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The boosted photocatalytic activity induced NAMPT-regulating therapy offers a promising way to address the important issue of penetration depth limitation induced cancer relapse and migration, providing more possibilities toward successful clinical application.Anode materials based on transition metal sulfides suffer from poor electrochemical reversibility, which limits their cycling stability. Herein, we synthesize hollow I-Cu2MoS4 nanocubes composed of ultrathin nanosheets using a solvothermal method with Cu2O nanocubes as sacrificial templates. The presence of a surfactant is a key factor that prevents the structural collapse of the hollow cubic structure of Cu2MoS4 and the formation of nanoplates. An ether-based electrolyte shows better compatibility with the Cu2MoS4 electrode than a carbonate-based electrolyte, which is reflected in high reversible capacity, superior rate performance, and remarkably improved cycling performance. Ex-situ XRD analysis demonstrates a highly reversible electrochemical reaction in the ether-based electrolyte, which enhances the cycling stability.To enhance the photocatalytic performance of titanium dioxide (TiO2) and reduce the photocorrosion of graphitic carbon nitride (g-C3N4), two-dimensional (2D) reduced graphene oxide (rGO) and g-C3N4 co-modified three-dimensional (3D) TiO2 nanotube arrays (rGO@g-C3N4/TNAs) photoelectrodes were fabricated by the combination of impregnation, annealing and electrochemical cathode deposition. The micromorphology and microstructure were observed by SEM and TEM. The crystalline structure and element composition were characterized by XRD, XPS and Raman spectra. The optical and photo-electrochemical properties were analyzed by UV-vis DRS, open circuit potential and photocurrent density. Results indicated that g-C3N4 and rGO were successfully loaded on the surface of the TNAs photoelectrodes and formed rGO@g-C3N4/TNAs heterostructure. The photocatalytic activity of the photoelectrodes was evaluated by the degradation rate of tetracycline hydrochloride (TC) under xenon lamp irradiation. The introduction of g-C3N4 and rGO reduced the band gap of TNAs photoelectrodes and promoted the separation of photo-induced electron-hole pairs. The rGO@g-C3N4/TNAs photoelectrodes exhibited higher photo-electrochemical properties and photocatalytic activity. The removal rate of TC by rGO@g-C3N4/TNAs photoelectrodes could reach 90% under 120 min photo-degradation and reaction kinetic constant was 2.38 times that of TNAs photoelectrodes. The active radicals capture and ESR experiments results showed that O2- radical and OH radical played the major role in photocatalytic degradation of TC. The possible photocatalytic mechanism of rGO@g-C3N4/TNAs photoelectrodes was presented.Bacterial biofilm represents a protected mode of bacterial growth that significantly enhances the resistance to antibiotics. Poly lactic-co-glycolic acid (PLGA)-based nanoparticle delivery systems have been intensively investigated to combat the bacterial biofilms-associated infections. However, some drawbacks associated with current PLGA-based nanoformulations (e.g. the relatively low drug loading capability, premature burst release and/or incapability of on-demand release of cargos at the site of action) restrict the transition from the lab research to the clinical applications. One potent strategy to overcome the above-mentioned limitations is exploiting the unique properties of carbon quantum dots (CQDs) and combining CQDs with the conventional PLGA nanoparticles. In the present study, the CQDs were innovatively incorporated into PLGA nanoparticles by using a microfluidic method. The resulting CQD-PLGA hybrid nanoparticles presented good loading capability of azithromycin (a macrolide antibiotic, AZI) and tobramycin (an aminoglycoside antibiotic, TOB), and stimuli-responsive release of the cargos upon laser irradiation. Consequently, AZI-loaded CQD-PLGA hybrid nanoparticles showed chemo-photothermally synergistic anti-biofilm effects against P. learn more aeruginosa biofilms. Additionally, the CQD-PLGA hybrid nanoparticles demonstrated good biocompatibility with the eukaryotic cells. Overall, the proof-of-concept of CQD-PLGA hybrid nanoparticles may open a new possibility in chemo-photothermal therapy against bacterial biofilms.The properties of clays and oxides govern many environmental processes, consequently, ongoing effort is invested in developing non-destructive, in-situ analytical tools that reflect these properties. Herein, the physicochemical properties of montmorillonite (MMT) and iron-oxide coated montmorillonite (FeOx-MMT) were characterized using common analytical techniques, and the results were compared to spectral induced polarization (SIP) measurements. FeOx-MMT particles showed a lower CEC, higher pH dependency of the surface charge, and lower suspension stability. Also, the size of the primary particles increased following iron-oxide deposition. SIP measurements over a range of salinities showed that the effective polarization length of the clays was in the order of several microns, suggesting the measurements of aggregates (not primary particles). Moreover, FeOx-MMT particles were more compact than MMT, and their size decreased with increasing salinity due to compaction of the EDL and arrangement of primary particles in the aggregate. The SIP-response to pH changes agreed with zeta potential measurements; at low pH values, MMT exhibited higher polarization due to the higher CEC. However, at a high pH, the differences diminish due to deprotonation of the Fe-OH surface groups. These findings suggest that SIP is a sensitive method that can detect changes in the surface chemistry of soil particles.The word "nanotribology" was introduced for the first time in the title of a paper and a book in 1995. This field encompasses fundamental studies of surface characterization, adhesion, friction, scratching, wear, and lubrication at the atomic scale. At most solid-solid interfaces of technological relevance, contact occurs at numerous asperities. It is of importance to investigate a single asperity contact in the fundamental tribological studies. A nanoprobe sliding on a surface in probe-based microscopies, including atomic force microscopy (AFM) at ultralow loads, simulates one such contact. AFMs and depth-sensing nanoindentation techniques are also used for nanomechanical characterization. The field is referred to as nanomechanics. AFMs can also be used for nanoelectrical characterization which includes electrical resistance, surface potential, and capacitance mapping. Research in the field of nanotribology and nanomechanics was initiated by or for the magnetic storage industry in the late 1980s. Later in the mid-1990s, nanotribology and nanomechanics research became important in bio/nanotechnology devices which involve relative motion, as well as ultrathin films.

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