Demystifying Trion Emission in CdSe Nanoplatelets.

At cryogenic temperatures, the photoluminescence spectrum of CdSe nanoplatelets (NPLs) usually consists of multiple emission lines, the origin of which is still under debate. While there seems to be consensus that both neutral excitons and trions contribute to the NPL emission, the prominent role of trions is rather puzzling. In this work, we demonstrate that Förster resonant energy transfer in stacks of NPLs combined with hole trap states in specific NPLs within the stack trigger trion formation, while single NPL spectra are dominated by neutral excitonic emission. This interpretation is verified by implementing copper (Cu+) dopants into the lattice as intentional hole traps. Trion emission gets strongly enhanced, and due to the large amount of hole trapping Cu+ states in each single NPL, trion formation does not necessarily require stacking of NPLs. Thus, the ratio between trion and neutral exciton emission can be controlled by either changing the amount of stacked NPLs during sample preparation or implementing copper dopants into the lattice which act as additional hole traps.

Facile construction of copper-doped metal organic framework as a novel visible light-responsive photocatalyst for contaminant degradation.

ABSTRACTMetal-organic frameworks (MOFs) with photocatalytic activity have garnered significant attentions in environmental remediation. Herein, copper-doped zeolitic imidazolate framework-7 (Cu-doped ZIF-7) was synthesized rapidly and easily using a microwave-assisted technique. Various analytical and spectroscopic methods were employed to access the framework, morphology, light absorption, photo-electrochemical and photocatalytic performance of the synthesized materials. Compared to ZIF-7, Cu/ZIF-7 (molar ratio of Cu2+ to Zn2+ is 1:1) demonstrates superior visible light absorption ability, narrower band gap, enhanced charge separation capability, and reduced electron-hole recombination performance. Under visible light irradiation, Cu/ZIF-7 serves as a Fenton-like catalyst and demonstrates exceptional activity for contaminant degradation, while virgin ZIF-7 remains inactive. With the addition of 9.8 mmol H2O2 and exposure to visible light for 30 min, 10 mg of Cu/ZIF-7 can completely decompose RhB solution (10 mg/L, 50 mL). The synergistic effect of the Cu/ZIF-7/H2O2/visible light system is attributed to visible light photocatalysis and Fenton-like reactions. Cu/ZIF-7 demonstrates excellent catalytic performance stability, with only a slight decrease in degradation efficiency from an initial 97.0% to 95.4% over four cycles. Additionally, spin-trapping ESR measurements and active species trapping experiments revealed that h+ and ·OH occupied a significant position for Rhodamine B (RhB) degradation. Degradation intermediate products of Rhodamine B have been identified using UPLC-MS, and the degradation pathways have been proposed and discussed. This work offers a facile and efficient technique for developing MOF-based visible light photocatalysts for water purification.

Synergistic Dual Doping of Sulfur and Copper for Improved Thermoelectric Properties of Silver Selenide Nanomaterials.

Research on flexible thermoelectric (TE) materials has typically focused on conducting polymers and conducting polymer-based composites. However, achieving TE properties comparable in magnitude to those exhibited by their inorganic counterparts remains a formidable challenge. This study focuses on the synthesis of silver selenide (Ag2Se) nanomaterials using solvothermal methods and demonstrates a significant enhancement in their TE properties through the synergistic dual doping of sulfur and copper. Flexible TE thin films demonstrating excellent flexibility are successfully fabricated using vacuum filtration and hot-pressing techniques. The resulting thin films also exhibited outstanding TE performance, with a high Seebeck coefficient (S = -138.5 µV K-1) and electrical conductivity (σ = 1.19 × 105 S m-1). The record power factor of 2296.8 µW m-1 K-2 at room temperature is primarily attributed to enhanced carrier transport and interfacial energy filtration effects in the composite material. Capitalizing on these excellent TE properties, the maximum power output of flexible TE devices reached 1.13 µW with a temperature difference of 28.6 K. This study demonstrates the potential of Ag2Se-based TE materials for flexible and efficient energy-harvesting applications.

