The sluggish reaction kinetics of the oxygen evolution reaction(OER)and methanol oxidation reaction(MOR)remain obstacles to the commercial promotion of water splitting and direct methanol fuel cells.Considering the vi...The sluggish reaction kinetics of the oxygen evolution reaction(OER)and methanol oxidation reaction(MOR)remain obstacles to the commercial promotion of water splitting and direct methanol fuel cells.Considering the vital role of noble metals in electrocatalytic activity,this work focuses on the rational synthesis of Ni-noble metal composite nanocatalysts for overcoming the drawbacks of high cost and susceptible oxidized surfaces of noble metals.The inherent catalytic activity is improved by the altered electronic structure and effective active sites of the catalyst induced by the size effect of noble metal clusters.In particular,a series of Ni-noble metal nanocomposites are successfully synthesized by partially introducing noble metal into Ni with porous interfacial defects derived from Ni-Al layered double hydroxide(LDH).The Ni_(10)Pd_(1)nanocomposite exhibits high OER catalytic activity with an overpotential of 0.279 V at 10 m A/cm^(2),surpassing Ni_(10)Ag_(1)and Ni_(10)Au_(1)counterparts.Furthermore,the average diameter of Pd clusters gradually increases from 5.57 nm to 44.44 nm with the increased proportion of doped Pd,leading to the passivation of catalytic activity due to the exacerbated surface oxidation of Pd in the form of Pd^(2+).After optimization,Ni_(10)Pd_(1)delivers significantly enhanced OER and MOR electroactivities and long-term stability compared to that of Ni_(2)Pd_(1),Ni_(1)Pd_(1)and Ni_(1)Pd_(2),which is conducive to the effective utilization of Pd and alleviation of surface oxidation.展开更多
Within the framework of carbon neutrality,lithium-ion batteries(LIBs)are progressively booming along with the growing utilization of green and clean energy.However,the extensive application of LIBs with limited lifesp...Within the framework of carbon neutrality,lithium-ion batteries(LIBs)are progressively booming along with the growing utilization of green and clean energy.However,the extensive application of LIBs with limited lifespan has brought about a significant recycling dilemma.The traditional hydrometallurgical or pyrometallurgical strategies are not capable to maximize the output value of spent LIBs and minimize the potential environmental hazards.Herein,to alternate the tedious and polluting treatment processes,we propose a high-temperature molten-salt strategy to directly regenerate spent cathodes of LIBs,which can also overcome the barrier of the incomplete defects'restoration with previous low-temperature molten salts.The high-energy and stable medium environment ensures a more thorough and efficient relithiation reaction,and simultaneously provides sufficient driving force for atomic rearrangement and grains secondary growth.In consequence,the regenerated ternary cathode(R-NCM)exhibits significantly enhanced structural stability that effectively suppresses the occurrence of cracks and harmful side reactions.The R-NCM delivers excellent cycling stability,retaining 81.2%of its capacity after 200 cycles at 1 C.This technique further optimizes the traditional eutectic molten-salt approach,broadening its applicability and improving regenerated cathode performance across a wider range of conditions.展开更多
Serpentine structured Co_(3)Si_(2)O_(5)(OH)_(4) is inexpensive,chemically stable,and electrochemically active in oxygen evolution reactions(OER).However,the OER activity of Co_(3)Si_(2)O_(5)(OH)_(4) materials is still...Serpentine structured Co_(3)Si_(2)O_(5)(OH)_(4) is inexpensive,chemically stable,and electrochemically active in oxygen evolution reactions(OER).However,the OER activity of Co_(3)Si_(2)O_(5)(OH)_(4) materials is still unfavorable due to the low active sites.Here,Mn^(2+)-doped Co_(3)Si_(2)O_(5)(OH)_(4) serpentine nanosheets with tuned d-band centers are achieved for efficient oxygen evolution in alkaline and neutral electrolytes.The Co_(x)Mn_(3−x)Si_(2)O_(5)(OH)_(4) serpentine nanosheets are synthesized by a simple hydrothermal method.The optimized Co_(2.4)Mn_(0.6)Si_(2)O_(5)(OH)_(4) serpentine nanosheets showed favorable OER overpotentials as well as stable durability in KOH solution and phosphate buffer solution,which were superior to most of the Co-based and Mn-based OER electrocatalysts.The in situ Raman spectroscopy shows that the materials are kept well in the electrochemical OER environments.Further density functional theory shows that the d-band center of Co_(x)Mn_(3−x)Si_(2)O_(5)(OH)_(4) serpentine nanosheets is shifted more upward in comparison with pristine Co_(3)Si_(2)O_(5)(OH)_(4).The changes in the d-band center increase the adsorption of intermediates,optimize the reaction steps,and lower the energy barriers of the OER.That is the main reason for the OER enhancement Mn^(2+)-doped Co_(3)Si_(2)O_(5)(OH)_(4).This work gives an efficient strategy to design cheap and stable electrocatalytic materials for OER in a broad pH environment.展开更多
Lithium metal batteries(LMBs)encounter substantial challenges related to hydrogen fluoride(HF)-induced degradation of electrode materials and interfacial instability.The predominant sources of HF are attributed to the...Lithium metal batteries(LMBs)encounter substantial challenges related to hydrogen fluoride(HF)-induced degradation of electrode materials and interfacial instability.The predominant sources of HF are attributed to the hydrolysis of lithium hexafluorophosphate(LiPF_(6))in the electrolyte and the decomposition of fluorine-containing solvents,which result in transition metal dissolution,rapid capacity fading,and overall battery performance deterioration.To mitigate these issues,we introduce a dual-protection strategy via the synergistic incorporation of pentafluorophenyl trifluoroacetate(PFTFA)and lithium difluoro(oxalato)borate(LiDFOB)additives,achieving both chemical HF capture and physical HF defense.The optimized electrolyte system not only promotes the formation of a robust cathode-electrolyte interphase layer enriched with LiF and LiB_(x)O_(y)compounds but also effectively scavenges HF through PFTFA coordination,thereby ensuring enhanced cathode stability.Consequently,the Li‖LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2)(NCM811)cells demonstrate remarkable cyclic stability with 80%capacity retention over 420 cycles at the cutoff voltage of 4.4 V under 1 C rate,whereas conventional carbonate-based electrolytes only retain 54.8%capacity after 150 cycles under identical conditions.Even under high voltage conditions(4.8 V,0.5 C),the developed electrolyte maintains 77.8%capacity retention over 200 cycles.This work provides valuable insights into the rational design of multifunctional electrolyte additives for high-performance LMBs.展开更多
The poor oxidation stability of ether-based solvents has long been a major challenge limiting their practical application.To enhance the oxidative stability of ether-based electrolytes,the physicochemical properties o...The poor oxidation stability of ether-based solvents has long been a major challenge limiting their practical application.To enhance the oxidative stability of ether-based electrolytes,the physicochemical properties of various glycol dimethyl ethers are screened,and diglyme(G2)is selected as the sole solvent for the electrolyte.Lithium bis(fluorosulfonyl)imide(LiFSI),a highly dissociative salt,is used as the primary salt;while lithium nitrate(LiNO_(3))and lithium difluorophosphate(LiDFP),which have small ionic sizes and strong binding energies,are added as secondary salts.The resulting electrolyte can modulate the electric double layer structure by NO_(3)^(-) and DFP^(-) on the cathode side,leading to an increased Liþconcentration that is originally repelled by the cathode.Additionally,the oxidation stability of the electrolyte is improved and the formed electrode-electrolyte interphase is more uniform and stable,thereby enhancing the electrochemical performance of the cells.As a result,cells assembled with a total of 1 M ternary lithium salts in G2 solvent can operate at high voltage of 4.4 V.The LijjNCM811 cells maintain 80.2%capacity retention after 270 cycles at room temperature,with an average Coulombic efficiency of 99.5%,and exhibit 88.4%capacity retention after 200 cycles at -30℃.展开更多
