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7 million km2 for restoration or altered management opportunities. The results suggest that current hazard mapping is inadequate for resilience planning; increased storm frequency and intensity necessitate modification of design standards, land-use policies, and infrastructure operation. Implementation of interventions can be guided by a greater understanding of social-ecological vulnerabilities within hazard and exposure areas.The nanoscale morphology of polymer blends is a key parameter to reach high efficiency in bulk heterojunction solar cells. Thereby, research typically focusing on optimal blend morphologies while studying nonoptimized blends may give insight into blend designs that can prove more robust against morphology defects. Here, we focus on the direct correlation of morphology and device performance of thieno[3,4-b]-thiophene-alt-benzodithiophene (PTB7)[6,6]phenyl C71 butyric acid methyl ester (PC71BM) bulk heterojunction (BHJ) blends processed without additives in different donor/acceptor weight ratios. We show that while blends of a 11.5 ratio are composed of large donor-enriched and fullerene domains beyond the exciton diffusion length, reducing the ratio below 10.5 leads to blends composed purely of polymer-enriched domains. Importantly, the photocurrent density in such blends can reach values between 45 and 60% of those reached for fully optimized blends using additives. We provide here direct visual evidence thats such as donor-enriched domains exceeding the exciton diffusion length.A complex alkali and alkaline-earth metal borate Li4Ca2B8O16 has been synthesized successfully via the high-temperature solution method. Li4Ca2B8O16 crystallizes into the space group P1̅ (No. 2) of the triclinic crystal system. The crystal structure exhibits a three-dimensional framework consisting of the [B8O16]∞ chains connected by the [LiOn] (n = 3, 4, 6) and [CaO7] polyhedra. The fundamental building block [B8O18] differs from those of other anhydrous octa-borates, which can be identified as a unique one. Furthermore, Li4Ca2B8O16 shows three different Li-O units, which is unique among all non-disordered anhydrous borates. It shows a short UV cutoff edge less than 190 nm. Eloxatin To better study the relationships between the crystal structure and properties, the DFT calculations were used for the evaluations of the optical band gap and birefringence.Our early studies demonstrated an impressive chemopreventive efficacy of dihydromethysticin (DHM), unique in kava, against tobacco carcinogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK)-induced lung tumorigenesis in A/J mice in which DHM was supplemented in the diet. The current work was carried out to validate the efficacy, optimize the dosing schedule, and further elucidate the mechanisms using oral bolus dosing of DHM. The results demonstrated a dose-dependent chemopreventive efficacy of DHM (orally administered 1 h before each of the two NNK intraperitoneal injections, 1 week apart) against NNK-induced lung adenoma formation. Temporally, DHM at 0.8 mg per dose (∼32 mg per kg body weight) exhibited 100% lung adenoma inhibition when given 3 and 8 h before each NNK injection and attained >93% inhibition when dosed at either 1 or 16 h before each NNK injection. The simultaneous treatment (0 h) or 40 h pretreatment (-40 h) decreased lung adenoma burden by 49.8% and 52.1%, respectively. However, post-NNK administration of DHM (1-8 h after each NNK injection) was ineffective against lung tumor formation. In short-term experiments for mechanistic exploration, DHM treatment reduced the formation of NNK-induced O6-methylguanine (O6-mG, a carcinogenic DNA adduct in A/J mice) in the target lung tissue and increased the urinary excretion of NNK detoxification metabolites as judged by the ratio of urinary NNAL-O-gluc to free NNAL, generally in synchrony with the tumor prevention efficacy outcomes in the dose scheduling time-course experiment. Overall, these results suggest DHM as a potential chemopreventive agent against lung tumorigenesis in smokers, with O6-mG and NNAL detoxification as possible surrogate biomarkers.The efficient utilization of solar energy is the actual task of the present and near future. Thus, the preparation of appropriate materials that are able to harvest and utilize the broad wavelength range of solar light (especially commonly ignored near-infrared light region-NIR) is the high-priority challenging mission. Our study provides a rationally designed two-dimensional (2D) flexible heterostructures with photocatalytic activity for the production of "clean" hydrogen under NIR illumination, with the hydrogen production rate exceeding most 2D materials and the ability to use the seawater as a starting material. The proposed design utilizes the hybrid bimetallic (Au/Pt) periodic structure, which is further covalently grafted with a metal-organic framework MIL-101(Cr). The periodic gold structure is able to efficiently support the plasmon-polariton wave and to excite the hot electrons, which is further injected in the Pt and MIL-101(Cr) layers. The Pt and MIL-101(Cr) structures provide catalytic sites, which are saturated with hot electrons and efficiently initiate water splitting and hydrogen production. The MIL-101(Cr) layer also serves for repelling generated hydrogen bubbles. The mechanistic studies reveal the catalytic role of every element of the 2D flexible heterostructures. The maximum hydrogen output was achieved under plasmon resonance excitation in the NIR range, and it could be actively controlled by the applied LED wavelength.Due to its unique structure and high porosity, metal-organic frameworks (MOFs) can act not only as nanozyme materials but also as carriers to encapsulate natural enzymes and thus have received extensive attention in recent years. However, a few research studies have been conducted to investigate MOF as a template to generate and tune nanozymes in the structure and performance. In this work, the "raisin