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41.
We investigate the pairing symmetry of the Kondo-Heisenberg model on triangular lattice, which is believed to capture the core competition of Kondo screening and local magnetic exchange interaction in heavy electron compounds. On the dominant background of the heavy fermion state, the introduction of the Heisenberg antiferromagnetic interaction (J H ) leads to superconducting pairing instability. Depending on the strength of the interactions, it is found that the pairing symmetry favours an extended s-wave for small J H and high conduction electron density but a chiral \(d_{x^2 - y^2 } + id_{xy}\)-wave for large J H and low conduction electron density, which provides a phase diagram of pairing symmetry from the calculations of the ground-state energy. The transition between these two pairing symmetries is found to be first-order. Furthermore, we also analyze the phase diagram from the pairing strengths and find that the phase diagram obtained is qualitatively consistent with that based on the ground-state energy. In addition, we propose an effective single-band BCS Hamiltonian, which is able to describe the low-energy thermodynamic behaviors of the heavy fermion superconducting states. These results further deepen the understanding of the antiferromagnetic interaction which results in a geometric frustration for the model studied. Our work may provide a possible scenario to understand the pairing symmetry of the heavy fermion superconductivity, which is one of active issues in very recent years.  相似文献   
42.
采用计算流体动力学(CFD)数值模拟方法分析了湍流与化学反应相互作用下MILD煤粉燃烧的微观特征。比较了涡耗散模型(EDM模型)和涡耗散概念模型(EDC模型)对MILD煤粉燃烧的影响,两者得到的速度场、温度场、烟气成分等结果与实验结果符合较好.在此基础上分析了MILD煤粉燃烧湍流和化学反应的微观特征尺度,发现采用EDC模型能更准确地反映MILD煤粉燃烧的微观特征,即山于强烈的烟气内部再循环导致的高湍流混合和烟气稀释后低氧浓度下的缓慢化学反应.  相似文献   
43.
席锋  秦岚  薛联  段莹 《强激光与粒子束》2013,25(04):1035-1039
位置敏感探测器(PSD)是基于半导体的横向光电效应的光电转换器件。根据横向光电效应的原理,增强光生载流子的寿命可提高光生载流子的扩散长度,从而实现横向光电效应的增强。利用缺陷和完整光子晶体设计了一维位置敏感探测器,并用传输矩阵法计算了缺陷光子晶体的透射率和完整光子晶体的反射率。从所设计的位置敏感探测器对入射光的响应理论研究表明,提高缺陷光子晶体的透射率和完整光子晶体的反射率可提高光生载流子的寿命,从而实现增强位置敏感探测器的横向光电效应。  相似文献   
44.
This paper investigates the development of an effective heuristic to solve the set covering problem (SCP) by applying the meta-heuristic Meta-RaPS (Meta-heuristic for Randomized Priority Search). In Meta-RaPS, a feasible solution is generated by introducing random factors into a construction method. Then the feasible solutions can be improved by an improvement heuristic. In addition to applying the basic Meta-RaPS, the heuristic developed herein integrates the elements of randomizing the selection of priority rules, penalizing the worst columns when the searching space is highly condensed, and defining the core problem to speedup the algorithm. This heuristic has been tested on 80 SCP instances from the OR-Library. The sizes of the problems are up to 1000 rows × 10,000 columns for non-unicost SCP, and 28,160 rows × 11,264 columns for the unicost SCP. This heuristic is only one of two known SCP heuristics to find all optimal/best known solutions for those non-unicost instances. In addition, this heuristic is the best for unicost problems among the heuristics in terms of solution quality. Furthermore, evolving from a simple greedy heuristic, it is simple and easy to code. This heuristic enriches the options of practitioners in the optimization area.  相似文献   
45.
Glycosylation reactions are significant as they provide access to model compounds that are useful for elucidating biochemical pathways. Herein, we describe the development of glycosyl ortho-alkynylbenzoates as novel, bench-top stable, and readily available glycosyl donors. Glycosylation is promoted by inexpensive trimethylsilyl triflate (TMSOTf) in combination with N-iodosuccinimide (NIS) under mild reaction conditions; hence, the novel glycosyl donors are promising reagents for the synthesis of glycosides.  相似文献   
46.
