Search Results (58)

Owing to the intramolecular push-pull electron effect between the electron donor (D) unit and electron acceptor (A) unit, the D-A type based polymer donors display outstanding device performance. However, the imperfect energy levels lead to the D-A-type-based polymer device exhibiting high voltage loss. In this study, an A1-A2-type copolymer M1 was developed with 1,3-bis(2-ethylhexyl)-5,7-di(thiophen-2-yl)benzo[1,2-c:4,5-c’]dithiophene-4,8-dione (BDD) as the A1 unit and dithieno[3′,2′:3,4;2″,3″:5,6]benzo[1,2-c][1,2,5]thiadiazole (DTBT) as the A2 unit. Compared with D-A-type-based polymer donor PM6, the A1-A2 type based M1 possesses lower energy levels, broader absorption, and stronger crystallinity. After introducing M1 to the PM6:L8-BO-based system as the guest material, the ternary blend films exhibited exceptional face-on molecular orientation and favorable active-layer morphology, which promotes exciton dissociation and suppresses charge recombination. Consequently, the PM6:M1(5%):L8-BO-based ternary device exhibited an impressive power conversion efficiency (PCE) of 19.70% with simultaneously enhanced photostability, which is superior to the PM6:L8-BO-based binary system. Our work offers an efficient approach to developing high-performance ternary devices by introducing a novel A1-A2 type polymer donors as the guest material. Full article

We study the optical susceptibility of a CdSe-based semiconductor quantum dot with a cascade exciton–biexciton configuration, which is coupled via the Coulomb interaction to a gold spheroidal nanoparticle, in the presence of a nearly resonant strong pump field and a weak probe field. We take both fields’ polarization vectors to be parallel to the interparticle axis, derive the equations of motion for the density matrix, and proceed with a perturbative expansion approach to calculate the components of the density matrix associated with the effective optical susceptibility, which describes processes to first order in the probe field and to all orders in the pump field. We present spectra of the effective susceptibility and examine their dependence on the metal nanoparticle’s geometric characteristics for various interparticle distances and pump field detunings, under both one- and two-photon resonance conditions. The role of the biexciton energy shift is also studied. Lastly, we introduce a dressed-state picture to elucidate the origin of the observed spectral features. Our calculations reveal that reducing the interparticle distance and increasing the metal nanoparticle aspect ratio enhance the exciton–plasmon coupling, leading to pronounced resonance splitting, spectral shifts, and broadened gain regions. Prolate nanoparticles aligned with the field polarization exhibit the strongest coupling and the widest gain bandwidth, whereas oblate geometries produce nearly overlapping resonances. Under exact resonance, the probe displays zero absorption with a negative dispersion slope, indicating slow-light behavior. These results demonstrate the tunability of hybrid CdSe-Au nanostructures for designing nanoscale optimal amplifiers, modulators, and sensors. Full article

We present a systematic study of the fundamental optical properties of indium selenide (InSe) single crystals over a temperature range of 17 K to 300 K. The high structural quality of the β-polytype crystals was confirmed through X-ray diffraction, Raman spectroscopy, and high-resolution transmission electron microscopy, demonstrating excellent crystallinity and a nearly stoichiometric In:Se ratio. The temperature-dependent absorption and photoluminescence (PL) spectra are characterized by a prominent free exciton (FX) resonance. At 17 K, the photoluminescence spectrum exhibits a distinct fine-structure splitting of the Wannier–Mott exciton, yielding a triplet state at 1.333 eV and a singlet state at 1.336 eV. Additionally, a biexciton (XX) is localized at an energy of 1.322 eV as confirmed by the nonlinear dependence of intensity on excitation power density. At low temperatures, the absorption spectrum exhibits the free exciton ground state (n = 1) at 1.338 eV together with the first excited state (n = 2) at 1.350 eV. We systematically tracked and analyzed the temperature evolution of these quasiparticle energies. These findings enhance our understanding of the intrinsic many-body interactions in high-quality InSe, providing essential parameters for advancing its applications in innovative optoelectronic and quantum light-emitting devices. Full article

