Stable Near-Infrared Photoluminescence of Hexagonal-Shaped PbS Nanoparticles with 1-Dodecanethiol Ligands.

In this study, lead(II) sulphide (PbS) nanoparticles of varying particle sizes were synthesized using the hot injection method, employing 1-octadecene (ODE) as a coordinating ligand in conjunction with oleylamine (OAm). This synthesis approach was compared with the preparation of hexagonal-shaped nanoparticles through the ligand of 1-Dodecanethiol (DT), resulting in DT-capped PbS nanoparticles. The prepared nanoparticles were characterized using multiple techniques including photoluminescence (PL), transmission electron microscopy (TEM), X-ray diffraction (XRD), and Fourier-transform infrared spectroscopy (FT-IR). The condensation reaction of DT ligands led to various nanoparticles within the range of 34.87 nm to 35.87 nm across different synthesis temperatures (120 °C, 150 °C, 180 °C, 210 °C, and 240 °C). The PbS with DT ligands exhibited a highly crystalline and superhydrophilic structure. Interestingly, near-infrared (NIR)-PL analysis revealed peaks at 1100 nm, representing the lowest-energy excitonic absorption peak of PbS nanoparticles for both ligands. This suggests their potential utility in various applications, including IR photoreactors, as well as in the development of non-toxic nanoparticles for potential applications in in vivo bioimaging.

Enhancing Stability in All-Vacuum-Evaporated Hybrid Perovskite Solar Cells via a Bipolar Host as a Hole-Transporting Layer.

Growing an ultrathin hybrid organic-inorganic perovskite film while maintaining high efficiency and addressing photostability challenges for commercial devices remains a significant hurdle. In this study, we explore the incorporation of organometallic copper phthalocyanine (CuPc) and MS-OC (a previously published spiro-based interfacial material for perovskite solar cells (PSCs), featuring an ortho-oriented carbazole donor) as an addition to the hole-transporting layer (HTL) in all-vacuum-deposited Cs0.06FA0.94Pb(I0.68Br0.32)3 PSCs. By innovatively introducing a 3 nm-thin MS-OC layer at the CuPc-perovskite interface, we achieve a deeper understanding of the crystallographic dynamics of perovskites, resulting in a uniform and pinhole-free film. We demonstrate that PSCs utilizing the CuPc HTL with an MS-OC interfacial layer in a p-i-n architecture achieve a power conversion efficiency (PCE) of up to 14.42%. Remarkably, the CuPc/MS-OC-based device exhibits outstanding long-term photostability, maintaining its initial PCE over 400 h (T100 = 400 h) under continuous sunlight illumination. By configuring the device architecture as ITO/MoO3/CuPc/MS-OC/perovskite/C60/BCP/Ag, we find that the evaporated MS-OC thin films effectively reduce nonradiative losses, passivate the perovskite, and enhance device performance. Our findings indicate that the polarity of the underlying surface significantly influences perovskite nucleation, underscoring the potential to improve photostability by controlling interfacial imperfections.

Engineering S. oneidensis for Performance Improvement of Microbial Fuel Cell-a Mini Review.

Microbial fuel cell (MFC) is a promising technology that utilizes exoelectrogens cultivated in the form of biofilm to generate power from various types of sources supplied. A metal-reducing pathway is utilized by these organisms to transfer electrons obtained from the metabolism of substrate from anaerobic respiration extracellularly. A widely established model organism that is capable of extracellular electron transfer (EET) is Shewanella oneidensis. This review highlights the strategies used in the transformation of S. oneidensis and the recent development of MFC in terms of intervention through genetic modifications. S. oneidensis was genetically engineered for several aims including the study on the underlying mechanisms of EET, and the enhancement of power generation and wastewater treating potential when used in an MFC. Through engineering S. oneidensis, genes responsible for EET are identified and strategies on enhancing the EET efficiency are studied. Overexpressing genes related to EET to enhance biofilm formation, mediator biosynthesis, and respiration appears as one of the common approaches.

Resonant energy transfer and light scattering enhancement of plasmonic random lasers embedded with silver nanoplates.

