Notes

Pinning-Induced Folding-Unfolding Asymmetry in Adhesive Wrinkles.
Nanoparticles (NPs) functionalized with antibodies (Abs) on their surface are used in a wide range of bioapplications. Whereas the attachment of antibodies to single NPs to trigger the internalization in cells via receptor-mediated endocytosis has been widely studied, the conjugation of antibodies to larger NP assemblies has been much less explored. Taking into account that NP assemblies may be advantageous for some specific applications, the possibility of incorporating targeting ligands is quite important. Herein, we performed the effective conjugation of antibodies onto a fluorescent NP assembly, which consisted of fluorinated Quantum Dots (QD) self-assembled through fluorine-fluorine hydrophobic interactions. Cellular uptake studies by confocal microscopy and flow cytometry revealed that the NP assembly underwent the same uptake procedure as individual NPs; that is, the antibodies retained their targeting ability once attached to the nanoassembly, and the NP assembly preserved its intrinsic properties (i.e., fluorescence in the case of QD nanoassembly).Aqueous rechargeable zinc ion batteries (ARZIBs) have gained wide interest in recent years as prospective high power and high energy devices to meet the ever-rising commercial needs for large-scale eco-friendly energy storage applications. The advancement in the development of electrodes, especially cathodes for ARZIB, is faced with hurdles related to the shortage of host materials that support divalent zinc storage. EPZ020411 price Even the existing materials, mostly based on transition metal compounds, have limitations of poor electrochemical stability, low specific capacity, and hence apparently low specific energies. Herein, NH4V4O10 (NHVO), a layered oxide electrode material with a uniquely mixed morphology of plate and belt-like particles is synthesized by a microwave method utilizing a short reaction time (~0.5 h) for use as a high energy cathode for ARZIB applications. The remarkable electrochemical reversibility of Zn2+/H+ intercalation in this layered electrode contributes to impressive specific capacity (417 mAh g-1 at 0.25 A g-1) and high rate performance (170 mAh g-1 at 6.4 A g-1) with almost 100% Coulombic efficiencies. Further, a very high specific energy of 306 Wh Kg-1 at a specific power of 72 W Kg-1 was achieved by the ARZIB using the present NHVO cathode. The present study thus facilitates the opportunity for developing high energy ARZIB electrodes even under short reaction time to explore potential materials for safe and sustainable green energy storage devices.Marine nano-ecotoxicology has emerged with the purpose to assess the environmental risks associated with engineered nanomaterials (ENMs) among contaminants of emerging concerns entering the marine environment. ENMs' massive production and integration in everyday life applications, associated with their peculiar physical chemical features, including high biological reactivity, have imposed a pressing need to shed light on risk for humans and the environment. Environmental safety assessment, known as ecosafety, has thus become mandatory with the perspective to develop a more holistic exposure scenario and understand biological effects. Here, we review the current knowledge on behavior and impact of ENMs which end up in the marine environment. A focus on titanium dioxide (n-TiO2) and silver nanoparticles (AgNPs), among metal-based ENMs massively used in commercial products, and polymeric NPs as polystyrene (PS), largely adopted as proxy for nanoplastics, is made. ENMs eco-interactions with chemical molecules including (bio)natural ones and anthropogenic pollutants, forming eco- and bio-coronas and link with their uptake and toxicity in marine organisms are discussed. An ecologically based design strategy (eco-design) is proposed to support the development of new ENMs, including those for environmental applications (e.g., nanoremediation), by balancing their effectiveness with no associated risk for marine organisms and humans.To improve the heat dissipation efficiency of batteries, the eutectic mass ratios of each component in the ternary low-melting phase change material (PCM), consisting of stearic acid (SA), palmitic acid (PA), and lauric acid (LA), was explored in this study. Subsequently, based on the principle of high thermal conductivity and low leakage, SA-PA-LA/expanded graphite (EG)/carbon fiber (CF) composite phase change material (CPCM) was prepared. A novel double-layer CPCM, with different melting points, was designed for the battery-temperature control test. Lastly, the thermal management performance of non-CPCM, single-layer CPCM, and double-layer CPCM was compared via multi-condition charge and discharge experiments. When the mass ratio of SA to PA is close to 82, better eutectic state is achieved, whereas the eutectic mass ratio of the components of SA-PA-LA in ternary PCM is 29.67.463. SA-PA-LA/EG/CF CPCM formed by physical adsorption has better mechanical properties, thermal stability, and faster heat storage and heat release rate than PCM. When the CF content in SA-PA-LA/EG/CF CPCM is 5%, and the mass ratio of SA-PA-LA to EG is 919, the resulting SA-PA-LA/EG/CF CPCM has lower leakage rate and better thermal conductivity. The temperature control effect of single-layer paraffin wax (PW)/EG/CF CPCM is evident when compared to the no-CPCM condition. However, the double-layer CPCM (PW/EG/CF and SA-PA-LA/EG/CF CPCM) can further reduce the temperature rise of the battery, effectively control the temperature and temperature difference, and primarily maintain the battery in a lower temperature range during usage. After adding an aluminum honeycomb to the double-layer CPCM, the double-layer CPCM exhibited better thermal conductivity and mechanical properties. Moreover, the structure showed better battery temperature control performance, while meeting the temperature control requirements during the charging and discharging cycles