An unprecedented stereoselective synthesis of trisubstituted vinylboronates is reported to proceed by direct borylation of lithium ketone enolates under transition‐metal‐free conditions. The stereospecific C?O borylation of lithium enolates was triggered by a carbonyl‐induced 1,3‐metalate rearrangement via a C‐bound boron enolate. DFT calculations and control experiments revealed that the stereoselectivity is controlled by sterics. A variety of stereospecific trisubstituted vinylboronates, together with several tetrasubstituted vinylboronates, were conveniently synthesized with the newly developed methodology. Based on the transformation of stereospecific vinylboronate, a single isomer of Dienestrol was efficiently obtained.  相似文献   
47.
48.
Three inorganic‐organic hybrid frameworks [Mn(HIMDC)(4,4′‐bipyo)0.5(H2O)]n (1) , [Cd(H2IMDC)2(2,2′‐bipyo)] (2) and [Ca(HIMDC)(H2O)2·H2O]n (3) (H3IMDC = 4,5‐imidazoledicarboxylate; 4,4′‐bipyo = 4,4′‐bipyridine‐N,N′‐dioxide; 2,2′‐bipyo= 2,2′‐bipyridine‐N,N′‐dioxide) have been hydrothermally synthesized and characterized by the elemental analyses, IR spectra, TG analysis and the single crystal diffraction. Both compounds 1 and 3 exhibit 2D layers while 2 is a monomer. It is noteworthy that compound 2 exhibits strong fluorescent emission in the solid state at room temperature.  相似文献   
49.
In this work, we innovatively assembled two types of traditional photosensitizers, that is pyridine ruthenium/ferrum (Ru(bpy)32+/Fe(bpy)32+) and porphyrin/metalloporphyrin complex (2HPor/ZnPor) by covalent linkage to get a series of dual photosensitizer-based three-dimensional metal-covalent organic frameworks (3D MCOFs), which behaved strong visible light-absorbing ability, efficient electron transfer and suitable band gap for highly efficient photocatalytic hydrogen (H2) evolution. Rubpy-ZnPor COF achieved the highest H2 yield (30 338 μmol g−1 h−1) with apparent quantum efficiency (AQE) of 9.68 %@420 nm, which showed one of the best performances among all reported COF based photocatalysts. Furthermore, the in situ produced H2 was successfully tandem used in the alkyne hydrogenation with ≈99.9 % conversion efficiency. Theoretical calculations reveal that both the two photosensitizer units in MCOFs can be photoexcited and thus contribute optimal photocatalytic activity. This work develops a general strategy and shows the great potential of using multiple photosensitive materials in the field of photocatalysis.  相似文献   
50.
Curcumin is the most important active component in turmeric extracts. Curcumin, a natural monomer from plants has received a considerable attention as a dietary supplement, exhibiting evident activity in a wide range of human pathological conditions. In general, curcumin is beneficial to human health, demonstrating pharmacological activities of anti-inflammation and antioxidation, as well as antitumor and immune regulation activities. Curcumin also presents therapeutic potential in neurodegenerative, cardiovascular and cerebrovascular diseases. In this review article, we summarize the advancements made in recent years with respect to curcumin as a biologically active agent in malignant tumors, Alzheimer’s disease (AD), hematological diseases and viral infectious diseases. We also focus on problems associated with curcumin from basic research to clinical translation, such as its low solubility, leading to poor bioavailability, as well as the controversy surrounding the association between curcumin purity and effect. Through a review and summary of the clinical research on curcumin and case reports of adverse effects, we found that the clinical transformation of curcumin is not successful, and excessive intake of curcumin may have adverse effects on the kidneys, heart, liver, blood and immune system, which leads us to warn that curcumin has a long way to go from basic research to application transformation.  相似文献   
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