Generalized Deligne-Hitchin Twistor Spaces: Construction and Properties

In this paper, we generalize the construction of Deligne-Hitchin twistor space by gluing two certain Hodge moduli spaces. We investigate such generalized Deligne-Hitchin twistor space as a complex analytic manifold. More precisely, we show it admits holomorphic sections with weight-one property and semi-negative energy, and it carries a balanced metric, and its holomorphic tangent bundle (for the case of rank one) is stable. Moreover, we also study the automorphism groups of the Hodge moduli spaces and the generalized Deligne-Hitchin twistor space.Comment: An update of the revised version with some gaps fixed in 2022, comments welcome

Moduli Spaces of Parabolic Bundles over P1\mathbb{P}^1 with Five Marked Points

This paper considers the moduli spaces (stacks) of parabolic bundles (parabolic logarithmic flat bundles with given spectrum, parabolic regular Higgs bundles) with rank $2$ and degree $1$ over $\mathbb{P}^1$ with five marked points. The foliation and stratification structures on these moduli spaces (stacks) are investigated. In paricular, we confirm Simpson's conjecture for moduli space of parabolic logarithmic flat bundles with certain non-special weight system

(Formato-κ2 O,O′)bis­(1,10-phenanthroline-κ2 N,N′)manganese(II) perchlorate

In the title complex, [Mn(CHO2)(C12H8N2)2]ClO4, the MnII cation is chelated by two 1,10-phenanthroline (phen) ligands and one formate anion in a distorted MnN4O2 octa­hedral geometry. The two phen planes are oriented at a dihedral angle of 57.48 (11)°. The perchlorate anion links with the Mn complex cation via weak C—H⋯O hydrogen bonding

[2-(Tetra­zol-1-yl)acetato-κO]tris­(tri­phenyl­phosphine-κP)silver(I) mono­hydrate

The AgI atom in the title compound, [Ag(C3H3N4O2)(C18H15P)3]·H2O, exists in a distorted tetra­hedral environment. The uncoordinated water mol­ecule forms only one hydrogen bond to the uncoordinated carbonyl O atom

Realization of edge states along a synthetic orbital angular momentum dimension

The synthetic dimension is a rising method to study topological physics, which enables us to implement high-dimensional physics in low-dimensional geometries. Photonic orbital angular momentum (OAM), a degree of freedom characterized by discrete yet unbounded, serves as a suitable synthetic dimension. However, a sharp boundary along a synthetic OAM dimension has not been demonstrated, dramatically limiting the investigation of topological edge effects in an open boundary lattice system. In this work, we make a sharp boundary along a Floquet Su-Schrieffer-Heeger OAM lattice and form approximate semi-infinite lattices by drilling a pinhole on the optical elements in a cavity. The band structures with zero ($\pm\pi$) energy boundary states are measured directly, benefiting from the spectra detection of the cavity. Moreover, we obtain the edge modes moving from the gap to the bulk by dynamically changing the boundary phase, and we reveal that interference near the surface leads to spectrum discretization. Our work provides a new perspective to observe edge effects and explore practical photonics tools

KIC 10417986: Spectroscopic confirmation of the nature of the binary system with a {\delta} Scuti component

KIC 10417986 is a short orbital period (0.0737 d) ellipsoidal variable star with a {\delta} Scuti and {\gamma} Doradus hybrid pulsations component discovered by Kepler. The ground-based spectroscopic observations were carried out in the winters of 2020 and 2021 to investigate the binary nature of this star. We derive the orbital parameters using the rvfit code with a result of K1 = 29.7 $\pm$ 1.5 km/s, {\gamma} = -18.7 $\pm$ 1.7 km/s, and confirm an orbital period of 0.84495 d instead of the result given by Kepler. The atmospheric parameters of the primary are determined by the synthetic spectra fitting technique with the estimated values of Teff = 7411 $\pm$ 187 K, log g = 4.2 $\pm$ 0.3 dex, [M/H] = 0.08 $\pm$ 0.09 dex and vsini = 52 $\pm$ 11 km/s. KIC 10417986 is a circular orbit binary system. From the single-lined nature and mass function of the star, the derived orbital inclination is 26 $\pm$ 6{\deg}, and the mass of the secondary is from 0.43 to 0.7 M_sun, which should be a late-K to early-M type star. Fourteen frequencies are extracted from Kepler light curves, of which six independent frequencies in the high-frequency region are identified as the p-mode pulsations of {\delta} Scuti star, and one independent frequency in the low-frequency region (f2 = 1.3033 c/d) is probably the rotational frequency due to the starspots rather than the ellipsoidal effect or g-mode of {\gamma} Doradus.Comment: 18 pages, 8 figure

Plasmonic photoluminescence for recovering native chemical information from surface-enhanced Raman scattering

表面增强拉曼光谱(SERS)可以提供高达单分子的检测灵敏度和特异的分子指纹信息，是一个非常有前景的分析技术。SERS增强主要源自贵金属纳米结构的局域表面等离激元共振(LSPR)效应。虽然SERS研究者早已意识到该效应强烈依赖于激光波长，并对不同频率的拉曼谱峰增强效果不同，但是迄今为止仍缺乏有效的方法对SERS谱峰相对强度进行可靠的矫正，也常有文献错误解读SERS强度信息，从而过度或错误地解释实验结果。 在该工作中，任斌教授课题组采用单粒子光谱技术从实验上直接检测SERS光谱和金属纳米粒子的光致发光谱(PL)，通过定量研究两者的关联，提出了一种普适的方法矫正LSPR对不同拉曼谱峰相对强度的影响，为理解表面物种构型和作用方式提供了本征的化学指纹信息。【Abstract】Surface-enhanced Raman scattering (SERS) spectroscopy has attracted tremendous interests as a highly sensitive label-free tool. The local field produced by the excitation of localized surface plasmon resonances (LSPRs) dominates the overall enhancement of SERS. Such an electromagnetic enhancement is unfortunately accompanied by a strong modification in the relative intensity of the original Raman spectra, which highly distorts spectral features providing chemical information. Here we propose a robust method to retrieve the fingerprint of intrinsic chemical information from the SERS spectra. The method is established based on the finding that the SERS background originates from the LSPR-modulated photoluminescence, which contains the local field information shared also by SERS. We validate this concept of retrieval of intrinsic fingerprint information in well controlled single metallic nanoantennas of varying aspect ratios. We further demonstrate its unambiguity and generality in more complicated systems of tip-enhanced Raman spectroscopy (TERS) and SERS of silver nanoaggregates.该工作得到国家自然科学基金委（项目批准号：21633005、21621091和J1310024）、科技部（项目批准号：2013CB933703、2016YFA0200601）、教育部等部门的大力资助与支持