Co-synthesis and Electrochemical Investigation of the Nitrogen-Doped Carbon Layer with Metallic Nano Beads on the SiOx Anode for Lithium Secondary Batteries.

The high theoretical capacity (∼2000 mAh g-1) of silicon suboxide (SiOx, with 1 < x < 2) can solve the energy density issue of the graphite anode in Li-ion batteries. In addition, it has an advantage in terms of volume expansion or side reactions compared to pure Si or Li metals, which are considered as next-generation anode materials. However, the loading content of SiOx is limited in commercial anodes because of its low cycle stability and initial coulombic efficiency. In this study, a nitrogen-doped carbon layer with Cu beads (N-C/Cu) derived from copper phthalocyanine (CuPc) is applied to a SiOx electrode to improve its electrochemical performance. The SiOx electrode is simultaneously coated with a Cu- and N-doped carbon layer using CuPc. N-C/Cu synergistically enhances the electric conductivity of the electrode, thus improving its electrochemical performance. The SiOx/N-C/Cu composite has better cyclability and higher capacity (1095.5 mAh g-1) than the uncoated electrode, even after 200 cycles in the 0.5 C condition. In full-cell cycling with NCM811 cathodes, the SiOx (60 wt % of SiOx, with a n/p ratio of 1.1) and graphite-mixed (7.8 wt % of SiOx, with a n/p ratio of 1.1) anodes also show improved electrochemical performances in the same conditions.

Optimal non-thermal inactivation methods by study of the microbial control effect in laver (Porphya sp.).

Laver (Porphya sp.) containing vitamins and minerals has a high total number of bacteria of 6-7 log CFU/g. Changes in microbial count in dried laver by light pulse, ultrahigh pressure, electron beam, and superheated steam treatment were compared. It was decreased by 1.3-1.7 log using IPL (Intense Pulsed Light) for 30-60 s at an irradiation distance of 80 mm in dried and wet laver. The key parameters of IPL are energy intensity, processing time and irradiation distance. Light pulse inactivation is based on destruction of microbial DNA structure. Electron beam irradiation at 7 and 10 kGy resulted reduction of 1.8-3.2 log CFU/g. Dried laver was treated at 500 MPa of ultra-high pressure for 3 min, total bacterial number showed no change. Applying superheated steam at 150 °C for 10 s, about 3.3 log CFU/g sterilized. However, it is difficult to apply due to severe damage to sensory quality such as browning.

Aqueous Quaternary Polymer Binder Enabling Long-Life Lithium-Sulfur Batteries by Multifunctional Physicochemical Properties.

Lithium-sulfur batteries (LSBs) have been considered promising candidates for application in high-density energy storage systems owing to their high gravimetric and volumetric energy densities. However, LSB technology faces many barriers from the intrinsic properties of active materials that need to be solved to realize high-performance LSBs. Herein, an aqueous binder, that is, PPCP, based on polyethyleneimine (PEI), polyvinylpyrrolidone (PVP), citric acid (CA), and polyethylene oxide (PEO), was developed. The synthesized PPCP binder has incredible mechanical properties, suitable viscosity, and essential functional groups for developing an effective and reliable LSB system. This study demonstrates that CA is crucial in cross-linking PEI-PVP polymer molecules, and PEO segments significantly enhance the flexibility of the PPCP binder; thus, the binder can mechanically stabilize the cathode structure over many operating cycles. The redistribution of active materials during the charge-discharge processes and reduction of the shuttle effect originate from the excellent chemical interactions of PPCP with lithium polysulfides, which is confirmed by the density functional theory calculation, enabling an ultra-long electrochemical cycle life of 1800 cycles with a low decay rate of 0.0278% cycle-1.

Novel inactivation methods of Doenjang (fermented soybean paste) by high pressure and ohmic heating.

The changes of the total cell number in doenjang (Korean traditional fermented soybean paste) by conventional conduction heating, high pressure non-thermal treatment, and ohmic heating were compared. A total of (101-102) CFU/g cells were decreased by heating at (100-105) °C for 10 min. The inactivation rate was improved when heated to a temperature higher than 110 °C, but the taste, color of doenjang were severely changed. Inactivation by high pressure at (200-800) MPa was not achieved, because the total cell did not reach a reduction of 101 CFU/g. The total bacterial counts of 103 CFU/g were decreased during ohmic heating at 15 V and 60 Hz for 10 min, and showed the most effective inactivation. Therefore, application of the ohmic heating in doenjang with high viscosity can kill target microorganisms related to quality deterioration, and rapid and uniform ohmic heating leads to reduction in sensory quality damage.

