Passively Q-switched mode-locking Erbium-doped fiber laser with net-normal dispersion using nonlinear polarization rotation technique

We experimentally demonstrate a passively Q-switched mode-locking (QML) operation in an Erbium-doped fiber ring laser with net normal dispersion by using nonlinear polarization rotation technique. A 2 m long section of dispersion compensating fiber (DCF) with extra large positive dispersion was inserted into the cavity to ensure the fiber laser working in the region of net positive dispersion. By carefully adjusting the polarization controller, both uniform dissipative mode-locking pulses with fundamental repetition rate and QML pulse trains with tunable repetition rate from 71.58 to 98.83 kHz are achieved. It is found that the QML operation is caused by the interaction between the polarization state of the pulse and the intracavity polarizer.     

Supramolecular control over LCST behavior of hybrid macrocyclic system based on pillar[5]arene and crown ether

A hybrid system containing a pillar[5]arene unit and ten crown ether moieties was developed. The LCST behavior and thermo-responsiveness were successfully introduced into this pillar[5]arene-crown ether system. Both host-guest interactions and salting-out effect displayed great effects in realizing the supramolecular control over LCST properties and thermo-responsiveness. Compared with the individual macrocycles, this hybrid macrocycle system dramatically amplified the supramolecular control effect over LCST behavior.     

A Disulfide Switch Providing Absolute Handedness Control in Double Helices via Conversion from the Antiparallel to Parallel Helical Pattern

A strategy to reversibly switch the parallel/antiparallel helical conformation of aromatic double helices through the formation/breakage of a disulfide bond is presented. Single-crystal X-ray structures, NMR, and circular dichroism spectroscopy demonstrate that the double helices with terminal thiol groups favor an antiparallel helical arrangement both in the solid state and in solution, while the P/M bias of helicity induced by chiral segments from another extremity of the sequence is weak in this structural motif. The antiparallel helices can be rearranged to parallel helices through the disulfide connection of the sequences. This change enhances the bias of helical handedness and results in absolute chirality control of the double helices. The handedness-mediated process can be governed by the oxidation-reduction cycle, thereby switching the structural arrangement and the enhancement of chiral bias. In addition, we find that the sequences can dimerize into an intermolecular double helix with the disulfide connection. And the helical handedness is also fully controlled due to the head-to-head structural motif.     

Facile and green synthesis of Co3O4 nanoplates/graphene nanosheets composite for supercapacitor

Journal of Solid State Electrochemistry - A series of Co3O4 nanoplates/graphene nanosheets (GNS) composites are fabricated using a facile and green method by hydrothermal treatment and subsequent...     

Synthesis of one-dimensional graphene-encapsulated TiO2 nanofibers with enhanced lithium storage capacity for lithium-ion batteries

Journal of Solid State Electrochemistry - The one-dimensional graphene/TiO2 composite nanofibers with the unique microstructures have been successfully synthesized via an efficient method and...     

A new class of multi-wavelet bases: V-system

The V-system is a complete orthogonal system of functions defined on the interval [0, 1], generated by finite Legendre polynomials and the dilation and translation of a function generator, which consists of a finite number of continuous and discontinuous functions. The V-system has interesting properties, such as orthogonality, symmetry, completeness and short compact support. It is shown in this paper that the V-system is essentially a special multi-wavelet basis. As a result, some basic properties of the V-system are established through the well-developed theory of multi-wavelets. From this point of view, more other V-systems are constructed.     

Synthesis of Layered Carbonitrides from Biotic Molecules for Photoredox Transformations

The construction of layered covalent carbon nitride polymers based on tri-s-triazine units has been achieved by using nucleobases (adenine, guanine, cytosine, thymine and uracil) and urea to establish a two-dimensional semiconducting structure that allows band-gap engineering applications. This biomolecule-derived binary carbon nitride polymer enables the generation of energized charge carrier with light-irradiation to induce photoredox reactions for stable hydrogen production and heterogeneous organosynthesis of C−O, C−C, C−N and N−N bonds, which may enrich discussion on chemical reactions in prebiotic conditions by taking account of the photoredox function of conjugated carbonitride semiconductors that have long been considered to be stable HCN-derived organic macromolecules in space.