The Distortion of Energy Deposit Distribution of (12)～C Ions in Water

The transport process of 12C ions in water was studied with SRIM code and Geant4 toolkit. The SRIM results indicate that the transverse diffusion of 12C ion beam causes distortion of energy deposit along the beam direction. The distortion becomes more notable as the transverse diffusion increases. The simulation results of Geant4 indicate that the influence of secondary fragments on energy deposit distribution would be the main factor causing the distortion in higher energy range. In the region adjacent to the beam line where the contribution from 12C ions domi- nates, the contributions from secondary fragments are ignorable. The further from the beam axis the region locates, the larger the contributions from secondary fragments, until the contributions from secondary fragments are ignorable. The further from the beam axis the region locates, the larger the contributions from secondary fragments, until the contributions from secondary frag- ments exceed that of 12C. Among all the secondary fragments, the contributions of H, He and B ions are mostly notable. It is also found that some positron-emitting secondary fragments could be very useful for position emitting tomography （PET）.

Influences of nitrogen flow rate on the structures and properties of Ti and N co-doped diamond-like carbon films deposited by arc ion plating

In this paper, Ti-C-N nanocomposite films are deposited under different nitrogen flow rates by pulsed bias arc ion plating using Ti and graphite targets in the Ar/N2 mixture gas. The surface morphologies, compositions, microstructures, and mechanical properties of the Ti-C-N films are investigated systematically by field emission scanning electron mi- croscopy （FE-SEM）, x-ray photoelectron spectroscopy （XPS）, grazing incident x-ray diffraction （GIXRD）, Raman spectra, and nano-indentation. The results show that the nanocrystalline Ti（C,N） phase precipitates in the film from GIXRD and XPS analysis, and Raman spectra prove the presence of diamond-like carbon, indicating the formation of nanocomposite film with microstructures comprising nanocrystalline Ti（C,N） phase embedded into a diamond-like matrix. The nitrogen flow rate has a significant effect on the composition, structure, and properties of the film. The nano-hardness and elastic modulus first increase and then decrease as nitrogen flow rate increases, reaching a maximum of 34.3 GPa and 383.2 GPa, at a nitrogen flow rate of 90 sccm, respectively.

C/Sn复合薄膜的磁控溅射制备及其作为锂离子电池负极材料的电化学性能

采用磁控溅射的方法在铜箔上制备了C/Sn复合薄膜并将其作为锂离子电池负极材料,研究了C/Sn复合薄膜中Sn质量分数对其电化学性能的影响。研究发现,随着复合薄膜中Sn质量分数的增加,其首圈放电比容量增加,在一定范围内增加Sn质量分数,首圈库仑效率增加,但当Sn质量分数过多时其库仑效率降低。Sn质量分数分别为89.20%、91.61%、93.85%、95.81%的四种复合薄膜,在电流密度为500 mA/g时的首圈放电比容量分别为1195.4、1372.97、1574.86、1642.30 mA·h/g,首圈库仑效率分别为86.84%、87.88%、94.06%、80.66%。循环200圈后,四种复合薄膜的比容量衰减率分别为0.70%、6.13%、11.32%、18.88%。研究结果表明,当复合薄膜中Sn质量分数为89.20%时,其具有最优的倍率性能和循环稳定性能,随着复合薄膜中Sn质量分数的增加,其倍率性能及循环稳定性变差。

硅碳负极的失效机理与FEC的改善作用

采用含和不含氟代碳酸乙烯酯(FEC)的电解液,研究了一种硅碳材料作为锂离子电池负极的充放电行为,对充放电循环前后的硅碳电极进行了组成和形貌的谱学表征,并通过计算比较了电解液主要成分的还原活性。结果表明:不含FEC的电解液,硅碳负极首次充放电库伦效率低、容量衰减快,这是因为硅碳表面不能形成稳定的SEI,嵌锂后体积膨胀使SEI开裂,电解液持续分解。相反,含FEC的电解液,因FEC比电解液其他组分更容易在硅碳负极上还原,生成含氟的聚合物,形成稳定的SEI,抑制电解液还原分解,并缓冲硅碳负极的体积膨胀,从而显著提高库伦效率和循环稳定性。添加5%的FEC,硅碳负极首次充放电库伦效率从83%提高到86%;添加10%的FEC,0.2 C充放电循环50次后,硅碳负极的容量保持率从28%提高到75%。

