Theoretical analysis of the double-differential cross-sections of neutron,proton,deuteron,^(3)He,andαfor the p+^(6) Li reaction

Based on the unified Hauser–Feshbach and exciton model,which can describe the particle emission processes between discrete energy levels with energy,angular momentum,and parity conservations,a statistical theory of light nucleus reaction(STLN)is developed to calculate the double-differential cross-sections of the outgoing neutron and light charged particles for the proton-induced^(6) Li reaction.A significant difference is observed between the p+^(6) Li and p+^(7) Li reactions owing to the discrepancies in the energy-level structures of the targets.The reaction channels,including sequential and simultaneous emission processes,are analyzed in detail.Taking the double-differential cross-sections of the outgoing proton as an example,the influence of contaminations(such as^(1) H,^(7)Li,^(12)C,and^(16)O)on the target is identified in terms of the kinetic energy of the first emitted particles.The optical potential parameters of the proton are obtained by fitting the elastic scattering differential cross-sections.The calculated total double-differential cross-sections of the outgoing proton and deuteron at E_(p)=14 MeV agree well with the experimental data for different outgoing angles.Simultaneously,the mixed double differential cross-sections of^(3) He andαare in good agreement with the measurements.The agreement between the measured data and calculated results indicates that the two-body and three-body breakup reactions need to be considered,and the pre-equilibrium reaction mechanism dominates the reaction processes.Based on the STLN model,a PLUNF code for the p+^(6) Li reaction is developed to obtain an ENDF-6-formatted file of the double-differential cross-sections of the nucleon and light composite charged particles.

通过成结模拟器研究n^(+)-n^(-)-p碲镉汞高温探测器

第三代红外探测器发展的一个重要方向是高工作温度探测器。对于碲镉汞n-on-p探测器而言,n^(+)-n^(-)-p结构以及良好的钝化工艺能够有效的抑制暗电流的产生,从而在高工作温度条件下获得较好的探测器性能。基于自行开发的成结模拟器,对n^(+)-n^(-)-p结构地高温器件进行了工艺仿真和器件仿真,获得成结过程的制备参数,并结合抑制表面漏电的组分梯度钝化工艺,将高工作温度下的暗电流抑制至理论极限,研制出可以在更高温度工作下的碲镉汞n-on-p红外焦平面探测器。经测试,中波n-on-p红外焦平面器件在不同工作温度下性能优异,在80 K工作温度下噪声等效温差(NETD)达到了6.1 mK,有效像元率为99.96%;而在150 K工作温度下噪声等效温差(NETD)为11.0 mK,有效像元率为99.50%,达到了同类器件的理论极限。

云南松苗木N、P、K元素含量间异速生长关系对N、P添加的响应

为了解云南松苗木不同器官N、P、K的分布特征,分析云南松不同器官N、P、K含量间的分配差异,进一步探讨各器官N、P、K元素间的异速生长关系。采用N、P二因素三水平的方法开展不同施肥试验,并对苗木采样测定,研究云南松苗木N、P、K元素含量间异速生长关系对N、P添加的响应。结果表明,云南松苗木对N、P、K在不同器官间具有不同的分配策略,总体K变动较小,N、P波动较大且相似,在各器官中N、K分配表现为萌条>叶>茎>根;P表现为萌条>茎>叶>根。与对照相比,单施N、P和N、P配施均对云南松苗木生长的影响产生一定差异,总体来看N、P配施更能促进苗木的养分合理分配,有效缓解单施N、P对植株的限制作用,使养分处于一个平衡状态,进而促进苗木的生长。随施肥时间的推移,各器官营养元素间的异速生长关系也随之发生变化,且各器官表现为N、P的积累速度相接近,总体表现为K的积累速度低于N、P。总体而言,随施肥时间的改变,云南松苗木各器官之间元素的异速生长轨迹发生了显著变化,形成不同的营养元素分配模式。

