Analysis of Light Load Efficiency Characteristics of a Dual Active Bridge Converter Using Wide Band-Gap Devices

In this paper, the zero voltage switching (ZVS) region of a dual active bridge (DAB) converter with wide band-gap (WBG) power semiconductor device is analyzed. The ZVS region of a DAB converter varies depending on output power and voltage ratio. The DAB converters operate with hard switching at light loads, it is difficult to achieve high efficiency. Fortunately, WBG power semiconductor devices have excellent hard switching characteristics and can increase efficiency compared to silicon (Si) devices. In particular, WBG devices can achieve ZVS at low load currents due to their low parasitic output capacitance (Co,tr) characteristics. Therefore, in this paper, the ZVS operating resion is analyzed based on the characteristics of Si, silicon carbide (SiC) and gallium nitride (GaN). Power semiconductor devices. WBG devices with low Co,tr operate at ZVS at lower load currents compared to Si devices. To verify this, experiments are conducted and the results are analyzed using a 3 kW DAB converter. For Si devices, ZVS is achieved above 1.4 kW. For WBG devices, ZVS is achieved at 700 W. Due to the ZVS conditions depending on the switching device, the DAB converter using Si devices achieves a power conversion efficiency of 91% at 1.1 kW output. On the other hand, in the case of WBG devices, power conversion efficiency of more than 98% is achieved under 11 kW conditions. In conclusion, it is confirmed that the WBG device operates in ZVS at a lower load compared to the Si device, which is advantageous in increasing light load efficiency.

Impedance Modeling and Stability Analysis of Dual Active Bridge Converter with LC Input Filter

The dual active bridge(DAB)converter is gaining more and more attention in various applications such as energy storage systems,electric vehicles and smart grids.To improve the quality of the input current,a LC filter is often cascaded at the input side of the DAB converter.However,there are instable problems of this cascaded system due to the impedance interactions of the DAB converter and the LC filter,although the DAB converter is stable at the individual operation mode.To assess the stability of the cascaded system of the DAB converter and the LC filter,the impedance model of the DAB converter is firstly developed based on generalized state-space averaging method.The developed impedance model can be used to accurately predict the stability of the DAB converter with its LC input filter.Based on the stability analysis,the optimum filter parameter design guideline is determined.The impedance model and stability analysis are validated by the simulation and experimental results.

Dual active sites over Cu-ZnO-ZrO_(2) catalysts for carbon dioxide hydrogenation to methanol

CO_(2) hydrogenation to methanol is a significant approach to tackle the problem of global warming and simultaneously meet the demand for the portable fuel.Cu-ZnO catalysts with various kinds of promoters have received wide attention.However,the role of promoter and the form of active sites in CO_(2) hydrogenation are still in debate.Here,various molar ratios of ZrO_(2) were added into the Cu-ZnO catalysts to tune the distributions of Cu^(0) and Cu+species.A volcano-like trend between the ratio of Cu+/(Cu++Cu^(0))and the amount of ZrO_(2) is presented,among which the CuZn10Zr(the molar ratio of ZrO_(2) is 10%)catalyst reaches the highest value.Correspondingly,the maximum value of space-time yield to methanol with 0.65 gMeOH/(gcat·hr)is obtained on CuZn10Zr at reaction conditions of 220°C and 3 MPa.Detailed characterizations demonstrate that dual active sites are proposed during CO_(2) hydrogenation over CuZn10Zr catalyst.The exposed Cu^(0) takes participate in the activation of H_(2),while on the Cu^(+) species,the intermediate of formate from the co-adsorption of CO_(2) and H_(2) prefers to be further hydrogenated to CH_(3)OH than decomposing into the by-product of CO,yielding a high selectivity of methanol.