Copper-doped bismuth oxychloride nanosheets assembled into sphere-like morphology for improved photocatalytic inactivation of drug-resistant bacteria.

The devastating microbiological contamination as well as emerging drug-resistant bacteria has posed severe threats to the ecosystem and public health, which propels the continuous exploitation of safe yet efficient disinfection products and technology. Here, copper doping engineered bismuth oxychloride (Cu-BiOCl) nanocomposite with a hierarchical spherical structure was successfully prepared. It was found that due to the exposure of abundant active sites for the adsorption of both bacteria cells and molecular oxygen in the structure, the obtained Cu-BiOCl with nanosheets assembled into sphere-like morphology exhibited remarkable photocatalytic antibacterial effects. In particular, compared to the pure BiOCl, composite Cu-BiOCl possessed improved antibacterial effects against Escherichia coli (E. coli), Staphylococcus aureus (S. aureus), and Methicillin-resistant Staphylococcus aureus (MRSA). The combination of physicochemical characterizations and theoretical calculations has revealed that copper doping significantly promoted the light absorbance, inhibited the recombination of electron-hole pairs, and enhanced molecular oxygen adsorption, which resulted in more generation of active species including reactive oxygen species (ROS) and h+ to achieve superior photocatalytic bacterial inactivation. Finally, transcriptome analysis on MRSA pinpointed photocatalytic inactivation induced by Cu-BiOCl may retard largely the development of drug-resistance. Therefore, the built spherical Cu-BiOCl nanocomposite has provided an ecofriendly, economical and robust strategy for the efficient removal of drug-resistant bacteria with promising potentials for environmental and healthcare utilizations.

Sol-Gel Prepared Spinel HTLs for Assembling 20% Efficiency Perovskite Solar Cell in Air Without Using Anti-Solvent and Toxic Solvent.

Low-temperature sol-gel prepared ZnCo2 O4 spinel-based thin films are developed as high-performance hole transporting layer (HTL) for coating perovskite film (NA-Psk) from the basic MAPbI3 /ACN/CH3 NH2 solution in air without using anti-solvent. Inverted PSC based on 2 mole% (vs Zn) Cu2+ doped ZnCo2 O4 (2%Cu@ZnCo2 O4 ) HTL and NA-Psk absorber exhibit the maximum power conversion efficiency (PCE) of 20.0% with no current hysteresis while the cell based on ZnCo2 O4 and PEDOT:PSS HTL (using NA-Psk absorber) achieves the PCE of 15.79% and 12.3% with a current hysteresis index of 9.8% and 32.4%, respectively. Without encapsulation, PSCs based on 2%Cu@ZnCo2 O4 , ZnCo2 O4 , and PEDOT:PSS HTLs maintain 90%, 77%, and 12%, respectively of the original efficiency by standing in ambient atmosphere (temperature: 20-25 °C, RH:30%-40%) for 1800 h. Large area (10 cm × 10 cm substrate) perovskite mini-module (PSM) with PCE over 15% is also demonstrated by using sol-gel prepared 2%Cu@ZnCo2 O4 HTL. The poor photovoltaic performance of PEDOT:PSS HTL is due to the basic MAPbI3 /ACN/CH3 NH2 solution will deprotonate the acidic PEDOT:PSS to reduce its conductivity whereas ZnCo2 O4 HTL are not affected by basic perovskite precursor solution.

Low-Temperature Synthesis of Cu-Doped Anatase TiO2 Nanostructures via Liquid Phase Deposition Method for Enhanced Photocatalysis.

