Engineering Mn‐Doped CdS Thin Films Through Chemical Bath Deposition for High‐Performance Photoelectrochemical Water Splitting

Engineering Mn-Doped CdS Thin Films Through Chemical Bath Deposition for High-Performance Photoelectrochemical Water Splitting

Single phase Mn-doped CdS thin films were successfully synthesized by the chemical bath deposition. Different morphologies like nano-cubes, nanoflakes, nano-worms, and nanosheets were obtained under different deposition conditions. The optimized Mn-doped CdS exhibited better photoelectrochemical (PEC) performance for oxygen evolution reaction (OER) than pure CdS films.


Abstract

Doping conventional materials with a second element is an exciting strategy for enhancing catalytic performance via electronic structure modifications. Herein, Mn-doped CdS thin films were successfully synthesized with the aid of the chemical bath deposition (CBD) by varying the pH value (8, 10, and 12) and the surfactant amount (20, 40, 60 mg). Different morphologies like nano-cubes, nanoflakes, nano-worms, and nanosheets were obtained under different deposition conditions. The optimized Mn-doped CdS synthesized at pH=8 exhibited better photoelectrochemical (PEC) performance for oxygen evolution reaction (OER) than pure CdS films, with a maximum photocurrent density of 300 μA/cm2 at an external potential of 0.5 V, under sunlight illumination. The observed performance is attributed to the successful Mn doping, porosity, high surface area, and nanosphere morphology.

Dynamic control of circumrotation of a [2]catenane by acid‐base switching

Dynamic control of circumrotation of a [2]catenane by acid-base switching

We reports a mechanical interlocking donor-acceptor [2]catenane, which is able to form varying degrees of self-complexed or decomplexed compounds that alter the cavity size of the crown ether and affecting the circumrotation behavior of CBPQT ⋅ 4PF6 ring of the catenane.


Abstract

Dynamic control of the motion in a catenane remains a big challenge as it requires precise design and sophisticated well-organized structures. This paper reports the design and synthesis of a donor-acceptor [2]catenane through mechanical interlocking, employing a crown ether featuring two dibenzylammonium salts on its side arms as the host and a cyclobis(paraquat-p-phenylene) (CBPQT ⋅ 4PF6) ring as the guest molecule. By addition of external acid or base, the catenane can form self-complexed or decomplexed compounds to alter the cavity size of the crown ether ring, consequently affecting circumrotation rate of CBPQT ⋅ 4PF6 ring of the catenane. This study offers insights for the design and exploration of artificial molecular machines with intricate cascading responsive mechanisms.

Electrochemical detection of miRNA using commercial and hand‐made screen‐printed electrodes: liquid biopsy for cancer management as case of study

Electrochemical detection of miRNA using commercial and hand-made screen-printed electrodes: liquid biopsy for cancer management as case of study

Screen-printed electrodes are able to offer potent tools for detecting miRNAs in liquid biopsy: commercial or handmade?


Abstract

The growth of liquid biopsy, i. e., the possibility of obtaining health information by analysing circulating species (nucleic acids, cells, proteins, and vesicles) in peripheric biofluids, is pushing the field of sensors and biosensors beyond the limit to provide decentralised solutions for nonspecialists. In particular, among all the circulating species that can be adopted in managing cancer evolution, both for diagnostic and prognostic applications, microRNAs have been highly studied and detected. The development of electrochemical devices is particularly relevant for liquid biopsy purposes, and the screen-printed electrodes (SPEs) represent one of the building blocks for producing novel portable devices. In this work, we have taken miR-2115-3p as model target (it is related to lung cancer), and we have developed a biosensor by exploiting the use of a complementary DNA probe modified with methylene blue as redox mediator. In particular, the chosen sensing architecture was applied to serum measurements of the selected miRNA, obtaining a detection limit within the low nanomolar range; in addition, various platforms were interrogated, namely commercial and hand-made SPEs, with the aim of providing the reader with some insights about the optimal platform to be used by considering both the cost and the analytical performance.

5‐Aryl Substituted 2‐(2‐Methoxyphenyl)benzoxazoles with Large Stokes Shifts: Synthesis, Crystal Structures and Optical Properties

5-Aryl Substituted 2-(2-Methoxyphenyl)benzoxazoles with Large Stokes Shifts: Synthesis, Crystal Structures and Optical Properties

Unlike 2-(2-hydroxyphenyl)benzoxales (HBOs), 2-(2-methoxyphenyl)benzoxazoles (MBOs) lack the sought-after large Stokes shifts of the former which are necessary in fluorescence microscopy. Herein, we demonstrate that the 5-aryl substitution of MBOs affords 2-(4-methoxy-[1,1’-biphenyl]-3-yl)benzoxazoles (MBBOs) dyes with large Stokes shifts.


Abstract

2-(2-methoxyphenyl)benzoxazole (MBO) displays similar photophysical properties to 2-(2-hydroxyphenyl)benzoxazole (HBO), but it lacks the large Stokes shifts necessary for fluorescence microscopy applications. In this paper, we report the 5-substitution of MBO with aryl groups to produce 2-(4-methoxy-[1,1’-biphenyl]-3-yl)benzoxazoles (MBBOs) with large Stokes shifts. The synthesis of MBBOs 615 was accomplished in moderate to good yields by microwave-assisted Sonogashira cross couplings. Crystal structures for compounds 69 and 15 are provided. MBBOs 610, 12, and 14 displayed considerably blue-shifted absorption maxima and slight bathochromic shifts of their fluorescence maxima relative to the unsubstituted MBO.

