Correction: Optimized Cu-doping in ZnO electro-spun nanofibers for enhanced photovoltaic performance in perovskite solar cells and photocatalytic dye degradation.

[This corrects the article DOI: 10.1039/D4RA01544D.].

Optimized Cu-doping in ZnO electro-spun nanofibers for enhanced photovoltaic performance in perovskite solar cells and photocatalytic dye degradation.

Perovskite solar cells (PSCs) compete with conventional solar cells regarding their low-temperature processing and suitable power conversion efficiency. In PSCs, the electron transport layer (ETL) plays a vital role in charge extraction and avoiding recombination; however, poor charge transport of ETL leads to high internal resistance and associated low fill factors. To successfully resolve this challenge, copper-doped zinc oxide nanofibers as an electron transport layer are prepared with various doping levels of 1, 2, and 3 wt% using the electrospinning sol-gel method. The 3 wt% doping of Cu revealed the optimum performance as an ETL, as it offers an electrically efficient transporting structure. SEM images revealed a randomly oriented distribution of nanofibers with different sizes having mesoporous uniformity. Optical properties of doped nanofibers examined using UV-visible analysis showed an extended light absorption due to heteroatom-doping. Adding Cu into the ZnO leads to enhanced charge mobility across the electron transport material. According to Hall measurements, dopant concentration favors the conductivity and other features essentially required for charge extraction and transport. The solar cell efficiency of ZnO doped with 0%, 1%, 2%, and 3% Cu is 4.94%, 5.97%, 6.89%, and 9.79%, respectively. The antibacterial and photocatalytic activities of the prepared doped and undoped ZnO are also investigated. The better light absorption of Cu-ZnO showed a pronounced improvement in the photocatalytic activity of textile electrodes loaded with doped ZnO. The dye degradation rate reaches 95% in 180 min under visible light. In addition, these textile electrodes showed strong antibacterial activity due to the production of reactive oxygen species under light absorption.

Correction: Carbon quantum dots (CQDs)-modified polymers: a review of non-optical applications.

Correction for 'Carbon quantum dots (CQDs)-modified polymers: a review of non-optical applications' by Zeeshan Latif et al., Nanoscale, 2024, 16, 2265-2288, https://doi.org/10.1039/D3NR04997C.

Carbon quantum dots (CQDs)-modified polymers: a review of non-optical applications.

Carbon quantum dots (CQDs) are a promising candidate to replace metal-based additives for polymer reinforcement and functionalization. Specifically, vast interest in CQDs for polymer functionalization stems from their cost effectiveness, sustainable organic precursors, and their non-toxicity. Although several reviews of optical devices based on CQDs have been reported, this mini-review covers the non-optical aspects of CQD-polymer composites. Applications of CQD-modified polymers for smart devices, mechanical reinforcement, textile surface-modification methods, membranes, protective coatings, and thermal resistance are summarized. The synthesis method of CQDs, their dispersion in a polymer matrix and the underlying mechanisms related to the enhanced performance of composites are outlined. Unlike nano-reinforcements, CQDs are self-stabilized and offer an extremely high surface area, which significantly alters the polymer properties at a 1-2% concentration. Finally, a comparative analysis of recent advances in CQD-polymer composites, their problems, and future directions are discussed.

Colorimetric Detection of Cu2+ and Ag+ Ions Using Multi-Responsive Schiff Base Chemosensor: A Versatile Approach for Environmental Monitoring.

In this study, we have synthesized a novel Schiff base-centered chemosensor, designated as SB, with the chemical name ((E)-1-(((6-methylbenzo[d]thiazol-2-yl) imino)methyl)naphthalen-2-ol). This chemosensor was structurally characterized by FT-IR, 1H NMR, UV-Vis and fluorescence spectroscopy. After structural characterization the chemosensor SB was subsequently employed for the detection of Cu2+ and Ag+, using fluorescence spectroscopy. The chemosensor SB showed excellent ability to recognize the target metal ions, leading to fluorescence enhancement and color change from yellow to yellowish orange for Cu2+ and yellow to radish for Ag+ ions. The detection capabilities of this chemosensor were impressive, showing excellent selectivity and an exceptionally low detection limit of 0.0016 µM for Cu2+ and 0.00389 µM for Ag+. Most notably, our approach enables the quantitative detection both metal ions in different water and soil samples at trace level. This achievement holds great promise for analytical applications and offers significant contributions to the field of chemical sensing and environmental protection.