C离子对AlGaAs/InGaAs异质结的辐照影响

基于SRIM软件计算了不同能量的C离子在AlGaAs/InGaAs异质结中的平均投影射程和辐照损伤区,仿真了能量为500keV、800keV、1100keV的C离子入射到AlGaAs/InGaAs异质结中的能量损失情况,发现随着入射离子能量的增加,电离能比例增加,非电离能比例降低,入射离子产生的电离能损远大于反冲原子产生的电离能损,反冲原子产生的声子能损远多于入射离子产生的声子能损;通过仿真还发现,当C离子的能量为800keV时,辐照损伤区在异质结处且在异质结处产生的空位缺陷最多。

离子推力器C-C复合栅多工况热态微位移研究

针对LIPS-100离子推力器C-C一体化复合栅极组件设计问题,利用热特性计算模型开展栅极热力学特性研究。采用Workbench瞬态热分析法研究了两种曲面朝向的C-C栅极热性能参数,并与传统金属钼栅进行了对比分析。结果表明:等工况、等球面构型、等栅间距条件下,C-C复合栅较钼栅组件质量减轻35.7%,热态分析温度上限降低19.6%,升温速率降低21.3%;C-C复合屏栅较钼栅微位移减小0.151 mm,加速栅微位移减小0.123 mm,具有更高的抗热冲击性,可有效缓解推力器工作前期栅间距波动较大的问题;同一C-C复合栅材料下,球面朝向结构不同,栅极中心-开孔区边缘热态微位移不同,凸型栅较凹型栅加速栅微位移量降低0.025~0.038 mm,可有效提升加速栅开孔区磨损寿命。对于小尺寸离子推力器,凸面C-C复合栅组件抗热冲击性优势明显。

蛋黄-壳NiCoP@N-C材料的制备及其储钠特性研究

NiCo基磷化物因其优异的导电性和较高的理论容量,被认为是最有潜力的钠离子电极材料.然而,NiCo基磷化物在钠离子嵌入/脱出时会发生严重的体积应变,导致NiCo基磷化物的倍率特性降低,循环稳定性大幅度衰减.针对这些问题,采用多巴胺包覆-煅烧-磷化处理法制备了蛋黄-壳结构的NiCoP@N-C材料,在该材料中,氮掺杂碳层有效地改善了电极材料固有的电导率和结构完整性;独特的蛋黄-壳结构显著减缓了在钠离子嵌入/脱出过程中的体积膨胀.当NiCoP@N-C作为钠离子电池负极材料时表现出优异的电化学性能.在0.1 A·g^(-1)电流密度下,循环100圈后的可逆比容量仍高达462.3 mAh·g^(-1).

基于PKC-P2X3信号通路观察电针对神经病理性疼痛小鼠神经修复的作用机制

目的:基于蛋白激酶C(PKC)-配体门控型非选择性离子通道3(P2X3)信号通路观察电针对神经病理性疼痛小鼠神经修复的作用机制。方法:48只小鼠随机分成假手术组、模型组、针刺组与电针组,每组12只。除假手术组外,其余小鼠构建坐骨神经慢性限制性损伤(CCI)模型。术后第8天针刺组与电针组接受针刺与电针干预,连续7 d。于术前、术后3 d、5 d、7 d、10 d、12 d、14 d对各组进行机械缩足反射阈值(MWT)与热刺激缩足反射潜伏期(TWL)测试。术后15 d处死所有小鼠,HE染色观察坐骨神经组织形态,ELISA检测脊髓组织IL-1β、TNF-α水平,Western blot检测脊髓组织PKC、P2X3水平,免疫荧光检测脊髓神经元PKC、P2X3表达情况。结果:假手术组神经元细胞大小不一,细胞膜完整,细胞质呈细小颗粒状,细胞核大而圆,核仁居中清晰可见;模型组可见萎缩的神经元,有髓神经纤维紊乱,轴突肿胀,神经元间形成间隙;与模型组相比,针刺组、电针组萎缩神经元数量减少(P<0.05),有髓神经纤维排布情况改善,电针组较针刺组改善更为明显。与相同时间点的假手术组相比,术后3 d、5 d、7 d、10 d、12 d、14 d模型组、针刺组、电针组患侧后肢的MWT、TWL值明显下降(P<0.05),IL-1β、TNF-α、PKC、P2X3表达量、PKC、P2X3阳性细胞数、平均光密度值升高(P<0.05);与模型组相比,术后10 d、12 d、14 d针刺组、电针组MWT、TWL值明显上升(P<0.05),IL-1β、TNF-α、PKC、P2X3表达量、PKC、P2X3阳性细胞数、平均光密度值降低(P<0.05);与针刺组相比,术后10 d、12 d、14 d电针组MWT、TWL值升高(P<0.05),IL-1β、TNF-α、PKC、P2X3表达量、PKC、P2X3阳性细胞数、平均光密度值降低(P<0.05)。结论:电针可能减轻CCI模型小鼠神经炎症反应,降低PKC、P2X3表达水平,改善坐骨神经细胞形态与有髓神经纤维排布情况,缩小神经元间间隙,提升MWT、TWL值,缓解神经病理性疼痛程度。