Titanium dioxide (TiO2) photocatalysis can harness the energy from sunlight, providing a solution to many green- and energy-related problems. In this study, we aimed to produce Cu doped TiO2 (Cu-TiO2) structures at a low temperature (~70 °C) under atmospheric pressure based on liquid phase deposition. The products prepared with Cu nitrate exhibited anatase-phase TiO2 with the presence of Cu, and the particles showed a waxberry-like structure. Changing the Cu nitrate concentration allowed control of the atomic concentration; we confirmed ~1.3 atm.% of Cu ions in the product when we applied 10 mM in the precursor solution. By doping Cu, the light absorption edge shifted to 440 nm (~2.9 eV), and we proved the photocatalytic reaction through action spectral measurement. We observed the decomposition of acetaldehyde into CO2 on Cu-TiO2 photocatalysts, which produced optimized improvements in photocatalytic activity at Cu dopant levels between 0.2 and 0.4 atm.%. This study demonstrates that the liquid phase deposition technique can be used for doping metallic ions into TiO2, which shows promise for preparing novel and unique nanomaterials as visible light photocatalysts.

Cu-Doped MoSi2 N4 Monolayer as a Potential NH3 Sensor.

Cu doped MoSi2 N4 monolayer (Cu-MoSi2 N4 ) was firstly proposed to analyze adsorption performances of common gas molecules including O2 , N2 , CO, NO, NO2 , CO2 , SO2 , H2 O, NH3 and CH4 via density functional theory (DFT) combining with non-equilibrium Green's function (NEGF). The electronic transport calculations indicate that Cu-MoSi2 N4 monolayer has high sensitivity for CO, NO, NO2 and NH3 molecules. However, only NH3 molecule adsorbs on the Cu-MoSi2 N4 monolayer with moderate strength (-0.55 eV) and desorbs at room temperature (2.36×10-3  s). Thus, Cu-MoSi2 N4 monolayer is demonstrated as a potential NH3 sensor.

Observation of Phonon Cascades in Cu-Doped Colloidal Quantum Wells.

Electronic doping has endowed colloidal quantum wells (CQWs) with unique optical and electronic properties, holding great potential for future optoelectronic device concepts. Unfortunately, how photogenerated hot carriers interact with phonons in these doped CQWs still remains an open question. Here, through investigating the emission properties, we have observed an efficient phonon cascade process (i.e., up to 27 longitudinal optical phonon replicas are revealed in the broad Cu emission band at room temperature) and identified a giant Huang-Rhys factor (S ≈ 12.4, more than 1 order of magnitude larger than reported values of other inorganic semiconductor nanomaterials) in Cu-doped CQWs. We argue that such an ultrastrong electron-phonon coupling in Cu-doped CQWs is due to the dopant-induced lattice distortion and the dopant-enhanced density of states. These findings break the widely accepted consensus that electron-phonon coupling is typically weak in quantum-confined systems, which are crucial for optoelectronic applications of doped electronic nanomaterials.

Tuning the Red Emission to Instigate Intrinsic White-Light Emission in Single-Phase Phosphor with Excellent Color Rendering Index.

There is ever-growing interest to develop intrinsic white light emitting single-phase phosphors that have high CRI, devoid of bluish tinge, ease of synthesis and are scalable. Herein, manipulating vacuum pressure to instigate white light emission in Cu2+ -doped-ZnS phosphors is reported. The detailed X-ray diffraction and electron microscopy confirm the cubic phase of Cu2+ -doped-ZnS phosphor having agglomerated particles (∼130-150 nm). The incorporation of Cu2+ in the ZnS lattice is substantiated by the anti-Stokes shift of Raman peaks and shifting of XRD peaks to higher 2θ values. Upon increasing Cu2+ doping concentration, the resulted decrease in the FWHM of XRD peaks implies shrinkage of the ZnS lattice. Interestingly, by tailoring the excitation wavelength, the stoichiometry of dopant ion, and defect states by varying the vacuum pressure, the optimized ZSC-3 (3% Cu2+ -doped-ZnS) displays the origin of clear blue, green and red emission bands, consequently giving rise to white light emission (CIE values: 0.345:0398). The PLQY and average lifetime calculated for ZSC-3 are 5.98% and 1.5 ms, respectively. Such intense white light emission prompted to fabricate a prototype using a 310 nm UV LED. It exhibits high CRI (97) and warm CCT (4538 K), meeting highly desired values for a white light-emitting phosphor for different lighting and electroluminescence applications.

