This work aimed to prepare nanostructures of ZnO with various lasers, testing them as photocatalysts, and comparing their morphology and activity in the degradation of organic pollutants in aqueous media. ZnO nanospheres (ns-ZnO) and ZnO nanorods (ms-ZnO) were prepared via the laser ablation of a Zn metal plate in water using nanosecond- and millisecond-pulsed lasers, respectively. The obtained materials were characterized using a set of optical, structural, and surface-science techniques, such as UV-vis spectroscopy, X-ray diffraction (XRD), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). Under visible-light irradiation, both nanostructures were found to be catalytically active toward the oxidation of methylene blue, which was used as a model compound. The ZnO nanorods fabricated with the millisecond laser showed better photocatalytic performance than their spherically shaped counterparts obtained by means of the nanosecond laser, which could be assigned to a larger number of defects on the ms-ZnO surface.
In the design of electron-transport layers (ETLs) to enhance the efficiency of planar perovskite solar cells (PSCs), facile electron extraction and transport are important features. Here, we consider the effects of different titanium oxide (TiO2) polymorphs, anatase and brookite. We design and fabricate high-phase-purity, single-crystalline, highly conductive, and low-temperature (<180 °C)-processed brookite-based TiO2 heterophase junctions on fluorine-doped tin oxide (FTO) as the substrate. We test and compare single-phase anatase (A) and brookite (B) and heterophase anatase–brookite (AB) and brookite–anatase (BA) as ETLs in PSCs. The power-conversion efficiencies (PCEs) of PSCs with low-temperature-processed single-layer FTO-B as the ETL were as high as 14.92%, which is the highest reported efficiency of FTO-B-based single-layer PSC. This implies that FTO-B serves as an active phase and can be a potential candidate as an n-type ETL scaffold in planar PSCs. Moreover, the surface of highly crystalline brookite TiO2 exhibits a tendency toward interparticle necking, leading to the formation of compact scaffolds. Furthermore, PSCs with heterophase junction FTO-AB ETLs exhibited PCEs as high as 16.82%, which is superior to those of PSCs with single-phase anatase (FTO-A) and brookite (FTO-B) as the ETLs (13.86% and 14.92%, respectively). In addition, the PSCs with FTO-AB exhibited improved efficiency and decreased hysteresis compared with those with FTO-BA (13.45%) due to the suitable band alignment with the perovskite layer, which resulted in superior photogenerated charge-carrier extraction and reduced charge accumulation at the interface between the heterophase junction and perovskite. Thus, the present work presents an effective strategy by which to develop heterophase junction ETLs and manipulate the interfacial energy band to further improve the performance of planar PSCs and enable the clean and eco-friendly fabrication of low-cost mass production.
The present work reports on room-temperature ethanol sensing performance of ZnO nanospheres and nanorods prepared using pulsed laser ablation in water. Nanosecond and millisecond lasers were used to prepare ZnO nanomaterials with hexagonal wurtzite crystal structure. The two contrasting nanostructures were tested as gas sensors towards volatile compounds such as ethanol, ammonia, and acetone. At room temperature, devices based on both ZnO nanomaterials demonstrated selectivity for ethanol vapor. The sensitivity of nanospheres was somewhat higher compared to that of nanorods, with response values of ∼19 and ∼14, respectively, towards 250 ppm. Concentrations as low as 50 ppm could be easily detected.
Electron-transport layer (ETL)/perovskite interface modification plays a key task for producing efficient planar perovskite solar cells (PSCs). In this study, interfacial modification of compact TiO2 using novel, one-step hydrothermally synthesized single-crystalline anatase (AT) titania nanoparticles (TiO2 NPs) (average diameter = 6–10 nm) was applied as an ETL bilayer to enhance the efficient charge generation and extraction and eliminate the electron–hole recombination ratio. We report here an easy approach for enhancing the performance of planar PSCs by introducing a compact TiO2/AT TiO2 NPs bilayer through spray pyrolysis (SP) deposition and spin-coating (SC) techniques, respectively. The enhanced performance of the devices with an SP-TiO2/SC-AT TiO2 NPs bilayer facilitated more efficient electron transport, charge extraction, and low interfacial recombination. Ultimately, the best device had a 17.05% power conversion efficiency resulting from the significant decrease in J–V hysteresis, presenting almost a 12% performance improvement compared to the TiO2 only layer-based counterpart. Thus, the present study provides an important advance to the design of photovoltaic devices with respect to charge transport and electron–hole recombination.
The photovoltaic performance of perovskite solar cells (PSCs) can be improved by utilizing efficient front contact. However, it has always been a significant challenge for fabricating high-quality, scalable, controllable, and cost-effective front contact. This study proposes a realistic multi-layer front contact design to realize efficient single-junction PSCs and perovskite/perovskite tandem solar cells (TSCs). As a critical part of the front contact, we prepared a highly compact titanium oxide (TiO2) film by industrially viable Spray Pyrolysis Deposition (SPD), which acts as a potential electron transport layer (ETL) for the fabrication of PSCs. Optimization and reproducibility of the TiO2 ETL were discreetly investigated while fabricating a set of planar PSCs. As the front contact has a significant influence on the optoelectronic properties of PSCs, hence, we investigated the optics and electrical effects of PSCs by three-dimensional (3D) finite-difference time-domain (FDTD) and finite element method (FEM) rigorous simulations. The investigation allows us to compare experimental results with the outcome from simulations. Furthermore, an optimized single-junction PSC is designed to enhance the energy conversion efficiency (ECE) by > 30% compared to the planar reference PSC. Finally, the study has been progressed to the realization of all-perovskite TSC that can reach the ECE, exceeding 30%. Detailed guidance for the completion of high-performance PSCs is provided.
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