Bacillus spores: a review of their properties and inactivation processing technologies.

Many factors determine the resistance properties of a Bacillus spore to heat, chemical and physical processing, including thick proteinaceous coats, peptidoglycan cortex and low water content, high levels of dipicolinic acid (DPA), and divalent cations in the spore core. Recently, attention has been focused on non-thermal inactivation methods based on high pressure, ultrasonic, high voltage electric fields and cold plasmas for inactivating Bacillus spores associated with deterioration in quality and safety. The important chemical sporicides are glutaraldehyde, chorine-releasing agents, peroxygens, and ethylene oxide. Some food-grade antimicrobial agents exhibit sporostatic and sporicidal activities, such as protamine, polylysine, sodium lactate, essential oils. Surfactants with hydrophilic and hydrophobic properties have been reported to have inactivation activity against spores. The combined treatment of physical and chemical treatment such as heating, UHP (ultra high pressure), PEF (pulsed electric field), UV (ultraviolet), IPL (intense pulsed light) and natural antimicrobial agents can act synergistically and effectively to kill Bacillus spores in the food industry.

Improving the quality of vegetable foodstuffs by microwave inactivation.

With the aim of improving the loss of quality in retorted vegetables, experiments on pretreatment inactivation using microwaves were carried out to allow the heating intensity to be reduced during retorting. Microwave heating reduced the bacteria level by 103 CFU/g, and was a more effective method considering the short processing time of 3 min and the required energy being 70-80% of that when using steam. The inactivation effect was due to dielectric heat generation by the high-frequency microwaves. The inactivation effect for heat-resistant Bacillus amyloliquefaciens was indicated by a reduction of 102 CFU/g after 3 min of microwave heating. The total bacteria counts for peeled potato and spicy sauce with vegetables decreased by 3-4 log CFU/g after 3 min using microwaves, and heat-resistant microorganisms were reduced by 2 log CFU/g. Combining microwave heating and mild retorting is expected to produce higher quality vegetable foodstuffs compared to conventional retorting.

Enabling reversible redox reactions in electrochemical cells using protected LiAl intermetallics as lithium metal anodes.

Rechargeable electrochemical cells with metallic anodes are of increasing scientific and technological interest. The complex composition, poorly defined morphology, heterogeneous chemistry, and unpredictable mechanics of interphases formed spontaneously on the anodes are often examined but rarely controlled. Here, we couple computational studies with experimental analysis of well-defined LiAl electrodes in realistic electrochemical environments to design anodes and interphases of known composition. We compare phase behavior, Li binding energies, and activation energy barriers for adatom transport and study their effects on the electrochemical reversibility of battery cells. As an illustration of potential practical benefits of our findings, we create cells in which LiAl anodes protected by Langmuir-Blodgett MoS2 interphases are paired with 4.1 mAh cm-2 LiNi0.8Co0.1Mn0.1O2 cathodes. These studies reveal that small- and larger-format (196 mAh, 294 Wh kg-1, and 513 Wh liter-1) cells based on protected LiAl anodes exhibit high reversibility and support stable Li migration during recharge of the cells.

Carbon Nitride Phosphorus as an Effective Lithium Polysulfide Adsorbent for Lithium-Sulfur Batteries.

Lithium-sulfur (Li-S) batteries are attracting substantial attention because of their high-energy densities and potential applications in portable electronics. However, an intrinsic property of Li-S systems, that is, the solubility of lithium polysulfides (LiPSs), hinders the commercialization of Li-S batteries. Herein, a new material, that is, carbon nitride phosphorus (CNP), is designed and synthesized as a superior LiPS adsorbent to overcome the issues of Li-S batteries. Both the experimental results and the density functional theory (DFT) calculations confirm that CNP possesses the highest binding energy with LiPS at a P concentration of ∼22% (CNP22). The DFT calculations explain the simultaneous existence of Li-N bonding and P-S coordination in the sulfur cathode when CNP22 interacts with LiPS. By introducing CNP22 into the Li-S systems, a sufficient charging capacity at a low cutoff voltage, that is, 2.45 V, is effectively implemented, to minimize the side reactions, and therefore, to prolong the cycling life of Li-S systems. After 700 cycles, a Li-S cell with CNP22 gives a high discharge capacity of 850 mA h g-1 and a cycling stability with a decay rate of 0.041% cycle-1. The incorporation of CNP22 can achieve high performance in Li-S batteries without concerns regarding the LiPS shuttling phenomenon.