基于VLPE技术的碲镉汞p-on-n双层异质结材料与器件研究进展

本文对比分析了碲镉汞p-on-n器件四种制备方式的优劣,其中,VLPE(Vertical Liquid Phase Epitaxy)技术具有原位As掺杂与高激活率的技术优势,是制备高性能p-on-n双层异质结器件的重要方式。针对该技术,从材料生长、器件工艺和器件性能方面回顾了国内外研究进展,讨论了国内外差距,明确了制约该技术发展的关键问题和技术难点,并提出了解决思路。最后,展望了VLPE技术pon-n异质结器件的发展趋势。

干旱胁迫对白枪杆幼苗生长生物量及C、N、P化学计量特征的影响

【目的】研究不同干旱胁迫程度对白枪杆幼苗生长、生物量积累与分配,以及不同器官C、N、P积累与分配,探究白枪杆对不同干旱环境的适应性。【方法】以1 a生白枪杆幼苗实生苗为试验材料,研究干旱胁迫处理分别是对照(CK)、轻度干旱胁迫(LS)、中度干旱胁迫(MS)和重度干旱胁迫(SS)对白枪杆幼苗生长、生物量的积累量与分配、根冠比、各器官C、N、P含量及化学计量特征的分析和各器官C、N、P的积累和分配规律等指标测定。【结果】随干旱胁迫程度的上升,白枪杆幼苗的苗高和地径的增长量显著降低(P<0.05)。叶片、茎和根的生物量及总生物量、叶片生物量占比降低,茎和根生物量占比和根冠比降低。白枪杆幼苗C、N和P的积累量随干旱胁迫程度的上升呈下降趋势;与适宜的水分处理相比,白枪杆幼苗各器官的C∶N均呈先下降后上升的趋势,叶片和根的C∶P呈先下降后上升的趋势;白枪杆幼苗各器官N∶P低于14,表明生长主要受N限制。【结论】白枪杆幼苗生长及生物量和C、N、P含量及化学计量特征对不同干旱胁迫程度的响应有差异,主要表现在随干旱胁迫程度的上升,白枪杆幼苗的苗高、地径增长量呈下降趋势,生物量的分配也倾向于地下部分,干旱胁迫处理下不利于白枪杆幼苗的生长,生物量的积累减少,C、N和P的积累量降低。

天坑森林植物叶-凋落物-土壤C、N、P生态化学计量特征

为探究广西乐业大石围天坑森林群落的C、N、P养分循环特征,比较了天坑内外森林群落的植物叶片-凋落物-土壤C、N、P含量及其化学计量比,采用相关性分析和冗余分析等统计方法研究其内在联系和相互影响。结果表明,与天坑外部森林相比,天坑内部森林植物叶片和凋落物呈现出C低N、P高,土壤为C、N低P高的格局。植物叶片C:N、C:P与凋落物C、N:P显著正相关,植物叶片C与土壤P显著负相关;天坑外部森林的植物叶片N、N:P与土壤N:P显著负相关,植物叶片C:N与土壤C、C:N显著正相关,说明天坑森林内部凋落物的C、P养分可能主要来源于植物叶片,而天坑外部森林的植物叶片C、N主要来自土壤。土壤C:N:P对植物叶、凋落物的C:N:P变化的解释率分别为90.7%和50.6%,其中土壤P对植物叶和凋落物的C:N:P计量特征变化的解释度最高,坑内生境植物对P含量变化更为敏感、坑外植物对于N含量变化更为敏感,表明天坑内部森林可能是P素受限位点、天坑外部森林是N素受限位点。喀斯特天坑内部森林和外部森林植物叶-凋落物-土壤的C:N:P的差异和联系,体现了天坑内外森林群落的养分循环特征和植物群落的适应性。

