杂化势对周期性安德森模型电子结构的影响

采用格林函数退耦合方法．研究了杂化势对周期性安德森模型电子结构的影响． 结果表明，费米能处的态密度随杂化势的增强而有系统的变化，可由单峰结构劈裂成双峰 结构，并在费米能附近形赝隙或能隙．

HSE方法研究Cd_(1-x)Zn_xTe合金的性质

采用HSE杂化势计算了Cd1-xZnxTe合金的性质,并获得了较传统GGA更为准确的光学带隙和形成焓.在构建超胞计算合金体系时,采用SQS模型.计算分析得出Cd1-xZnxTe合金的光学带隙下凹参数为0.266 eV,这与已报道实验结果 0.254 eV非常吻合.同时,计算得出的形成焓较高,特别是在Cd0.5Zn0.5Te合金组分时(25.60 meV/at-om).对合金中键长的分析后得出Cd-Te键和Zn-Te键的局域键长与CdTe和ZnTe体材料的值非常接近,但二者之间相差较大,从而导致合金材料中各个原子存在较大的弛豫,这也是该合金具有较大形成焓的主要原因.

Density ＇Functional Theory Study on Mechanism of Forming Spiro-Geheterocyclic Ring Compound from Me2Ge--Ge： and Acetaldehyde

The H2Ge=Ge：, as well as and its derivatives （X2Ge=Ge：, X=H, Me, F, C1, Br, Ph, At, ...） is a kind of new species. Its cycloaddition reactions is a new area for the study of germylene chemistry. The mechanism of the cycloaddition reaction between singlet Me2Ge=Ge： and acetaldehyde was investigated with the B3LYP/6-31G＊ method in this work. From the potential energy profile, it could be predicted that the reaction has one dominant reaction pathway. The reaction rule is that the two reactants firstly form a four-membered Ge-heterocyclic ring germylene through the [2＋2] cycloaddition reaction. Because of the 4p unoccupied orbital of Ge： atom in the four-membered Ge-heterocyclic ring germylene and the ~ orbital of acetaldehyde forming a r^--~p donor-acceptor bond, the four-membered Ge-heterocyclic ring germylene further combines with acetaldehyde to form an intermedi- ate. Because the Ge atom in intermediate happens sp3 hybridization after transition state, then, intermediate isomerizes to a spiro-Ge-heterocyclic ring compound via a transition state. The research result indicates the laws of cycloaddition reaction between Me2Ge=Ge： and ac- etaldehyde, and lays the theory foundation of the cycloaddition reaction between H2Ge=Ge： and its derivatives （X2Ge=Ge：, X=H, Me, F, C1, Br, Ph, At, ...） and asymmetric ^-bonded compounds, which are significant for the synthesis of small-ring and spiro-Ge-heterocyclic ring compounds.

Ab initio Study on Formation Mechanism of Spiro-Si-Heterocyclic Ring Compound Involving Ge from H2Ge=Si： and Formaldehyde

H2Ge=Si： and its derivatives （X2Ge=Si：, X=H, Me, F, C1, Br, Ph, Ar, ...） are new species. Its cycloaddition reactions are new area for the study of silylene chemistry. The cycloaddition reaction mechanism of singlet H2Ge=Si： and formaldehyde has been investigated with the MP2/aug-cc-pVDZ method. From the potential energy profile, it could be predicted that the reaction has one dominant reaction pathway. The reaction rule is that two reactants firstly form a four-membered Ge-heterocyclic ring silylene through the [2＋2] cycloaddition reaction. Because of the 3p unoccupied orbital of Si： atom in the four-membered Ge-heterocyclic ring silylene and the π orbital of formaldehyde forming a π--p donor-acceptor bond, the four-membered Ge-heterocyclic ring silylene further combines with formaldehyde to form an intermediate. Because the Si： atom in the intermediate undergoes sp3 hybridization after transition state, then the intermediate isomerizes to a spiro-Si-heterocyclic ring compound involving Ge via a transition state. The result indicates the laws of cycloaddition reaction between H2Ge=Si： or its derivatives （X2Ge=Si：, X=H, Me, F, Cl, Br, Ph, Ar, ...） and asymmetric π-bonded compounds are significant for the synthesis of small-ring involving Si and Ge and spiro-Si-heterocyclic ring compounds involving Ge.