Two-Dimensional WS2@Nitrogen-Doped Graphite for High-Performance Lithium Ion Batteries: Experiments and Molecular Dynamics Simulations.

As promising candidates for anode materials in lithium ion batteries (LIB), two-dimensional tungsten disulfide (WS2) and WS2@(N-doped) graphite composites were synthesized, and their electrochemical properties were comprehensibly studied in conjunction with calculations. The WS2 nanosheets, WS2@graphite, and WS2@N-doped graphite (N-graphite) exhibit outstanding cycling performance with capacities of 633, 780, and 963 mA h g-1, respectively. To understand their lithium storage mechanism, first-principles calculations involving a series of ab initio NVT- NPT molecular dynamics simulations were conducted. The calculated discharge curves for amorphous phase are well matched with the experimental ones, and the capacities reach 620, 743, and 915 mA h g-1 for WS2, WS2@graphite, and WS2@N-graphite, respectively. The large capacities of the two composites can be attributed to the tendency of W and Li atoms to interact with graphite, suppressing the formation of W metal clusters. In the case of WS2@N-graphite, vigorous amorphization of the N-graphite enhances the interaction of W and Li atoms with the fragmented N-graphite in such a way that unfavorable Li-W repulsion is avoided at very early stage of lithiation. As a result, the volume expansion in WS2@graphite and WS2@N-graphite is calculated to be remarkably small (only 6 and 44%, respectively, versus 150% for WS2). Therefore WS2@(N-)graphite composites are expected to be almost free of mechanical pulverization after repeated cycles, which makes them promising and excellent candidates for high-performance LIBs.

Arsenic for high-capacity lithium- and sodium-ion batteries.

We report arsenic (As) as a promising alternative to graphite anode materials in lithium- and sodium-ion batteries (LIBs and SIBs). The electrochemical properties of the As/carbon nanocomposite for both LIBs and SIBs were investigated using experimental and theoretical approaches. The LIBs showed excellent cycling performance, with a reversible capacity of 1306 mA h g-1 (after 100 cycles), which is much higher than that of Li3As (1072 mA h g-1). In the corresponding SIBs, the measured reversible capacity was 750 mA h g-1 (after 200 cycles), which is lower than that of Na3As. Extensive first-principles calculations were performed employing a structure prediction method for crystalline LixAs and NaxAs (x = 1-6) phases, as well as ab initio molecular dynamics simulations for their amorphous phases. In good agreement with the experimental LIB data, our calculations successfully predict the discharge capacity versus voltage curves, showing that the capacity of the amorphous phase reaches up to that of Li4As. In contrast, the SIB exhibited difficulty in reaching the predicted capacity (x = 3.5), probably due to significant volume expansion. Comparison of the theoretical discharge curves with the experimental data provides valuable information for the development of high-performance LIBs and SIBs.

Antimicrobial effect of a combination of herb extract and organic acid against Bacillus subtilis spores.

The sporicidal activities of the herbs were investigated to screen for novel antimicrobial substances against Bacillus subtilis spores. The bacterial inactivation effects of ethanol extracts of coriander, caraway, mace at concentrations of 0.5% (w/v) and 1.0-2.5% were about 10- and 100-fold respectively against spores. At pH 5, the antimicrobial activity was about 92%, but at pH 4 the sporicidal activity was particularly high, reducing the spore count by 99.99%. The 0.1-2.5% ethanol extract of herbs adjusted to pH 4-5 exhibited significantly marked deactivation effects, with 3-4 log CFU/mL reductions. The herb-acid combination exerted a further increase in sporicidal activity, with an additional 1-3 log CFU/mL reduction. The sporicidal mechanism was assumed to involve a two-step: (1) the hydrophobic binding of surfactants in the herbs onto the spore coat destroys its protein, and (2) the acid then penetrates into the interior, generating unstable growth conditions.

Enhanced electrochemical performance of a ZnO-MnO composite as an anode material for lithium ion batteries.