Direct Growth of Nitrogen-Doped Carbon Quantum Dots on Co9S8 Passivated on Cotton Fabric as an Efficient Photoelectrode for Water Treatment.

Heterogeneous growth of photocatalysts on different porous substrates is a solution to avoid secondary pollution caused by composite photocatalysts themselves. However, the heterogeneous growth of composite photocatalysts with nitrogen-doped carbon quantum dots (NCQDs) inclusions-introduced during synthesis-impedes the direct growth on the substrate. To overcome this problem, NCQDs were grown on a Co9S8 (NCQDs-G@Co9S8) layer, decorated on cotton fabric. This optimal coupling mode of NCQDs and Co9S8 showed 54% degradation, compared to 33% dye degradation via NCQDs-doped Co9S8 (NCQDs-D@Co9S8). The change in the crystal structure and its lower loading on fabric results in significantly lower performance of NCQDs-D@Co9S8. Even with the combination of both surface growth and doping (NCQDs-DG@Co9S8), the performance was still limited to 42%. In addition, the optimum growth concentration of NCQDs on Co9S8 was observed for 7.5 w/w %, resulting in 92% photocatalytic activity (PCA) in 80 min. Comparing different surface states formed in NCQDs using different solvents, water-based surface states (oxygen-rich surface) are most suitable for the dye degradation. NCQDs-G@Co9S8 also offers 67% Cr-VI reduction to Cr-III, showing its suitability for both inorganic and organic compounds. Better electrode performance was related to suitable charge separation of the composite, where -OH groups mainly contribute in the photocatalytic dye degradation..

Recent Advances in Organic Sensors for the Detection of Ag+ Ions: A Comprehensive Review (2019-2023).

Recently, organic sensors for the detection of Ag+ and other metal ions have experienced significant advancements. This is because there is a growing demand for reliable and sensitive tools to monitor various environmental pollutants. Organic sensors have O-, S-, and N-donor atoms, which can act as a ligand and coordinate with different metal ions, hence stabilizing them in a variety of oxidation states. This interaction gives colorimetric and fluorescence changes, which are used to monitor Ag+ and other metal ions. This comprehensive review highlights the latest developments in organic sensors for the recognition of Ag+. We present an in-depth analysis of the underlying principles and mechanisms governing Ag+ ion recognition. Various organic sensing platforms, such as fluorescent and colorimetric sensors, are discussed, shedding light on their unique advantages and limitations. Special attention is given to the diverse range of organic ligands, receptors, and functional materials used to achieve high sensitivity, selectivity, and quantification accuracy. Additionally, we delve into real-world applications of organic sensors for Ag+ ion detection, examining their performance in complex matrices such as biological, environmental, industrial and agricultural matrices.

Sunlight-Driven Photocatalytic Active Fabrics through Immobilization of Functionalized Doped Titania Nanoparticles.

Frequent washing of textiles poses a serious hazard to the ecosystem, owing to the discharge of harmful effluents and the release of microfibers. On one side, the harmful effluents from detergents are endangering marine biota, while on the other end, microplastics are observed even in breastfeeding milk. This work proposes the development of sunlight-driven cleaning and antibacterial comfort fabrics by immobilizing functionalized Zn-doped TiO2 nanoparticles. The research was implemented to limit the use of various detergents and chemicals for stain removal. A facile sol-gel method has opted for the fabrication of pristine and Zn-doped TiO2 nanoparticles at three different mole percentages of Zn. The nanoparticles were successfully functionalized and immobilized on cotton fabric using silane coupling agents via pad-dry-cure treatment. As-obtained fabrics were characterized by their surface morphologies, availability of chemical functionalities, and crystallinity. The sunlight-assisted degradation potential of as-functionalized fabrics was evaluated against selected pollutants (eight commercial dyes). The 95-98% degradation of dyes from the functionalized fabric surface was achieved within 3 h of sunlight exposure, estimated by color strength analysis with an equivalent exposition of bactericidal activities. The treated fabrics also preserved their comfort and mechanical properties. The radical trapping experiment was performed to confirm the key radicals responsible for dye degradation, and h+ ions were found to be the most influencing species. The reaction pathway followed the first order kinetic model with rate constant values of 0.0087 min-1 and 0.0131 min-1 for MB and MO dyes, respectively.

