Publications by authors named "Jiangbin Zhang"

A photonic lantern is a low-loss device that connects a single multimode waveguide to multiple single-mode waveguides and can enhance the beam quality of a fiber laser by adaptively controlling the optical parameters (amplitude, phase, polarization) at the input. In this work, we combined the gains and losses of individual modes within the fiber amplifier and introduced a mode content parameter at the amplifier's output as an evaluation function to simulate mode control effects. Mode competition within the gain fiber can degrade the control effect of the fundamental mode and lead to it taking a longer time for the control to converge.

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Article Synopsis
  • Understanding hot carrier relaxation in metal nanostructures is crucial for their use in energy conversion and photocatalysis.
  • Research shows two distinct relaxation channels for hot carriers in gold plasmonic nanostructures, with faster relaxation from surface plasmon resonance (SPR) compared to interband transitions (IBTs).
  • The findings highlight different scattering mechanisms for hot carriers, with surface-mediated scattering occurring in large structures from SPR and bulk scattering for IBT-induced carriers, enhancing our grasp of hot carrier dynamics.
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The photodarkening (PD) and transverse mode instability (TMI) effects are two main factors limiting the power increase and long-term stability of high-power fiber lasers. A prolonged burn-in test for an all-fiber laser oscillator below the TMI threshold was carried out. We observed the PD-induced TMI effects, which manifested as a sudden decrease in the output power due to higher-order mode leakage.

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Laser dazzling on complementary metal oxide semiconductor (CMOS) image sensors is an effective method in optoelectronic countermeasures. However, previous research mainly focused on the laser dazzling under far fields, with limited studies on situations that the far-field conditions were not satisfied. In this paper, we established a Fresnel diffraction model of laser dazzling on a CMOS by combining experiments and simulations.

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Disordered polymer chain entanglements within all-polymer blends limit the formation of optimal donor-acceptor phase separation. Therefore, developing effective methods to regulate morphology evolution is crucial for achieving optimal morphological features in all-polymer organic solar cells (APSCs). In this study, two isomers, 4,5-difluorobenzo-c-1,2,5-thiadiazole (SF-1) and 5,6-difluorobenzo-c-1,2,5-thiadiazole (SF-2), were designed as solid additives based on the widely-used electron-deficient benzothiadiazole unit in nonfullerene acceptors.

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We carry out a detailed investigation of TMI mitigation by pump modulation based on multiple current waveforms in a fiber laser oscillator. Compared with continuous wave (CW), the modulation of various waveforms, including sinusoidal wave, triangular wave, and pulse wave with a duty cycle of 50% and 60%, can increase the TMI threshold. The average output power of a stabilized beam is boosted via the adjustment of phase difference between the signal channels.

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The demand for both strength and toughness is perpetual in fiber-reinforced composites. Unfortunately, both properties are often mutually exclusive. As the mechanical properties of the composites are highly dependent on their interfacial properties, engineering interfaces between the fiber and matrix would be vital to overcome the conflict between strength and toughness.

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We report on the generation of single transverse mode output in large-mode-area fiber with a core diameter of 50 µm using a 3×1 photonic-lantern-based adaptive spatial mode control system. We have designed and fabricated the photonic lantern composed of a single mode fibers bundle taper region and a multi-segment multimode fiber splicing region. From simulation and experiments, we demonstrate that the quality of the output beam is significantly influenced by the size of the fibers bundle's waist and the segmented splicing scheme of the multimode fiber.

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Boron-nitrogen substitutions in polycyclic aromatic hydrocarbons (PAHs) have a strong impact on the optical properties of the molecules due to a significantly more heterogeneous electron distribution. However, besides these single-molecule properties, the observed optical properties of PAHs critically depend on the degree of intermolecular interactions such as π-π-stacking, dipolar interactions, or the formation of dimers in the excited state. Pyrene is the most prominent example showing the latter as it exhibits a broadened and strongly bathochromically shifted emission band at high concentrations in solution compared to the respective monomers.

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Exploration of upconversion luminescence from lanthanide emitters through energy migration has profound implications for fundamental research and technology development. However, energy migration-mediated upconversion requires stringent experimental conditions, such as high power excitation and special migratory ions in the host lattice, imposing selection constraints on lanthanide emitters. Here we demonstrate photon upconversion of diverse lanthanide emitters by harnessing triplet exciton-mediated energy relay.