Zonal activation of molecular carbon dioxide and hydrogen over dual sites Ni-Co-MgO catalyst for CO_(2) methanation:Synergistic catalysis of Ni and Co species

An in-depth mechanism in zonal activation of CO_(2)and H2molecular over dual-active sites has not been revealed yet.Here,Ni-Co-MgO was rationally constructed to elucidate the CO_(2)methanation mechanism.The abundant surface nickel and cobalt components as active sites led to strong Ni-Co interaction with charge transfer from nickel to cobalt.Notably,electron-enriched Coδ-species participated in efficient chemisorption and activation of CO_(2)to generate monodentate carbonate.Simultaneously,plentiful available Ni0sites facilitated H2dissociation,thus CO_(2)and H2were smoothly activated at zones of Coδ-species and Ni0,respectively.Detailed in situ DRIFTS,quasi situ XPS,TPSR,and DFT calculations substantiated a new formate evolution mechanism via monodentate carbonate instead of traditional bidentate carbonate based on synergistic catalysis of Coδ-species and Ni0.The zonal activation of CO_(2)and H2by tuning electron behaviors of double-center catalysts can boost heterogeneous catalytic hydrogenation performance.

Molybdenum phosphide(MoP) with dual active sites for the degradation of diclofenac in Fenton-like system

The leaching and non-recoverability of mental ions have always limited the practical application of Fenton-like processes. For the first time, we synthesized molybdenum phosphide (MoP) with dual active sites for the degradation of diclofenac (DCF) in the Fenton-like process. The DCF degradation rate constant (k) of MoP + H_(2)O_(2) process was calculated to be 0.13 min^(-1) within 40 min, indicating a highly efficient catalytic ability of MoP. In addition, this catalyst exhibits a stable structure and good activity, which could apply in a broad pH range, different ions solution and real wastewater condition. Accordingly, this efficient catalytic capability may be attributed to the presence of the metal sites Mo^(δ+) and the electron-rich sites P^(δ-) in MoP, which could induce the generation of hydroxyl radical (^(·)OH) and superoxide radical (^(·)O_(2)^(-)) through electron transfer, resulting in the effective removal of DCF. This study provides an idea for the optimization of Fenton-like technologies and environmental remediation.

One-step conversion of methane and formaldehyde to ethanol over SA-FLP dual-active-site catalysts: A DFT study

One-step conversion of methane and formaldehyde into ethanol is a 100% atom-efficient process for carbon resources utilization and environment protection but still faces eminent challenges due to the lacking of efficient catalysts. Therefore, developing active and stable catalysts is crucial for the co-conversion of methane and formaldehyde. Herein, twelve kinds of “Single-Atom”-“Frustrated Lewis Pair”(SA-FLP)dual-active-site catalysts are designed for the direct conversion of methane and formaldehyde to ethanol based on density functional theory(DFT) calculations and microkinetic simulations. The results show that the SA-FLP dual active sites can simultaneously activate methane at the SA site and activate formaldehyde at the FLP site. Among the twelve designed SA-FLP catalysts, Fe1-FLP shows the best performance in the co-conversion of methane and formaldehyde to ethanol with the rate-determining barrier of 1.15 e V.Ethanol is proved as the main product with the turnover frequency of 1.32 × 10^(-4)s^(-1)at 573 K and 3 bar.This work provides a universal strategy to design dual active sites on metal oxide materials and offers new insights into the effective conversion of methane and formaldehyde to desired C_(2) chemicals.

Highly active and stable Co nanoparticles embedded in nitrogen-doped mesoporous carbon nanofibers for aqueous-phase levulinic acid hydrogenation

Developing a highly active and durable non-noble metal catalyst for aqueous-phase levulinic acid(LA)hydrogenation to g-valerolactone(GVL)is an appealing yet challenging task.Herein,we report well-dispersed Co nanoparticles(NPs)embedded in nitrogen-doped mesoporous carbon nanofibers as an efficient catalyst for aqueous-phase LA hydrogenation to GVL.The Co zeolitic imidazolate framework(ZIF-67)nanocrystals were anchored on the sodium dodecyl sulfate modified wipe fiber(WF-S),yielding one-dimensional(1-D)structured composite(ZIF-67/WF-S).Subsequently,Co NPs were uniformly embedded in nitrogen-doped mesoporous carbon nanofibers(Co^(R)NC/SMCNF)through a pyrolysis-reduction strategy using ZIF-67/WF-S as the precursor.Benefiting from introducing modified wipe fiber WF-S to enhance the dispersion of Co NPs,and Co^(0) with Co-N_xdual active sites,the resulting Co^(R)NC/SMCNF catalyst shows brilliant catalytic activity(206 h^(-1) turnover frequency).Additionally,the strong metal-support interactions greatly inhibited the Co NPs from aggregation and leaching from the mesoporous carbon nanofibers,and thus increasing the reusability of the Co^(R)NC/SMCNF catalyst(reusable nine times without notable activity loss).