Si/C复合锂离子电池负极材料的制备及其性能

从电池性能的角度出发,合理设计电池负极材料是必要的,为此提出Si/C复合锂离子电池负极材料的制备及电化学性能分析研究。准备实验材料和仪器后,分别按照Si:石墨为1:9、2:8、3:7和4:6的比例准备混合料,按照料液比1:4加入无水乙醇作为球磨介质,在球磨机中进行球磨处理,干燥后得到Si含量分别为10%、20%、30%和40%的复合材料;按照质量比为90:5:2:3的比例活性物质(Si/C复合材料)、导电剂碳黑、分散剂乙二醇和粘结剂PVDF配置浆料,涂抹于锂箔表面,经热压成型机对极片进行压实处理,得到Si/C复合锂离子电池负极。在采用电池测试系统在100 mA/g下对硅含量分别为10%、20%、30%和40%的复合材料电极电化学性质进行测试,得出结论Si/C复合锂离子电池负极材料的放电容量受硅含量影响明显,并且不存在直接的线性相关关系;硅含量也会影响Si/C复合锂离子电池负极材料的库伦效率,过高或高低都会导致库伦效率下降。

脓毒症心肌病对大鼠心室肌细胞的损伤及维生素C的干预效果

目的:研究脓毒症对大鼠心肌的损伤及维生素C的干预效果。方法:选取90只SD雄性大鼠随机分成三组,将其中两组进行脓毒症造模,一组予维生素C干预(A组)、另一组作为脓毒症组(B组)及第三组为对照组(C组),造模成功后24 h和48 h检测降钙素原(procalcitonin,PCT)、脂多糖(lipopolysaccharide,LPS)及超氧化物歧化酶(superoxide dismutase,SOD)水平;造模后24 h检测大鼠左室射血分数以及左心室收缩末期和舒张末期容积和心肌细胞动作电位及离子通道电压与密度变化。结果:A组及B组PCT、LPS均升高且高于C组,而B组在造模后48 h的PCT及LPS高于A组。超声提示A、B两组大鼠左室射血分数、收缩及舒张末期容积均降低,但B组更为显著;与C组相比,A、B两组的心肌细胞动作电位显著延长、而B组延长更为明显;与C组相比,A组与B组的I_(Ca-L)和I_(to)密度明显降低、B组更为显著(均P<0.05);造模后48 h SOD检测发现A组较C组相比升高、B组与C组比较降低(均P<0.05)。结论:脓毒症大鼠PCT、LPS升高,维生素C干预可以降低其水平;脓毒症大鼠SOD降低,维生素C干预可以减轻SOD降低水平。脓毒症大鼠心脏功能下降,且心肌细胞动作电位明显延长,同时脓毒症大鼠I Ca-L和I to密度降低,而进行维生素C干预后均可改善。

Biological effects of low-energy C ion implantation on sesame(Sesamum indicum L.)

Field cultivation experiments on white sesame(Sesamum indicum L.)seeds implanted with low-energy C ion showed that different dosages of C ion implantation pro-duce different biological effects.Sesame plants in 6 different dosage groups with C ion density respectively at 1×10^(11),1×10^(12),1×10^(15),5×10^(15),1×10^(16),5×10^(16)ion/cm2 were superior to the control group in plant height,leaf number,stalk diameter and leaf size.Further,sesame plants in these groups flower and seed earlier than those in the control group,and single plant yield also increased.Of all the groups,the 5×10^(15)ion/cm2 dosage group yielded the best effect,whereas the 1×10^(17)/cm^(2)dosage group showed an evident inhibitory effect of ion implantation on the germination and growth of the sesame seeds.