The resonant energy transfer enhancement from a plasmonic random laser (PRL) has been investigated by means of a dye-covered PVA film with embedded silver nanoplates (DC-PVA/AgNPs). Different sizes and morphologies of AgNPs were adopted to shift the localized surface plasmon resonance (LSPR) and intensify recurrent light scattering between the AgNPs. For better overlap between surface plasmon resonance and the photoluminescence of fluorescent molecules with appropriately-sized silver nanoprisms, the slope efficiency of the PRL was greatly enhanced and the lasing threshold was obviously reduced. In addition, the photon lifetime for the DC-PVA/AgNPs film reveals an apparent decline around 1.39 ns owing to better coupling with LSPR. The stronger light scattering of samples with bigger-sized silver nanoprisms has been demonstrated by coherent back scattering measurements, which reveals a smaller transport mean free path around 3.3 µm. With α-stable analysis, it has been successfully demonstrated that the tail exponent α can be regarded as an identifier of the threshold of random lasing.

The production of an efficient visible light photocatalyst for CO oxidation through the surface plasmonic effect of Ag nanoparticles on SiO2@α-Fe2O3 nanocomposites.

A process for the photo deposition of noble Ag nanoparticles on a core-shell structure of SiO2@α-Fe2O3 nanocomposite spheres was performed to produce a CO photo oxidation catalyst. The structural analyses were carried out for samples produced using different Ag metal nanoparticle weight percentages on SiO2@α-Fe2O3 nanocomposite spheres by X-ray diffraction (XRD), field emission-scanning electron microscopy (FE-SEM), UV-vis spectroscopy, Raman spectroscopy and Fourier transform infrared spectroscopy (FTIR). A computational study was also performed to confirm the existence of the synergic effect of surface plasmon resonance (SPR) for different weight percentages of Ag on the SiO2@α-Fe2O3 nanocomposites. The mechanism for CO oxidation on the catalyst was explored using diffuse reflectance infrared Fourier transform spectroscopy (DRFIT). The CO oxidation results for the Ag (2 wt%)-SiO2@α-Fe2O3 nanocomposite spheres showed 48% higher photocatalytic activity than α-Fe2O3 and SiO2@α-Fe2O3 at stable temperature.

Degradation of Methylene Blue Dye in the Presence of Visible Light Using SiO2@α-Fe2O3 Nanocomposites Deposited on SnS2 Flowers.

Semiconductor materials have been shown to have good photocatalytic behavior and can be utilized for the photodegradation of organic pollutants. In this work, three-dimensional flower-like SnS2 (tin sulfide) was synthesized by a facile hydrothermal method. Core-shell structured SiO2@α-Fe2O3 nanocomposites were then deposited on the top of the SnS2 flowers. The as-synthesized nanocomposites were characterized by X-ray diffraction (XRD), Raman spectroscopy, field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), UV⁻Vis Spectroscopy, Brunauer⁻Emmett⁻Teller (BET) surface area analysis, and photoluminescence (PL) spectroscopy. The photocatalytic behavior of the SnS2-SiO2@α-Fe2O3 nanocomposites was investigated by observing the degradation of methylene blue (MB). The results show an effective enhancement of photocatalytic activity for the degradation of MB especially for the 15 wt % SiO2@α-Fe2O3 nanocomposites on SnS2 flowers.

The Preparation of Porous Sol-Gel Silica with Metal Organic Framework MIL-101(Cr) by Microwave-Assisted Hydrothermal Method for Adsorption Chillers.

Abstract: Metal organic framework (MOF) of MIL-101(Cr)-Silica (SiO2) composites with highly mesoporous and uniform dispersions were synthesized by a microwave-assisted hydrothermal method followed by the sol-gel technique. Water vapor adsorption experiments were conducted on the MIL-101(Cr)-SiO2 composites for industrial adsorption chiller applications. The effects of MIL-101(Cr)-SiO2 mixing ratios (ranging from 0% to 52%), the surface area and amount of Lewis and Brønsted sites were comprehensively determined through water vapor adsorption experiments and the adsorption mechanism is also explained. The BET and Langmuir results indicate that the adsorption isotherms associated with the various MIL-101(Cr)-SiO2 ratios demonstrated Type I and IV adsorption behavior, due to the mesoporous structure of the MIL-101(Cr)-SiO2. It was observed that the increase in the amount of Lewis and Brønsted sites on the MIL-101(Cr)-SiO2 composites significantly improves the water vapor adsorption efficiency, for greater stability during the water vapor adsorption experiments.