水曲柳叶片功能性状及C、N、P化学计量对海拔的响应

【目的】水曲柳是小陇山主要珍贵的用材树种,探讨其叶片性状对小生境变化的适应性,可为深入研究影响该树种的主要环境因子提供理论基础。【方法】以黑河保护区天然水曲柳为研究对象,分析4个海拔梯度(1268,1529,1741,1926 m)间14种叶片功能性状和叶片营养元素含量的差异显著性及其相关性。【结果】(1)随海拔升高,叶片厚度、干物质含量和叶绿素含量逐渐增大,并分别在海拔1741 m、1926 m、1741 m处达到最大,比叶面积、最大净光合速率、蒸腾速率、叶C和N含量则逐渐减少,除叶C含量外均在海拔1268 m达到最大。叶面积、气孔导度和叶C∶N随着海拔升高呈先增后降的趋势,胞间CO_(2)浓度、C∶P和N∶P呈先降后升的趋势。(2)海拔平均每上升200 m,叶片功能性状和C∶N平均增加1.13%~30.72%,比叶面积、最大净光合速率和C、N含量减小2.22%~15.75%。(3)各海拔叶N∶P为4.36~6.89,与最大净光合速率呈极显著正相关。最大净光合速率与比叶面积、C和N含量、C∶P和N∶P呈极显著正相关,与叶片厚度、干物质含量和叶绿素含量呈极显著负相关,比叶面积与干物质含量呈极显著负相关,与C和N含量和C∶P呈极显著正相关。【结论】海拔显著影响水曲柳叶片功能性状及元素含量,海拔1700 m以下有利于叶的发育和养分的积累。

Current Status and Perspectives of Dual-Atom Catalysts Towards Sustainable Energy Utilization

The exploration of sustainable energy utilization requires the imple-mentation of advanced electrochemical devices for efficient energy conversion and storage,which are enabled by the usage of cost-effective,high-performance electro-catalysts.Currently,heterogeneous atomically dispersed catalysts are considered as potential candidates for a wide range of applications.Compared to conventional cata-lysts,atomically dispersed metal atoms in carbon-based catalysts have more unsatu-rated coordination sites,quantum size effect,and strong metal-support interactions,resulting in exceptional catalytic activity.Of these,dual-atomic catalysts(DACs)have attracted extensive attention due to the additional synergistic effect between two adja-cent metal atoms.DACs have the advantages of full active site exposure,high selectiv-ity,theoretical 100%atom utilization,and the ability to break the scaling relationship of adsorption free energy on active sites.In this review,we summarize recent research advancement of DACs,which includes(1)the comprehensive understanding of the synergy between atomic pairs;(2)the synthesis of DACs;(3)characterization meth-ods,especially aberration-corrected scanning transmission electron microscopy and synchrotron spectroscopy;and(4)electrochemical energy-related applications.The last part focuses on great potential for the electrochemical catalysis of energy-related small molecules,such as oxygen reduction reaction,CO_(2) reduction reaction,hydrogen evolution reaction,and N_(2) reduction reaction.The future research challenges and opportunities are also raised in prospective section.

Ga-N共同掺杂CoP催化氨硼烷制氢机理的理论研究

本文通过密度泛函理论(DFT),计算研究了金属原子Ga和非金属原子N共同掺杂磷化钴(CoP)作为催化剂催化氨硼烷(NH_(3) BH_(3))的脱氢过程.在这里,我们设计了四条可行的反应路径,并且计算了每条路径中间体过渡态的能量.通过研究结果得出结论,路径Ⅱ为最优反应路径.这将为金属和非金属共同掺杂CoP催化NH_(3) BH_(3)脱氢反应提供一定的理论基础.

Effects of drought on non-structural carbohydrates and C,N,and P stoichiometric characteristics of Pinus yunnanensis seedlings

To study non-structural carbohydrate character-istics and nutrient utilization strategies of Pinus yunnanen-sis under continuous drought conditions,2-year-old seed-lings were planted in pots with appropriate water,light and moderate and severe drought treatments[(80±5),(65±5),(50±5),and(35±5)%of field water-holding capacity].Non-structural carbohydrates,carbon(C),nitrogen(N),and phosphorus(P)concentrations were measured in each plant component.The results show that:(1)With increasing drought,non-structural carbohydrates gradually increased in leaves,stems,and coarse roots,while gradually decreased in fine roots;(2)C concentrations of all were relatively stable under different stress levels.Phosphorous utilization of each component increased under light and moderate drought conditions,while N and P utilization efficiency of each plant component decreased under severe drought.Growth was mainly restricted by N,first decreasing and then increasing with increased drought;(3)There was a correlation between the levels of non-structural carbohydrates and C,N,and P in each component.Changes in N concentration affected the interconversion between soluble sugar and starch,which play a regulatory role in the fluctuation of the concentration of non-structural carbohydrates;and,(4)Plasticity analysis showed that P.yunnanensis seedlings responded to drought mainly by altering starch concentration,the ratio of soluble sugar to starch in leaves and stems,and further by alter-ing N and P utilization efficiencies.Overall,these results suggest that the physiological activities of all organs of P.yunnanensis seedlings are restricted under drought and that trade-offs exist between different physiological indicators and organs.Our findings are helpful in understanding non-structural carbohydrate and nutrient adaptation mechanisms under drought in P.yunnanensis seedlings.

