Wastewater Treatment Using High-Performance In Situ Formed Double-Heterojunction Janus Photocatalyst Microparticles Shaped via a Microfluidic Device.

In this work, a heterogeneous photocatalysis system is fabricated for treating wastewater containing organic dyes and pharmaceutical substances. Double-heterojunction Janus photocatalysts are formed on the surface of size-tunable polydimethylsiloxane (PDMS) microparticles shaped via simple and low-cost coflow microfluidic devices. Ag0/Ag0-TiO2/TiO2 Janus-like photocatalysts are synthesized on the surface of porous PDMS microparticles as the support in which the metal-semiconductor heterojunction of Ag0/Ag0-TiO2 and the second heterojunction of Ag0-TiO2/TiO2 are created in situ, leading to the formation of Ag0/Ag0-TiO2/TiO2@PDMS photocatalysis systems. To form the heterojunctions on the PDMS surface, the polymer chain etching method is employed as a desired strategy to have half of the TiO2 nanoparticles on the surface of microparticles, which are treated by a Ag source. Using salt additives and the etching method, PDMS microparticles are made porous, providing more surface area for photoreactions. Surprisingly, the highest decomposition efficiencies of 94.4 and 91.1% are achieved for rhodamine B(RhB) and tetracycline (TC), respectively, under visible light for 60 min pH 11, a light source at a distance of 2 cm, 5 mM AgNO3, 10 wt % TiO2, 7 wt % NaCl, and 20 gm/L photocatalyst, which are conditions that result in the best performance for RhB degradation. Regarding the stability of the photocatalysts, no significant change is observed in the performance after five cycles.

Enhancing the efficiency and stability of perovskite solar cells based on moisture-resistant dopant free hole transport materials by using a 2D-BA2PbI4 interfacial layer.

In this work, the photovoltaic performance and stability of perovskite solar cells (PSCs) based on a dopant-free hole transport layer (HTL) are efficiently improved by inserting a two-dimensional (2D) interfacial layer. The benzyl ammonium lead iodide (BA2PbI4) 2D perovskite is used as an interfacial layer between the 3D CH3NH3PbI3 perovskite and two moisture-resistant dopant-free HTLs including poly[[2,3-bis(3-octyloxyphenyl)-5,8-quinoxalinediyl]-2,5-thiophenediyl] (TQ1) and poly(3-hexylthiophene) (P3HT). TQ1 with a facile synthesis procedure has a higher moisture resistivity compared to P3HT which can improve the stability of PSCs. The 2D BA2PbI4 perovskite with a less-volatile bulkier organic cation efficiently passivates the defects at the perovskite/HTL interface, leading to 11.95% and 15.04% efficiency for the modified TQ1 and P3HT based cells, respectively. For a better understanding, the structural, optical, and electrical properties of PSCs comprising P3HT and TQ1 HTLs with and without interface modification are studied. The interface modified PSCs show slower open-circuit voltage decay and longer carrier lifetimes compared to unmodified cells. In addition, impedance spectroscopy reveals lower charge transport resistance and higher recombination resistance for the modified devices, which could be associated with the modification of the interface between the 3D CH3NH3PbI3 perovskite and HTL caused by the 2D interfacial layer. Also after aging under ambient conditions for about 800 hours, the modified PCSs retain more than 80% of their initial PCEs. These results give us the hope of achieving simpler, cheaper, and more stable PSCs with dopant-free HTLs through 2D interfacial layers, which have great potential for commercialization.

High-Performance Solar Steam Generator Using Low-Cost Biomass Waste Photothermal Material and Engineering of the Structure.

In this work, high-performance, low-cost, environmentally friendly multilayered solar steam generation systems are fabricated by engineering the structure and using a biomass photothermal material. Remarkably, the biomass photothermal material is extracted from the pyrolysis waste of linseed (flax) grains. The introduced system desalinates water using solar energy as the renewable source of energy, and its light absorber is from the waste of a renewable source. The biomass waste powder possesses a mesoporous structure, providing high light absorption through photon scattering and its high surface area. Moreover, to harvest the incident light efficiently and manage the thermal energy generated, devices including light absorbers with cone and cubic configurations and different water manager layers are fabricated and compared to each other. To confirm the high performance of the introduced photothermal material, different systems comprising graphite, graphene oxide, and carbon nanotube light absorbers are also fabricated. Using a biomass light absorber combined with harvesting of the light in different directions (cone configuration), the system with a water evaporation rate of 1.59 kg/m2h corresponding to an efficiency of 92.9% is achieved. Furthermore, by depositing a thin layer of the transparent thermal superinsulator silica aerogel on the light absorber layer, the generated heat is localized and the heat losses are prevented, leading to a 7.5% enhancement of the water evaporation rate of the biomass system. The eco-friendly biomass-based system shows no significant change in its performance through operation for 40 desalination cycles of Persian Gulf water.