Developing detectors to enhance the timing resolution of positron emission tomography scanners can help reduce radioactive doses absorbed by patients and improve spatial resolution in medical imaging. Time resolution may be enhanced in heterostructures comprising a heavy scintillator for attenuation of 511 keV γ-quanta, as well as a fast scintillator converting recoiled electrons from the heavy scintillator to prompt light photons. In this study, ZnO films as fast scintillators with different thicknesses were obtained on substrates of a heavy bismuth germanate (Bi₄Ge₃O₁₂, BGO) scintillator using several film preparation techniques, such as spray-coating, drop-casting, and spin-coating. The design of heterostructures combined the key advantage of a low-cost film preparation technique with environmentally friendly and available precursors. This work proposes synthesis methods of highly nanocrystalline ZnO films on BGO, where a film thickness ranges from 6 to 18 μm. All ZnO studied films exhibit exciton luminescence peaked in UV (353 nm) and defect luminescence in the green (657 nm) range under 325 nm excitation. The best coincidence time resolution of 158 ± 8 ps was obtained with BGO@ZnO heterostructures fabricated by the spray-coating. The proposed approach allowed obtaining BGO@ZnO heterostructures for potential use as ultrafast scintillation detectors. Full article

This study of the BaSO₄-Bi phosphor has revealed that the accumulated energy after external optical excitation exhibits specific characteristics. During irradiation with photon energy exceeding the bandgap, in addition to the intrinsic ultraviolet emission of the Bi³⁺ ion, several recombination emissions and emission from the Bi²⁺ ion are observed. At 80 K, the recombination luminescence states and Bi²⁺ ion emission form combined electronic states. Upon heating of the BaSO₄-Bi phosphor, these combined electronic states decay into recombination emissions at 2.34 eV, 2.4 eV, 3.1 eV, and 2.7 eV, as well as Bi²⁺ ion emission at 1.97 eV. It is assumed that the 2.34 eV, 2.4 eV, and 3.1 eV emissions are associated with the recombination of electrons released from ionized ${SO}_4^{3-}$ electron trapping centers with nonequivalently localized holes in the host lattice. The 2.7 eV emission is attributed to the decay of an exciton formed by electron–hole recombination near a Bi³⁺ ion. Full article

Efficient photocatalysts based on composite materials are essential for addressing environmental pollution and enhancing water purification. This study presents a novel BiOI/V₂O₅ nanocomposite (BVNC) with a flower-like layered structure, synthesized via a low-temperature solvothermal process followed by high-pressure annealing for visible light (VL)-driven dye degradation and antibacterial activities. Compared to individual BiOI nanoparticles (BOINP) and V₂O₅ nanoparticles (VONP), under VL, the BVNC demonstrated significantly enhanced photocatalytic and antibacterial activity. The best-performing BVNC achieved a remarkable methylene blue degradation efficiency of 95.7% within 140 min, with a rate constant value 439% and 430% of those of BOINP and VONP, respectively. Additionally, BVNC exhibited high photocatalytic efficiencies for rhodamine 6G (94.0%), methyl orange (90.4%), and bisphenol A (69.5%) over 160 min, highlighting the superior performance of the composite materials for cationic and anionic dyes. Furthermore, BVNC established outstanding antibacterial capability against Staphylococcus aureus and Escherichia coli, demonstrating zones of inhibition of 12.24 and 11.62 mm, respectively. The improved catalytic and antibacterial capability is ascribed to the presence of a robust p-n heterojunction between BOINP and VONP, which broadens the photo-absorption range, reduces bandgap energy, and facilitates the significant separation of excitons and faster release of reactive oxygen species. Full article

Exciton generation and separation play an important role in the photoelectric properties and the luminescence performance of materials. In order to tailor the defects and grain boundaries and improve the exciton separation and light harvesting of the graphitic carbon nitride (g-C₃N₄) nanosheets, a C₃N₄/bismuth sulfide (Bi₂S₃) nanocomposite was synthesized. The photoelectric properties of the 405, 532, 650, 780, 808, 980 and 1064 nm light sources were studied using Au electrodes and graphite electrodes with 4B and 5B pencil drawings. The results indicate that the C₃N₄/Bi₂S₃ nanocomposite exhibited photocurrent switching behavior in the broadband light spectrum range. It is noted that even with zero bias applied, a good photoelectric signal was still measured. The resulting nanocomposite exhibited good photophysical stability. Physical mechanisms are discussed herein. It is suggested that the interfacial interaction of C₃N₄ and Bi₂S₃ in the nanocomposite creates a strong built-in electric field, which accelerates the separation of excitons. Therefore, as a dynamic process of photoexcitation, fluorescence, the photoelectric effect, and scattering are three main competing processes; the separation of excitons and the extraction of free photogenerated charge can be used as a reference for the fluorescent materials or other photoelectric materials studies as photophysical properties. This study also serves as an important reference for the design, defect and grain boundary modulation or interdisciplinary application of functional nanocomposites, especially for the bandgap modulation and suppression of photogenerated carrier recombination. Full article