p-Si/n-Ga_(2)O_(3)异质结制备与特性研究

本实验采用金属有机化学气相沉积(MOCVD)工艺,在p(111)型Si衬底上制备了p-Si/n-Ga_(2)O_(3)结构的PN结。通过X射线衍射仪、原子力显微镜等对样品进行了晶体结构、表面形貌、表面粗糙度等的表征分析;通过磁控溅射与蒸镀方法在样品上生长Ti/Au电极并进行I-V特性曲线、开启电压、开关电流比、反向饱和电流、理想因子、零偏压下的势垒高度等结特性测试,研究了掺杂浓度与薄膜厚度对PN结特性的影响,并对其原因进行了分析;通过二步生长法和缓冲层温度优化实验,减少了Si衬底与β-Ga_(2)O_(3)之间的晶格失配与热失配带来的影响,对薄膜与器件特性进行了优化。最终获得了表面粗糙度最低可达到4.21 nm的高质量n型β-Ga_(2)O_(3)薄膜,以及具有较低理想因子(42.1)的PN结。

Study on the optimal incident proton energy of ^(7)Li(p,n)^(7)Be neutron source for boron neutron capture therapy

Boron neutron capture therapy(BNCT)is recognized as a precise binary targeted radiotherapy technique that effectively eliminates tumors through the^(10)B(n,α)^(7)Li nuclear reaction.Among various neutron sources,accelerator-based sources have emerged as particularly promising for BNCT applications.The^(7)Li(p,n)^(7)Be reaction is highly regarded as a potential neutron source for BNCT,owing to its low threshold energy for the reaction,significant neutron yield,appropriate average neutron energy,and additional benefits.This study utilized Monte Carlo simulations to model the physical interactions within a lithium target subjected to proton bombardment,including neutron moderation by an MgF_(2)moderator and subsequent BNCT dose analysis using a Snyder head phantom.The study focused on calculating the yields of epithermal neutrons for various incident proton energies,finding an optimal energy at 2.7 MeV.Furthermore,the Snyder head phantom was employed in dose simulations to validate the effectiveness of this specific incident energy when utilizing a^(7)Li(p,n)^(7)Be neutron source for BNCT purposes.

PIG3启动子结合元件(TGYCC)n与肿瘤易感性的研究进展

PIG3是受p53调控的下游靶基因,通过参与合成活性氧及对氧化应激的调控参与细胞凋亡过程。PIG3的启动子区有一段串联重复序列(TGYCC)n(Y=C或T),其转录调控与这段五核苷酸重复序列密切相关。本文对(TGYCC)n这段串联重复序列在PIG3转录调控中的作用进行综述,探讨其多态性与肿瘤易感性的关系。

Microbial synthesis of N, P co-doped carbon supported PtCu catalysts for oxygen reduction reaction

Developing highly efficient and stable platinum-based electrocatalyst for oxygen reduction reaction(ORR) is critical to expediting commercialization of fuel cells.Herein,several PtCu alloy nanocatalysts supported on N,P co-doped carbon(PtCu/NPC) were prepared by microbial-sorption and carbonization-reduction.Among them,PtCu/NPC-700 ℃ exhibits excellent catalytic performance for ORR with a mass activity of 0.895 A mg_(pt)^(-1)(@0.9 V) which is 8.29 folds of commercial Pt/C.Additionally,the ECSA and MA of PtCu/NPC-700℃ only decrease by 14.2% and 18.7% respectively,while Pt/C decreases by 35.2% and 52.8% after 10,000 cycles of ADT test.Moreover,the PtCu/NPC-700℃ catalyst emanates a maximum power density of 715 mW cm^(-2) and only 11.1% loss of maximum power density after 10,000 ADTs in single-cell test,indicating PtCu/NPC-700℃ also manifests higher activity and durability in actual single-cell operation than Pt/C.This research provides an easy and novel strategy for developing highly active and durable Pt-based alloy catalyst.