Three-dimensional(3D)covalent organic frameworks(COFs)have attracted extensive attention as photocatalysts for CO_(2)reduction reactions.Introducing metal atoms is essential for enhancing activity,but previous metal s...Three-dimensional(3D)covalent organic frameworks(COFs)have attracted extensive attention as photocatalysts for CO_(2)reduction reactions.Introducing metal atoms is essential for enhancing activity,but previous metal sites in 3D COFs predominantly exhibit symmetrical coordination,making them unsuitable for CO_(2)activation.Here,we design a 3D COF with 2,2'-pyridine linked around tetra-(4-anilyl)methane(TCM-Bpy-COF),where Co^(2+)is asymmetrically coordinated by bipyridine and acetates(TCMBpy-COF-CoAc).The TCM-Bpy-COF-CoAc exhibits outstanding photocatalytic CO_(2)reduction performance under weak visible light,achieving a CO evolution rate of 26,650μmol g^(-1)h^(-1)under 5 W of lightemitting-diode(LED)lamp and high apparent quantum efficiency.The performance far exceeds that of symmetrically coordinated bipyridine-Co-bipyridine TCM-Bpy-COF and surpasses most reported COF-based photocatalysts.In-situ spectral characterizations and theoretical calculations show that asymmetric N,O-coordination around the Co^(2+)center polarizes electron density and lowers reaction energy barriers of^(*)COOH intermediates,enhancing the conversion of CO_(2)to CO.This work inspires the design of 3D COF-based photocatalysts with highly catalytic efficiency.展开更多
Strategy of anchoring alloy nanoparticles made up of the efficient catalytic element(e.g.,Ni,Fe)on dodecyl sulfate(DS^(-))-intercalated NiFe layered double hydroxides(DS^(-)-NiFe LDH)obtained by a convenient one-step ...Strategy of anchoring alloy nanoparticles made up of the efficient catalytic element(e.g.,Ni,Fe)on dodecyl sulfate(DS^(-))-intercalated NiFe layered double hydroxides(DS^(-)-NiFe LDH)obtained by a convenient one-step hydrothermal coprecipitation method for essentially enhancing oxygen evolution reaction(OER)performance was proposed.The results of structural characterization indicate Pt_(2)FeNi alloy nanoparticles evenly distribute on the surface of DS^(-)-NiFe LDH.The sizes of the Pt_(2)FeNi nanoparticles,closely related to their OER performance,could be wellcontrolled by adjusting the amount of H;PtCl;addition.The composite structure of as-prepared product was stable during processes of synthesis,exfoliation,self-assembly,and subsequent electrocatalytic OER.Rigorous electrochemical test proving the contributing catalytic active sites was located at the interface between Pt_(2)FeNi and DS^(-)-NiFe LDH,and the Ni and Fe were the major active elements while O atoms are adsorption sites.The formation of Pt_(2)FeNi nanoparticles could greatly prompt the reduction of Tafel slope.The best-performing Pt_(2)FeNi/DS^(-)-NiFe LDH with a Pt content of 0.98 wt%achieved low overpotential of 204 mV at 10 mA cm^(-2)and 262 mV at 50 mA cm^(-2).This work provides a convenient and effective strategy to create additional active sites for enhancing OER performance of NiFe LDH and make contribution to its wide application.展开更多
The d-band state of materials is an important descriptor for activity of oxygen evolution reaction(OER).For NiO materials,there is rarely concern about tuning their d-band states to tailor the OER behaviors.Herein,NiO...The d-band state of materials is an important descriptor for activity of oxygen evolution reaction(OER).For NiO materials,there is rarely concern about tuning their d-band states to tailor the OER behaviors.Herein,NiO nanocrystals with doping small amount of La^(3+)were used to regulate d-band states for promoting OER activity.Density of states calculations based on density functional theory revealed that La^(3+)doping produced upper shift of d-band center,which would induce stronger electronic interaction between surface Ni atoms and species of oxygen evolution reaction intermediates.Further density functional theory calculation illustrated that La^(3+)doped NiO possessed reduced Gibbs free energy in adsorbing species of OER intermediate.Predicted by theoretical calculations,trace La^(3+)was introduced into crystal lattice of NiO nanoparticles.The La^(3+)doped NiO nanocrystal showed much promoted OER activity than corresponding pristine NiO product.Further electrochemical analysis revealed that La^(3+)doping into NiO increased the intrinsic activity such as improved active sites and reduced charge transfer resistance.The in-situ Raman spectra suggested that NiO phase in La^(3+)doped NiO could be better maintained than pristine NiO during the OER.This work provides an effective strategy to tune the d-band center of NiO for efficient electrocatalytic OER.展开更多
BACKGROUND Sarcopenia may be associated with hepatocellular carcinoma(HCC)following hepatectomy.But traditional single clinical variables are still insufficient to predict recurrence.We still lack effective prediction...BACKGROUND Sarcopenia may be associated with hepatocellular carcinoma(HCC)following hepatectomy.But traditional single clinical variables are still insufficient to predict recurrence.We still lack effective prediction models for recent recurrence(time to recurrence<2 years)after hepatectomy for HCC.AIM To establish an interventable prediction model to estimate recurrence-free survival(RFS)after hepatectomy for HCC based on sarcopenia.METHODS We retrospectively analyzed 283 hepatitis B-related HCC patients who underwent curative hepatectomy for the first time,and the skeletal muscle index at the third lumbar spine was measured by preoperative computed tomography.94 of these patients were enrolled for external validation.Cox multivariate analysis was per-formed to identify the risk factors of postoperative recurrence in training cohort.A nomogram model was developed to predict the RFS of HCC patients,and its predictive performance was validated.The predictive efficacy of this model was evaluated using the receiver operating characteristic curve.RESULTS Multivariate analysis showed that sarcopenia[Hazard ratio(HR)=1.767,95%CI:1.166-2.678,P<0.05],alpha-fetoprotein≥40 ng/mL(HR=1.984,95%CI:1.307-3.011,P<0.05),the maximum diameter of tumor>5 cm(HR=2.222,95%CI:1.285-3.842,P<0.05),and hepatitis B virus DNA level≥2000 IU/mL(HR=2.1,95%CI:1.407-3.135,P<0.05)were independent risk factors associated with postoperative recurrence of HCC.Based on the sarcopenia to assess the RFS model of hepatectomy with hepatitis B-related liver cancer disease(SAMD)was established combined with other the above risk factors.The area under the curve of the SAMD model was 0.782(95%CI:0.705-0.858)in the training cohort(sensitivity 81%,specificity 63%)and 0.773(95%CI:0.707-0.838)in the validation cohort.Besides,a SAMD score≥110 was better to distinguish the high-risk group of postoperative recurrence of HCC.CONCLUSION Sarcopenia is associated with recent recurrence after hepatectomy for hepatitis B-related HCC.A nutritional status-based prediction model is first established for postoperative recurrence of hepatitis B-related HCC,which is superior to other models and contributes to prognosis prediction.展开更多
