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For all tested strains and both tested QAACs, the presence of smectite increased apparent MIC values while kaolinite had no effect on MICs. Sorption curves without bacteria showed that smectite sorbed larger amounts of QAACs than kaolinite. Correcting nominal QAAC concentrations employed in toxicity tests for QAAC sorption using the sorption curves explained well the observed shifts in apparent MICs. Transmission electron microscopy (TEM) demonstrated that the interlayer space of smectite expanded from 13.7 ± 1 Å to 19.9 ± 1.5 Å after addition of BAC-C12. This study provides first evidence that low charge 21 expandable layer silicates can play an important role for buffering QAAC toxicity in soils.[Formula see text] and [Formula see text] are well known materials in the field of photocatalysis due to their exceptional electronic structure, high chemical stability, non-toxicity and low cost. However, owing to the wide band gap, these can be utilized only in the UV region. Thus, it's necessary to expand their optical response in visible region by reducing their band gap through doping with metals, nonmetals or the combination of different elements, while retaining intact the photocatalytic efficiency. We report here, the codoping of a metal and a nonmetal in anatase [Formula see text] and [Formula see text] for efficient photocatalytic water splitting using hybrid density functional theory and ab initio atomistic thermodynamics. The latter ensures to capture the environmental effect to understand thermodynamic stability of the charged defects at a realistic condition. We have observed that the charged defects are stable in addition to neutral defects in anatase [Formula see text] and the codopants act as donor as well as acceptor depending on the nature of doping (p-type or n-type). However, the most stable codopants in [Formula see text] mostly act as donor. Our results reveal that despite the response in visible light region, the codoping in [Formula see text] and [Formula see text] cannot always enhance the photocatalytic activity due to either the formation of recombination centers or the large shift in the conduction band minimum or valence band maximum. Amongst various metal-nonmetal combinations, [Formula see text] (i.e. Mn is substituted at Ti site and S is substituted at O site), [Formula see text] in anatase [Formula see text] and [Formula see text], [Formula see text] in [Formula see text] are the most potent candidates to enhance the photocatalytic efficiency of anatase [Formula see text] and [Formula see text] under visible light irradiation.Active meta polarizers based on phase-change materials have recently led to emerging developments in terahertz devices and systems for imaging, security, and high-speed communications. Existing technologies of adaptive control of meta polarizers are limited to the complexity of external stimuli. Here, we introduce an active terahertz polarizer consisting of a single layer of large array patterns of vanadium dioxide material integrated with metallic patch matrix to dynamically reconfigure the polarization of the terahertz waves. The proposed active polarizer is simple in structure and can independently manipulate the polarization of the incident THz waves in two orthogonal directions. In addition, the device can also be performing as a highly efficient reflector at the same frequencies. We demonstrate that efficient and fast polarization changes of THz waves can be achieved over a wide operating bandwidth. Compared with other active polarizers using mechanical, optical and thermal controls, it can be conveniently manipulated with DC bias without any external actuators, intense laser source or heater. Therefore, with the advantages of high efficiency, compact size, low loss, low cost and fast response, the proposed polarizer can be highly integrative and practical to operate within adaptive terahertz circuits and systems.Optical polarization is an indispensable component in photonic applications, the orthogonality of which extends the degree of freedom of information, and strongly polarized and highly efficient small-size emitters are essential for compact polarization-based devices. We propose a group III-nitride quantum wire for a highly-efficient, strongly-polarized emitter, the polarization anisotropy of which stems solely from its one-dimensionality. We fabricated a site-selective and size-controlled single quantum wire using the geometrical shape of a three-dimensional structure under a self-limited growth mechanism. We present a strong and robust optical polarization anisotropy at room temperature emerging from a group III-nitride single quantum wire. Based on polarization-resolved spectroscopy and strain-included 6-band k·p calculations, the strong anisotropy is mainly attributed to the anisotropic strain distribution caused by the one-dimensionality, and its robustness to temperature is associated with an asymmetric quantum confinement effect.Ruthenium complexes have been extensively explored as potential molecules for cancer treatment. Considering our previous findings on the remarkable cytotoxic activity exhibited by the ruthenium (II) complex 3-hydroxy-4-methoxybenzoate (hmxbato)-cis-[RuII(ŋ2-O2CC7H7O2)(dppm)2]PF6 against Leishmania promastigotes and also the similar metabolic characteristics between trypanosomatids and tumor cells, the present study aimed to analyze the anticancer potential of hmxbato against lung tumor cells, as well as the partial death mechanisms involved. Hmxbato demonstrated selective cytotoxicity against A549 lung tumor cells. Cefodizime manufacturer In addition, this complex at a concentration of 3.8 µM was able to expressively increase the generation of reactive oxygen species (ROS) in tumor cells, causing an oxidative stress that may culminate in (1) reduction in cellular proliferation; (2) changes in cell morphology and organization patterns of the actin cytoskeleton; (3) cell arrest in the G2/M phase of the cell cycle; (4) apoptosis; (5) changes in the mitochondrial membrane potential and (6) initial DNA damage. Furthermore, we demonstrated that the induction of programmed cell death can occur by the intrinsic apoptotic pathway through the activation of caspases. It is also worth highlighting that hmxbato exhibited predominant actions on A549 tumor cells in comparison to BEAS-2B normal bronchial epithelium cells, which makes this complex an interesting candidate for the design of new drugs against lung cancer.