Operationally Simple Enantioselective Silane Reduction of Ketones by the [Ir(OMe)(cod)]2/Azolium Catalytic System

An operationally simple protocol was designed for the enantioselective silane reduction (ESR) of ketones using air- and moisture-stable [Ir(OMe)(cod)]2 (cod = 1,5-cyclooctadiene) (3) as a metal catalyst precursor. This reaction was driven by chiral hydroxyamide-functionalized azolium salt 2. The catalytic ESR reaction could be performed under benchtop conditions at room temperature. Treatment of 2 with 3 in THF yielded the monodentate IrCl(NHC)(cod) (NHC = N-heterocyclic carbene) complex 4 in 93% yield, herein the anionic methoxy ligand of 3 serves as an internal base that deprotonates the azolium ring of 2. The well-defined Ir complex 4 catalyzed the ESR reaction of propiophenone (6) with (EtO)2MeSiH using the pre-mixing reaction procedure. Based on this success, the catalytic ESR reaction was designed and implemented using an in situ-generated NHC/Ir catalyst derived from 2 and 3. Thus, a wide variety of aryl ketones could be reduced to the corresponding optically active alcohols in moderate to excellent stereoselectivities at room temperature without temperature control. Since the high catalytic activity of 3 was observed, we next evaluated several other transition metal catalyst precursors for the catalytic ESR reaction under the influence of 2. This evaluation revealed that Ir(acac)(cod) (acac = acetylacetonate) (28) and [IrCl(cod)]2 (5) can be successfully used as metal catalyst precursors in the ESR reaction.

Pd nanoparticles embedded in N-Enriched MOF-Derived architectures for efficient oxygen reduction reaction in alkaline media

Developing high efficient Pd-based electrocatalysts for oxygen reduction reaction(ORR) is still challenging for alkaline membrane fuel cell,since the strong oxygen adsorption energy and easy agglomerative intrinsic properties. In order to simultaneously solve these problems, Pd/Co_(3)O_(4)–N–C multidimensional materials with porous structures is designed as the ORR catalysts. In details, the ZIF-67 with polyhedral structure was firstly synthesized and then annealed at high-temperature to prepare the N-doped Co_(3)O_(4)carbon-based material, which was used to homogeneously confine Pd nanoparticles and obtained the Pd/Co_(3)O_(4)–N–C series catalysts. The formation of Co–N and C–N bond could provide efficient active sites for ORR. Simultaneously, the strong electronic interaction in the interface between the Pd and N-doped Co_(3)O_(4)could disperse and avoid the agglomeration of Pd nanoparticles and ensure the exposure of active sites, which is crucial to lower the energy barrier toward ORR and substantially enhance the ORR kinetics. Hence, the Pd/Co_(3)O_(4)–N–C nanocompounds exhibited excellent ORR catalytic performance, ideal Pd mass activity, and durability in 0.1 mol L-1KOH solution compared with Co_(3)O_(4)–N–C and Pd/C. The scalable synthesis method, relatively low cost, and excellent electrochemical ORR performance indicated that the obtained Pd/Co_(3)O_(4)–N–C electrocatalyst had the potential for application on fuel cells.

Investigation on Breakdown Characteristics of Various Surface Terminal Structures for GaN-Based Vertical P-i-N Diodes

GaN-based vertical P-i-N diode with mesa edge terminal structure due to electric field crowding effect, the breakdown voltage of the device is significantly reduced. This work investigates three terminal structures, including deeply etched, bevel, and stepped-mesas terminal structures, to suppress electric field crowding effects at the device and junction edges. Deeply-etched mesa terminal yields a breakdown voltage of 1205 V, i.e., 89% of the ideal voltage. The bevel-mesa terminal achieves about 89% of the ideal breakdown voltage, while the step-mesa terminal is less effective in mitigating electric field crowding, at about 32% of the ideal voltage. This work can provide an important reference for the design of high-power, high-voltage GaN-based P-i-N power devices, finding a terminal protection structure suitable for GaNPiN diodes to further enhance the breakdown performance of the device and to unleash the full potential of GaN semiconductor materials.

