宽波段连续调谐全固态CW PPMgLN光学参量振荡器

利用半导体激光泵浦输出1064 nm波长的全固态连续Nd:YVO4激光器作为泵浦源,采用周期调谐和温度调谐组合调谐技术,对基于掺氧化镁周期性极化铌酸锂晶体（MgO:LiNbO3, PPMgLN）准相位匹配（QPM）的全固态连续波（CW）光学参量振荡器（OPO）宽波段无分立连续调谐输出特性进行研究。实验采用连续工作模式和外腔结构,基于多周期PPMgLN晶体的30.2,30.4和30.6 m周期,在改变晶体的极化周期的基础上,同时在30～100 ℃范围内调节晶体工作温度。实验结果表明:CW PPMgLN OPO的泵浦阈值仅为0.22 W;不同极化周期需要的温度调谐范围不同;信号光在1 559.8～1 597.2 nm近红外波段和闲频光在3 187.3~3 347.3 nm中红外波段连续调谐输出。实现了外腔式全固态CW OPO在信号光和闲频光波段的无分立连续调谐输出。     

Superconvergence and a posteriori error estimates for the Stokes eigenvalue problems

In this paper we consider the finite element approximation of the Stokes eigenvalue problems based on projection method, and derive some superconvergence results and the related recovery type a posteriori error estimators. The projection method is a postprocessing procedure that constructs a new approximation by using the least squares strategy. The results are based on some regularity assumptions for the Stokes equations, and are applicable to the finite element approximations of the Stokes eigenvalue problems with general quasi-regular partitions. Numerical results are presented to verify the superconvergence results and the efficiency of the recovery type a posteriori error estimators.     

Coulomb‐enhanced spin–orbit coupling and semiconductor to half‐metal transition under pressure in Sr2CrReO6

Ordered Sr₂CrReO₆ has been synthesized recently. It is measured to be ferrimagnetic semiconductor, in contrary to the previous reports of metallic properties. To solve the discrepancy, we have investigated the compound by using the density functional theory. The semiconducting behavior is reproduced by including the electron correlation and spin–orbit coupling simultaneously. The calculated band gap is 0.22 eV, close to the experimental value of 0.21 eV. A large orbital moment of 0.69µ_B is found for Re, which is caused by the Coulomb‐enhanced spin–orbit coupling. By applying pressure, a semiconductor to half‐metal transition is observed through 5% volume compression.

     

Surface modification of hollow microsphere Li1.2Ni1/3Co1/3Mn1/3O2 cathode by coating with CoAl2O4

Journal of Solid State Electrochemistry - Li1.2Ni1/3Co1/3Mn1/3O2 was synthesized as a cathode material for lithium-ion batteries and coated with various amounts of CoAl2O4 (0–5 wt%)...     

Electroactive Metal–Organic Frameworks as Emitters for Self-Enhanced Electrochemiluminescence in Aqueous Medium

Metal–organic frameworks (MOFs) have limited applications in electrochemistry owing to their poor conductivity. Now, an electroactive MOF (E-MOF) is designed as a highly crystallized electrochemiluminescence (ECL) emitter in aqueous medium. The E-MOF contains mixed ligands of hydroquinone and phenanthroline as oxidative and reductive couples, respectively. E-MOFs demonstrate excellent performance with surface state model in both co-reactant and annihilation ECL in aqueous medium. Compared with the individual components, E-MOFs significantly improve the ECL emission due to the framework structure. The self-enhanced ECL emission with high stability is realized by the accumulation of MOF cation radicals via pre-reduction electrolysis. The self-enhanced mechanism is theoretically identified by DFT. The mixed-ligand E-MOFs provide a proof of concept using molecular crystalline materials as new ECL emitters for fundamental mechanism studies.     

高次Galerkin有限元法的超收敛性

通过局部误差估计,对具有光滑边界的二阶常系数椭圆型方程,给出了高次Ｇａｌｅｒｋｉｎ 有限元法的超收敛性． 运用对称技巧和积分恒等式技巧,在局部对称矩形网格或三角形网格上,我们得到了改进的超收敛性（提高１－ ３ 阶）．     

Low-entropy lattices engineered through bridged DNA origami frames

The transformation from disorder to order in self-assembly is an autonomous entropy-decreasing process. The spatial organization of nanoscale anisotropic building blocks involves the intrinsic heterogeneity in three dimensions and requires sufficiently precise control to coordinate intricate interactions. Only a few approaches have been shown to achieve the anisotropic extension from components to assemblies. Here, we demonstrate the ability to engineer three-dimensional low-entropy lattices at the nucleotide level from modular DNA origami frames. Through the programmable DNA bridging strategy, DNA domains of the same composition are periodically arranged in the crystal growth directions. We combine the site-specific positioning of guest nanoparticles to reflect the anisotropy control, which is validated by small-angle X-ray scattering and electron microscopy. We expect that our DNA origami-mediated crystallization method will facilitate both the exploration of refined self-assembly platforms and the creation of anisotropic metamaterials.

Through the bridging principle, DNA origami building blocks are integrated into ordered self-assembled structures. Periodically arranged DNA domains can locate the nanoparticles in a uniform site to achieve precise control of the contents.