Dual-active-site Fe/Cu single-atom nanozymes with multifunctional specific peroxidase-like properties for S^(2-)detection and dye degradation

Designing single-atom nanozymes with densely exposed metal atom active sites and enhancing catalytic activity to detect pollutants remain a serious challenge.Herein,we reported a single-atom nanozyme with layered stacked Fe/Cu dual active sites(Fe/Cu-NC SAzyme)synthesized via hydrothermal and hightemperature pyrolysis using folic acid as a template.Compared with Fe-NC and Cu-NC SAzyme,Fe/Cu-NC SAzyme has higher peroxidase-like activity,which indicates that the doping of synthesized Fe/Cu bimetals can improve the catalytic activity and that the atomic loading of Fe and Cu in Fe/Cu-NC is 5.5 wt%and 2.27 wt%,respectively.When S^(2-)is added to the Fe/Cu-NC catalytic system,a high-sensitivity and high-selectivity S^(2-)colorimetric sensing platform can be established,with a wide linear range(0.09-6μmol/L)and a low detection limit(30 nmol/L),which can be used to detect S^(2-)in environmental water samples.What’s more,the Fe/Cu-NC SAzyme can activate peroxymonosulfate(PMS)to degrade 99.9%of rhodamine B(Rh B)within 10 min with a degradation kinetics of 0.5943 min^(-1).This work details attractive applications in Fe/Cu-NC SAzyme colorimetric sensing and dye degradation.

Relationship of familial cytochrome P450 4V2 gene mutation with liver cirrhosis:A case report and review of the literature

BACKGROUND Many genetic and metabolic diseases affect the liver,but diagnosis can be difficult because these diseases may have complex clinical manifestations and diverse clinical patterns.There is also incomplete clinical knowledge of these many different diseases and limitations of current testing methods.CASE SUMMARY We report a 53-year-old female from a rural area in China who was hospitalized for lower limb edema,abdominal distension,cirrhosis,and hypothyroidism.We excluded the common causes of liver disease(drinking alcohol,using traditional Chinese medicines,hepatitis virus infection,autoimmunity,and hepatolenticular degeneration).When she was 23-years-old,she developed night-blindness that worsened to complete blindness,with no obvious cause.Her parents were first cousins,and both were alive.Analysis of the patient’s family history indicated that all 5 siblings had night blindness and impaired vision;one sister was completely blind;and another sister had night-blindness complicated with cirrhosis and subclinical hypothyroidism.Entire exome sequencing showed that the patient,parents,and siblings all had mutations in the cytochrome P450 4V2gene(CYP4V2).The CYP4V2 mutations of the parents and two sisters were heterozygous,and the others were homozygous.Two siblings also had heterozygous dual oxidase activator 2(DUOXA2) mutations.CONCLUSION Mutations in the CYP4V2 gene may affect lipid metabolism and lead to chronic liver injury,fibrosis,and cirrhosis.

A Pincer Cobalt Complex as Catalyst with Dual Hydrogenation Activities for Hydrodeoxygenation of Ketones with H2

Reductive deoxygenation of ketones using H_(2) is a highly desirable but also challenging transformation in both chemical synthesis,industrial-scale petroleum and biomass feedstock reforming processes.Herein,we report a cooperative cobalt/Lewis acid (LA)-catalyzed hydrodeoxygenation of ketones using H_(2) as the reductant.In particular,the newly developed pincer cobalt catalyst possesses dual hydrogenation activities for both ketones and alkenes under the same reaction conditions.This reaction features a broad substrate scope,excellent functional-group compatibility,and potential applicability.