Perovskite materials, as emerging semiconductors, have attracted significant attention for their exceptional optoelectronic properties, tunable bandgaps, ease of fabrication, and cost-effectiveness, making them promising candidates for next-generation optoelectronic devices. The all-inorganic perovskite Cs₂AgBiBr₆ distinguishes itself from other perovskite materials due to its remarkable optical absorption and emission properties, excellent stability, prolonged carrier recombination lifetime, and nontoxic characteristics. However, a deeper understanding of its unique luminescent properties and a further optimization of its structure and performance are still necessary. This study systematically investigates the optimization of Cs₂AgBiBr₆ double perovskite films through A-site Na⁺ doping. At an optimal Na⁺ doping concentration of 3.5% (Na_0.07Cs_1.93AgBiBr₆), the film shows 1.4 times and 2.7 times enhancement in light absorption and photoluminescence intensity, compared to the undoped film. Low-temperature spectroscopy measurements indicate that Na_0.07Cs_1.93AgBiBr₆ exhibits higher exciton binding energy and phonon energy. Based on Na_0.07Cs_1.93AgBiBr₆, the photodetectors demonstrate significant performance improvements, with a high photocurrent response of 10⁻² A, a photo-to-dark current ratio (PDCR) of 7.57 × 10⁴, a responsivity (R) of 16.23 A/W, a detectivity (D*) of 2.92 × 10¹² Jones, a linear dynamic range (LDR) of 98.75 dB, and a fast response time of 943 ms. This work provides a promising strategy for optimizing all-inorganic perovskite materials through doping and offers guidance for enhancing high-performance photodetectors. Full article

Spherical quantum wells (SQWs) have proven to be excellent materials for suppressing Auger recombination due to their expanded confinement volume. However, research on the factors and mechanisms of their high-intensity optical properties, such as multiexciton properties and third-order optical nonlinearities, remains incomplete, limiting further optimization of these properties. Here, a series of CdS/CdSe (xML)/CdS SQWs with varying CdSe layer thicknesses were prepared. The modulation effects of CdSe shell variations on the PL properties, defect distribution, biexciton binding energy, and third-order optical nonlinearities of the SQWs were investigated, and their impact on the material’s multiexciton properties was further analyzed. Results showed that the typical CdS/CdSe(3ML)/CdS sample exhibited a large volume-normalized two-photon absorption cross-section (18.17 × 10² GM/nm³) and favorable biexciton characteristics. Optical amplification was observed at 12.4 μJ/cm² and 1.02 mJ/cm² under one-photon (400 nm) and two-photon (800 nm) excitation, respectively. Furthermore, different amplified spontaneous emission spectra were observed for the first time under one/two-photon excitation. This phenomenon was attributed to thermal effects overcoming the biexciton binding energy. This study provides valuable insights for further optimizing multiexciton gain characteristics in SQWs and developing optical gain applications. Full article

Singlet fission (SF), as an effective way to break through the Shockley–Queisser limit, can dramatically improve energy conversion efficiency in solar cell areas. The formation, separation, and relaxation of triplet-pair excitons directly affect the triplet yield, especially triplet-pair separation; thus, how to enhance the triplet-pair separation rate becomes one of the key points to improve SF efficiency; the decay mechanism where the singlet state is converted into two triplet states is significant for the study of the SF mechanism. Herein, we employ ultrafast transient absorption spectroscopy to study the singlet-fission process of nano-amorphous 6, 13-bis(triisopropylsilylethynyl)-Pentacene (TIPS-pentacene) films in a diamond anvil cell (DAC). A kinetics model related to the structural geometric details, as well as an evaluation of the pressure manipulation impacts, is demonstrated based on the experimental results. The results indicate that pressure manipulation enhanced the triplet-pair separation rates of SF-based materials according to their structural micro-environmental improvement when compressed in DAC, while the triplet-exciton transportation lifetime is prolonged. This work shows that pressure may effectively optimize the structural disorder of SF materials, which were found to improve triplet-pair separation efficiency and potentially offer an effective way to further improve SF efficiency. Full article

Phototransistors are three-terminal photodetectors that usually have a higher photocurrent gain than photodiodes due to the amplification of the gate electrode. In this work, a broad spectral phototransistor based on copper phthalocyanine (CuPc) and a Cs₃Bi₂I₉ (CBI) heterojunction is fabricated by the full vacuum evaporation method. Due to the complementary UV–visible absorption of CuPc and CBI, the device exhibits superior performance under three different types of visible light illumination. The experimental results show that the structure of the organic/perovskite heterojunction active layer has the characteristics of good compatibility and a simple process. Meanwhile, by utilizing the superior light-absorption characteristics of perovskite materials and the strong exciton dissociation efficiency of a hetero-type heterojunction interface, the CuPc/CBI-PT exhibits a higher photoresponsivity, photosensitivity, specific detection rate, and lower operating voltage than the CuPc reference device. The stability test shows that the CuPc/CBI-PT can still obtain a 0.73 A/W photoresponsivity under 660 nm light illumination after being stored in the air for 360 h without any packaging. This indicates that the organic/perovskite heterojunction PT may be a good choice for the preparation of high-performance photodetectors. Full article

