Effect of Ultraviolet Irradiation on 4H-SiC PiN Diodes Characteristics

In this paper, the effect of ultraviolet (UV) irradiation on the static characteristics of high voltage 4H-SiC PiN is investigated. No significant change is observed in the forward on state characteristic of 4H-SiC PiN diodes before and after ultraviolet light irradiation. However, it is found that the blocking voltage is significantly increased with UV irradiation, which is resulted from the depletion region width extension with the collection of positive charges under the increase of the surface negative charge density. The deep level transient spectroscopy reveals that the UV irradiation induced deep-level defects play a dominant role over the trapped negative charges, and therefore leads to the increase of blocking voltage of 4H-SiC PiN Diodes.

Rear side dielectrics on interdigitating p+-(i)-n+ back-contact solar cells − hydrogenation vs. charge effects

Polysilicon-on-oxide (POLO) passivating contacts and interdigitated back-contact (IBC) cell technologies have recently attracted a lot of interest as candidates for the implementation in the next generation of solar cells. An IBC cell with POLO junctions for both polarities − a POLO2-IBC cell − has to electrically isolate the highly defective p+ and n+ poly-Si regions on the rear side of the cell to avoid parasitic recombination. Inserting an initially undoped, intrinsic (i) region between the p+ and n+ poly-Si regions was demonstrated to successfully prevent the parasitic recombination in the transition region of ISFH's 26.1%-efficient POLO2-IBC cell. In order to further improve the conversion efficiency towards 27%, we apply hydrogen-donating dielectric layer stacks to the p+-(i)-n+ POLO interdigitating rear side to enhance the passivation quality of the POLO junctions. We indeed show a significant improvement of POLO junctions on symmetrical full-area homogenously doped reference samples, but when we apply a hydrogen-donating layer stack on the p+-(i)-n+ POLO interdigitating rear side, we observe a strong degradation in the performance of the POLO2-IBC cell. We attribute this to the formation of a conductive channel between the p+ and n+ poly-Si regions due to the strong negative charge density of the hydrogen-donating layer stack.

Remarkably Enhanced Ion-Exchange Capacity of H2O2-Intercalated Layered Titanate

The H2O2-intercalated layered titanate H1.07Ti1.73O4 (H2O2-HTO) exhibits a dramatically enhanced ion-exchange capacity and remarkably improved reaction rate with various divalent cations. The intercalation can increase negative charge density of TiO6...

Determination of Bacterial Surface Charge Density Via Saturation of Adsorbed Ions

ABSTRACTBacterial surface charge is a critical characteristic of the cell’s interfacial physiology that influences how the cell interacts with the local environment. A direct, sensitive, and accurate experimental technique capable of quantifying bacterial surface charge is needed to better understand molecular adaptations in interfacial physiology in response to environmental changes. We introduce here the method of second harmonic light scattering (SHS) which is capable of detecting the number of molecular ions adsorbed as counter charges on the exterior bacterial surface, thereby providing a measure of the surface charge. In this first demonstration, we detect the small molecular cation, malachite green, electrostatically adsorbed on the surface of representative strains of Gram-positive and Gram-negative bacteria. Surprisingly, the SHS deduced molecular transport rates through the different cellular ultra-structures are revealed to be nearly identical. However, the adsorption saturation densities on the exterior surfaces of the two bacteria were shown to be characteristically distinct. The negative charge density of the lipopolysaccharide coated outer surface of Gram-negative E. coli (8.7±1.7 nm−2) was deduced to be seven times larger than that of the protein surface layer of Gram-positive L. rhamnosus (1.2±0.2 nm−2). The feasibility of SHS deduced bacterial surface charge density for Gram-type differentiation is presented.STATEMENT of SIGNIFICANCEBacterial surface charge density is an important physiological characteristic which determines how the cell interacts with its local environment. Directly measuring the surface charge density, however, is experimentally non-trivial. In this work, we report an experimental method, second harmonic light scattering, that can directly and accurately quantify the surface charge density of individual living bacteria. This is achieved by measuring the number of molecular ions electrostatically adsorbed on the exterior cellular surface as counter charges. It is found that the negative charge density of a representative Gram-negative bacterium is 7 times larger than a representative Gram-positive bacterium. It is suggested that this disparity of surface charge density can be exploited as a basis for Gram-classification of bacteria.

