The investigation of the unseen interrelationship of grain size, ionic defects, device physics and performance of perovskite solar cells

Controlling the phenomenological morphology effects on the performance of the perovskite solar cell (PSC) is a continuing concern due to its photo-physical complexity and the existing contrary reports. Distinguishing the effect of the formed electron and hole traps in the bulk and at surface/interfaces of the perovskite layer from their impact on the performance of the device can be beneficial in optimizing fabrication methods. Here, the transient AC and steady state DC measurements, and morphology characterizations confirm the variation of performance parameters with respect to grain boundaries growth. The device physics is uncovered with respect to the grain size (GS) of the perovskite layer employing the theoretical drift-diffusion framework incorporating the electronic and ionic contributions. The increase of open circuit voltage (V-oc) for devices with large GS can be associated to the density of defect states. The findings here suggest a more pronounced role of interfaces in efficiency enhancement of the PSCs with the emphasis on the impact of the hole transport layer (HTL)/perovskite layer interface which is also found to be accountable to the difference between the device internal voltage and the terminal voltage and minimizing this difference can lead to an enhancement of approximately 100 mV in V-oc. Additionally, the electron traps in the bulk of the perovskite layer play a distinguishable role in the reduction of V-oc for the device with the smallest GS. The ionic defect density is also estimated. Considering our results and previous reports, the performance of the PSC is remarkably dependent on the method of fabrication and the associated perovskite conversion mechanism, and not necessarily on GS. The results are expected to deliver important guidelines for the development of more efficient PSCs by further enhancement of the V-oc towards its thermodynamic limit of 1.32V, via creating optimal interfaces

ZnO-SrAl2O4:Eu Nanocomposite-Based Optical Sensors for Luminescence Thermometry

Conventional thermometers fail to operate in a variety of medical procedures due to the harsh and sensitive environments required for such applications, and therefore, the development of optical fiber thermometers has gained significant attention. In this study, a ZnO-SrAl2O4:Eu (ZnO-SAO:Eu) nanocomposite has been synthesized by using a CO2 laser, which showed enhanced optical properties and a dynamic range in comparison with the crystalline ones. XRD, EDAX, SEM, and PL spectroscopy investigated the crystalline and optical properties of precursors, and the final nanostructure, and the findings were in agreement with references. Further analysis of the PL spectra in a 0-100 degrees C range suggests that the optical properties of the ZnO-SAO:Eu nanocomposite show a linear behavior toward temperature alterations. Considering this inter-relation and measuring the decay time for various frequencies helped us calibrate the temperature based on phase angle shift alterations. The curve obtained at 30 Hz frequency exhibits the highest linearity and accuracy (0.33%) due to its relatively high phase shift (60 degrees C) in the studied temperature range. The fabricated sensor exhibited great sensitivity and repeatability while maintaining an unprecedented structure. Finally, the thermometer's applicability for future industries was tested by measuring the interior temperature of a dead muscle tissue as it was being heated by a diode laser and it was accompanied by remarkable results. This achievement could make this device a promising addition to the drug delivery science and industry as it could aid the study and optimization of medications that increase the targeted tissues temperature and therefore can be employed in treating tumors that are formed in organic tissues