三维Ni/NiO@C/GN复合材料的制备及其锂离子电池性能

将醋酸镍和葡萄糖溶于水中,与氧化石墨烯(GO)水悬浮液均匀混合,在180℃下水热处理24 h,再在Ar中700℃下炭化3 h,然后在空气中300℃下煅烧3 h得到三维Ni/NiO@C/GN。结果表明,水热处理过程中葡萄糖衍生的炭层将Ni(OH)2完全包裹,并在炭化过程中转化为金属Ni,部分金属Ni在空气中煅烧中被氧化为NiO。当作为锂离子电池的负极材料时,其初始容量为711.6 mA h g^(-1),300次循环后增加到772.1 mA h g^(-1)。作为对比,没有添加GO的材料的初始容量较低,仅为584.7 mA h g^(-1),300次循环后下降到148.8 mA h g^(-1)。这些结果表明炭层可以抑制Ni/NiO纳米颗粒的团聚,有效缓解锂化过程中的体积膨胀,抑制循环过程中的电极开裂。GO的加入可形成丰富的导电网络,提高导电性。较大的比表面积可增加活性位点,有利于电解液快速浸润电极材料。这些因素显著改善了Ni/NiO@C/GN负极的电化学性能。

Tribological Properties of DLC Film Prepared by C^+ Ion Beam-assisted Deposition (IBAD)

C ^＋ ion beam-assisted deposition was utilized to prepare deposit diamond-like carbon （ DLC ） film. With the help of a series of experiments such as Raman spectroscopy, FT-IR spectroscopy, AFM and nanoindentation , the DLC film has been recognized as hydrogenated DLC film and its tribologicul properties have been evaluated. The bull-on-disc testing results show that the hardness and the tribologicul properties of the DLC film produced by C^ ＋ ion beam- assisted deposition are improved significantly. DLC film produced by C ^＋ ion beam- assisted deposition is positive to have a prosperous tribologicul application in the near future.

Synergistic responses of NHX, AKT1, and SOS1 in the control of Na^+ homeostasis in sweet sorghum mutants induced by ^(12)C^(6+)-ion irradiation

Sweet sorghum mutants induced by^(12)C(6+)-ion irradiation were planted under different soil salinity conditions to investigate the mechanisms maintaining the transport and spatial distribution of Na^+. The functions of the synergistic responses of NHX, AKT1, and SOS1 related to Na^+ accumulation were investigated in control(KFJT-CK) sorghum and KF1210-3 and KF1210-4 mutants. The results indicated that the NHX, AKT1, and SOS1 proteins in sweet sorghum are mainly involved in the transport, exclusion, and spatial distribution of Na^+,respectively. In addition to physiological parameters, we also measured the expression levels of NHX, AKT1, and SOS1 genes. The experimental results indicated that 150 m M Na Cl induced marked increases in the transcripts of NHX and SOS1 after 8 and 12 h in the KF1210-3,KF1210-4, and KFJT-CK cultivars. In contrast, however, a decrease in AKT1 was observed. On the basis of our results, we propose a model in which cooperation amongNHX, AKT1, and SOS1 facilitates Na^+ homeostasis in sweet sorghum in response to an increase in salt concentration. Accordingly, study of the regulatory mechanisms in sweet sorghum generated by carbon ion irradiation is essential for the selection of salt-tolerant cultivars.

Preparation and electrochemical properties of LiFePO_4/C composite with network structure for lithium ion batteries

The bare LiFePO4 and LiFePO4/C composites with network structure were prepared by solid-state reaction. The crystalline structures, morphologies and specific surface areas of the materials were investigated by X-ray diffractometry(XRD), scanning electron microscopy(SEM) and multi-point brunauer emmett and teller(BET) method. The results show that the LiFePO4/C composite with the best network structure is obtained by adding 10% phenolic resin carbon. Its electronic conductivity increases to 2.86×10-2 S/cm. It possesses the highest specific surface area of 115.65 m2/g, which exhibits the highest discharge specific capacity of 164.33 mA·h/g at C/10 rate and 149.12 mA·h/g at 1 C rate. The discharge capacity is completely recovered when C/10 rate is applied again.

Structural and electrical properties of carbon-ion-implanted ultrananocrystalline diamond films

We investigate the structural and electrical properties of carbon-ion-implanted ultrananocrystalline diamond（UNCD）films. Impedance spectroscopy measurements show that the impedance of diamond grains is relatively stable, while that of grain boundaries（GBs）（Rb） significantly increases after the C~＋ implantation, and decreases with the increase in the annealing temperature（Ta） from 650℃ to 1000℃. This implies that the C~＋ implantation has a more significant impact on the conductivity of GBs. Conductive atomic force microscopy demonstrates that the number of conductive sites increases in GB regions at Ta above 900℃, owing to the formation of a nanographitic phase confirmed by high-resolution transmission electronic microscopy. Visible-light Raman spectra show that resistive trans-polyacetylene oligomers desorb from GBs at Ta above 900℃, which leads to lower Rb of samples annealed at 900 and 1000℃. With the increase in Ta to 1000℃, diamond grains become smaller with longer GBs modified by a more ordered nanographitic phase, supplying more conductive sites and leading to a lower Rb.

