In气氛下晶体生长对Mg掺杂p-Al_xGa_(1-x)N激活能的影响

Ⅲ-Ⅴ族氮化物宽禁带半导体材料体系中,普通方法生长的p型外延层电导率一般都很低,成为了制约器件性能提高的瓶颈。在p-AlxGa1-xN材料中,Mg受主的激活能较大,并且随Al组份增加而增大。通过在p-AlxGa1-xN材料生长过程中引入三甲基铟(TMIn),发现能有效地降低AlxGa1-xN材料中受主态的激活能。为研究不同In气氛下生长的p-AlxGa1-xN材料的性质,在使用相同二茂基镁(CP2Mg)的情况下,改变TMIn流量,生长了A,B,C和D四块样品。X射线衍射(XRD)组份分析表明:在1100℃下生长AlxGa1-xN外延层时,In的引入不会影响晶体组份。利用变温霍尔(Hall)测试研究了p-AlxGa1-xN材料中受主的激活能,结果表明:In气氛下生长的外延层相比无In气氛下生长的外延层,受主激活能明显降低,电导率显著提高。采用这种方法改进深紫外发光二极管(LED)的p-AlxGa1-xN层后,LED器件性能明显提高。     

Hierarchical nanowires for high-performance electrochemical energy storage

Nanowires are promising candidates for energy storage devices such as lithium-ion batteries, su- per（：apa.citors and lithium-air batteries. However, simple-structured nanowires have some limitations hence the strategies to make improvements need to be explored and investigated. Hierarchical nanowires with enhanced periormanee have been considered as an ideal candidate for energy storage due to the novel structures and/or synergistic properties. This review describes some of the recent progresses in the hierarchical nanowire merits, classification, synthesis and performance in energy storage applieat, ions. Herein we discuss the hierarchical nanowires based on their structural design from three major categories, including exterior design, interior design and aligned nanowire assembly. This review also briefly outlines the prospects of hierarchical nanowires in morphology control, property enhancement and application versatility.     

The work function of hydrothermally synthesized UO2 and the implications for semiconductor device fabrication

The photoelectric work function of nearly stoichiometric (111) and (100) hydrothermally grown UO₂ was measured to be 6.28 ± 0.36 eV and 5.80 ± 0.36 eV, respectively. Candidate metals for electrical contacts are identified for both rectifying and non‐rectifying contacts based on work function, lattice compatibility, and electrical conductivity.     

双原子分子振动能级半量子化及量子理论的数值计算

利用半经典量子化理论和量子理论，分别采用Ｌｅｎｎａｒｄ－Ｊｏｎｅｓ势和Ｍｏｒｓｅ势，对双原子分子的振动能级给予了较为详细的数值计算。并将所得结果与部分实验数据进行比较，峄双原子分子的振动能级作了较为详细的 讨论。     

爆电换能脉冲大电流输出研究

 基于爆电换能原理,使用掺铌的PZT 95/5陶瓷组装换能器件,在垂直工作模式下,对爆电电源LRC电路响应进行了理论分析,并开展了脉冲大电流输出实验研究。实验采用多组PZT 95/5铁电陶瓷并联,利用平面波发生器作为冲击加载手段,获得了峰值5 kA以上的脉冲大电流,初始电流上升速率可达10~20 GA/s。实验结果与理论设计符合较好。     

丝电爆过程的电流导入机理

丝电爆制备纳米粉时, 电流从电极导入金属丝的过程直接影响电极烧损和粉末中微米级大颗粒产生. 分别通过接触和气体放电两种方式导入电流进行电爆试验. 结果表明, 光测量装置检测到的丝端部光电流几乎与回路放电电流同时产生, 而中间位置的光电流则要滞后一段时间; 由探针收集的产物确定, 金属丝端部主要形成熔融粒子, 中间部分主要形成气相粒子. 分析可知, 接触方式导入电流时, 丝端部也存在气体放电现象, 大电流主要通过气体放电形成的等离子体导入. 等离子体对电流的旁路作用会阻碍能量向金属丝沉积, 这是产生微米级大颗粒和"积瘤"主要原因. 通过气体放电方式导入电流时, 电极烧损明显减轻, 并可以避免"积瘤"产生.     