The lattice-oxygen-mediated mechanism is considered as a reasonable mechanism for the electrochemical catalytic oxygen evolution reaction(OER)of NiFe layered double hydroxides(LDHs).A NiFe LDH with distinct lattice co...The lattice-oxygen-mediated mechanism is considered as a reasonable mechanism for the electrochemical catalytic oxygen evolution reaction(OER)of NiFe layered double hydroxides(LDHs).A NiFe LDH with distinct lattice contraction and microcrystallization was synthesized via a simple one-step method using sodium gluconate.The lattice contraction is attributed to the interaction of carbon in sodium gluconate and iron in NiFe LDH.The NiFe LDH with optimized microcrystallization and lattice contraction shows a low overpotential of 217 mV at a current density of 10 mA cm^(−2) and excellent durability of 20 h at a high current density of 100 mA cm^(−2).The results revealed that a contractive metal–oxygen bond could boost the intrinsic activity of active sites and the microcrystallization promotes an increase in the number of active sites in terms of unit area.The chemical environment of oxygen elemental characterization and resistance at different chronopotentiometry times confirm that the lattice oxygen element is indeed involved in the process of OER,supporting the lattice-oxygen-mediated mechanism of NiFe LDH.Density functional theory calculations reveal that contractive metal–oxygen bonds induced a reduction of the adsorption energy barrier of intermediate products,thus improving the intrinsic catalytic activity.The special characteristics of microcrystallization and lattice contraction of NiFe LDH provide a strategy to improve both the number and the intrinsic activity of active sites in a versatile manner.展开更多
Ion cyclotron wave resonance heating(ICRH) is one of the most important auxiliary methods to heat plasma in the Experimental Advanced Superconducting Tokamak(EAST). Several megawatts of power is transmitted through se...Ion cyclotron wave resonance heating(ICRH) is one of the most important auxiliary methods to heat plasma in the Experimental Advanced Superconducting Tokamak(EAST). Several megawatts of power is transmitted through separate coaxial lines and coupled with the plasma through arrays of loop antennas. The parameters of the ICRH system, including the injected power and phasing between antenna straps, are critical to the coupling efficiency of the power as well as the resulting impact on the heating efficiency. In this paper, we present a system for feedback control of the phase between the current straps and the ICRH power on EAST. The feedback control system was tested using both a matched dummy load and a plasma load, and it successfully maintained stable operation in the 2016 EAST campaign. Good control of the injected power and wave phases was achieved during edgelocalized mode operation.展开更多
The SC200 proton therapy superconducting cyclotron was developed by ASIPP (Hefei, China) and JINR (Dubna, Russia). A measurement system was designed to assess the average radial component of the magnetic field (Brav) ...The SC200 proton therapy superconducting cyclotron was developed by ASIPP (Hefei, China) and JINR (Dubna, Russia). A measurement system was designed to assess the average radial component of the magnetic field (Brav) with 15 search coils in the median plane. The winding differences of the search coils affect the measurement accuracy of the Brav. Based on the electromagnetic induction principle, to measure the Brav accurately, this paper focuses on the design and commissioning of the Brav measurement system. The preliminary results confirm that the system design is reasonable and suitable. After testing the search coil at different speeds, the optimal speed was determined as 2.5 mm/s. The relative error was approximately 0.1% under the maximum radial component of the magnetic field Br of 7 G. The measurement precision was up to 1.0×10^-3, which can provide the required measurement tolerance of 3–7 G for Br in the median plane. The commissioning of the Brav measurement system is an important step for Br measurement. It can check and adjust the asymmetry of the superconducting coils (SCs).展开更多
Silicon(Si)has been attracting extensive attention for rechargeable lithium(Li)‐ion batteries due to its high theoretical capacity and low potential vs Li/Li+.However,it remains challenging and problematic to stabili...Silicon(Si)has been attracting extensive attention for rechargeable lithium(Li)‐ion batteries due to its high theoretical capacity and low potential vs Li/Li+.However,it remains challenging and problematic to stabilize the Si materials during electrochemical cycling because of the huge volume expansion,which results in losing electric contact and pulverization of Si particles.Consequently,the Si anode materials generally suffer from poor cycling,poor rate performance,and low coulomb efficiency,preventing them from practical applications.Up‐to‐date,there are numerous reports on the engineering of Si anode materials at microscale and nanoscale with significantly improved electrochemical performances.In this review,we will concentrate on various precisely designed protective layers for silicon‐based materials,including carbon layers,inorganic layers,and conductive polymer protective layer.First,we briefly introduced the alloying and failure mechanism of Si as anode materials upon electrochemical reactions.Following that,representative cases have been introduced and summarized to illustrate the purpose and advancement of protective coating layers,for instance,to alleviate pulverization and improve conductivity caused by volume expansion of Si particles during charge/discharge process,and maintain the surface stability of Si particles to form a stable solid‐electrolyte interphase layer.At last,possible strategies on the protective coating layer for stabilizing silicon anode materials that can be applied in the future have been indicated.展开更多
Traditional synthetic methodologies are confronted with great challenges to fabricate complex nanomaterials with delicate design,high efficiency and excellent sustainability.During the past decade,bio-inspired synthes...Traditional synthetic methodologies are confronted with great challenges to fabricate complex nanomaterials with delicate design,high efficiency and excellent sustainability.During the past decade,bio-inspired synthesis has been extensively applied as an effective and efficient strategy for the fabrication of nanomaterials and nanostructures.Mimicking electrode materials at nanoscale in the aspect of either structure or functionality has been receiving surging interest because of their incomparable advantages and outperforming properties.In this review,we summarize the recent progresses on bio-inspired synthesis of nanomaterials and smart structures in the field of energy storage and conversion.Firstly,an overall introduction of bio-inspired synthetic strategies will be presented,with focus on the biotemplates and bio-resources.Following that,a library of complex mimicking structures featured by high-order,hierarchical porosity,or bionic function are introduced,with discussion on their chemical and physical properties associated with the structure.The enhanced electrochemical properties such as energy density,cycling stability,etc.in different electrochemical systems will be also discussed.At last,we will expand the perspectives regarding the advantages and limitations of bioinspired strategy and possible solutions in the future.展开更多
Silicon(Si)is regarded as a promising anode material for next-generation lithium-ion batteries due to its ultrahigh theoretical capacity.However,the drastic volume change and the continuous solid electrolyte interphas...Silicon(Si)is regarded as a promising anode material for next-generation lithium-ion batteries due to its ultrahigh theoretical capacity.However,the drastic volume change and the continuous solid electrolyte interphase(SEI)formation during the lithiation/delithiation process seriously hinder its practical application as commercial anodes.Herein,macrocyclic betacyclodextrin(β-CD)has been designed as the diffusion channel for lithium ions at the molecular scale.The diameter of molecular channel is approximately comparable with the solvated lithium ions,which enables the transport of lithium ions and prevents the penetration of solvent molecules.Moreover,the addition ofβ-CD changes the formation behavior of SEI layer and stabilizes the Si nanoparticles.The enhanced electrochemical performances in terms of fast kinetics and improved stability have been achieved.The Si anode with the particularly selected lithium-ion diffusion channel and stabilized SEI layer exhibits a high reversible capability of 2562 m Ah g-1 after 50 cycles at the current density of 500 m A g-1,1944 m Ah g-1 after 200 cycles at the current density of 1 A g-1,and high rate performance.The novel strategy of molecular channel for lithium-ion diffusion offers new insights into the design of alloy-typed anode electrodes with high capacity for lithium-ion batteries.展开更多