Covalent organic framework containing dual redox centers as an efficient anode in Li-ion batteries

Covalent organic frameworks(COFs)with periodic channels and tunable chemical structures have been widely considered as promising electrode materials in rechargeable batteries.However,the design and construction of high-performance COFs-based electrodes still face some challenges in the introduction of multiple efficient redox centers as well as the reduction of dead mass.To address these issues,a unique COF containing double active centers(C═N and N═N)is developed as an anode in rechargeable lithium-ion batteries(LIBs).The as-prepared COF displays excellent electrochemical performance due to its remarkable structural stability and the existence of many active groups.Meanwhile,its electrochemical performance is significantly better than that of the small molecule compound or the linear polymer with the same construction units.Even at a high current density of 5 A/g,the LIBs with COF electrodes remain at a high discharge capacity of 227 mAh/g after 2000 cycles.Moreover,the distinction in electrochemical performances of these three materials is further revealed by calculation.This study illustrates the importance of molecular structure design for improving the performance of organic electrodes.

Photocatalytic uranium extraction boosted by dual effective active sites of porphyrin metal-organic frameworks

Porphyrinoid metal-organic frameworks(MOFs)with dual effective uranium uptake sites were synthesized through combined insitu and post-synthetic method.The MOF10@5 demonstrates the uptake amount of uranium reaches 1476 mg/g under visiblelight irradiation.The PN-MOF10@5 with dual uranyl uptake sites yields the amount of extracting uranyl of 1590 mg/g under visible-light irradiation.The density functional theory(DFT)calculations reveal strong interaction between uranyl and dual uranyl effective active sites.These MOFs demonstrate a powerful synthesis strategy for uranium extraction materials with dual effective active sites.

High efficacy of chlorfenapyr-based net Interceptor■G2 against pyrethroid-resistant malaria vectors from Cameroon

Background The increasing reports of resistance to pyrethroid insecticides associated with reduced efficacy of pyrethroid-only interventions highlight the urgency of introducing new non-pyrethroid-only control tools.Here,we investigated the performance of piperonyl-butoxide(PBO)-pyrethroid[Permanet 3.0(P3.0)]and dual active ingredients(AI)nets[Interceptor G2(IG2):containing pyrethroids and chlorfenapyr and Royal Guard(RG):containing pyrethroids and pyriproxyfen]compared to pyrethroid-only net Royal Sentry(RS)against pyrethroid-resistant malaria vectors in Cameroon.Methods The efficacy of these tools was firstly evaluated onAnopheles gambiae s.l.andAnopheles funestus s.l.from Gounougou,Mibellon,Mangoum,Nkolondom,and Elende using cone/tunnel assays.In addition,experimental hut trials(EHT)were performed to evaluate the performance of unwashed and 20 times washed nets in semi-field conditions.Furthermore,pyrethroid-resistant markers were genotyped in dead vs alive,blood-fed vs unfed mosquitoes after exposure to the nets to evaluate the impact of these markers on net performance.The XLSTAT software was used to calculate the various entomological outcomes and the Chi-square test was used to compare the efficacy of various nets.The odds ratio and Fisher exact test were then used to establish the statistical significance of any association between insecticide resistance markers and bed net efficacy.Results Interceptor G2 was the most effective net against wild pyrethroid-resistantAn.funestus followed by Permanet 3.0.In EHT,this net induced up to 87.8%mortality[95%confidence interval(CI):83.5-92.1%)and 55.6%(95%CI:48.5-62.7%)after 20 washes whilst unwashed pyrethroid-only net(Royal Sentry)killed just 18.2%(95%CI:13.4-22.9%)of host-seekingAn.funestus.The unwashed Permanet 3.0 killed up to 53.8%(95%CI:44.3-63.4%)of field-resistant mosquitoes and 47.2%(95%CI:37.7-56.7%)when washed 20 times,and the Royal Guard 13.2%(95%CI:9.0-17.3%)for unwashed net and 8.5%(95%CI:5.7-11.4%)for the 20 washed net.Interceptor G2,Permanet 3.0,and Royal Guard provided better personal protection(blood-feeding inhibition 66.2%,77.8%,and 92.8%,respectively)compared to pyrethroid-only net Royal Sentry(8.4%).Interestingly,a negative association was found betweenkdrw and the chlorfenapyr-based net Interceptor G2(χ^(2)=138;P<0.0001)with homozygote-resistant mosquitoes predominantly found in the dead ones.Conclusions The high mortality recorded with Interceptor G2 against pyrethroid-resistant malaria vectors in this study provides first semi-field evidence of high efficacy against these major malaria vectors in Cameroon encouraging the implementation of this novel net for malaria control in the country.However,the performance of this net should be established in other locations and on other major malaria vectors before implementation at a large scale.