Effect of Magnesium on the C-S-H Nanostructure Evolution and Aluminate Phases Transition in Cement-Slag Blend

The microstructural study was conducted on cement and cement-slag pastes immersed in different concentrations of Mg（NO3）2 solutions utilizing ^29Si, ^27Al NMR spectroscopy and XRD techniques. The results show that the hydration of both the cement and cement-slag pastes is delayed when the pastes are cured in Mg（NO3）2 solutions as compared to the pastes cured in water. Moreover, Mg^2＋ ions also exhibit an decalcifying and dealuminizing effect on the C-A-S-H in cement and cement-slag pastes, and thereby decrease Ca/Si and Al[4]/Si ratios of the C-A-S-H. The dealuminization of C-A-S-H is mitigated for cement-slag paste as compared to pure cement paste. The depolymerized calcium and aluminum ions from C-A-S-H gel mainly enter the pore solution to maintain the pH value and form Al^[6] in TAH, respectively. On the other hand, Mg^2＋ ions exert an impact on the intra-transition between Al^[6] species, from AFm and hydrogarnet to hydrotalcite-like phase. NO3^-ions are interstratified in the layered Mg-Al structure and formed nitrated hydrotalcite-like phase（Mg1-xAlx（OH）2（NO3）x·nH2O）. Results from both ^27Al NMR and XRD data show that ettringite seems not to react with Mg^2＋ ions.

SnS_2@C Hollow Nanospheres with Robust Structural Stability as High?Performance Anodes for Sodium Ion Batteries

Constructing unique and highly stable structures with plenty of electroactive sites in sodium storage materials is a key factor for achieving improved electrochemical properties through favorable sodium ion di usion kinetics. An SnS_2@carbon hollow nanospheres(SnS_2@C) has been designed and fabricated via a facile solvothermal route, followed by an annealing treatment. The SnS_2@C hybrid possesses an ideal hollow structure, rich active sites, a large electrode/electrolyte interface, a shortened ion transport pathway, and, importantly, a bu er space for volume change, generated from the repeated insertion/extraction of sodium ions. These merits lead to the significant reinforcement of structural integrity during electrochemical reactions and the improvement in sodium storage properties, with a high specific reversible capacity of 626.8 mAh g^(-1) after 200 cycles at a current density of 0.2 A g^(-1) and superior high-rate performance(304.4 mAh g^(-1) at 5 A g^(-1)).

Theoretical study on photorecombination of C V ion

The partial and total photorecombination cross sections of the ground-state C V ion in the KLL and KLM resonant energy regions were calculated in detail by using the Dirac atomic R-matrix code based on a fully relativistic R-matrix method. Meanwhile, the principal resonant lines in each photorecombination channel have been classified according to the calculated transition energies and probabilities from the KLL and KLM resonant states to the 1s2nl（n = 2, 3 and l = s, p, d）final states. The validity of these calculations is assessed by comparison with previously published experimental and theoretical data. The good agreement between the present calculated results and those obtained using different approaches confirms the accuracy of the present results. In addition, it is found that the damping effect can be neglected for the KLL resonant, but not for the KLM resonant.

Hydrogen cold plasma for synthesizing Pd/C catalysts: the effect of support-metal ion interaction

It has been found that cold plasma is a facile and environmentally benign method for synthesizing supported metal catalysts, and great efforts have been devoted to enlarging its applications. However, little work has been done to disclose the influence mechanism, which is significant for controllable synthesis. In this work, hydrogen cold plasma was adopted to synthesize a palladium catalyst supported on activated carbon （Pd/C-P） using HzPdC14 as a Pd precursor followed by calcination in hydrogen gas to remove the chlorine ions. The Pd/C-P catalyst was found to be made of larger Pd nanoparticles showing a decreased migration to the support outer surface than that prepared by the conventional thermal hydrogen reduction method （Pd/C-C）. Meanwhile, the pore diameter of the activated carbon support is small （,-~4 nm）. Therefore, Pd/C-P exhibits lower CO oxidation activity than Pd/C-C. It was proposed that the strong interaction between the activated carbon and PdC142-, and the enhanced metal-support interaction caused by hydrogen cold plasma reduction made it difficult for Pd nanoparticles to migrate to the support outer surface. The larger-sized Pd nanoparticles for Pd/C-P may be due to the Coulomb interaction resulting in the disturbance of the metal-support interaction. This work has important guiding significance for the controllable synthesis of supported metal catalysts by hydrogen cold plasma.