Due to its high theoretical capacity and appropriate potential platform,tin-based alloy materials are expected to be a competitive candidate for the next-generation high performance anodes of lithium-ion batteries.Nev...Due to its high theoretical capacity and appropriate potential platform,tin-based alloy materials are expected to be a competitive candidate for the next-generation high performance anodes of lithium-ion batteries.Nevertheless,the immense volume change during the lithium-ion insert process leads to severe disadvantages of structural damage and capacity fade,which limits its practical application.In this work,a three-dimensional(3 D)multicore-shell hollow nanobox encapsulated by carbon layer is obtained via a three-step method of hydrothermal reaction,annealing and alkali etching.During the electrochemical reactions,the CoSn@void@C nanoboxes provide internal space to compensate the volumetric change upon the lithiation of Sn,while the inactive component of Co acts as chemical buffers to withstand the anisotropic expansion of nanoparticles.Owing to the above-mentioned advantages,the elaborated anode delivers an excellent capacity of 788.2 m Ah/g at 100 m A/g after 100 cycles and considerable capacity retention of 519.2 mAh/g even at a high current density of 1 A/g after 300 cycles.The superior stability and high performance indicate its capability as promising anodes for lithium-ion batteries.展开更多
Ion cyclotron wave resonance heating system(ICRH)which is one of the most important auxiliary system in EAST provides conditions for heating the plasma.In order to make the whole transmission network of ICRH form the ...Ion cyclotron wave resonance heating system(ICRH)which is one of the most important auxiliary system in EAST provides conditions for heating the plasma.In order to make the whole transmission network of ICRH form the required state,the coaxial switching system was developed,which mainly consists of 11 same coaxial switches.Each coaxial switch has a controller with an RS485 communication interface and is able to switch between two states.All controllers are integrated to an RS485 hub which connects to the computer.A master computer software is developed to control the coaxial switching system so as to achieve the state needs of ICRH.Moreover,several rounds of experiments show that the coaxial switching system operates reliably.The coaxial switching system has already been applied to normal use currently.展开更多
In this study,we aimed to evaluate the toxic effects,changes in life span,and expression of various metabolismrelated genes in Caenorhabditis elegans,using RNA interference(RNAi)and mutant strains,after 3-bromopyruvat...In this study,we aimed to evaluate the toxic effects,changes in life span,and expression of various metabolismrelated genes in Caenorhabditis elegans,using RNA interference(RNAi)and mutant strains,after 3-bromopyruvate(3-BrPA)treatment.C.elegans was treated with various concentrations of 3-BrPA on nematode growth medium(NGM)plates,and their survival was monitored every 24 h.The expression of genes related to metabolism was measured by the real-time fluorescent quantitative polymerase chain reaction(qPCR).Nematode survival in the presence of 3-BrPA was also studied after silencing three hexokinase(HK)genes.The average life span of C.elegans cultured on NGM with 3-BrPA was shortened to 5.7 d compared with 7.7 d in the control group.hxk-1,hxk-2,and hxk-3 were overexpressed after the treatment with 3-BrPA.After successfully interfering hxk-1,hxk-2,and hxk-3,the 50%lethal concentration(LC50)of all mutant nematodes decreased with 3-BrPA treatment for 24 h compared with that of the control.All the cyp35 genes tested were overexpressed,except cyp-35B3.The induction of cyp-35A1 expression was most obvious.The LC50 values of the mutant strains cyp-35A1,cyp-35A2,cyp-35A4,cyp-35B3,and cyp-35C1 were lower than that of the control.Thus,the toxicity of 3-BrPA is closely related to its effect on hexokinase metabolism in nematodes,and the cyp-35 family plays a key role in the metabolism of 3-BrPA.展开更多
Ion cyclotron range of frequency（ICRF） heating has been used in tokamaks as one of the most successful auxiliary heating tools and has been adopted in the EAST. However, the antenna load will fluctuate with the chan...Ion cyclotron range of frequency（ICRF） heating has been used in tokamaks as one of the most successful auxiliary heating tools and has been adopted in the EAST. However, the antenna load will fluctuate with the change of plasma parameters in the ICRF heating process. To ensure the steady operation of the ICRF heating system in the EAST, fast ferrite tuner（FFT） has been carried out to achieve real-time impedance matching. For the requirements of the FFT impedance matching system, the magnet system of the ferrite tuner（FT） was designed by numerical simulations and experimental analysis, where the biasing magnetic circuit and alternating magnetic circuit were the key researched parts of the ferrite magnet. The integral design goal of the FT magnetic circuit is that DC bias magnetic field is 2000 Gs and alternating magnetic field is±400 Gs. In the FTT, E-type magnetic circuit was adopted. Ferrite material is Nd Fe B with a thickness of 30 mm by setting the working point of Nd Fe B, and the ampere turn of excitation coil is 25 through the theoretical calculation and simulation analysis. The coil inductance to generate alternating magnetic field is about 7 m H. Eddy-current effect has been analyzed, while the magnetic field distribution has been measured by a Hall probe in the medium plane of the biasing magnet. Finally, the test results show the good performance of the biasing magnet satisfying the design and operating requirements of the FFT.展开更多
基金support by the National Natural Science Foundation of China(Nos.U20A20123,51874357,22379166)Natural Science Foundation for Distinguished Young Scholars of Hunan Province(No.2022JJ10089)。
文摘The sluggish reaction kinetics of the oxygen evolution reaction(OER)and methanol oxidation reaction(MOR)remain obstacles to the commercial promotion of water splitting and direct methanol fuel cells.Considering the vital role of noble metals in electrocatalytic activity,this work focuses on the rational synthesis of Ni-noble metal composite nanocatalysts for overcoming the drawbacks of high cost and susceptible oxidized surfaces of noble metals.The inherent catalytic activity is improved by the altered electronic structure and effective active sites of the catalyst induced by the size effect of noble metal clusters.In particular,a series of Ni-noble metal nanocomposites are successfully synthesized by partially introducing noble metal into Ni with porous interfacial defects derived from Ni-Al layered double hydroxide(LDH).The Ni_(10)Pd_(1)nanocomposite exhibits high OER catalytic activity with an overpotential of 0.279 V at 10 m A/cm^(2),surpassing Ni_(10)Ag_(1)and Ni_(10)Au_(1)counterparts.Furthermore,the average diameter of Pd clusters gradually increases from 5.57 nm to 44.44 nm with the increased proportion of doped Pd,leading to the passivation of catalytic activity due to the exacerbated surface oxidation of Pd in the form of Pd^(2+).After optimization,Ni_(10)Pd_(1)delivers significantly enhanced OER and MOR electroactivities and long-term stability compared to that of Ni_(2)Pd_(1),Ni_(1)Pd_(1)and Ni_(1)Pd_(2),which is conducive to the effective utilization of Pd and alleviation of surface oxidation.
