence of metal nanoparticles in the structure may be used as a catalyst to convert the captured CO2 into useful products, e.g., fuels or other chemical compounds, at high temperatures. It was found that B-PEI-PCP has a larger surface area and higher CO2 capture capacity with a surface area of 32.84 m2/g and a CO2 capture capacity of 1.05 mmol CO2/g adsorbent compared to L-PEI-PCP. Amongst metal-nanoparticle-embedded PEI-PCPs (M@PEI-PCPs, M: Ni, Co, Cu), Ni@L-PEI-PCP was found to have higher CO2 capture capacity, 0.81 mmol CO2/g adsorbent, and a surface area of 225 m2/g. These data are significant as they will steer future studies for the conversion of captured CO2 into useful fuels/chemicals.

Schottky heterojunction-based photocatalysis-in-situ-self-Fenton system: Removal of tetracycline hydrochloride and biotoxicity evaluation of intermediates

Efficiently removing tetracycline hydrochloride (TC) while minimizing the formation of toxic intermediates is a significant challenge. A novel photocatalysis-in-situ-self-Fenton catalyst, RF/EA-Fe@Ti3C2, removed 92 % of TC (20 mg L−1, 100 mL) under visible light irradiation within 80 min. The results of optical thickness and local volumetric rate of photon absorption demonstrated that RF/EA-Fe@Ti3C2 had superior light capture ability than that of RF/EA-Fe. TC significantly inhibited wheat seed germination, seedling growth, and chlorophyll and carotenoid generation, whereas its intermediates had a lesser effect. Additionally, TC damaged the photosystem II (PSII) of wheat seedlings, reducing light response ability and energy capture efficiency, while TC intermediates caused damage similar to deionized water. The rapid TC degradation and low-ecotoxic intermediates stem from the synergistic effects between photogenerated holes and hydroxyl radicals. This study advanced the design of photocatalysis-in-situ-self-Fenton systems for antibiotic degradation and detoxification.

Freestanding molybdenum carbide nanowires electrode for high specific capacity and superior rate performance Li–CO2 batteries

Li–CO2 batteries have attracted wide attention owing to unique CO2 capture ability and potential power source for Mars exploration. However, the practical application of Li–CO2 batteries are severely restricted by the sluggish reaction kinetics of 4–electron Li2CO3 as discharged products. Herein, we design efficient freestanding Mo2C nanowires electrode following low electron Li2C2O4–product route to achieve high–performance Li–CO2 batteries. More importantly, we propose a regulation and evolution mechanism of discharge products Li2C2O4 and Li2CO3 on Mo2C cathode in Li–CO2 battery with different discharge depths. Based on reasonable regulation of discharge products, Li–CO2 batteries with the Mo2C nanowires exhibit excellent electrochemical performance with an ultra–low overpotential 0.35 V at 0.05 mA cm–2 and a cycle life of 165 cycles below charge potential of 3.8 V. The Mo2C nanowires electrode also delivers high discharge capacity of 8.47 mAh cm–2 and superior rate capability compared to a conventional Mo2C cathode reported. Moreover, the superior flexibility and stability of the binder–free Mo2C nanowires electrode under different deformations assists in the development of wearable Li–CO2 batteries with safety and sustainability.

Biomimetic hydrogel evaporator with excellent salt-rejection performance via edge-preferential crystallization and ion-transport effects

Solar steam generation has been considered a compellent desalination technology due to its environmental friendliness and sustainability, while interfacial salt crystallization and low freshwater yield are two serious issues that constrain its widespread application. In this work, inspired by lotus seedpod, a biomimetic evaporator containing conductive hydrogel was fabricated through 3D printing. The printed evaporator has excellent solar absorption, good mechanical properties, high water capture ability, and reduced vaporization enthalpy, which are exactly desired by good evaporators. Furthermore, the vertical micro-channels and networks inside hydrogel promote the transport of ions from the interface to bulk seawater, and the constructed edge petals drive salt ions to crystallize at the edges, both of these strategies suppress the salt crystallization and ensure long-term continuous operation of the evaporator in concentrated (25 wt%) seawater. Due to these positive effects, the evaporator can achieve 2.413 and 1.889 kg·m−2·h−1 steam yield under one sun in pure water and concentrated (25 wt%) seawater, which is much higher than the 2D evaporator and competitive among the reported evaporators. This work paves the road for the practical utilization of hydrogel in solar desalination.