Exploring the Potential of Alternate Inorganic Fibers for Automotive Composites.

Composites are a promising material for high-specific strength applications; specifically, fiber-reinforced polymer composites (FRPCs) are in the limelight for their extraordinary mechanical properties. Amongst all FRPCs, carbon fiber reinforcements are dominant in the aerospace and automotive industry; however, their high cost poses a great obstacle in commercial-scale manufacturing. To this end, we explored alternate low-cost inorganic fibers such as basalt and rockwool as potential replacements for carbon fiber composites. In addition to fibrous inclusions to polymers, composites were also fabricated with inclusions of their respective particulates formed using ball milling of fibers. Considering automotive applications, composites' mechanical and thermo-mechanical properties were compared for all samples. Regarding mechanical properties, rockwool fiber and basalt fiber composites showed 30.95% and 20.77% higher impact strength than carbon fiber, respectively. In addition, rockwool and basalt fiber composites are less stiff than carbon and can be used in low-end applications in the automotive industry. Moreover, rockwool and basalt fiber composites are more thermally stable than carbon fiber. Thermogravimetric analysis of carbon fiber composites showed 10.10 % and 9.98 % higher weight loss than basalt and rockwool fiber composites, respectively. Apart from better impact and thermal properties, the low cost of rockwool and basalt fibers provides a key advantage to these alternate fibers at the commercial scale.

Investigation of the anticorrosion and adsorption properties of two polymer compounds on the corrosion of SABIC iron in 1 M HCl solution by practical and computational approaches.

The anticorrosion efficiency of two polymer compounds, namely polystyrene (PS), polybutylene terephthalate (PBT), against the corrosion of SABIC iron (S-Fe) in 1.0 M HCl solution was investigated. The anticorrosion efficiency was estimated by chemical and electrochemical measurements. The anticorrosion efficiency increased with the increase in the concentration of the polymer compounds and reduction in temperature. All the obtained corrosion data confirmed the anticorrosion strength in the presence of PS and PBT compounds, such as the decreasing values of the corrosion current density, capacity of the double layer, and weight reduction, while the values of the charge-transfer resistance increased. Also, the pitting potential values moved in the noble (+) direction. The anticorrosion efficiency of the PBT compound was higher than that of the PS compound, which was 95.98% at 500 ppm concentration for PBT while for PS it was 93.34% according to polarization measurements. The anticorrosion activity occurred by the adsorption of PS and PBT compounds on the surface of S-Fe according to the Langmuir isotherm. The polarization curves indicated that the PS and PBT compounds were mixed-type inhibitors. Density functional theory (DFT) and Monte Carlo simulation (MC) were performed for the two polymer compounds. The computational quantum functions were found to be in agreement with the experimental results.

Synthesis of (tricyanofuran-3-ylmethylene)hydrazinyl thiazole-containing chromophore: A study of its photophysical properties, solvatochromism, and TD-DFT computations.

The chromophore 2-2-(3-cyano-5,5-dimethyl-4-((2-[thiazol-2-yl]hydrazono)methyl)-furan-2(5H)-ylidene)malononitrile (TzHTCF) was prepared by diazo-coupling of diazotized 2-aminothiazole with 3-cyano-2-(dicyanomethylene)-4,5,5-trimethylfuran (TCF). The TzHTCF absorption solvatochromism, in different polarity solvents, demonstrated a ΔEmax = +4.74 in which the positive sign implied the occurrence of a red shift and the TzHTCF lowest excited state was more polar than its ground state. In addition, the TzHTCF fluorescence spectrum produced a λem in the 416-670 nm range and was more dependent on the solvent polarity than the absorption λmax , despite both exhibiting a red shift of 24 and 254 nm, respectively. To discover the Stokes shift ( ∆ ν ¯ ) behaviour of the TzHTCF derivative, Lippert-Mataga and linear solvation-energy relationship (LSER) formulations were utilized in which the LSER approach displayed better results than the Lippert-Mataga method (R2 = 0.9931). Furthermore, the LSER showed that the absorption and fluorescence solvatochromic behaviours were dependent on the solvent's hydrogen-bond donor (α) and acceptor (ß), along with the solvent's polarizability (π*). Moreover, DFT calculations showed that TzHTCF has a planar configuration and its simulated absorption and emission spectra in dimethyl sulphoxide revealed that λmax primarily originated from the HOMO→LUMO and HOMO-1→LUMO transitions, respectively.

