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Our device represents a microfluidic tool for electronic assessment of immune activation states and, hence, a portable diagnostic for quantitative evaluation of immunity and disease state. Further, its ability to achieve label-free enrichment of activated immune cells promises clinical utility in cell-based immunotherapies.Many COVID-19 patients are presenting with atypical clinical features. Happy hypoxemia with almost normal breathing, anosmia in the absence of rhinitis or nasal obstruction, and ageusia are some of the reported atypical clinical findings. Based on the clinical manifestations of the disease, we are proposing a new hypothesis that SARS-CoV-2 mediated inflammation of the nucleus tractus solitarius may be the reason for happy hypoxemia in COVID-19 patients.In this work, o-phenylenediamine is utilized as a precursor to synthesize the fluorescent emission wavelength switchable carbon dots (o-CDs). Our investigation reveals that ferrous ions (Fe2+) can effectively induce fluorescence quenching of o-CDs by chelation and aggregation. After the addition of hydrogen peroxide (H2O2), the fluorescence of o-CDs recovers and the fluorescent color changes from yellow to green. As far as we know, o-CDs are the first reported CDs with switchable fluorescence emission wavelength. In order to fabricate an enzyme-free immunosensor, an amino-functionalized dendritic mesoporous silica nanoparticle (DMSN)-gold nanoparticle (Au NP) nanostructure was fabricated as a glucose oxidase mimetic nanoenzyme by in situ coating of the Au NPs on the surface of the DMSNs. Then, the functionalized DMSN-Au NPs were modified on the detection antibody and hydrolyzed with glucose to produce H2O2. This immune induced recognition strategy combines with the o-CDs+Fe2+ signal generation system to achieve specific and sensitive detection of the target. The replacement of glucose oxidase by DMSN-Au NPs not only reduces the cost but also provides significantly amplified signals due to DMSNs haing a high specific surface area. We show the detection of carcinoembryonic antigen (CEA) as an example target to evaluate the analytical figure of merits of the proposed strategy. Under the optimal conditions, two-photon-based o-CDs displayed excellent performances for CEA and the limit of detection as low as 74.5 pg/mL with a linear range from 0.1 to 80 ng/mL. The proposed fluorescent immunosensor provides an optional and potential scheme for low cost, high sensitivity, and versatile discovery of clinical biomarkers.One of the main challenges for next-generation electric power systems and electronics is to avoid premature dielectric breakdown in insulators and capacitors and to ensure reliable operations at higher electric fields and higher efficiencies. However, dielectric breakdown is a complex phenomenon and often involves many different processes simultaneously. Here we show distinctly different defect-related and intrinsic breakdown processes by studying individual, single-crystalline TiO2 nanoparticles using in situ transmission electron microscopy (TEM). As the applied electric field intensity rises, rutile-to-anatase phase transition, local amorphization/melting, and ablation are identified as the corresponding breakdown processes, the field intensity thresholds of which are found to be related to the position of the intensified field and the duration of the applied bias relative to the time of charged defects accumulation. Our observations reveal an intensity-dependent dielectric response of crystalline oxides at breakdown and suggest possible routes to suppress the initiation of premature dielectric breakdown. Hence, they will aid the design and development of next-generation robust and efficient solid dielectrics.Solid foams with micrometric pores are used in different fields (filtering, 3D cell culture, etc.), but today, controlling their foam geometry at the pore level, their internal structure, and the monodispersity, along with their mechanical properties, is still a challenge. Existing attempts to create such foams suffer either from slow speed or size limitations (above 80 μm). In this work, by using a temperature-regulated microfluidic process, 3D solid foams with highly monodisperse open pores (PDI lower than 5%), with sizes ranging from 5 to 400 μm and stiffnesses spanning 2 orders of magnitude, are created for the first time. These features open the way for exciting applications, in cell culture, filtering, optics, etc. Here, the focus is set on photonics. Numerically, these foams are shown to open a 3D complete photonic bandgap, with a critical index of 2.80, thus compatible with the use of rutile TiO2. In the field of photonics, such structures represent the first physically realizable self-assembled FCC (face-centered cubic) structure that possesses this functionality.Quick and effective sterilization of drug-resistant bacteria inevitably became an ever-growing global challenge. In this study, a multifunctional composite (PDA/Cu-CS) hydrogel mainly composed of polydopamine (PDA) and copper-doped calcium silicate ceramic (Cu-CS) was prepared. It was confirmed that PDA/copper (PDA/Cu) complexing in the composite hydrogel played a key role in enhancing the photothermal performance and antibacterial activity. Through a unique "hot ions effect", created by the heating of Cu ions through the photothermal effect of the composite hydrogel, the hydrogel showed high-efficiency, quick, and long-term inhibition of methicillin-resistant Staphylococcus aureus and Escherichia coli. In addition, the hydrogel possessed remarkable bioactivity to stimulate angiogenesis. The in vivo results confirmed that the "hot ions effect" of the composite hydrogel removed existing infection in the wound area efficiently and significantly promoted angiogenesis and collagen deposition during infectious skin wound healing. Our results suggested that the design of multifunctional hydrogels with "hot ions effect" may be an effective therapeutic approach for the treatment of infectious wounds.Utilization of the lithium (Li) metal anode is seriously prevented by the undesirable side reactions with electrolyte solvents due to their mismatched energy gaps and easily lacerated SEI layer. In this work, we develop a transplantable carbonaceous membrane with a particular ability of filtrating Li+ ions by blocking organic solvents and use it as an independent protective component to isolate lithium metal anode from the electrolytes. This graphene-supported N-doped membrane (GNM) can separate organic carbonates of dimethyl carbonate (DMC) and diethyl carbonate (DEC) from H2O-DMC/DEC mixtures by holding back the organic solvents. When this membrane is used in a Li-Cu cell, a high Li Coulombic efficiency (CE) of 98.5% is maintained in carbonate electrolyte over 400 cycles. Application of GNM in Li-O2 full cell provides a sustainable use of Li metal for more than 200 cycles (2000 h) by keeping its shiny metal luster. selleck chemicals llc Our results demonstrate that the use of an independent component with Li+ filtrating ability, such as the transplantable membrane of GNM developed in this work, should be a feasible remedy to protect Li metal anode in practical Li metal batteries.