In Vivo Analysis of the Immune Response to Strontium- and Copper-doped Bioglass.

BACKGROUND: Bioglass is a highly adoptable bone substitute material which can be combined with so-called therapeutic ions. However, knowledge is poor regarding the influence of therapeutic ions on immune reactions and associated bone healing. Thus, the aim of this work was to investigate the influence of strontium- and copper-doped bioglass on the induction of M1 and M2 macrophages, as well as vascularization. MATERIALS AND METHODS: Two types of alkali glass were produced based on ICIE16 bioglass via the melt-quench method with the addition of 5 wt% copper or strontium (ICIE16-Cu and ICIE16-Sr). Pure ICIE16 and 45S5 bioglass were used as control materials. The ion release and chemical composition of the bioglass were investigated, and an in vivo experiment was subcutaneously performed on Sprague-Dawley rats. RESULTS: Scanning electron microscopy revealed significant differences in the surface morphology of the bioglass materials. Energy dispersive X-ray spectroscopy confirmed the efficiency of the doping process by showing the ion-release kinetics. ICIE16-Cu exhibited a higher ion release than ICIE16-Sr. ICIE16-Cu induced low immune cell migration and triggered not only a low number of M1 and M2 macrophages but also of blood vessels. ICIE16-Sr induced higher numbers of M1 macrophages after 30 days. Both bioglass types induced numbers of M2 macrophages comparable with those found in the control groups. CONCLUSION: Bioglass doping with copper and strontium did not significantly influence the foreign body response nor vascularization of the implantation bed in vivo. However, all the studied bioglass materials seemed to be biocompatible.

Optical Dynamics of Copper-Doped Cadmium Sulfide (CdS) and Zinc Sulfide (ZnS) Quantum-Dots Core/Shell Nanocrystals.

Recently, quantum-dot-based core/shell structures have gained significance due to their optical, optoelectronic, and magnetic attributes. Controlling the fluorescence lifetime of QDs shells is imperative for various applications, including light-emitting diodes and single-photon sources. In this work, novel Cu-doped CdS/ZnS shell structures were developed to enhance the photoluminescence properties. The objective was to materialize the Cu-doped CdS/ZnS shells by the adaptation of a two-stage high-temperature doping technique. The developed nanostructures were examined with relevant characterization techniques such as transmission electron microscopy (TEM) and ultraviolet-visible (UV-vis) emission/absorption spectroscopy. Studying fluorescence, we witnessed a sharp emission peak at a wavelength of 440 nm and another emission peak at a wavelength of 620 nm, related to the fabricated Cu-doped CdS/ZnS core/shell QDs. Our experimental results revealed that Cu-doped ZnS shells adopted the crystal structure of CdS due to its larger bandgap. Consequently, this minimized lattice mismatch and offered better passivation to any surface defects, resulting in increased photoluminescence. Our developed core/shells are highly appropriate for the development of efficient light-emitting diodes.

Microtexture analysis of copper-doped iron oxide thin films prepared by air pneumatic spray.

The stereometric and fractal concepts are crucial tools to analyse, to verify, to report 3-D microtexture of thin film surfaces on the nanometre scale and thereby to generate useful topographic characteristics for better understanding and steering them toward further improvements and rational use in modern applications. At first, the present work aimed to prepare hematite α-Fe2 O3 thin films with (0, 2, 4, 6 and 8 wt%) of Cu doping by using the air pneumatic spray method. Subsequently, the obtained pure α-Fe2 O3 and Cu-doped α-Fe2 O3 thin films were characterised by XRD device, which determines their polycrystalline nature with the rhombohedral hematite structure. Analysis by UV-VIS absorption showed that the transmittance of the thin films is extinct in the wavelength from approximately 500 to 800 nm, revealing that the films have good optical absorbance in the visible region. The obtained bandgap values varied between 2.23 and 2.21 eV. At second stage, the stereometric and fractal analysis are applied on 3-D image data of pure α- Fe2 O3 and Cu-doped α-Fe2 O3 thin films, which in prior generated using AFM device. Accordingly, the obtained statistical parameters such as surface roughness, density distribution of peaks, depths etc. were used to understand the influence of Cu doping on the 3D microtexture of pure α- Fe2 O3 and Cu-doped α- Fe2 O3 thin film surfaces.