Properties of Zr hypernuclei in deformed Skyrme Hartree-Fock approach

Properties of the even-N Zr isotopes and their corresponding single-Λ and double-Λ hypernuclei are studied in the deformed Skyrme-Hartree-Fock approach. Binding energy, the two-neutron separation energies, radii are studied from beta-stable zone to the neutron drip line in this paper. The neutron drip line nuclei predicted with SLy4 and SkI4 interactions are ¹²²Zr and ¹³⁸Zr, respectively. The neutron drip line of single-Λ and double-Λ hypernuclei are ¹³⁹_ΛZr and ¹⁴²_2ΛZr with SkI4 interaction, respectively. The predicted hyperon drip line hypernuclei with ⁸⁰Zr and ¹³⁸Zr cores are ¹⁰⁰_20ΛZr and ¹⁸⁸_50ΛZr, respectively.     

TX-100和CTAB交换动力学的核磁共振研究

运用核磁共振(NMR)方法分别测定了表面活性剂辛基苯聚氧乙烯醚(TX-100)和十六烷基三甲溴化铵(CTAB)在不同温度下的临界胶束浓度.阐述了应用1D NMR线型分析方法对表面活性剂快交换体系平均停留时间的定量测量.实验测量了TX-100和CTAB胶束溶液中表面活性剂分子在不同温度下的平均停留时间.结果显示,平均停留时间随温度的增加逐渐减小,说明TX-100和CTAB分子进出胶束的速率随温度的增加逐渐加快.利用阿伦尼乌斯公式拟合,获得了TX-100和CTAB的表观交换活化能,TX-100的表观交换活化能为17.6 k J/mol,CTAB的表观交换活化能为75.3 k J/mol.对TX-100和CTAB平均停留时间和表观交换活化能进行分析,得出平均停留时间和表观交换活化能与分子结构的关系:表观交换活化能反映的是疏水相互作用和静电斥力的大小;而平均停留时间不仅受活化能的影响,还与分子结构有关.     

Coadsorption of water and CO molecules on Ru(0 0 1) at high CO coverages: comparisons with a Ru(0 0 1) electrode surface

The coadsorption of carbon monoxide (CO) and water molecules on a Ru(0 0 1) surface has been studied by infrared spectroscopy, LEED and STM. At high CO coverage phases, a 2×2-(2CO+D₂O) structure was observed on both UHV and electrode surfaces. Electrode potential dependent structures from CO and water adlayers on an electrode surface were reproduced on a UHV surface by controlling molecular orientations of the first layer and second over-layer water molecules. At lower CO coverages, a CO band center showed coverage dependent shift down to 1444 cm⁻¹ due to an electron transfer from a lone pair of a water molecule to CO 2π^*.     

关于量子体系的高效相干能量转移的最优初始化的研究

For an energy transfer network, the irreversible depletion of excited electron energy occurs through either an efficient flow into an outer energy sink or an inefficient decay. With a small decay rate, the energy transfer efficiency is quantitatively reflected by the average life time of excitation energy before being trapped in the sink where the decay process is omitted. In the weak dissipation regime, the trapping time is analyzed within the exciton population subspace based on the secular Redfield equation. The requirement of the noise-enhanced energy transfer is obtained, where the trapping time follows an exact or approximate 1/Γ-scaling of the dissipation strength Γ. On the opposite side, optimal initial system states are conceptually constructed to suppress the 1/Γ-scaling of the trapping time and maximize the coherent transfer efficiency. Our theory is numerically testified in four models, including a biased two-site system, a symmetric three-site branching system, a homogeneous onedimensional chain, and an 8-chromophore FMO protein complex.