Two Lineages of Pseudomonas aeruginosa Filamentous Phages: Structural Uniformity over Integration Preferences

Pseudomonas aeruginosa filamentous (Pf) bacteriophages are important factors contributing to the pathogenicity of this opportunistic bacterium, including biofilm formation and suppression of bacterial phagocytosis by macrophages. In addition, the capacity of Pf phages to form liquid crystal structures and their high negative charge density makes them potent sequesters of cationic antibacterial agents, such as aminoglycoside antibiotics or host antimicrobial peptides. Therefore, Pf phages have been proposed as a potential biomarker for risk of antibiotic resistance development. The majority of studies describing biological functions of Pf viruses have been performed with only three of them: Pf1, Pf4, and Pf5. However, our analysis revealed that Pf phages exist as two evolutionary lineages (I and II), characterized by substantially different structural/morphogenesis properties, despite sharing the same integration sites in the host chromosomes. All aforementioned model Pf phages are members of the lineage I. Hence, it is reasonable to speculate that their interactions with P. aeruginosa and impact on its pathogenicity may be not completely extrapolated to the lineage II members. Furthermore, in order to organize the present numerical nomenclature of Pf phages, we propose a more informative approach based on the insertion sites, that is, Pf-tRNA-Gly, -Met, -Sec, -tmRNA, and -DR (direct repeats), which are fully compatible with one of five types of tyrosine integrases/recombinases XerC/D carried by these viruses. Finally, we discuss possible evolutionary mechanisms behind this division and consequences from the perspective of virus–virus, virus–bacterium, and virus–human interactions.

The Changes of Surface Potential and Built-in Charge in Alumina Films After the Anodization Process

We have shown that the surface potential of anodic alumina films changes in time: immediately after the anodization process it was positively followed by the substantial decrease to negative values. Such variations of the surface potential can be associated with the negative built-in electric charge in alumina. The highest negative charge density occurs in the films formed in citric and phosphoric electrolytes.

Enhancement of colloidal particle and lignin removal from pre-hydrolysis liquor by pectinase pre-treatment – Study on model substances

Removal of colloidal particle and lignin from pre-hydrolysis liquor (PHL) is important for the subsequent processing and utilization of the saccharides in the PHL. Cationic polymers treatment is a common method for the purpose, and pectinase pre-treatment of PHL can improve the efficiency of the treatment with cationic polymers. To investigate the mechanism of pectinase pre-treatment for improvement of the cationic polymer efficiency, polygalacturonic acid (PGA) was added in the colloidal lignin and dissolved lignin model substances systems, respectively, and the effects of polygalacturonic acid (PGA) and its pectinase pre-treatment on the removal of colloidal and dissolved lignin in the following cationic polymer treatment process were studied. The results showed that the presence of PGA caused the increase of negative charge density of the colloidal lignin and dissolved lignin systems, which lowered the efficiency of the cationic polymers and negatively affected the removal of both the colloidal lignin and the dissolved lignin. After pectinase treatment, the PGA present in the colloidal and dissolved lignin system was degraded and the negative effects on the cationic polymers were eliminated, and the efficiency of the cationic polymers was improved. Compared to the colloidal lignin and dissolved lignin systems with PGA, less cationic polymers were needed for the same systems with pectinase treatment to obtain the similar lignin removal level.

Effect of the ammonium ion on proton conduction in porous ionic crystals based on Keggin-type silicododecatungstate

Proton conduction in crystalline porous materials has received much attention from basic scientific research through to practical applications. Polyoxometalates (POMs) can efficiently transport protons because of their small superficial negative charge density. A simple method for enhancing proton conductivity is to introduce NH4 + into the crystal structure, because NH4 + can form hydrogen bonds and function as a proton carrier. According to these considerations, NH4 + was introduced into the porous structure of A 2[Cr3O(OOCH)6(etpy)3]2[α-SiW12O40]·nH2O (A = Li, Na, K and Cs; etpy = 4-ethylpyridine) (I-A+ ) via topotactic cation exchange. The resulting compound, diammonium tris(4-ethylpyridine)hexaformatooxidotrichromium α-silicododecatungstate hexahydrate, (NH4)2[Cr3(CHO2)6O(C7H9N)3]2[α-SiW12O40]·6H2O, showed high proton conductivity and low activation energy under high relative humidity (RH), suggesting that protons migrate efficiently via rearrangement of the hydrogen-bonding network formed by the NH4 + cations and the waters of crystallization (Grotthuss mechanism). The proton conductivity and activation energy greatly decreased and increased, respectively, with the decrease in RH, suggesting that protons migrate as NH4 + and/or H3O+ under low RH (vehicle mechanism).

Influence of the negative charge density of metalate nanosheets on their bottom-up synthesis

Low negative charge density is required for the bottom-up synthesis of metalate nanosheets by an aqueous solution process.