Recent Advances in Copper-Doped Titanium Implants.

Titanium (Ti) and its alloys have been extensively used as implant materials in clinical practice due to their high corrosion resistance, light weight and excellent biocompatibility. However, the insufficient intrinsic osteogenic capacity of Ti and its alloys impedes bone repair and regeneration, and implant-related infection or inflammation remains the leading cause of implant failure. Bacterial infections or inflammatory diseases constitute severe threats to human health. The physicochemical properties of the material are critical to the success of clinical procedures, and the doping of Cu into Ti implants has been confirmed to be capable of enhancing the bone repair/regeneration, angiogenesis and antibacterial capability. This review outlines the recent advances in the design and preparation of Cu-doped Ti and Ti alloy implants, with a special focus on various methods, including plasma immersion implantation, magnetron sputtering, galvanic deposition, microarc oxidation and sol-gel synthesis. More importantly, the antibacterial and mechanical properties as well as the corrosion resistance and biocompatibility of Cu-doped Ti implants from different methods are systematically reviewed, and their prospects and limitations are also discussed.

Peroxidase-Mimetic Copper-Doped Carbon-Dots for Oxidative Stress-Mediated Broad-Spectrum and Efficient Antibacterial Activity.

Carbon dots (CDs) have recently emerged as antibacterial agents and have attracted considerable attention owing to their fascinating merits of small size, facile fabrication, and surface functionalization. Most of them are involved in external light activation or hybridization with other functional nanomaterials. Herein, we present peroxidase-like Cu-doped CDs (Cu-CDs) for in vitro antibacterial applications. The unique peroxidase-mimicking property of the Cu-CDs was demonstrated by tetramethylbenzidine chromogenic assay, electron paramagnetic resonance spectra, and hydroxy radical probe. Escherichia coli and Staphylococcus aureus were chosen as representative gram-negative/positive models against which Cu-CDs exhibited superior antimicrobial activity even at a dosage down to 5 µg/mL. A possible mechanism of action was that the Cu-CDs triggered a catalytic redox reaction of endogenous H2 O2 and glutathione depletion in the bacteria cells, with subsequent oxidative stress and membrane disruption. This work provides a new strategy for the design of microenvironment-responsive antimicrobial nano-agents.

Photocatalytic, self-cleaning and antibacterial properties of Cu(II) doped TiO2.

In the study, sol-gel based TiO2 nanoparticles (NPs) were doped by Cu(II), and the surface of cotton fabric was coated with Cu-doped TiO2 NPs to develop self-cleaning and antibacterial properties. Coffee stains were introduced on the modified cotton fabric and under suntest illumination; a decrease in the color of coffee stain was followed over time via K/S value to determine self-cleaning performance. The photocurrent in a photoelectrocatalytic reactor was measured to evaluate the photocatalytic effect of Cu(II) doping. TiO2 NPs showed self-cleaning and antibacterial effects under UV-illuminated conditions. However, no effects were observed under dark (non-illuminated) conditions. The modified textiles with Cu(II) doped TiO2 NPs showed antibacterial activity against E. coli under light and dark conditions. Under the 2 h illumination period, fluctuating color changes were observed on the raw cotton fabric, and stains remained on the fabric while 78% and 100% color removals were achieved in the cotton fabrics coated by Cu doped TiO2 NPs in 1 h and 2 h, respectively.

Copper doped terbium metal organic framework as emitter for sensitive electrochemiluminescence detection of CYFRA 21-1.