Prolonged Lifetime of Perovskite Solar Cells Using a Moisture-Blocked and Temperature-Controlled Encapsulation System Comprising a Phase Change Material as a Cooling Agent.

Although the power conversion efficiency of perovskite solar cells (PSCs) reached up to 25% that made them comparable to the commercial solar cells, they are facing issues toward commercialization, especially their short lifetime. Remarkably, the most important key factors that regulate the durability of the devices are moisture, light, and heat. In this work, prolonging the device lifetime is focused by designing a flexible moisture-blocked and temperature-controlled encapsulation system. In this regard, a thermally adjusted phase change material is embedded in a polymer encapsulation layer to avoid the moisture diffusion, rapid temperature fluctuation, and undesired crystalline phase change of the perovskite layer in the PSCs under the operation condition. As a result, a 2 year stable device is achieved, whereas the reference device loses more than 50% of its performance after 10 days. Surprisingly, the charge transport resistance and recombination rate show no significant change during 450 days of storage, which confirms no increase in the defect density.

High-Brightness Perovskite Light-Emitting Diodes Using a Printable Silver Microflake Contact.

Achieving efficient devices while maintaining a high fabrication yield is a key challenge in the fabrication of solution-processed, perovskite-based light-emitting diodes (PeLEDs). In this respect, pinholes in the solution-processed perovskite layers are a major obstacle. These are usually mitigated using organic electron-conducting planarization layers. However, these organic interlayers are unstable under applied bias in air and suffer from limited charge carrier mobility. In this work, we present a high brightness p-i-n PeLED based on a novel blade-coated silver microflake (SMF) rear electrode, which allows for a low-cost nanocrystalline ZnO inorganic electron-transporting layer to be used. This novel SMF contact is crucial for achieving high performance as it prevents the electrical shorting suffered when standard thermally evaporated silver rear contacts are used. The fabricated PeLEDs exhibit an excellent maximum luminance of 98,000 cd/m2, a maximum current efficiency of 22.3 cd/A, and a high external quantum efficiency of 4.6% under 5.9 V forward bias. The SMF rear contact can be printed and scaled at low cost to large areas and applied to flexible devices.

High Power UV-Light Irradiation as a New Method for Defect Passivation in Degraded Perovskite Solar Cells to Recover and Enhance the Performance.

Although the power conversion efficiency (PCE) of perovskite solar cells (PSCs) reached up to 23%, their short lifetime and fast degradation still remain as the main challenges. In this work, a new facile optical method based on the high power UV-irradiation is presented for the recovery of the degraded PSCs. Addition to the full recovery of the performance, about 20% PCE enhancement and hystersis reduction are also achieved by UV-irradiation. UV-treatment causes modifications in both the bulk properties of the perovskite layer and the energy equilibrium at the interfaces. It is shown that UV-treatment effectively passivates the surface and grain boundaries defects in different types of the devices comprising normal and inverted configurations that is confirmed by the reduction of the density of defect states (DOS). It is proposed that UV-light passivates the shallow and deep defects by dissociation of adsorbed hydroxyl groups and water molecules during the device storage.

Enhancing Lifetime and Efficiency of Organic Solar Cell by Applying an In Situ Synthesized Low-Crystalline ZnO Layer.

By introducing an in situ synthesized low-crystalline ZnO (LC-ZnO) (amorphous) layer between the cathode and the active layer of PCPDTBT:CdSe solar cell {PCPDTBT: poly[2,6-(4,4-bis(2-ethylhexyl)-4H-cyclopenta [2,1-b:3,4-b']dithiophene)-alt-4,7(2,1,3-benzothiadiazole)]}, the device keeps more than 80 and 40 % of its initial lifetime after 180 and 360 days without any encapsulation, respectively. In this regard, 180 days is the highest lifetime achieved for polymer-based solar cells with direct configuration. In addition, the power conversion efficiency (PCE) is improved up to 70 % in the presence of the LC-ZnO interfacial layer. The LC-ZnO layer is synthesized during polymer annealing after solution-deposition of the precursor at a low temperature (140 °C) and a short time. Highly crystalline ZnO (HC-ZnO) nanoparticles are also synthesized and applied as an interfacial layer. The results show that the LC-ZnO is superior to the HC-ZnO in acting as cathode interfacial layer and moisture scavenger because of the high coverage and surface area provided by the in situ synthesis method.