ABSTRACT
Improving solar energy collection in aquatic environments would allow for superior environmental monitoring and remote sensing, but the identification of optimal photovoltaic technologies for such applications is challenging as evaluation requires either field deployment or access to large water tanks. Here, we present a simple bench-top characterization technique that does not require direct access to water and therefore circumvents the need for field testing during initial trials of development. Employing LEDs to simulate underwater solar spectra at various depths, we compare Si and CdTe solar cells, two commercially available technologies, with GaInP cells, a technology with a wide bandgap close to ideal for underwater solar harvesting. We use this method to show that while Si cells outperform both CdTe and GaInP cells under terrestrial AM1.5G solar irradiance, CdTe and GaInP cells outperform Si cells at depths >2 m, with GaInP cells operating with underwater efficiencies approaching 54%.
ABSTRACT
Near-infrared photodetectors (NIR-PDs) are widely used in communications, biomedical imaging, and national defense. Here we report a new strategy to prepare a short wavelength light filter based NIR-PDs by introducing an interface layer between the perovskite layer and the polymer layer to achieve the selective passage of carriers. Through the synergistic effect of the perovskite and the interface layer, the short wavelength light component in the signal spectrum is effectively filtered out. The organic polymer layer with a bulk heterojunction structure is applied to realize the absorption and conversion of near-infrared light. The prepared device achieves a maximum external quantum efficiency of 83.7% without bias, a high specific detectivity of 1.52 × 1013 Jones, an NIR responsivity of 0.577A/W, and a short response time of 1.73/0.97 µs within the detection range from 770 to 900 nm. All these properties show great advantages compared with other perovskite/polymer hybrid NIR photodetectors that have been reported. This innovative strategy provides a new way to prepare high-performance near-infrared photodetectors.
ABSTRACT
The storage of charges in organic light-emitting diodes (OLEDs) has drawn much attention for its damage to device performance as well as the loss to carriers. Thus, it is essential to address the issue and do further investigation. The traditional approach to storage analysis is mainly based on transient measurement since it is sensitive to transient instead of steady signal. In this paper, we proposed a new benchmark to investigate the single-layer OLEDs capable of stored charges with poly (methyl methacrylate) (PMMA), which is just based on electrical and optical characteristics. Since the stored charges contribute both to luminance and current of the devices with PMMA, the area between them can be taken as a benchmark and evaluated the storage of charges. In our experiment, the areas of 4 nm, 6 nm, 8 nm, and 10 nm PMMA devices are 0.348, 0.554, 0.808, and 0.894, respectively, indicating a higher capability of storage in thicker PMMA. It is exactly in line with the results taken from transient electroluminescence (EL) measurement. Thus, this new benchmark is practical and provides a more accessible approach to investigate the storage of charges in OLEDs.
Subject(s)
Electricity , Light , Optical Phenomena , Polymethyl Methacrylate/chemistry , Semiconductors , Benchmarking , Equipment DesignABSTRACT
In this paper, capacitance/conductance-voltage characteristics (C/G-V) under illumination was achieved to investigate the dynamic mechanism of stored charges in OLEDs with a structure of ITO/ PEDOT:PSS/PMMA/Alq3/Al. For all devices, at least two peaks presented in the optical capacitance-voltage curve. Compared to curves of devices under dark, the first peak increased remarkably with a deviation to Vbi, which can be explained in the form of stored charges combined with the optical conductance characteristics. It was also found that a great decrease in capacitance is followed by the collapse of the first peak with PMMA thickness increased. It can account for the presence of interfacial charges, which is proved further by the conductance curves. To the device with 10 nm PMMA, a third peak took place in optical capacitance and it was due to the storage of electrons by PMMA. Also, the first capacitance peak enhanced approximate linearly as the illumination power increased, which can verify the contribution of the stored charges. Additionally, it shows the potential for the stored charges in optical detections.
Subject(s)
Electric Capacitance , Light , Lighting , SemiconductorsABSTRACT
The power conversion efficiencies (PCEs) of potential polymer solar cells have been shown to rapidly exceed 15%. However, these high-performance devices are based on halogenated solvents that pose a significant hazard to the atmospheric environment and human beings. The use of nonhalogenated solvents makes the device less efficient because of its solubility issues. In this work, we report high-efficiency devices utilizing PffBT4T-2OD and [6,6]-phenyl C71 butyric acid methyl ester system from nonhalogenated solvents such as o-xylene ( o-XY) and 1-methylnaphthalene (Me) hydrocarbon solvent. When Me was used as the additive, the PCE of prepared devices improved from 1.83 to 10.13%, which is rather higher than that of the devices processed with traditional solvents combined with chlorobenzene and 1,8-diiodooctane (8.18%). Both atomic force microscopy and transmission electron microscopy confirmed that after nonhalogen solvents are treated, a more finely phase-separated dense morphology of active layers than after halogen solvents. At the same time, grazing incident wide-angle X-ray scattering patterns show that the combination of nonhalogenated solvents o-XY and Me ingeniously formed an ordered crystal and π-π stacking. Also, the stability of devices prepared from nonhalogenated solvents was significantly better than that of halogenated solvents under continuous illumination in the air without encapsulation.
ABSTRACT
The grain size of perovskite films is a key factor to optimize the performance of perovskite photovoltaic devices. Herein, a new route is developed in this paper to prepare CH3NH3PbI3 (MAPbI3) films with a better morphology and crystallization. This method includes the spin coating deposition of perovskite films with a precursor solution of PbI2 and CH3NH3I at the molar ratio 1 : 1 and thermal annealing (TA). The thermal annealing is conducted with a thermal-induced process to realize grain growth with solvent evaporation. In addition, a mixed solvent vapor treatment in acetic acid with chlorobenzene (HAc/CB) improves the morphology and crystallization of films further. As a result, the photovoltaic device based on the perovskite film treated by mixed HAc/CB solvent exhibits the best efficiency of 13.15% in comparison to the control device with 11.44% under AM 1.5G irradiation (100 mW cm-2).