Photocatalytic degradation of low-concentration gaseous benzene in air via bifunctional tin-doped titanium dioxide catalyst

Benzene, a common volatile organic compound (VOC) detected in indoor environments, poses challenges for its removal because of its stable molecular structure and low-concentration. In this study, we successfully synthesized tin-doped titanium dioxide (Sn-TiO2) using a simple hydrothermal method. Various characterization techniques including X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Brunner–Emmet–Teller (BET) and molecular probes were employed to analyze the phase composition, structure and morphology, as well as photocatalytic properties of TiO2 and Sn-TiO2. The characterization results showed that moderate addition of tin doping not only effectively enhanced the capture ability of benzene molecules but also promoted hydroxyl radicals (·OH) generation, which was further validated by in-situ diffuse reflectance infrared Fourier transform (DRIFT) spectra and density function theory (DFT) calculations. Degradation experiments on gaseous benzene revealed that under 15 W ultraviolet (UV) light irradiation in humid and closed conditions for 60 min, 1 % Sn-TiO2 achieved a benzene degradation efficiency of 93.14 %, with almost complete mineralization. Furthermore, flow system experiments demonstrated efficient decomposition of trace amounts of benzene (∼10 mg/m3) in the air to satisfy emission standards when employing 1 % Sn-TiO2 at a flow rate of 100 L/min.

Advancing drinking water safety: Facile fabrication of nanofiltration membrane for enhanced antibiotics removal and efficient water softening

Long-term water consumption with contaminated antibiotics and high levels of hardness threatens the health of humans and animals. In this study, a novel positively charged nanofiltration membrane was designed for the dual purpose of efficiently removing antibiotics and softening hard water. The membrane was fabricated by casting P84 polymer solution onto non-woven fabrics, followed by immersion in the polyethyleneimine (PEI) solution for phase inversion and cross-linking, and finalized interfacial polymerization with trimesoyl chloride. Notably, the rapid immersion of the P84 substrate into PEI drastically reduces preparation time by 95 % compared to the regular method while maximizing PEI storage, resulting in uniform pore sizes and a positively charged surface. The optimal membrane showed a high water permeance of 11.3 L m−2 h−1 bar−1 and exceptional antibiotic rejection, i.e., 99.6 % for enrofloxacin, 99.2 % for ciprofloxacin, and 96.3 % for sulfamethoxazole, as well as a highly effective removal in water hardness (over 96 % of Ca2+ and Mg2+) at 4 bar. Simulated water separation tests showed that the optimal membrane effectively controls hard water salinity within optimum drinking water ranges (Ca2+ ≤ 80 mg/L; Mg2+ ≤ 30 mg/L), providing efficient water softening and antibiotic capture ability. Additionally, the optimal membrane demonstrated a superior anti-bacterial and long-term stability performance. This study has significant potential for improving drinking water supply safety and addressing pressing public health and environmental concerns.

Interface coupling of octahedron Cu2O with reduced graphene oxide for enhanced photocatalytic and photoelectrochemical activity

Graphene oxide (GO) has been recognized as an ideal substrate material of semiconductor photocatalysts to achieve superior properties. Herein, Cu2O/reduced graphene oxide hetero-structures (Cu2O/rGO), featured by octahedron Cu2O with highly exposed {111} facets in-situ anchored on the framework of rGO nanosheets, were constructed via a green wet chemistry route at room temperature. During the reactions, Cu2+ ions that were adsorbed on GO could act as the nucleation sites of Cu2O while GO was further converted into rGO under the reduction of glucose, forming a robust hetero-interface of C–O–Cu bonding. Owning to the improved photon capture ability and carrier separation efficiency, the optimized Cu2O/rGO exhibits about 3.5 and 9.3 times enhancement of photocurrent intensity and photocatalytic activity, respectively, as compared to those of pure Cu2O. Meanwhile, the correlation among rGO content, structure and photocatalytic activity of Cu2O/rGO was demonstrated. This work presents a rational route and deep insight for the interface coupling within metal oxide/carbon material hetero-structures for advanced catalytic applications.

Construction of La1−xSrxNiO3/g-C3N4 type-Z heterojunctions with enhanced visible-light photocatalytic degradation of organic pollutants

Lanthanum nickelate (LaNiO3), known for its high visible-light absorption, is a promising photocatalyst for water purification. However, the low conduction band position and high photogenerated carrier complexation rate of pure LaNiO3 limit its photocatalytic activity. To address this issue, we investigated the synergistic effects of doping and constructing heterojunctions. A La0.9Sr0.1NiO3 (20%)/g-C3N4 (L2CN8) heterojunction was successfully created. In addition, various characterisation techniques were then employed to analyse the structure–performance relationships of these heterojunction photocatalysts in degrading organic dyes. Results revealed that at a 10% Sr doping level, the oxygen vacancy content was 0.68, which is significantly higher than that of LaNiO3 (0.05). The increased number of oxygen vacancies enhanced the electron capture ability and improved the separation efficiency of photogenerated carriers. Furthermore, the optimised L2CN8 (20 mg) achieved 81.2% and 73.8% removal of methylene blue (50.0 mL, 10 mg L−1) and tetracycline (50.0 mL, 10 mg L−1) under simulated visible-light irradiation (λ > 420 nm). Furthermore, an active species capture experiment confirmed the significant role of superoxide radicals (·O2−) in the degradation process. Based on these experimental findings, we proposed a rational Z-type charge transfer mechanism. This study holds great importance for water pollution control and environmental protection.