Synergistic applications of nanocomposite, ultrasound, and on‐water synthesis for efficient and green synthesis of spirooxindole derivatives via cascade C–N, C–O, and C–S bond formation

Synergistic applications of nanocomposite, ultrasound, and on-water synthesis for efficient and green synthesis of spirooxindole derivatives via cascade C–N, C–O, and C–S bond formation

A highly efficient, green, and multicomponent reaction for 32 spirooxindole derivatives via the formation of cascade C–N, C–O, and C–S bonds using starch-capped zinc oxide nanocomposite as an effective heterogeneous catalyst with the synergistic application of ultrasound and on-water synthesis has been developed.


A highly efficient, green, and multicomponent reaction method has been developed for the diversity-oriented synthesis of 32 spirooxindole derivatives via the formation of cascade C–N, C–O, and C–S bonds. The synthesis involved starch-capped zinc oxide nanocomposite as an effective heterogeneous catalyst with the synergistic application of ultrasound and on-water synthesis. By employing this approach, all desired products were successfully obtained with high yields and comparatively short reaction times. Furthermore, the catalyst employed in the process exhibited excellent recyclability, allowing for its recovery and reuse for up to eight consecutive runs without any loss of catalytic activity. The greenness of the protocol was evaluated by various green metrics such as E-factor and eco-score, and the result showed the acceptability of the present method in organic synthesis.

Green synthesis of bovine serum albumin–tailored silver nanoparticles from Aspergillus fumigatus: Statistical optimization, characterization, antioxidant, and cytotoxicity evaluation on colon cancer cells

Green synthesis of bovine serum albumin–tailored silver nanoparticles from Aspergillus fumigatus: Statistical optimization, characterization, antioxidant, and cytotoxicity evaluation on colon cancer cells

This study aimed to synthesize silver nanoparticles from biological method like fungi, as it is an easy, nontoxic, cost-effective process. A design expert software was utilized for optimization through Box-Behnken design. BSA AgNPs were characterized for DLS studies, antioxidant studies like DPPH, Ferrous ion chelation, lipid peroxidation were carried out and it exhibited good antioxidant results for BSA AgNPs and AgNPs. Cytotoxicity test was performed on HT-29 cells and the results exhibited that AgNPs and BSA AgNPs showed the IC50 value of 120 and 100 μg/ml. Hence, our formulations are favouring the  good antioxidant and cytotoxicity leads to better clinical outcomes.


Nanobiotechnology has evolved as a promising technology in developing therapeutically active materials. This study involved the biological synthesis of silver nanoparticles (AgNPs) from extracellular filtrate from the fungal species Aspergillus fumigatus to assess their antioxidant and cytotoxic activity under in-vitro conditions. This method has become more reliable than physical and chemical approaches, attributed to its use of ecologically clean and non-toxic methods. These synthesized nanoparticles are then characterized by UV–visible spectroscopy, Fourier transform infrared spectroscopy (FTIR), dynamic light scattering, scanning electron microscope (SEM), differential scanning calorimetry, and X-ray diffraction (XRD). Design optimization was done to optimize the selected variables to choose the best-fit ratios for the experiment. UV spectroscopy showed the absorption peaks for AgNPs and bovine serum albumin (BSA) AgNPs at 300 and 315 nm. FTIR spectroscopy showed amide, carboxyl, and ester groups in BSA AgNPs, indicating their role in stabilizing nanoparticles. The particle size and zeta potential for AgNPs and BSA AgNPs were found to be 124.81 and 152.92 nm; zeta potentials for AgNPS and BSA AgNPs were found to be −13.3 and −15.6 mV. Various antioxidant studies like 2,2-Diphenyl-1-picrylhydrazyl (DPPH), 2,2-azinobis-(3-ethylbenzothiazoline-6-sulfonate) (ABTS), ion chelating assay, lipid peroxide assay, and malondialdehyde were carried out, indicating good antioxidant activity for synthesized nanoparticles. SEM images advocated good spherical images and are well dispersed. The cytotoxic assay performed on HT-29 colon cancer cells exhibited good inhibition activity for AgNPs and BSA AgNPs, with an IC50 value of 120 and 100 μg/ml. These study results revealed that the synthesized AgNPs, on optimization through Box-Behnken design, exhibited good antioxidant and cytotoxic activity.

“Steric Armor” Strategy of Blue Fluorescent Emitters against Photooxidation‐Induced Degradation

“Steric Armor” Strategy of Blue Fluorescent Emitters against Photooxidation-Induced Degradation


Comprehensive Summary

Stability against oxygen is an important factor affecting the performance of organic semiconductor devices. Improving photooxidation stability can prolong the service life of the device and maintain the mechanical and photoelectric properties of the device. Generally, various encapsulation methods from molecular structure to macroscopic device level are used to improve photooxidation stability. Here, we adopted a crystallization strategy to allow 14H-spiro[dibenzo[c,h]acridine-7,9′-uorene] (SFDBA) to pack tightly to resist fluorescence decay caused by oxidation. In this case, the inert group of SFDBA acts as a “steric armor”, protecting the photosensitive group from being attacked by oxygen. Therefore, compared with the fluorescence quenching of SFDBA powder under 2 h of sunlight, SFDBA crystal can maintain its fluorescence emission for more than 8 h under the same conditions. Furthermore, the photoluminescence quantum yields (PLQYs) of the crystalline film is 327% higher than that of the amorphous film. It shows that the crystallization strategy is an effective method to resist oxidation.