pudding"-type ZIF-67/Cu0.76Co2.24O4 nanospheres (ZIF-67/Cu0.76Co2.24O4 NSs) were obtained by rationally regulating the weight ratio of ZIF-67 and Cu(NO3)2 in the synthesis process. Here, ZIF-67 not only acts as a template but also provides a cobalt source for the synthesis of cobalt copper oxide on the surface of ZIF-67/Cu0.76Co2.24O4 NSs with multiple enzyme-like activities. The ZIF-67/Cu0.76Co2.24O4 NSs can mimic four kinds of enzymes with peroxidase-like, glutathione peroxidase-like, superoxide dismutase-like, and laccase-like activities. Based on its laccase-like activity, an online electrochemical system for continuous monitoring of 3,4-dihydroxyphenylacetic acid with good linearity in the range of 0.5-20 μM and a detection limit of 0.15 μM was established. Furthermore, the alteration of DOPAC in the brain microdialysate before and after ischemia of the rats' brain was also successfully recorded. This work not only raises a new idea for the synthesis of nanozyme materials with multiple enzyme activities but also provides a new solution for the detection of neurotransmitters in living brains.The fouling of surfaces submerged in a liquid is a serious problem for many applications including lab-on-a-chip devices and marine sensors. Inspired by the versatility of cilia in manipulating fluids and particles, it is experimentally demonstrated that surfaces partially covered with magnetic artificial cilia (MAC) have the capacity to efficiently prevent attachment and adhesion of real biofouling agents-microalgae Scenedesmus sp. Actuation of the MAC resulted in over 99% removal of the algae for two different scenarios (1) actuating the MAC immediately after injecting the algae into a microfluidic chip, demonstrating antifouling and (2) starting to actuate the MAC 1 week after injecting the algae into the chip and leaving them to grow in static conditions, showing self-cleaning. It is shown that the local and global flows generated by the actuated MAC are substantial, resulting in hydrodynamic shear forces acting on the algae, which are likely to be key to efficient antifouling and self-cleaning. These findings and insights will potentially lead to novel types of self-cleaning and antifouling strategies, which may have a relevant practical impact on different fields and applications including lab-on-a-chip devices and water quality analyzers.Bioinspired nanofibril-humped fibers (BNFs) are fabricated by using thermoplastic polyester elastomer and chitosan, via combining the electrospinning technique and fluid coating method to achieve periodic humps composed of interlaced random nanofibrils and a joint composed of aligned nanofibrils, which are highly similar to the micro/nanostructures of wetted spider silk. Especially, nanofibrils can increase the specific area of the hump to capture fog droplets effectively and transport water in channels between the nanofibrils under humid conditions, and thus the fog droplets can coalesce and be highly efficiently transported toward humps for water collection directionally. Such an ability of highly efficient fog capture is attributed to cooperation of an efficient transportation inside the outer shell of BNFs and outside transportation. Inside transportation is induced by anisotropic capillary channels between nanofibrils. When BNFs are wetted, the inside transportation mode is dominated for water collection, induced by anisotropic capillary channels between nanofibrils. BNF web is also used to investigate the droplet transportation in different cross-fiber contact modes in the process of fog capture on a large scale. This study offers an insight into the design of novel materials, which is expected to be developed for some realms of applications, such as fog harvesting engineering, filtration, and others.Mechano-bactericidal nanomaterials rely on their mechanical or physical interactions with bacteria and are promising antimicrobial strategies that overcome bacterial resistance. However, the real effect of mechanical versus chemical action on their activity is under debate. In this paper, we quantify the forces necessary to produce critical damage to the bacterial cell wall by performing simultaneous nanoindentation and fluorescence imaging of single bacterial cells. Our experimental setup allows puncturing the cell wall of an immobilized bacterium with the tip of an atomic force microscope (AFM) and following in real time the increase in the fluorescence signal from a cell membrane integrity marker. We correlate the forces exerted by the AFM tip with the fluorescence dynamics for tens of cells, and we find that forces above 20 nN are necessary to exert critical damage. Moreover, a similar experiment is performed in which bacterial viability is assessed through physiological activity, in order to gain a more complete view of the effect of mechanical forces on bacteria. Our results contribute to the quantitative understanding of the interaction between bacteria and nanomaterials.Self-heating in light-emitting electrochemical cells (LECs) has been long overlooked, while it has a significant impact on (i) device chromaticity by changing the electroluminescent band shape, (ii) device efficiency because of thermal quenching and exciton dissociation reducing the external quantum efficiency (EQE), and (iii) device stability because of thermal degradation of excitons and eliminate doped species, phase separation, and collapse of the intrinsic emitting zone. Herein, we reveal, for the first time, a direct relationship between self-heating and the early changes in the device chromaticity as well as the magnitude of the error comparing theoretical/experimental EQEs-that is, an overestimation error of ca. 35% at usual pixel working temperatures of around 50 °C. This has been realized in LECs using a benchmark nanographene-that is, a substituted hexa-peri-hexabenzocoronene-as an emerging class of emitters with outstanding device performance compared to the prior art of small-molecule LECs-for example, luminances of 345 cd/m2 and EQEs of 0.