High selective epoxidation of 2-methylpropene over a Mo-based oxametallacycle reinforced nano composite

Compared with the gas-solid phase reactions,the epoxidation of light olefins in the liquid phase could realize the highly selective preparation of epoxides at a lower temperature.Nevertheless,the C=C bond of light olefins is more difficult to activate,and it is still a challenge to realize the dual activation of the oxidant and light olefins in one reaction system.In this contribution,an oxametallacycle reinforced nanocomposite(Mo(O_(2))_(2)@RT)is prepared via an oxidative pretreatment strategy,and its epoxidation performance to 2-methylpropene in liquid-phase with tert-butyl hydroperoxide(TBHP)as an oxidant is evaluated.A set of advanced characterizations including field emission scanning electron microscopy,X-ray photoelectron spectroscopy,in-situ Fourier transform infrared spectroscopy(FT-IR),electron spin-resonance spectroscopy,and high-resolution mass spectrometer are implemented to confirm the physicochemical properties and the catalytic behaviors of Mo(O_(2))_(2)@RT.This catalyst has a fast kinetic response and exhibits excellent catalytic activity in 2-methylpropene epoxidation to produce 2-methylpropylene oxide(MPO;select.:99.7%;yield:92%),along with good reusability and scalability.Moreover,the main epoxidation mechanism is deduced that TBHP is activated by Mo(O_(2))_(2)@RT to generate the highly active tert-butyl peroxide radical,which realizes the epoxidation of 2-methylpropene to yield MPO.

Intramolecularly lactam stapled oxyntomodulin analogues inhibit cancer cell proliferation in vitro

As a glucagon(GCG) receptor(GCGR) and glucagon-like peptide 1(GLP-1) receptor(GLP-1R) dual agonist, oxyntomodulin(OXM) has been attracting scientific attentions due to its efficacies of suppressing appetite, increasing energy expenditure, and inducing body weight loss in obese humans. Based on the scaffold of native OXM, specific helix-favoring amino acids substitutions and the consequent salt bridge formations were believed to offer enhanced and balanced GCGR/GLP-1R activations through increasing α-helical conformation. Novel OXM analogues are obtained by intramolecular lactam stapling of positions[Glu16 & Lys20] or [Lys17 & Glu21] to further strengthen conformationally constrained stabilization. Even though the lactam staple does not provide additional dual GCGR/GLP-1R activations in vitro, the stapled OXM analogues are firstly reported to have higher or lower anti-PANC-1 cell proliferation activity, meanwhile which has no obvious inhibitory effect on the proliferation of He La cells. Therefore, it is speculated that the stapled analogues may have the potential to inhibit the proliferation of specific cancer cell types.Among the stapled peptides as well as their precursors, analogue 6 has the most prominent anti-PANC-1 proliferation activity with the IC50value of 115.1 μmol/L. Its mechanism of actions including effective signal pathways should be worth further investigations in future.

Upcycling electroplating sludge into bioengineering-enabled highly stable dual-site Fe-Ni_(2)P@C electrocatalysts for efficient oxygen evolution

The advancement of bimetallic catalysts holds significant promise for the innovation of oxygen evolution reaction(OER)catalysts.Drawing from adsorbate evolution mechanism(AEM)and lattice oxygen oxidation mechanism(LOM),the incorporation of dual active sites has the potential to foster novel OER pathways,such as the coupled oxygen evolution mechanism(COM),which can surpass the limitations of OER and elevate catalytic performance.In this study,uniformly distributed Fe/Ni dual-site Fe-Ni_(2)P@C electrocatalysts are crafted by upcycling metals in electroplating sludge via an eco-friendly and sustainable microbial engineering technique.Our findings indicate that a substantial number of defects emerge at the Ni2P crystal during the OER process,laying the groundwork for lattice oxygen involvement.Moreover,the displacement of Ni/Fe in the crystal lattice intensifies the asymmetry of the electronic structure at the metal active sites,facilitating the deprotonation process.This research introduces an innovative paradigm for the synthesis of effective and robust transition metal-based OER catalysts,with implications for sustainable energy generation technologies.

