Numerical investigation of GHz repetition rate fundamentally mode-locked all-fiber lasers

GHz repetition rate fundamentally mode-locked lasers have attracted great interest for a variety of scientific and practical applications. A passively mode-locked laser in all-fiber format has the advantages of high stability, maintenance-free operation, super compactness, and reliability. In this paper, we present numerical investigation on passive mode-locking of all-fiber lasers operating at repetition rates of 1-20 GHz. Our calculations show that the reflectivity of the output coupler, the small signal gain of the doped fiber, the total net cavity dispersion, and the modulation depth of the saturable absorber are the key parameters for producing stable fundamentally mode-locked pulses at GHz repetition rates in very short all-fiber linear cavities. The instabilities of GHz repetition rate fundamentally mode-locked all-fiber lasers with different parameters were calculated and analyzed. Compared to a regular MHz repetition rate mode-locked all-fiber laser, the pump power range for the mode-locking of a GHz repetition rate all-fiber laser is much larger due to the several orders of magnitude lower accumulated nonlinearity in the fiber cavity The presented numerical study provides valuable guidance for the design and development of highly stable mode-locked all-fiber lasers operating at GHz repetition rates.National Science Foundation Engineering Research Center for Integrated Access Networks [EEC-0812072]; Technology Research Initiative Fund (TRIF) Photonics Initiative of the University of Arizona; National Natural Science Foundation of China (NSFC) [61575075]Open access journalThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at [email protected]

Aggravated myocardial infarction-induced cardiac remodeling and heart failure in histamine-deficient mice

Histamine has pleiotropic pathophysiological effects, but its role in myocardial infarction (MI)-induced cardiac remodeling remains unclear. Histidine decarboxylase (HDC) is the main enzyme involved in histamine production. Here, we clarified the roles of HDC-expressing cells and histamine in heart failure post-MI using HDC-EGFP transgenic mice and HDC-knockout (HDC−/−) mice. HDC+CD11b+ myeloid cell numbers markedly increased in the injured hearts, and histamine levels were up-regulated in the circulation post-MI. HDC−/− mice exhibited more adverse cardiac remodeling, poorer left ventricular function and higher mortality by increasing cardiac fibrogenesis post-MI. In vitro assays further confirmed that histamine inhibited heart fibroblast proliferation. Furthermore, histamine enhanced the signal transducer and activator of transcription (STAT)-6 phosphorylation level in murine heart fibroblasts, and the inhibitive effects of histamine on fibroblast proliferation could be blocked by JAK3/STAT6 signaling selective antagonist. STAT6-knockout (STAT6−/−) mice had a phenotype similar to that of HDC−/− mice post-MI; however, in contrast to HDC−/− mice, the beneficial effects of exogenous histamine injections were abrogated in STAT6−/− mice. These data suggest that histamine exerts protective effects by modulating cardiac fibrosis and remodeling post-MI, in part through the STAT6-dependent signaling pathway

Investigations of Different Ion Intercalations on the Performance of FBG Hydrogen Sensors Based on Pt/MoO3

α-MoO3 has been used as a hydrogen sensing material due to its excellent properties and unique crystalline layer structure. However, the low repeatability of α-MoO3 based hydrogen sensor restricts its practical application. In this paper, the effect of intercalated ion species and the amount in α-MoO3 is experimentally investigated and discussed. It is concluded that the repeatability of the sensor depends on the radius of intercalated ions and amount of ionic bonds. The optimal ion species is Na+ and the optimal amount of precursor is 1 mmol

Ho3+-Doped All-Fiber Laser Q-Switched by D-Shaped Fiber Carbon-Nanotube Saturable Absorber

D-shaped fiber deposited with single-wall carbon-nanotubes was used as fiber-optic saturable absorber to achieve Q-switched Ho3+-doped fluoride fiber laser in all-fiber configuration with superior compactness and reliability. Stable Q-switched operation at 1192 nm was established at the pump power of 290 mW. When the pump power was increased to 1280 mW, Q-switched laser with a pulse duration of 1.1 mu s and pulse energy of 0.11 mu J at a repetition rate of 127 kHz was obtained. This all-fiber laser exhibits high stability with a radio-frequency signal-to-noise ratio > 50 dB.This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at [email protected]

A Porphyrin--Fullerene Dyad with a Supramolecular Double-Cable Structure as a Novel Electron Acceptor for Bulk Heterojunction Polymer Solar Cells

With a supramolecular “double-cable” structure in the solid state, a light harvesting porphyrin-fullerene dyad is demonstrated to be a promising candidate for new electron acceptors in high-performance bulk heterojunction (BHJ) polymer solar cells (PSCs). It has long-lived mobile carriers, a high short circuit current, and a large open circuit voltage

PCBM Disperse-Red Ester with Strong Visible-Light Absorption: Implication of Molecular Design and Morphological Control for Organic Solar Cells

A new dyad of fullerene/disperse-red, denoted as PCBDR, strongly absorbs visible light in the range of 400–600 nm. PCBDR showed advantages over PCBM in several aspects such as enhanced visible-light absorption, improved solubility, and the possibility to facilitate cascaded electron transfer. P3HT:PCBDR bulk heterojunction (BHJ) solar cells, nevertheless, so far have not outperformed P3HT:PCBM BHJ solar cells under similar conditions. Among factors that affect the efficiency of P3HT:PCBDR BHJ solar cells, the suppression of the interchain interaction of P3HT in the P3HT:PCBDR blend played a major role, presumably due to better interfacial miscibility between P3HT and PCBDR than that in blends of P3HT:PCBM. In contrast, benzoporphyrin (BP), due to its unique crystallinity, morphology, and nonsolubility, afforded a better control of the morphology and the interface of the p/n junctions. As a consequence, the performance of solar cells with BP/PCBDR as the active layer was comparable to that of BP/PCBM solar cells. These results suggest that a synergistic approach of synthetic design and morphological control in devices is critical to develop new electron acceptors for highly efficient organic/polymer solar cells