Optical Detection of Acetone Using "Turn-Off" Fluorescent Rice Straw Based Cellulose Carbon Dots Imprinted onto Paper Dipstick for Diabetes Monitoring.

Persistent bad breath has been reported as a sign of serious diabetes health conditions. If an individual's breath has a strong odor of acetone, it may indicate high levels of ketones in the blood owing to diabetic ketoacidosis. Thus, acetone gas in the breath of patients with diabetes can be detected using the current easy-to-use fluorescent test dipstick. In another vein, rice straw waste is the most well-known solid pollutant worldwide. Thus, finding a simple technique to change rice straw into a valuable material is highly important. A straightforward and environmentally friendly approach for reprocessing rice straw as a starting material for the creation of fluorescent nitrogen-doped carbon dots (NCDs) has been established. The preparation process of NCDs was carried out via one-pot hydrothermal carbonization using NH4OH as a passivation substance. A testing strip was developed on the basis of cellulose CD nanoparticles (NPs) immobilized onto cellulose paper assay. The NCDs demonstrated a quantum yield of 23.76%. A fluorescence wavelength was detected at 443 nm upon applying an excitation wavelength of 354 nm. NCDs demonstrated remarkable selectivity for acetone gas as their fluorescence was definitely exposed to quenching by acetone as a consequence of the inner filter effect. A linear correlation was observed across the concentration range of 0.5-150 mM. To detect and measure acetone gas, the present cellulose paper strip has a "switch off" fluorescent signal. A readout limit was accomplished for an aqueous solution of acetone as low as 0.5 mM under ambient conditions. The chromogenic fluorescence of the cellulose assay responsiveness depends on the fluorescence quenching characteristic of the cellulose carbon dots in acetone. A thin fluorescent cellulose carbon dot layer was deposited onto the surface of cellulose strips by a simple impregnation process. CDs were made using NP morphology and analyzed using infrared spectroscopy and transmission electron microscopy. The carbon dot distribution on the paper strip was evaluated by scanning electron microscope and energy-dispersive X-ray analysis. The absorption and fluorescence spectral analyses were investigated. The paper sheets' mechanical qualities were also examined.

Simple Preparation of Photoluminescent and Color-Tunable Polyester Resin Blended with Alkaline-Earth-Activated Aluminate Nanoparticles.

A simple inorganic/organic nanocomposite was used to generate long-lasting phosphorescent pebbles for easy commercial manufacturing of smart products. An organic/inorganic nanocomposite was made from low-molecular-weight unsaturated polyester and rare-earth-activated strontium aluminum oxide nanoparticles doped with europium and dysprosium. The polyester resin was mixed with phosphorescent strontium aluminate oxide nanoparticles and methylethyl ketone peroxide as a cross-linking agent to create a viscous mixture that can be hardened in a few minutes at room temperature. Before adding the hardener catalyst, the phosphorescent strontium aluminate nanoparticles were dispersed throughout the polyester resin in a homogeneous manner to ensure that the pigment did not accumulate. Long-lasting, reversible luminescence was shown by the photoluminescent substrates. The emission was reported at 515 nm upon exciting the pebble at 365 nm. In normal visible light, both blank and luminescent pebbles had a translucent appearance. As a result of UV irradiation, the photoluminescent pebbles produced an intense green color. The three-dimensional CIE Lab (International Commission on Illumination) color coordinates and luminescence spectra were used to investigate the color changing characteristics. Photophysical characteristics, including excitation, emission, and lifetime, were also investigated. Scanning electron microscopy, wavelength-dispersive X-ray fluorescence spectroscopy, and energy-dispersive X-ray analysis were employed to report the surface morphologies and elemental content. Without impairing the pebbles' original physico-mechanical characteristics, the pebbles showed improved superhydrophobic activity. The current simple colorless long-lasting phosphorescent nanocomposite can be applied to a variety of surfaces, like ceramics, glassware, tiles, and metals.