The achievement of size uniformity and monodispersity in perovskite quantum dots (QDs) requires the implementation of precise temperature control and the establishment of optimal reaction conditions. Nevertheless, the accurate control of a range of reaction variables represents a considerable challenge. This study addresses the aforementioned challenge by employing manganese (Mn) doping to achieve size uniformity in CsPbBr₃ perovskite QDs without the necessity for the precise control of the reaction conditions. By optimizing the Mn:Pb ratio, it is possible to successfully dope CsPbBr₃ QDs with the appropriate concentrations of Mn²⁺ and achieve a uniform size distribution. The spectroscopic measurements on single QDs indicate that the appropriate Mn²⁺ concentrations can result in a narrower spectral linewidth, a longer photoluminescence (PL) lifetime, and a reduced biexciton Auger recombination rate, thus positively affecting the PL properties. This study not only simplifies the size control of perovskite QDs but also demonstrates the potential of Mn-doped CsPbBr₃ QDs for narrow-linewidth light-emitting diode applications. Full article

Strain-free GaAs cone-shell quantum dots have a unique shape, which allows a wide tunability of the charge-carrier probability densities by external electric and magnetic fields. Here, the influence of a lateral electric field on the optical emission is studied experimentally using simulations. The simulations predict that the electron and hole form a lateral dipole when subjected to a lateral electric field. To evaluate this prediction experimentally, we integrate the dots in a lateral gate geometry and measure the Stark-shift of the exciton energy, the exciton intensity, the radiative lifetime, and the fine-structure splitting (FSS) using single-dot photoluminescence spectroscopy. The respective gate voltage dependencies show nontrivial trends with three pronounced regimes. We assume that the respective dominant processes are charge-carrier deformation at a low gate voltage U, a vertical charge-carrier shift at medium U, and a lateral charge-carrier polarization at high U. The lateral polarization forms a dipole, which can either enhance or compensate the intrinsic FSS induced by the QD shape anisotropy, dependent on the in-plane orientation of the electric field. Furthermore, the data show that the biexciton peak can be suppressed by a lateral gate voltage, and we assume the presence of an additional vertical electric field induced by surface charges. Full article

Monolayer two-dimensional transition metal dichalcogenide (TMD)-based materials have become one of the ideal platforms for the study of multibody interactions due to their rich excitonic complexes. The coupling between optical nanocavity and material has become an important means for manipulating the optical properties of materials, but there are few studies on the coupling of nanocavities and the multi-body effect in materials. In this study, we investigate the optical properties of silver nanodisk (Ag ND) arrays covering a monolayer WS₂. In the experimental sample, we observed a ~114.3-fold photoluminescence enhancement of charged biexciton in the heterostructure region, as compared to the monolayer WS₂ region, a value which is much higher than those for exciton (~2.2-fold) and trion (~16.4-fold), a finding which is attributed to the Fano resonant coupling between monolayer WS₂ and the Ag ND. By means of time-resolved spectroscopy, we studied the carrier dynamics in the hybrid system. Our findings reveal that resonant coupling promotes the formation and radiation recombination processes of the charged biexciton, significantly reducing the radiative recombination lifetime by ~15-fold, which is much higher than the measurement in exciton (~2-fold). Our results provide an opportunity to understand the multibody physics of coupling with nanocavities, which could facilitate the application of multi-body excitons in the fields of light-emitting devices and lasers, etc. Full article

Strong coupling of quantum states with electromagnetic modes of topological matter offer an interesting platform for the exploration of new physics and applications. In this work, we report a novel hybrid mode, a surface topological plexciton, arising from strong coupling between the surface topological plasmon mode of a ${\mathrm{Bi}}_2{\mathrm{Se}}_3$ topological insulator nanoparticle and the exciton of a two-level quantum emitter. We study the power absorption spectrum of the system by working within the dipole and rotating-wave approximations, using a density matrix approach for the emitter, and a classical dielectric-function approach for the topological-insulator nanoparticle. We show that a Rabi-type splitting can appear in the spectrum suggesting the presence of strong coupling. Furthermore, we study the dependence of the splitting on the separation of the two nanoparticles as well as the dipole moment of the quantum emitter. These results can be useful for exploring exotic phases of matter, furthering research in topological insulator plasmonics, as well as for applications in the far-infrared and quantum computing. Full article