Analysis of F_1 Heterosis of Agronomic Traits and Chemical Components on Selfbred Highpotassium New Lines

F1 heterosis of agronomic characters and chemical components of 8 fluecured tobacco varieties and 6 self-bred high-potassium new lines was studied. The results showed that 4-5 weeks after transplanting was the main changing period of agronomic traits. Compared with the comparative heterosis, among the proportions of combinations showing positive comparative heterosis at the significant level, the heterosis proportions of plant height （97.92%）, internode length （100%） and stem girth （58.33%） were larger, these of total nitrogen （83.33%）, protein （79.17%）, nicotine （79.17%） and potassium （95.83%） in upper leaves were larger, these of total sugar （64.58%）, total nitrogen （68.75%）, protein （72.92%） and nicotine （64.58%） in middle leaves were larger, and in lower leaves, except that the proportion of chlorine was smaller （12.50%）, the proportions of other chemical components all exceeded 40%. Compared with average heterosis, among the proportions of combinations showing positive comparative heterosis at the significant level, the heterosis proportions of plant height （54.17%）, leaf width （43.75%）, stem girth （43.75%） and internode length （72.92%） were larger, these of total sugar （47.92%） and reducing sugar （54.17%） in upper leaves were larger, these of all the chemical components in middle leaves exceeded 30%, and these of all the chemical components in lower leaves were in the range of 27.08%-41.67%. Compared with heterobeltiosis, among the proportions of combinations showing positive comparative heterosis at the significant level, that of the internode length （60.42%） was larger, these of chemical components in upper leaves were in the range of 8.33%-29.17%, these of chemical components in middle leaves were in the range of 20.83%-39.58%, and these of chemical components in lower leaves were in the range of 16.67%-35.42%. It was indicated that rational effective control of water and fertilizer in this sensitive period could significantly enhance heterosis.

In situ growth of minimal Ir-incorporated CoxNi1-xO nanowire arrays on Ni foam with improved electrocatalytic activity for overall water splitting

Exploration of cost-effective electrocatalysts for boosting the overall water-splitting efficiency is vitally important for obtaining renewable fuels such as hydrogen.Here,earth-abundant CoxNi1-xO nanowire arrays were used as a structural framework to dilute Ir incorporation for fabricating electrocatalysts for water splitting.Minimal Ir-incorporated CoxNi1-xO nanowire arrays were synthesized through the facile hydrothermal method with subsequent calcination by using Ni foam(NF)as both the substrate and source of Ni.The electrocatalytic water-splitting performance was found to crucially depend on the Ir content of the parent CoxNi1-xO nanowire arrays.As a result,for a minimal Ir content,as low as 0.57 wt%,the obtained Ir-CoxNi1-xO/NF electrodes exhibited optimal catalytic activity in terms of a low overpotential of 260 mV for the oxygen evolution reaction and 53 mV for the hydrogen evolution reaction at 10 mA cm?2 in 1 mol L–1 KOH.When used as bifunctional electrodes in water splitting,the current density of 10 mA cm–2 was obtained at a low cell voltage of 1.55 V.Density functional theory calculations revealed that the Ir-doped CoxNi1-xO arrays exhibited enhanced electrical conductivity and low Gibbs free energy,which contributed to the improved electrocatalytic activity.The present study presents a new strategy for the development of transition metal oxide electrocatalysts with low levels of Ir incorporation for efficient water splitting.

First-principles Study on the Magnetic,Half-metal and Thermoelectric Transport Properties of Inorganic-Organic Hybrid Compounds [C_4N_2H_(12)][Fe_4~Ⅱ(HPO_3)_2(C_2O_4)_3]

The electronic structure, magnetic and half-metal properties of inorganic-organic hybrid compound [C4N2H12][FeoI （HP03）2 （（72 04）3] are investigated by using the full-potential linearized augmented plane wave （FPLAPW） method within density-functional theory （DFT） calculations. The density of states （DOS）, the total energy of the cell and the spontaneous magnetic moment of [C4N2H12][FeII （HP03）2 （C2 04）3] are calculated. The calculation results reveal that the low-temperature phase of [C4N2H12][FeII （HP03）2（C204）3] exhibits a stable ferromagnetic （FM） ground state, and we find that this organic compound is a half-metal in FM state. In addition, we have calculated antiferromagnetically coupled interactions, revealing the existence of antiferromagnetic （AFM）, which is in agreement with the experiment. We have also found that [C4N2HI2][Fe4II （HP03）2（C204）3] is a semiconductor in the AFM state with a band gap of about 0.40 eV. Subsequently, the transport properties for potential thermoelectric applications have been studied in detail based on the Boltzmann transport theory.