Lanthanide metal organic frameworks (L-MOFs) are emerging as promising electrochemiluminescence (ECL) emitters for bioanalysis. This work proposed a copper doped terbium MOF as a luminescent tag for construction of a "signal-on" ECL immunosensing method. The Tb-Cu-PA MOF was prepared using Tb3+ and Cu2+ ions as metal linkers and m-phthalic acid as bridge ligand, and exhibited strong ECL emission with K2S2O8 as a coreactant. The immunosensor was prepared by immobilizing capture antibody on Pd nanoparticles modified Ni-Co layered double hydroxide (Pd-ZIF-67@LDH) nanoboxes, which showed strong electrocatalytic activity toward the reduction of S2O82- for amplifying the ECL signal. Upon the sandwich-typed immunoreactions, Tb-Cu-PA MOF labeled antibody was introduced onto the immunosensor for sensitive ECL detection of target protein. Using cytokeratin 19 fragment 21-1 (CYFRA21-1), a representative lung cancer biomarker, as target model, the ECL immunosensing method showed a linear range of 0.01-100 ng/mL and a detection limit of 2.6 pg/mL (S/N = 3). This immunosensing strategy highlighted the advances of using luminescent and electroactive MOFs in the developments of highly efficient immunosensors for bioanalysis.

Structural, Optical, and Electronic Properties of Cu-Doped TiNxOy Grown by Ammonothermal Atomic Layer Deposition.

Copper-doped titanium oxynitride (TiNxOy) thin films were grown by atomic layer deposition (ALD) using the TiCl4 precursor, NH3, and O2 at 420 °C. Forming gas was used to reduce the background oxygen concentration and to transfer the copper atoms in an ALD chamber prior to the growth initiation of Cu-doped TiNxOy. Such forming gas-mediated Cu-doping of TiNxOy films had a pronounced effect on their resistivity, which dropped from 484 ± 8 to 202 ± 4 µΩ cm, and also on the resistance temperature coefficient (TCR), which decreased from 1000 to 150 ppm °C-1. We explored physical mechanisms causing this reduction by performing comparative analysis of atomic force microscopy, X-ray photoemission spectroscopy, X-ray diffraction, optical spectra, low-temperature transport, and Hall measurement data for the samples grown with and without forming gas doping. The difference in the oxygen concentration between the films did not exceed 6%. Copper segregated to the TiNxOy surface where its concentration reached 0.72%, but its penetration depth was less than 10 nm. Pronounced effects of the copper doping by forming gas included the TiNxOy film crystallite average size decrease from 57-59 to 32-34 nm, considerably finer surface granularity, electron concentration increase from 2.2(3) × 1022 to 3.5(1) × 1022 cm-3, and the electron mobility improvement from 0.56(4) to 0.92(2) cm2 V-1 s-1. The DC resistivity versus temperature R(T) measurements from 4.2 to 300 K showed a Cu-induced phase transition from a disordered to semimetallic state. The resistivity of Cu-doped TiNxOy films decreased with the temperature increase at low temperatures and reached the minimum near T = 50 K revealing signatures of the quantum interference effects similar to 2D Cu thin films, and then, semimetallic behavior was observed at higher temperatures. In TiNxOy films grown without forming gas, the resistivity decreased with the temperature increase as R(T) = - 1.88T0.6 + 604 µΩ cm with no semimetallic behavior observed. The medium range resistivity and low TCR of Cu-doped TiNxOy make this material an attractive choice for improved matching resistors in RF analog circuits and Si complementary metal-oxide-semiconductor integrated circuits.

Copper-Doped Biphasic Calcium Phosphate Powders: Dopant Release, Cytotoxicity and Antibacterial Properties.