基金support by National Natural Science Foundation of China(22379166)Natural Science Foundation for Distinguished Young Scholars of Hunan Province(2022JJ10089)Central South University Innovation-Driven Research Programme(2023CXQD034).
文摘Within the framework of carbon neutrality,lithium-ion batteries(LIBs)are progressively booming along with the growing utilization of green and clean energy.However,the extensive application of LIBs with limited lifespan has brought about a significant recycling dilemma.The traditional hydrometallurgical or pyrometallurgical strategies are not capable to maximize the output value of spent LIBs and minimize the potential environmental hazards.Herein,to alternate the tedious and polluting treatment processes,we propose a high-temperature molten-salt strategy to directly regenerate spent cathodes of LIBs,which can also overcome the barrier of the incomplete defects'restoration with previous low-temperature molten salts.The high-energy and stable medium environment ensures a more thorough and efficient relithiation reaction,and simultaneously provides sufficient driving force for atomic rearrangement and grains secondary growth.In consequence,the regenerated ternary cathode(R-NCM)exhibits significantly enhanced structural stability that effectively suppresses the occurrence of cracks and harmful side reactions.The R-NCM delivers excellent cycling stability,retaining 81.2%of its capacity after 200 cycles at 1 C.This technique further optimizes the traditional eutectic molten-salt approach,broadening its applicability and improving regenerated cathode performance across a wider range of conditions.
基金supported by the National Natural Science Foundation of China(No.22072183)the Natural Science Foundation of Hunan Province,China(No.2022JJ30690)the High Performance Computing Center of Central South University.
文摘Serpentine structured Co_(3)Si_(2)O_(5)(OH)_(4) is inexpensive,chemically stable,and electrochemically active in oxygen evolution reactions(OER).However,the OER activity of Co_(3)Si_(2)O_(5)(OH)_(4) materials is still unfavorable due to the low active sites.Here,Mn^(2+)-doped Co_(3)Si_(2)O_(5)(OH)_(4) serpentine nanosheets with tuned d-band centers are achieved for efficient oxygen evolution in alkaline and neutral electrolytes.The Co_(x)Mn_(3−x)Si_(2)O_(5)(OH)_(4) serpentine nanosheets are synthesized by a simple hydrothermal method.The optimized Co_(2.4)Mn_(0.6)Si_(2)O_(5)(OH)_(4) serpentine nanosheets showed favorable OER overpotentials as well as stable durability in KOH solution and phosphate buffer solution,which were superior to most of the Co-based and Mn-based OER electrocatalysts.The in situ Raman spectroscopy shows that the materials are kept well in the electrochemical OER environments.Further density functional theory shows that the d-band center of Co_(x)Mn_(3−x)Si_(2)O_(5)(OH)_(4) serpentine nanosheets is shifted more upward in comparison with pristine Co_(3)Si_(2)O_(5)(OH)_(4).The changes in the d-band center increase the adsorption of intermediates,optimize the reaction steps,and lower the energy barriers of the OER.That is the main reason for the OER enhancement Mn^(2+)-doped Co_(3)Si_(2)O_(5)(OH)_(4).This work gives an efficient strategy to design cheap and stable electrocatalytic materials for OER in a broad pH environment.
基金financial support by the National Natural Science Foundation of China(22379166)the Natural Science Foundation for Distinguished Young Scholars of Hunan Province(2022JJ10089)+2 种基金the Central South University Innovation-Driven Research Programme(2023CXQD034)support from the 100 Talented program of Hunan Provincesupported in part by the HighPerformance Computing Center of Central South University。
文摘Lithium metal batteries(LMBs)encounter substantial challenges related to hydrogen fluoride(HF)-induced degradation of electrode materials and interfacial instability.The predominant sources of HF are attributed to the hydrolysis of lithium hexafluorophosphate(LiPF_(6))in the electrolyte and the decomposition of fluorine-containing solvents,which result in transition metal dissolution,rapid capacity fading,and overall battery performance deterioration.To mitigate these issues,we introduce a dual-protection strategy via the synergistic incorporation of pentafluorophenyl trifluoroacetate(PFTFA)and lithium difluoro(oxalato)borate(LiDFOB)additives,achieving both chemical HF capture and physical HF defense.The optimized electrolyte system not only promotes the formation of a robust cathode-electrolyte interphase layer enriched with LiF and LiB_(x)O_(y)compounds but also effectively scavenges HF through PFTFA coordination,thereby ensuring enhanced cathode stability.Consequently,the Li‖LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2)(NCM811)cells demonstrate remarkable cyclic stability with 80%capacity retention over 420 cycles at the cutoff voltage of 4.4 V under 1 C rate,whereas conventional carbonate-based electrolytes only retain 54.8%capacity after 150 cycles under identical conditions.Even under high voltage conditions(4.8 V,0.5 C),the developed electrolyte maintains 77.8%capacity retention over 200 cycles.This work provides valuable insights into the rational design of multifunctional electrolyte additives for high-performance LMBs.