Waste bio-tar based N-doped porous carbon for supercapacitors under dual activation:performance,mechanism,and assessment

Bio-tar extra-produced from biomass pyrolysis is prone to pose a threat to environment and human health.A novel N-doped porous electrode from bio-tar was produced under dual-activation of urea and KOH in this study.Onepot dual-activation played significant roles in N-functional group and micro-mesoporous structure,which resulted in the carbon material with the highest of nitrogen content(4.08%)and the special surface area(1298.26 m^(2)·g^(−1)).Specifically,the potential mechanisms of pore formation and N-doping in the one-pot dual-activation strategy were also proposed as a consequence,the one-pot dual-activated carbon material displayed excellent electrochemical performance with the highest capacitance of 309.5 F·g^(−1) at 0.5 A·g^(−1),and the unipolar specific capacitance remained with cyclic characteristics of 80.1%after 10,000 cycles in two-electrode symmetric system.Furthermore,the one-pot dual-activation strategy could create a profit of$1.64-$2.38 per kilogram of bio-tar processed without considering the initial investment and labor costs,which provides new perspectives for the utilization of waste bio-tar.

Reduced water dissociation barrier on constructing Pt-Co/CoO_(x)interface for alkaline hydrogen evolution

Water dissociation process is generally regarded as the rate-limiting step for alkaline hydrogen evolution reaction(HER),and severely inhibits the catalytic efficiency of Pt based catalysts.To overcome this problem,the in-situ constructed interfaces of PtCo alloy and amorphous cobalt oxide(CoO_(x))on the carbon powder are designed.The amorphous CoO_(x)at Pt-Co/CoO_(x)interfaces not only provide active sites for water dissociation to facilitate Volmer step,but also produce the strong electronic transfer with Pt-Co.Accordingly,the obtained interfacial catalysts exhibit outstanding alkaline HER performance with a Tafel slope of 29.3 mV·dec^(−1)and an ultralow overpotential of only 28 mV at 10 mA·cm^(−2).Density functional theory(DFT)reveals that the electronic accumulation on the interfacial Co atom in Pt-Co/CoO_(x)constructing the novel active site for water dissociation.Compared to the Pt-Co,all of the energy barriers for water adsorption,water dissociation and hydrogen adsorption/desorption are reduced in Pt-Co/CoO_(x)interfaces,suggesting a boosted HER kinetics for alkaline HER.

A System Identification-based Modeling Framework of Bidirectional DC-DC Converters for Power Grids

This paper proposes a system identification framework based on eigensystem realization to accurately model power electronic converters.The proposed framework affords an energy-based optimal reduction method to precisely identify the dynamics of power electronic converters from simulated or actual raw data measured at the converter’s ports.This method does not require any prior knowledge of the topology or internal parameters of the converter to derive the system modal information.The accuracy and feasibility of the proposed method are exhaustively evaluated via simulations and practical tests on a software-simulated and hardware-implemented dual active bridge(DAB)converter under steady-state and transient conditions.After various comparisons with the Fourier series-based generalized average model,switching model,and experimental measurements,the proposed method attains a root mean square error(RMSE)of less than 1%with respect to the actual raw data.Moreover,the computational effort is reduced to 1/8.6 of the Fourier series-based model.

Common-mode Electromagnetic Interference Mitigation for Solid-state Transformers

Solid-state transformers(SSTs)have been widely used in many areas owing to their advantages of high-frequency isolation and high power density.However,high-frequency switching causes severe electromagnetic interference(EMI)problems.Particularly,the common-mode(CM)EMI caused by the switching of the dual active bridge(DAB)converter is conducted through the parasitic capacitances in the high-frequency transformer and impacts the system reliability.With the understanding of the CM EMI model in SSTs,CM EMI mitigation methods have been studied.For passive mitigation,the coupled inductor can be integrated with the phase-shift inductor function to reduce CM EMI.For active mitigation,variations in the DAB switching frequency can help reduce the CM EMI peak.An active EMI filter can also be designed to sample and compensate for CM EMI.Using these methods,CM EMI can be reduced in SSTs.