A ZnO-MnO composite was synthesized using a simple solvothermal method combined with a high-temperature treatment. To observe the phase change during the heating process, in situ high-temperature XRD analysis was performed under vacuum conditions. The results indicated that ZnMn2O4 transformed into the ZnO-MnO composite phase starting from 500 °C and that this composite structure was retained until 700 °C. The electrochemical performances of the ZnO-MnO composite electrode were evaluated through galvanostatic discharge-charge tests and cyclic voltammetry analysis. Its initial coulombic efficiency was significantly improved to 68.3% compared to that of ZnMn2O4 at 54.7%. Furthermore, the ZnO-MnO composite exhibited improved cycling performance and enhanced rate capability compared with untreated ZnMn2O4. To clarify the discharge-charge mechanism of the ZnO-MnO composite electrode, the structural changes during the charge and discharge processes were also investigated using ex situ XRD and TEM.

Sporicidal Activities of Various Surfactant Components against Bacillus subtilis Spores.

The sporicidal activities against Bacillus subtilis spores of surfactant components with hydrophilic and hydrophobic properties that can lead to the denaturation of various proteins comprising the spore structure were investigated. The reduction in spore numbers by each of the surfactant components bornyl acetate, geranyl acetate, pinene, p-cymene, camphene, citral, 2,3-dihydrobenzofuran, polylysine, and thiamine dilaurylsulfate at 1% was estimated at 1 to 2 log CFU/ml. The average hydrophilelipophile balance value of surfactants with sporicidal activity causing a reduction of 1 to 2 log CFU/ml was 9.3, with a range from 6.7 to 15.8, which is similar to the values of various chemical surfactants of 9.6 to 16.7. The results also showed that the surfactants that were hydrophobic were more effective than those that were hydrophilic in killing B. subtilis spores. Furthermore, the sporicidal effect of surfactants like geranyl acetate and γ-terpinene was significantly enhanced in the presence of a germinant, because L-alanine and synergistic cofactors (e.g., K(+) ions) trigger cortex hydrolysis in spores.

The study of heat penetration of kimchi soup on stationary and rotary retorts.

The aim of this study was to determine the heat-penetration characteristics using stationary and rotary retorts to manufacture Kimchi soup. Both heat-penetration tests and computer simulation based on mathematical modeling were performed. The sterility was measured at five different positions in the pouch. The results revealed only a small deviation of F 0 among the different positions, and the rate of heat transfer was increased by rotation of the retort. The thermal processing of retort-pouched Kimchi soup was analyzed mathematically using a finite-element model, and optimum models for predicting the time course of the temperature and F 0 were developed. The mathematical models could accurately predict the actual heat penetration of retort-pouched Kimchi soup. The average deviation of the temperature between the experimental and mathematical predicted model was 2.46% (R(2)=0.975). The changes in nodal temperature and F 0 caused by microbial inactivation in the finite-element model predicted using the NISA program were very similar to that of the experimental data of for the retorted Kimchi soup during sterilization with rotary retorts. The correlation coefficient between the simulation using the NISA program and the experimental data was very high, at 99%.

Determination of Li(+) diffusion coefficients in the LixV2O5 (x = 0 - 1) nanocrystals of composite film cathodes.

The Li(+) ion diffusion coefficients (DLi+) in V2O5 (2.12 × 10(-12) cm(2) s(-1)) and in the intermediate α-, ε-, and δ-LixV2O5 phases (1.6 × 10(-14), 8.0 × 10(-15), and 8.5 × 10(-15) cm(2) s(-1), respectively), reversibly formed during charging/discharging processes of the crystalline-V2O5 and PEDOT (poly-3,4-ethylenedioxythiophene) composite-film electrode, are precisely determined by the galvanostatic intermittent titration technique. The specific surface area of the composite film is estimated to be 13.600 m(2) g(-1), where the external surface area and the nanopore area are 10.704 and 2.896 m(2) g(-1), respectively. The V2O5 crystals are coated and interconnected by a conductive polymer network in the composite film, thereby improving the electrode characteristics. V2O5 and PEDOT composite-film cathodes showed high specific capacities (290 mA h g(-1) at a 1 C rate), excellent rate capabilities (178 mA h g(-1) at a 10 C rate), and superior cycling stabilities (ca. 15% degradation after 500 consecutive cycles).