文摘The poor oxidation stability of ether-based solvents has long been a major challenge limiting their practical application.To enhance the oxidative stability of ether-based electrolytes,the physicochemical properties of various glycol dimethyl ethers are screened,and diglyme(G2)is selected as the sole solvent for the electrolyte.Lithium bis(fluorosulfonyl)imide(LiFSI),a highly dissociative salt,is used as the primary salt;while lithium nitrate(LiNO_(3))and lithium difluorophosphate(LiDFP),which have small ionic sizes and strong binding energies,are added as secondary salts.The resulting electrolyte can modulate the electric double layer structure by NO_(3)^(-) and DFP^(-) on the cathode side,leading to an increased Liþconcentration that is originally repelled by the cathode.Additionally,the oxidation stability of the electrolyte is improved and the formed electrode-electrolyte interphase is more uniform and stable,thereby enhancing the electrochemical performance of the cells.As a result,cells assembled with a total of 1 M ternary lithium salts in G2 solvent can operate at high voltage of 4.4 V.The LijjNCM811 cells maintain 80.2%capacity retention after 270 cycles at room temperature,with an average Coulombic efficiency of 99.5%,and exhibit 88.4%capacity retention after 200 cycles at -30℃.
基金financial support from the National Natural Science Foundation of China(No.22072183)the Natural Science Foundation of Hunan Province,China(No.2022JJ30690)supported in part by the High Performance Computing Center of Central South University。
文摘Three-dimensional(3D)covalent organic frameworks(COFs)have attracted extensive attention as photocatalysts for CO_(2)reduction reactions.Introducing metal atoms is essential for enhancing activity,but previous metal sites in 3D COFs predominantly exhibit symmetrical coordination,making them unsuitable for CO_(2)activation.Here,we design a 3D COF with 2,2'-pyridine linked around tetra-(4-anilyl)methane(TCM-Bpy-COF),where Co^(2+)is asymmetrically coordinated by bipyridine and acetates(TCMBpy-COF-CoAc).The TCM-Bpy-COF-CoAc exhibits outstanding photocatalytic CO_(2)reduction performance under weak visible light,achieving a CO evolution rate of 26,650μmol g^(-1)h^(-1)under 5 W of lightemitting-diode(LED)lamp and high apparent quantum efficiency.The performance far exceeds that of symmetrically coordinated bipyridine-Co-bipyridine TCM-Bpy-COF and surpasses most reported COF-based photocatalysts.In-situ spectral characterizations and theoretical calculations show that asymmetric N,O-coordination around the Co^(2+)center polarizes electron density and lowers reaction energy barriers of^(*)COOH intermediates,enhancing the conversion of CO_(2)to CO.This work inspires the design of 3D COF-based photocatalysts with highly catalytic efficiency.
基金the financial support by the National Natural Science Foundation of China(51874357,51872333,U20A20123)Innovative Research Group of Hunan Provincial Natural Science Foundation of China(2019JJ10006)support from Shenghua Scholar Program of Central South University.R.M.acknowledges support from JSPS KAKENNHI(18H03869)。
文摘Strategy of anchoring alloy nanoparticles made up of the efficient catalytic element(e.g.,Ni,Fe)on dodecyl sulfate(DS^(-))-intercalated NiFe layered double hydroxides(DS^(-)-NiFe LDH)obtained by a convenient one-step hydrothermal coprecipitation method for essentially enhancing oxygen evolution reaction(OER)performance was proposed.The results of structural characterization indicate Pt_(2)FeNi alloy nanoparticles evenly distribute on the surface of DS^(-)-NiFe LDH.The sizes of the Pt_(2)FeNi nanoparticles,closely related to their OER performance,could be wellcontrolled by adjusting the amount of H;PtCl;addition.The composite structure of as-prepared product was stable during processes of synthesis,exfoliation,self-assembly,and subsequent electrocatalytic OER.Rigorous electrochemical test proving the contributing catalytic active sites was located at the interface between Pt_(2)FeNi and DS^(-)-NiFe LDH,and the Ni and Fe were the major active elements while O atoms are adsorption sites.The formation of Pt_(2)FeNi nanoparticles could greatly prompt the reduction of Tafel slope.The best-performing Pt_(2)FeNi/DS^(-)-NiFe LDH with a Pt content of 0.98 wt%achieved low overpotential of 204 mV at 10 mA cm^(-2)and 262 mV at 50 mA cm^(-2).This work provides a convenient and effective strategy to create additional active sites for enhancing OER performance of NiFe LDH and make contribution to its wide application.
基金financial support from the National Natural Science Foundation of China(No.22072183)the Natural Science Foundation of Hunan Province,China(No.2022JJ30690)。
文摘The d-band state of materials is an important descriptor for activity of oxygen evolution reaction(OER).For NiO materials,there is rarely concern about tuning their d-band states to tailor the OER behaviors.Herein,NiO nanocrystals with doping small amount of La^(3+)were used to regulate d-band states for promoting OER activity.Density of states calculations based on density functional theory revealed that La^(3+)doping produced upper shift of d-band center,which would induce stronger electronic interaction between surface Ni atoms and species of oxygen evolution reaction intermediates.Further density functional theory calculation illustrated that La^(3+)doped NiO possessed reduced Gibbs free energy in adsorbing species of OER intermediate.Predicted by theoretical calculations,trace La^(3+)was introduced into crystal lattice of NiO nanoparticles.The La^(3+)doped NiO nanocrystal showed much promoted OER activity than corresponding pristine NiO product.Further electrochemical analysis revealed that La^(3+)doping into NiO increased the intrinsic activity such as improved active sites and reduced charge transfer resistance.The in-situ Raman spectra suggested that NiO phase in La^(3+)doped NiO could be better maintained than pristine NiO during the OER.This work provides an effective strategy to tune the d-band center of NiO for efficient electrocatalytic OER.
基金Supported by Guizhou Provincial Science and Technology Projects,No.[2021]013 and No.[2021]053Doctor Foundation of Guizhou Provincial People's Hospital,No.GZSYBS[2021]07.
文摘BACKGROUND Sarcopenia may be associated with hepatocellular carcinoma(HCC)following hepatectomy.But traditional single clinical variables are still insufficient to predict recurrence.We still lack effective prediction models for recent recurrence(time to recurrence<2 years)after hepatectomy for HCC.AIM To establish an interventable prediction model to estimate recurrence-free survival(RFS)after hepatectomy for HCC based on sarcopenia.METHODS We retrospectively analyzed 283 hepatitis B-related HCC patients who underwent curative hepatectomy for the first time,and the skeletal muscle index at the third lumbar spine was measured by preoperative computed tomography.94 of these patients were enrolled for external validation.Cox multivariate analysis was per-formed to identify the risk factors of postoperative recurrence in training cohort.A nomogram model was developed to predict the RFS of HCC patients,and its predictive performance was validated.The predictive efficacy of this model was evaluated using the receiver operating characteristic curve.RESULTS Multivariate analysis showed that sarcopenia[Hazard ratio(HR)=1.767,95%CI:1.166-2.678,P<0.05],alpha-fetoprotein≥40 ng/mL(HR=1.984,95%CI:1.307-3.011,P<0.05),the maximum diameter of tumor>5 cm(HR=2.222,95%CI:1.285-3.842,P<0.05),and hepatitis B virus DNA level≥2000 IU/mL(HR=2.1,95%CI:1.407-3.135,P<0.05)were independent risk factors associated with postoperative recurrence of HCC.Based on the sarcopenia to assess the RFS model of hepatectomy with hepatitis B-related liver cancer disease(SAMD)was established combined with other the above risk factors.The area under the curve of the SAMD model was 0.782(95%CI:0.705-0.858)in the training cohort(sensitivity 81%,specificity 63%)and 0.773(95%CI:0.707-0.838)in the validation cohort.Besides,a SAMD score≥110 was better to distinguish the high-risk group of postoperative recurrence of HCC.CONCLUSION Sarcopenia is associated with recent recurrence after hepatectomy for hepatitis B-related HCC.A nutritional status-based prediction model is first established for postoperative recurrence of hepatitis B-related HCC,which is superior to other models and contributes to prognosis prediction.