Insights into the adsorption and corrosion inhibition properties of newly synthesized diazinyl derivatives for mild steel in hydrochloric acid: synthesis, electrochemical, SRB biological resistivity and quantum chemical calculations.

Two azo derivatives, 4-((4-hydroxy-3-((4-oxo-2-thioxothiazolidin-5-ylidene)methyl)phenyl) diazinyl) benzenesulfonic acid (TODB) and 4-((3-((4,4-dimethyl-2,6-dioxocyclohexylidene) methyl)-4-hydroxyphenyl)diazinyl) benzenesulfonic acid (DODB) were synthesized and characterized using Fourier-transform infrared spectroscopy (FTIR), proton nuclear magnetic resonance (1H-NMR) and mass spectral studies. Gravimetric methods, potentiodynamic polarization (PDP), electrochemical impedance spectroscopy (EIS), electrochemical frequency modulation (EFM) techniques and inductive coupled plasma-optical emission spectroscopy were used to verify the above two compounds' ability to operate as mild steel (MS) corrosion inhibitors in 1 M HCl. Tafel data suggest that TODB and DODB have mixed-type characteristics, and EIS findings demonstrate that increasing their concentration not only alters the charge transfer (R ct) of mild steel from 6.88 Ω cm2 to 112.9 Ω cm2 but also changes the capacitance of the adsorbed double layer (C dl) from 225.36 to 348.36 µF cm-2. At 7.5 × 10-4 M concentration, the azo derivatives showed the highest corrosion inhibition of 94.9% and 93.6%. The inhibitory molecule adsorption on the metal substrate followed the Langmuir isotherm. The thermodynamic activation functions of the dissolution process were also calculated as a function of inhibitor concentration. UV-vis, scanning electron microscopy (SEM), and energy dispersive X-ray spectroscopy (EDX) techniques were used to confirm the adsorption phenomenon. The quantum chemical parameters, inductively coupled plasma atomic emission spectroscopy (ICPE) measurements, and the anti-bacterial effect of these new derivatives against sulfate-reducing bacteria (SRB) were also investigated. Taken together, the acquired results demonstrate that these compounds can create an appropriate preventing surface and regulate the corrosion rate.

Ethyl ester/acyl hydrazide-based aromatic sulfonamides: facile synthesis, structural characterization, electrochemical measurements and theoretical studies as effective corrosion inhibitors for mild steel in 1.0 M HCl.

In this research paper, aromatic sulfonamide-derived ethyl ester (p-TSAE) and its acyl hydrazide (p-TSAH) were directly synthesized, characterized, and employed for the first time as prospective anticorrosive agents to protect mild steel in 1.0 M HCl conditions. The corrosion efficiency was probed by electrochemical methods including polarization, impedance, and frequency modulation measurements. Optimal efficiencies of 94% and 92% were detected for the hydrazide and ester, respectively, revealing excellent corrosion inhibition. Moreover, both the hydrazide and ester molecules combat the cathodic and anodic reactions correspondingly in a mixed-type manner. The electron transfer (ET) at the inhibitor/metal interface was evaluated using DFT at the B3LYP/6-31g(d,p) level. Natural bond orbital analysis (NBO) and frontier molecular orbital analysis (FMO) calculations showed superior capabilities of the synthesized inhibitors to easily reallocate charge into the metal surface. However, the hydrazide molecules showed slightly better inhibition efficiency than the ester due to the strong interaction between the lone pairs of the nitrogen atoms and the d-orbitals of the metal. The chemical hardness of the hydrazide and ester are 2.507 and 2.511 eV, respectively, in good accordance with the recorded electrochemical inhibition efficiencies for both molecules. Good and straightforward correlations between the experiments and calculations are obtained.