Tetragonal phase germanium nanocrystals in lithium ion batteries.

Various germanium-based nanostructures have recently demonstrated outstanding lithium ion storage ability and are being considered as the most promising candidates to substitute current carbonaceous anodes of lithium ion batteries. However, there is limited understanding of their structure and phase evolution during discharge/charge cycles. Furthermore, the theoretical model of lithium insertion still remains a challenging issue. Herein, we performed comparative studies on the cycle-dependent lithiation/delithiation processes of germanium (Ge), germanium sulfide (GeS), and germanium oxide (GeO2) nanocrystals (NCs). We synthesized the NCs using a convenient gas phase laser photolysis reaction and attained an excellent reversible capacity: 1100-1220 mAh/g after 100 cycles. Remarkably, metastable tetragonal (ST12) phase Ge NCs were constantly produced upon lithiation and became the dominant phase after a few cycles, completely replacing the original phase. The crystalline ST12 phase persisted through 100 cycles. First-principles calculations on polymorphic lithium-intercalated structures proposed that the ST12 phase Ge12Lix structures at x ≥ 4 become more thermodynamically stable than the cubic phase Ge8Lix structures with the same stoichiometry. The production and persistence of the ST12 phase can be attributed to a stronger binding interaction of the lithium atoms compared to the cubic phase, which enhanced the cycling performance.

Sulfur/graphitic hollow carbon sphere nano-composite as a cathode material for high-power lithium-sulfur battery.

The intrinsic low conductivity of sulfur which leads to a low performance at a high current rate is one of the most limiting factors for the commercialization of lithium-sulfur battery. Here, we present an easy and convenient method to synthesize a mono-dispersed hollow carbon sphere with a thin graphitic wall which can be utilized as a support with a good electrical conductivity for the preparation of sulfur/carbon nano-composite cathode. The hollow carbon sphere was prepared from the pyrolysis of the homogenous mixture of the mono-dispersed spherical silica and Fe-phthalocyanine powder in elevated temperature. The composite cathode was manufactured by infiltrating sulfur melt into the inner side of the graphitic wall. The electrochemical cycling shows a capacity of 425 mAh g-1 at 3 C current rate which is more than five times larger than that for the sulfur/carbon black nano-composite prepared by simple ball milling.

Sulfur-infiltrated micro- and mesoporous silicon carbide-derived carbon cathode for high-performance lithium sulfur batteries.

Novel nanostructured sulfur (S)-carbide derived carbon (CDC) composites with ordered mesopores and high S content are successfully prepared for lithium sulfur batteries. The tunable pore-size distribution and high pore volume of CDC allow for an excellent electrochemical performance of the composites at high current densities. A higher electrolyte molarity is found to enhance the capacity utilization dramatically and reduce S dissolution in S-CDC composite cathodes during cycling.

Germanium-tin alloy nanocrystals for high-performance lithium ion batteries.

Germanium-tin (Ge(1-x)Sn(x)) alloy nanocrystals were synthesized using a gas-phase laser photolysis reaction of tetramethyl germanium and tetramethyl tin. A composition tuning was achieved using the partial pressure of precursors in a closed reactor. For x < 0.1, cubic phase alloy nanocrystals were exclusively produced without separation of the tetragonal phase Sn metal. In the range of x = 0.1-0.4, unique Ge(1-x)Sn(x)-Sn alloy-metal hetero-junction nanocrystals were synthesized, where the Sn metal domain becomes dominant with x. Thin graphitic carbon layers usually sheathed the nanocrystals. We investigated the composition-dependent electrochemical properties of these nanocrystals as anode materials of lithium ion batteries. Incorporation of Sn (x = 0.05) significantly increased the capacities (1010 mA h g(-1) after 50 cycles) and rate capabilities, which promises excellent electrode materials for the development of high-performance lithium batteries.

Germanium sulfide(II and IV) nanoparticles for enhanced performance of lithium ion batteries.

Germanium sulfide (GeS and GeS2) nanoparticles were synthesized by novel gas-phase laser photolysis and subsequent thermal annealing. They showed excellent cycling performance for lithium ion batteries, with a maximum capacity of 1010 mA h g(-1) after 100 cycles. Metastable tetragonal phase Ge nanoparticles were suggested as active materials for a reversible lithium insertion-extraction process.