基金National Natural Science Foundation of China,Grant/Award Numbers:51874357,51872333,U20A20123。
文摘The lattice-oxygen-mediated mechanism is considered as a reasonable mechanism for the electrochemical catalytic oxygen evolution reaction(OER)of NiFe layered double hydroxides(LDHs).A NiFe LDH with distinct lattice contraction and microcrystallization was synthesized via a simple one-step method using sodium gluconate.The lattice contraction is attributed to the interaction of carbon in sodium gluconate and iron in NiFe LDH.The NiFe LDH with optimized microcrystallization and lattice contraction shows a low overpotential of 217 mV at a current density of 10 mA cm^(−2) and excellent durability of 20 h at a high current density of 100 mA cm^(−2).The results revealed that a contractive metal–oxygen bond could boost the intrinsic activity of active sites and the microcrystallization promotes an increase in the number of active sites in terms of unit area.The chemical environment of oxygen elemental characterization and resistance at different chronopotentiometry times confirm that the lattice oxygen element is indeed involved in the process of OER,supporting the lattice-oxygen-mediated mechanism of NiFe LDH.Density functional theory calculations reveal that contractive metal–oxygen bonds induced a reduction of the adsorption energy barrier of intermediate products,thus improving the intrinsic catalytic activity.The special characteristics of microcrystallization and lattice contraction of NiFe LDH provide a strategy to improve both the number and the intrinsic activity of active sites in a versatile manner.
基金supported in part by the National Magnetic Confinement Fusion Science Program(No.2015GB101001)the National Natural Science Foundation of China(Nos.11375236 and11375235)
文摘Ion cyclotron wave resonance heating(ICRH) is one of the most important auxiliary methods to heat plasma in the Experimental Advanced Superconducting Tokamak(EAST). Several megawatts of power is transmitted through separate coaxial lines and coupled with the plasma through arrays of loop antennas. The parameters of the ICRH system, including the injected power and phasing between antenna straps, are critical to the coupling efficiency of the power as well as the resulting impact on the heating efficiency. In this paper, we present a system for feedback control of the phase between the current straps and the ICRH power on EAST. The feedback control system was tested using both a matched dummy load and a plasma load, and it successfully maintained stable operation in the 2016 EAST campaign. Good control of the injected power and wave phases was achieved during edgelocalized mode operation.
基金supported by the Natural Science Foundation of Anhui under Grant(No.1908085QA25)the Research Initiation Foundation of Anhui Polytechnic University(No.2018YQQ001)+3 种基金the PreResearch National Natural Science Foundation of China of Anhui Polytechnic University(No.2019yyzr13)the National Natural Science Foundation of China(Nos.11575237 and 11775258)the National Magnetic Confinement Fusion Science Program(No.2015GB101001)the International Scientific and Technological Cooperation Project of Anhui(No.1704e1002207)
文摘The SC200 proton therapy superconducting cyclotron was developed by ASIPP (Hefei, China) and JINR (Dubna, Russia). A measurement system was designed to assess the average radial component of the magnetic field (Brav) with 15 search coils in the median plane. The winding differences of the search coils affect the measurement accuracy of the Brav. Based on the electromagnetic induction principle, to measure the Brav accurately, this paper focuses on the design and commissioning of the Brav measurement system. The preliminary results confirm that the system design is reasonable and suitable. After testing the search coil at different speeds, the optimal speed was determined as 2.5 mm/s. The relative error was approximately 0.1% under the maximum radial component of the magnetic field Br of 7 G. The measurement precision was up to 1.0×10^-3, which can provide the required measurement tolerance of 3–7 G for Br in the median plane. The commissioning of the Brav measurement system is an important step for Br measurement. It can check and adjust the asymmetry of the superconducting coils (SCs).
基金Japan Society for the Promotion of Science,Grant/Award Number:18H03869National Natural Science Foundation of China,Grant/Award Numbers:51872333,51874357。
文摘Silicon(Si)has been attracting extensive attention for rechargeable lithium(Li)‐ion batteries due to its high theoretical capacity and low potential vs Li/Li+.However,it remains challenging and problematic to stabilize the Si materials during electrochemical cycling because of the huge volume expansion,which results in losing electric contact and pulverization of Si particles.Consequently,the Si anode materials generally suffer from poor cycling,poor rate performance,and low coulomb efficiency,preventing them from practical applications.Up‐to‐date,there are numerous reports on the engineering of Si anode materials at microscale and nanoscale with significantly improved electrochemical performances.In this review,we will concentrate on various precisely designed protective layers for silicon‐based materials,including carbon layers,inorganic layers,and conductive polymer protective layer.First,we briefly introduced the alloying and failure mechanism of Si as anode materials upon electrochemical reactions.Following that,representative cases have been introduced and summarized to illustrate the purpose and advancement of protective coating layers,for instance,to alleviate pulverization and improve conductivity caused by volume expansion of Si particles during charge/discharge process,and maintain the surface stability of Si particles to form a stable solid‐electrolyte interphase layer.At last,possible strategies on the protective coating layer for stabilizing silicon anode materials that can be applied in the future have been indicated.
基金the 100 Talented Team of Hunan Province(XiangZu[2016]91)the“Huxiang high-level talents”program(no.2018RS3077,no.2019RS1007).
文摘Traditional synthetic methodologies are confronted with great challenges to fabricate complex nanomaterials with delicate design,high efficiency and excellent sustainability.During the past decade,bio-inspired synthesis has been extensively applied as an effective and efficient strategy for the fabrication of nanomaterials and nanostructures.Mimicking electrode materials at nanoscale in the aspect of either structure or functionality has been receiving surging interest because of their incomparable advantages and outperforming properties.In this review,we summarize the recent progresses on bio-inspired synthesis of nanomaterials and smart structures in the field of energy storage and conversion.Firstly,an overall introduction of bio-inspired synthetic strategies will be presented,with focus on the biotemplates and bio-resources.Following that,a library of complex mimicking structures featured by high-order,hierarchical porosity,or bionic function are introduced,with discussion on their chemical and physical properties associated with the structure.The enhanced electrochemical properties such as energy density,cycling stability,etc.in different electrochemical systems will be also discussed.At last,we will expand the perspectives regarding the advantages and limitations of bioinspired strategy and possible solutions in the future.