Cytotoxicity and antibacterial properties associated with the dopant release of Cu-doped Biphasic Calcium Phosphate (BCP) powders, mainly composed of hydroxyapatite mixed with ß-tricalcium phosphate powders, were investigated. Twelve BCP ceramics were synthesized at three different sintering temperatures (600 °C, 900 °C and 1200 °C) and four copper doping rates (x = 0.0, 0.05, 0.10 and 0.20, corresponding to the stoichiometric amount of copper in Ca10Cux(PO4)6(OH)2-2xO2x). Cytotoxicity assessments of Cu-doped BCP powders, using MTT assay with human-Mesenchymal Stem Cells (h-MSCs), indicated no cytotoxicity and the release of less than 12 ppm of copper into the biological medium. The antibacterial activity of the powders was determined against both Gram-positive (methicillin-sensitive (MS) and methicillin resistant (MR) Staphylococcus aureus) and Gram-negative (Escherichia coli and Pseudomonas aeruginosa) bacteria. The Cu-doped biomaterials exhibited a strong antibacterial activity against MSSA, MRSA and E. coli, releasing approximatively 2.5 ppm after 24 h, whereas 10 ppm were required to induce an antibacterial effect against P. aeruginosa. This study also demonstrated that the culture medium used during experiments can directly impact the antibacterial effect observed; only 4 ppm of Cu2+ were effective for killing all the bacteria in a 1:500 diluted TS medium, whereas 20 ppm were necessary to achieve the same result in a rich, non-diluted standard marrow cell culture medium.

A facile electroless preparation of Cu, Sn and Sb oxides coated Ti electrode for electrocatalytic degradation of organic pollutants.

Electrocatalytic degradation of organic pollutants is an encouraging technology for wastewater treatment. To achieve practical application, electrode plate with cost effective fabrication, high catalytic efficiency and long service life is urgently required. This work prepared a CuO-SnO2-SbOX electrode on Ti substrate, which is achieved by ultrasonic assisted deposition of Cu layer, followed by electroless deposition of SnSb layer and finalized by calcination at 500 °C. The obtained electrode (Ti/CuO-SnO2-SbOX) exhibited high catalytic degradation activity and a high oxygen evolution potential (OEP) of 2.13 V, which is 0.4 V greater than that of the widely recognized Ti/SnO2-SbOX electrode. The oxygen evolution reaction (OER) models of active oxygen intermediate adsorption was optimized by density functional theory (DFT) calculations. The results revealed that (1) the ΔG of the OER rate-determining step was raised to 2.30 eV after Cu doping on 101 plane; (2) binding energies of the optimized surface with reactive oxygen species (ROS) were substantially decreased. Furthermore, the as-prepared electrode has a high yield of hydroxyl radical generation as evidenced by terephthalic acid detection. The potential for hydroxyl radical generation was measured to be 1.8 V at pH = 12 and 2.6 V at pH = 2.The catalytic degradation rate of methylene blue (MB) follows pseudo first order reaction kinetics, and the reaction constant K value reached 0.02964 -k/min-1, twice as much as that obtained from electrodeposition electrode (Ti/Cu/SnO2-SbOX). A degradation rate of 94.6% was achieved for MB in 100 min in the first run, and the value remained over 85% in the subsequent 10 runs. At the same conditions, the degradation rate of p-nitrophenol was over 90% in 100 min and complete mineralization was achieved in 4 h.

Defect enrich ultrathin TiO2 nanosheets for rapid adsorption and visible light mediated PPCPs degradation.

Recently, PPCPs have attracted extensive attention as emerging pollutants. Due to the strong hydrophilicity and small molecular weight, PPCPs are difficult to be fully removed by adsorption and other processes, posing a serious threat to the ecological environment. Here, we demonstrate solvothermal synthesis of defect enrich TiO2 nanosheets through simple copper doping. Novel TiO2 nanosheets were found to be mesoporous with high specific surface area and exhibited excellent visible light response. Performance of the developed TiO2 nanosheets were evaluated towards photocatalytic degradation of two model pollutants, tetracycline and acetaminophen. Results showed robust degradation of tetracycline and acetaminophen under visible-light irradiation within 100 min. Meanwhile, the potential relationship between the structural characteristics and excellent ability of the catalyst was discussed, as well as probable mechanism. Additionally, a study on the toxicity of tetracycline solution to human skin epidermal cells showed that the toxicity of the treated solution to cells is greatly reduced. The prepared catalysts show good repeatability (a slightly decrease ca.3% after 5 cycles) and applicability, providing a reasonable design for water remediation.