Dopant Mediated Surface Charge Imbalance in Enhancing Performance of Metal Oxide Chemiresistive Gas Sensors

Chemically pristine and untailored metal oxide based gas sensors usually suffer the brunt of poor sensitivity and selectivity. Doping with suitable element has been an efficient strategy to encounter above...

Mathematical Modeling and Performance Evaluation of Switched-Capacitor-Based Battery Equalization Systems

The battery storage system (BSS) is one of the key components in many modern power applications, such as in renewable energy systems and electric vehicles. However, charge imbalance among batteries is very common in BSSs, which may impair the power efficiency, reliability, and safety. Hence, various battery equalization methods have been proposed in the literature. Among these techniques, switched-capacitor (SC)-based battery equalizers (BEs) have attracted much attention due to their low cost, small size, and controllability. In this paper, seven types of SC-based BEs are studied, including conventional, double-tiered, modularized, chain structure types I and II, series-parallel, and single SC-based BEs. Mathematical models that describe the charge–discharge behaviors are first derived. Next, a statistical analysis based on MATLAB simulation is carried out to compare the performance of these seven BEs. Finally, a summary of the circuit design complexity, balancing speed, and practical implementation options for these seven topologies is provided.

The quantitative metabolome is shaped by abiotic constraints

Living systems formed and evolved under constraints that govern their interactions with the inorganic world. These interactions are definable using basic physico-chemical principles. Here, we formulate a comprehensive set of ten governing abiotic constraints that define possible quantitative metabolomes. We apply these constraints to a metabolic network of Escherichia coli that represents 90% of its metabolome. We show that the quantitative metabolomes allowed by the abiotic constraints are consistent with metabolomic and isotope-labeling data. We find that: (i) abiotic constraints drive the evolution of high-affinity phosphate transporters; (ii) Charge-, hydrogen- and magnesium-related constraints underlie transcriptional regulatory responses to osmotic stress; and (iii) hydrogen-ion and charge imbalance underlie transcriptional regulatory responses to acid stress. Thus, quantifying the constraints that the inorganic world imposes on living systems provides insights into their key characteristics, helps understand the outcomes of evolutionary adaptation, and should be considered as a fundamental part of theoretical biology and for understanding the constraints on evolution.

Symmetry decomposition of negativity of massless free fermions

We consider the problem of symmetry decomposition of the entanglement negativity in free fermionic systems. Rather than performing the standard partial transpose, we use the partial time-reversal transformation which naturally encodes the fermionic statistics. The negativity admits a resolution in terms of the charge imbalance between the two subsystems. We introduce a normalised version of the imbalance resolved negativity which has the advantage to be an entanglement proxy for each symmetry sector, but may diverge in the limit of pure states for some sectors. Our main focus is then the resolution of the negativity for a free Dirac field at finite temperature and size. We consider both bipartite and tripartite geometries and exploit conformal field theory to derive universal results for the charge imbalance resolved negativity. To this end, we use a geometrical construction in terms of an Aharonov-Bohm-like flux inserted in the Riemann surface defining the entanglement. We interestingly find that the entanglement negativity is always equally distributed among the different imbalance sectors at leading order. Our analytical findings are tested against exact numerical calculations for free fermions on a lattice.

Research on Molecular Structure and Electronic Properties of Ln3+ (Ce3+, Tb3+, Pr3+)/Li+ and Eu2+ Co-Doped Sr2Si5N8 via DFT Calculation

We use density functional theory (DFT) to study the molecular structure and electronic band structure of Sr2Si5N8:Eu2+ doped with trivalent lanthanides (Ln3+ = Ce3+, Tb3+, Pr3+). Li+ was used as a charge compensator for the charge imbalance caused by the partial replacement of Sr2+ by Ln3+. The doping of Ln lanthanide atom causes the structure of Sr2Si5N8 lattice to shrink due to the smaller atomic radius of Ln3+ and Li+ compared to Sr2+. The doped structure’s formation energy indicates that the formation energy of Li+, which is used to compensate for the charge imbalance, is the lowest when the Sr2 site is doped. Thus, a suitable Li+ doping site for double-doped lanthanide ions can be provided. In Sr2Si5N8:Eu2+, the doped Ce3+ can occupy partly the site of Sr12+ ([SrN8]), while Eu2+ accounts for Sr12+ and Sr22+ ([SrN10]). When the Pr3+ ion is selected as the dopant in Sr2Si5N8:Eu2+, Pr3+ and Eu2+ would replace Sr22+ simultaneously. In this theoretical model, the replacement of Sr2+ by Tb3+ cannot exist reasonably. For the electronic structure, the energy level of Sr2Si5N8:Eu2+/Li+ doped with Ce3+ and Pr3+ appears at the bottom of the conduction band or in the forbidden band, which reduces the energy bandgap of Sr2Si5N8. We use DFT+U to adjust the lanthanide ion 4f energy level. The adjusted 4f-CBM of CeSr1LiSr1-Sr2Si5N8 is from 2.42 to 2.85 eV. The energy range of 4f-CBM in PrSr1LiSr1-Sr2Si5N8 is 2.75–2.99 eV and its peak is 2.90 eV; the addition of Ce3+ in EuSr1CeSr1LiSr1 made the 4f energy level of Eu2+ blue shift. The addition of Pr3+ in EuSr2PrSr2LiSr1 makes part of the Eu2+ 4f energy level blue shift. Eu2+ 4f energy level in EuSr2CeSr1LiSr1 is not in the forbidden band, so Eu2+ is not used as the emission center.

Regulation of Neutrophil Functions by Hv1/VSOP Voltage-Gated Proton Channels

The voltage-gated proton channel, Hv1, also termed VSOP, was discovered in 2006. It has long been suggested that proton transport through voltage-gated proton channels regulate reactive oxygen species (ROS) production in phagocytes by counteracting the charge imbalance caused by the activation of NADPH oxidase. Discovery of Hv1/VSOP not only confirmed this process in phagocytes, but also led to the elucidation of novel functions in phagocytes. The compensation of charge by Hv1/VSOP sustains ROS production and is also crucial for promoting Ca2+ influx at the plasma membrane. In addition, proton extrusion into neutrophil phagosomes by Hv1/VSOP is necessary to maintain neutral phagosomal pH for the effective killing of bacteria. Contrary to the function of Hv1/VSOP as a positive regulator for ROS generation, it has been revealed that Hv1/VSOP also acts to inhibit ROS production in neutrophils. Hv1/VSOP inhibits hypochlorous acid production by regulating degranulation, leading to reduced inflammation upon fungal infection, and suppresses the activation of extracellular signal-regulated kinase (ERK) signaling by inhibiting ROS production. Thus, Hv1/VSOP is a two-way player regulating ROS production. Here, we review the functions of Hv1/VSOP in neutrophils and discuss future perspectives.