基金financial support by the National Natural Science Foundation of China(51874357,51872333)Innovative Research Group of Hunan Provincial Natural Science Foundation of China(2019JJ10006)+3 种基金the support from the 100 Talented Program of Hunan Province“Huxiang high-level talents”program(2019RS1007)support from Shenghua Scholar Program of Central South Universitysupport from JSPS KAKENNHI(18H03869)
文摘Silicon(Si)is regarded as a promising anode material for next-generation lithium-ion batteries due to its ultrahigh theoretical capacity.However,the drastic volume change and the continuous solid electrolyte interphase(SEI)formation during the lithiation/delithiation process seriously hinder its practical application as commercial anodes.Herein,macrocyclic betacyclodextrin(β-CD)has been designed as the diffusion channel for lithium ions at the molecular scale.The diameter of molecular channel is approximately comparable with the solvated lithium ions,which enables the transport of lithium ions and prevents the penetration of solvent molecules.Moreover,the addition ofβ-CD changes the formation behavior of SEI layer and stabilizes the Si nanoparticles.The enhanced electrochemical performances in terms of fast kinetics and improved stability have been achieved.The Si anode with the particularly selected lithium-ion diffusion channel and stabilized SEI layer exhibits a high reversible capability of 2562 m Ah g-1 after 50 cycles at the current density of 500 m A g-1,1944 m Ah g-1 after 200 cycles at the current density of 1 A g-1,and high rate performance.The novel strategy of molecular channel for lithium-ion diffusion offers new insights into the design of alloy-typed anode electrodes with high capacity for lithium-ion batteries.
基金the financial support by National Natural Science Foundation of China(Nos.U20A20123,51874357,52002405)Innovative Research Group of Hunan Provincial Natural Science Foundation of China(No.2019JJ10006)the support from the 100 Talented Program of Hunan Province and“Huxiang High-level Talents”Program(No.2019RS1007)。
文摘Due to its high theoretical capacity and appropriate potential platform,tin-based alloy materials are expected to be a competitive candidate for the next-generation high performance anodes of lithium-ion batteries.Nevertheless,the immense volume change during the lithium-ion insert process leads to severe disadvantages of structural damage and capacity fade,which limits its practical application.In this work,a three-dimensional(3 D)multicore-shell hollow nanobox encapsulated by carbon layer is obtained via a three-step method of hydrothermal reaction,annealing and alkali etching.During the electrochemical reactions,the CoSn@void@C nanoboxes provide internal space to compensate the volumetric change upon the lithiation of Sn,while the inactive component of Co acts as chemical buffers to withstand the anisotropic expansion of nanoparticles.Owing to the above-mentioned advantages,the elaborated anode delivers an excellent capacity of 788.2 m Ah/g at 100 m A/g after 100 cycles and considerable capacity retention of 519.2 mAh/g even at a high current density of 1 A/g after 300 cycles.The superior stability and high performance indicate its capability as promising anodes for lithium-ion batteries.
基金supported by National Natural Science Foundation of China(Nos.11575237,11775258)National Key Research and Development Program(Nos.2016YFA0400600 and 2016YFA0400601)China Fusion Engineering Experimental Reactor General Integration and Engineering Design(No.2017YFE0300503).
文摘Ion cyclotron wave resonance heating system(ICRH)which is one of the most important auxiliary system in EAST provides conditions for heating the plasma.In order to make the whole transmission network of ICRH form the required state,the coaxial switching system was developed,which mainly consists of 11 same coaxial switches.Each coaxial switch has a controller with an RS485 communication interface and is able to switch between two states.All controllers are integrated to an RS485 hub which connects to the computer.A master computer software is developed to control the coaxial switching system so as to achieve the state needs of ICRH.Moreover,several rounds of experiments show that the coaxial switching system operates reliably.The coaxial switching system has already been applied to normal use currently.
基金Project supported by the National Natural Science Foundation of China(Nos.31172174 and 81460677)the Fundamental Research Funds for the Central Universities of China(No.31920170039)the Natural Science Found of Gansu Province(No.18JR3RA283),China
文摘In this study,we aimed to evaluate the toxic effects,changes in life span,and expression of various metabolismrelated genes in Caenorhabditis elegans,using RNA interference(RNAi)and mutant strains,after 3-bromopyruvate(3-BrPA)treatment.C.elegans was treated with various concentrations of 3-BrPA on nematode growth medium(NGM)plates,and their survival was monitored every 24 h.The expression of genes related to metabolism was measured by the real-time fluorescent quantitative polymerase chain reaction(qPCR).Nematode survival in the presence of 3-BrPA was also studied after silencing three hexokinase(HK)genes.The average life span of C.elegans cultured on NGM with 3-BrPA was shortened to 5.7 d compared with 7.7 d in the control group.hxk-1,hxk-2,and hxk-3 were overexpressed after the treatment with 3-BrPA.After successfully interfering hxk-1,hxk-2,and hxk-3,the 50%lethal concentration(LC50)of all mutant nematodes decreased with 3-BrPA treatment for 24 h compared with that of the control.All the cyp35 genes tested were overexpressed,except cyp-35B3.The induction of cyp-35A1 expression was most obvious.The LC50 values of the mutant strains cyp-35A1,cyp-35A2,cyp-35A4,cyp-35B3,and cyp-35C1 were lower than that of the control.Thus,the toxicity of 3-BrPA is closely related to its effect on hexokinase metabolism in nematodes,and the cyp-35 family plays a key role in the metabolism of 3-BrPA.
基金supported by National Natural Science Foundation of China(Grant No.11575237)the National Magnetic Confinement Fusion Science Program(Grant No.2015GB101001)the International Scientific and Technological Cooperation Project of Anhui(Grant No.1704e1002207)
文摘Ion cyclotron range of frequency（ICRF） heating has been used in tokamaks as one of the most successful auxiliary heating tools and has been adopted in the EAST. However, the antenna load will fluctuate with the change of plasma parameters in the ICRF heating process. To ensure the steady operation of the ICRF heating system in the EAST, fast ferrite tuner（FFT） has been carried out to achieve real-time impedance matching. For the requirements of the FFT impedance matching system, the magnet system of the ferrite tuner（FT） was designed by numerical simulations and experimental analysis, where the biasing magnetic circuit and alternating magnetic circuit were the key researched parts of the ferrite magnet. The integral design goal of the FT magnetic circuit is that DC bias magnetic field is 2000 Gs and alternating magnetic field is±400 Gs. In the FTT, E-type magnetic circuit was adopted. Ferrite material is Nd Fe B with a thickness of 30 mm by setting the working point of Nd Fe B, and the ampere turn of excitation coil is 25 through the theoretical calculation and simulation analysis. The coil inductance to generate alternating magnetic field is about 7 m H. Eddy-current effect has been analyzed, while the magnetic field distribution has been measured by a Hall probe in the medium plane of the biasing magnet. Finally, the test results show the good performance of the biasing magnet satisfying the design and operating requirements of the FFT.