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The generation, control and transfer of triplet excitons in molecular and hybrid systems is of great interest owing to their long lifetime and diffusion length in both solid-state and solution phase systems, and to their applications in light emission, optoelectronics, photon frequency conversion and photocatalysis. Molecular triplet excitons (bound electron-hole pairs) are 'dark states' because of the forbidden nature of the direct optical transition between the spin-zero ground state and the spin-one triplet levels. Hence, triplet dynamics are conventionally controlled through heavy-metal-based spin-orbit coupling or tuning of the singlet-triplet energy splitting via molecular design.

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The doublet-spin nature of radical emitters is advantageous for applications in organic light-emitting diodes, as it avoids the formation of triplet excitons that limit the electroluminescence efficiency of non-radical emitters. However, radicals generally show low optical absorption and photoluminescence yields. Here we explain the poor optical properties of radicals based on alternant hydrocarbons, and establish design rules to increase the absorption and luminescence yields for donor-acceptor-type radicals.

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Article Synopsis
  • Recent advancements in perovskite light-emitting diodes (PeLEDs) have revealed a need for improvements in both efficiency and stability, prompting the search for better strategies.
  • Researchers developed perovskite-molecule composite thin films that integrate high-quality perovskite nanocrystals within an electron-transport molecular matrix, achieving a peak external quantum efficiency of 17.3% and a half-lifetime of about 100 hours.
  • Additionally, the study found that the degradation mechanisms of the PeLEDs vary depending on whether they are operated at high or low driving voltages, providing insights for future development.
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Recent progress in organic photovoltaics (OPVs) has been enabled by optimization of the energetic driving force for charge separation, and thus maximization of open-circuit voltage, using non-fullerene acceptor (NFA) materials. In spite of this, the carrier dynamics and relative energies of the key states controlling the photophysics of these systems are still under debate. Herein, we report an in-depth ultrafast spectroscopic study of a representative OPV system based on a polymer donor PffBT4T-2OD and a small-molecule NFA EH-IDTBR.

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Semiconductor quantum dots (QDs) are among the most promising next-generation optoelectronic materials. QDs are generally obtained through either epitaxial or colloidal growth and carry the promise for solution-processed high-performance optoelectronic devices such as light-emitting diodes (LEDs), solar cells, etc. Herein, a straightforward approach to synthesize perovskite QDs and demonstrate their applications in efficient LEDs is reported.

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The open-circuit voltage of organic solar cells is usually lower than the values achieved in inorganic or perovskite photovoltaic devices with comparable bandgaps. Energy losses during charge separation at the donor-acceptor interface and non-radiative recombination are among the main causes of such voltage losses. Here we combine spectroscopic and quantum-chemistry approaches to identify key rules for minimizing voltage losses: (1) a low energy offset between donor and acceptor molecular states and (2) high photoluminescence yield of the low-gap material in the blend.

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Herein, we report on the charge dynamics of photovoltaic devices based on two novel small-molecule nonfullerene acceptors featuring a central ketone unit. Using ultrafast near-infrared spectroscopy with optical and photocurrent detection methods, we identify one of the key loss channels in the devices as geminate recombination (GR) of interfacial charge transfer states (CTSs). We find that the magnitude of GR is highly sensitive to the choice of solvent and annealing conditions.

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Organic solar cell optimization requires careful balancing of current-voltage output of the materials system. Here, such optimization using ultrafast spectroscopy as a tool to optimize the material bandgap without altering ultrafast photophysics is reported. A new acceptor-donor-acceptor (A-D-A)-type small-molecule acceptor NCBDT is designed by modification of the D and A units of NFBDT.

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In solar energy harvesting devices based on molecular semiconductors, such as organic photovoltaics (OPVs) and artificial photosynthetic systems, Frenkel excitons must be dissociated via charge transfer at heterojunctions to yield free charges. What controls the rate and efficiency of charge transfer and charge separation is an important question, as it determines the overall power conversion efficiency (PCE) of these systems. In bulk heterojunctions between polymer donor and fullerene acceptors, which provide a model system to understand the fundamental dynamics of electron transfer in molecular systems, it has been established that the first step of photoinduced electron transfer can be fast, of order 100 fs.

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ZnO nanocrystals with a particle size of 20-30 nm have been synthesised for the first time using a template-free method. Chalcopyrite Cu0.28In1.

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CuIn(0.7)Ga(0.3)S2 quantum dots (QDs) with particle size of 2-5 nm were directly synthesised by a vacuum one-pot-nanocasting process and homogeneously anchored on TiO2 nanocrystals (<50 nm) for the first time.

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