of the battery.The potential of an innovation for establishing a simultaneous mechanical, thermal, and electrical connection between two metallic surfaces without requiring a prior time-consuming and expensive surface nanoscopic planarization and without requiring any intermediate conductive material has been explored. The method takes advantage of the intrinsic nanoscopic surface roughness on the interconnecting surfaces the two surfaces are locked together for electrical interconnection and bonding with a conventional die bonder, and the connection is stabilized by a dielectric adhesive filled into nanoscale valleys on the interconnecting surfaces. This "nano-locking" (NL) method for chip interconnection and bonding is demonstrated by its application for the attachment of high-power GaN-based semiconductor dies to its device substrate. The bond-line thickness of the present NL method achieved is under 100 nm and several hundred times thinner than those achieved using mainstream bonding methods, resulting in a lower overall device thermal resistance and reduced electrical resistance, and thus an improved overall device performance and reliability. Different bond-line thickness strongly influences the overall contact area between the bonding surfaces, and in turn results in different contact resistance of the packaged devices enabled by the NL method and therefore changes the device performance and reliability. The present work opens a new direction for scalable, reliable, and simple nanoscale off-chip electrical interconnection and bonding for nano- and micro-electrical devices. Besides, the present method applies to the bonding of any surfaces with intrinsic or engineered surface nanoscopic structures as well.Potassium ion batteries (KIBs) are considered as promising alternatives to lithium ion batteries (LIBs), following the rapid increase of demand for portable devices, and the development of electric vehicles and smart grids. Though there has been a promising breakthrough in KIB tech niques, exploring the promising anode materials for KIBs is still a challenge. Rational design with first-principle methods can help to speed up the discovery of potential anodes for KIBs. With density functional calculations, GeC with graphene-like 2D structure (g-GeC) is shown to be a desired anode material for applications in KIBs. The results show that the 2D g-GeC with a high concentration of K ions is thermodynamically stable, due to the strong interaction between C and Ge in GeC layer with the proper interaction between K and GeC. The storage capacity can be about 320 mAh/g, higher than that (279 mAh/g) in graphite. The low energy barrier (0.13 eV) of K ions diffusion on the honeycomb structure with proper voltage profile indicates the fast charge transfer. These theoretical finds are expected to stimulate the future experimental works in KIBs.The β-cyclodextrin shell of synthesized silver nanoparticles (βCD-AgNPs) are found to enhance the detection of hydrogen peroxide in urine when compared to the Horse Radish Peroxidase assay kit. Nanoparticles are confirmed by the UV-Vis absorbance of their localized surface plasmonic resonance (LSPR) at 384 nm. The mean size of the βCD-AgNPs is 53 nm/diameter; XRD analysis shows a face-centered cubic structure. The crystalline structure of type 4H hexagonal nature of the AgNPs with 2.4 nm β-CD coating onto is confirmed using aberration corrected high-resolution transmission electron microscopy (HRTEM). A silver atomic lattice at 2.50 Å and 2.41 Å corresponding to (100) and (101) Miller indices is confirmed using the HRTEM. The scope of βCD-AgNPs to detect hydrogen peroxide (H2O2) in aqueous media and human urine is investigated. The test is optimized by examining the effect of volumes of nanoparticles, the pH of the medium, and the kinetic and temperature effect on H2O2 detection. The βCD-AgNPs test is used as a refined protocol, which demonstrated improved sensitivity towards H2O2 in urine compared to the values obtained by the Horse Radish Assay kit. Direct assessment of H2O2 by the βCD-AgNPs test presented always with a linear response in the nM, μM, and mM ranges with a limit of detection of 1.47 nM and a quantitation limit of 3.76 nM. While a linear response obtained from 1.3 to 37.3 nmoles of H2O2/mole creatinine with a slope of 0.0075 and regression coefficient of 0.9955 when the βCD-AgNPs is used as refined test of creatinine. Values ranging from 34.62 ± 0.23 nmoles of H2O2/mole of creatinine and 54.61 ± 1.04 nmoles of H2O2/mole of creatinine when the matrix is not diluted and between 32.16 ± 0.42 nmoles of H2O2/mole of creatinine and 49.66 ± 0.80 nmoles of H2O2/mole of creatinine when the matrix is twice diluted are found in freshly voided urine of seven apparent healthy men aged between 20 and 40 years old.Molecular Doping (MD) involves the deposition of molecules, containing the dopant atoms and dissolved in liquid solutions, over the surface of a semiconductor before the drive-in step. The control on the characteristics of the final doped samples resides on the in-depth study of the molecule behaviour once deposited. It is already known that the molecules form a self-assembled monolayer over the surface of the sample, but little is known about the role and behaviour of possible multiple layers that could be deposited on it after extended deposition times. In this work, we investigate the molecular surface coverage over time of diethyl-propyl phosphonate on silicon, by employing high-resolution morphological and electrical characterization, and examine the effects of the post-deposition surface treatments on it. We present these data together with density functional theory simulations of the molecules-substrate system and electrical measurements of the doped samples. The results allow us to recognise a difference in the bonding types involved in the formation of the molecular layers and how these influence the final doping profile of the samples.
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