One‑Step Gas-Solid‑Phase Diffusion‑Induced Elemental Reaction for Bandgap‑Tunable Cu_(a)Agm_(1)Bim_(2)I_(n)/CuI Thin Film Solar Cells

Lead-free inorganic copper-silver-bismuth-halide materials have attracted more and more attention due to their environmental friendliness,high element abundance,and low cost.Here,we developed a strategy of one-step gas-solid-phase diffusioninduced reaction to fabricate a series of bandgap-tunable Cu_(a)Agm_(1)Bim_(2)I_(n)/CuI bilayer films due to the atomic diffusion effect for the first time.By designing and regulating the sputtered Cu/Ag/Bi metal film thickness,the bandgap of Cu_(a)Agm_(1)Bim_(2)I_(n)/CuI could be reduced from 2.06 to 1.78 eV.Solar cells with the structure of FTO/TiO_(2)/Cu_(a)Agm_(1)Bim_(2)I_(n)/CuI/carbon were constructed,yielding a champion power conversion efficiency of 2.76%,which is the highest reported for this class of materials owing to the bandgap reduction and the peculiar bilayer structure.The current work provides a practical path for developing the next generation of efficient,stable,and environmentally friendly photovoltaic materials.

Numerical Analysis on the Effect of n-Si on Cu(In, Ga)Se2 Based Thin-Films for High-Performance Solar Cells by 1D-SCAPS

We report the performances of a chalcopyrite Cu(In, Ga)Se2 CIGS-based thin-film solar cell with a newly employed high conductive n-Si layer. The data analysis was performed with the help of the 1D-Solar Cell Capacitance Simulator (1D-SCAPS) software program. The new device structure is based on the CIGS layer as the absorber layer, n-Si as the high conductive layer, i-In2S3, and i-ZnO as the buffer and window layers, respectively. The optimum CIGS bandgap was determined first and used to simulate and analyze the cell performance throughout the experiment. This analysis revealed that the absorber layer’s optimum bandgap value has to be 1.4 eV to achieve maximum efficiency of 22.57%. Subsequently, output solar cell parameters were analyzed as a function of CIGS layer thickness, defect density, and the operating temperature with an optimized n-Si layer. The newly modeled device has a p-CIGS/n-Si/In2S3/Al-ZnO structure. The main objective was to improve the overall cell performance while optimizing the thickness of absorber layers, defect density, bandgap, and operating temperature with the newly employed optimized n-Si layer. The increase of absorber layer thickness from 0.2 - 2 µm showed an upward trend in the cell’s performance, while the increase of defect density and operating temperature showed a downward trend in solar cell performance. This study illustrates that the proposed cell structure shows higher cell performances and can be fabricated on the lab-scale and industrial levels.

非金属P掺杂对In_(2)O_(3)电催化CO_(2)还原性能的影响机制

利用可再生的电能将CO_(2)还原为高附加值的化学品和燃料,对于缓解温室效应并实现碳中和具有重要的意义。开发了一种简单有效的方法制备非金属P元素掺杂的In_(2)O_(3)纳米颗粒,并将其用于电催化CO_(2)还原制甲酸盐。在H型电解池中,在-1.45 V vs.RHE电位下,P掺杂的In_(2)O_(3)纳米催化剂的产甲酸法拉第效率达到88.2%,同时具有优异的稳定性。进一步的实验分析和理论研究表明,掺杂在In_(2)O_(3)晶格中的P元素显著促进了CO_(2)分子的吸附和活化,降低了形成*HCOO中间体的吉布斯自由能,同时加强了对*HCOO的吸附作用,最终促进了甲酸盐的合成。阐明了非金属元素P掺杂对提升CO_(2)还原反应性能的分子机制,同时也为其他金属氧化物基的高性能电催化剂的设计提供了一种可行的策略。