Ag doped Sn3O4 nanostructure and immobilized on hyperbranched polypyrrole for visible light sensitized photocatalytic, antibacterial agent and microbial detection process.

Ag doped Sn3O4 Nanostructure and immobilized on hyperbranched polypyrrole is investigated in this project. The product was synthesized by the hydrothermal synthesis method. The surface and structural characteristics of the product was studied by different instrumental analysis. The fabricated nanocomposites was utilized as a nano photocatalyst in the removal of methylene blue dye. The crystallography results depicts the triclinic phase of Sn3O4 with the crystallite size 36.3 nm. The band gap of the Ag-Sn3O4/hyperbranched polypyrrole was found 1.50 eV from kubelka-munk measurements. The specific surface area was increased in the presence of the hyperbranched polypyrrole as compared to Ag-Sn3O4 samples. The photo-catalytic activity of composites was found 100.0% degradation of CR in 30 min under visible light irradiation. The catalytic kinetic was followed from the first kinetic model. Moreover, the Ag/Sn3O4/hyperbranched polypyrrole was applied as a bactericidal agent against Streptococcus pneumoniae, and Pseudomonas aeruginosa bacteria. Determination of Streptococcus pyogenes as a pathogenic bacteria was investigated by using aptamer/Ag/Sn3O4/hyperbranched polypyrrole in peroxidase activity. The detection limit of S. pyogenes was 71.0 CFU/mL by using the nano-aptamer.

Photoelectrochemical Water-Splitting Using CuO-Based Electrodes for Hydrogen Production: A Review.

The cost-effective, robust, and efficient electrocatalysts for photoelectrochemical (PEC) water-splitting has been extensively studied over the past decade to address a solution for the energy crisis. The interesting physicochemical properties of CuO have introduced this promising photocathodic material among the few photocatalysts with a narrow bandgap. This photocatalyst has a high activity for the PEC hydrogen evolution reaction (HER) under simulated sunlight irradiation. Here, the recent advancements of CuO-based photoelectrodes, including undoped CuO, doped CuO, and CuO composites, in the PEC water-splitting field, are comprehensively studied. Moreover, the synthesis methods, characterization, and fundamental factors of each classification are discussed in detail. Apart from the exclusive characteristics of CuO-based photoelectrodes, the PEC properties of CuO/2D materials, as groups of the growing nanocomposites in photocurrent-generating devices, are discussed in separate sections. Regarding the particular attention paid to the CuO heterostructure photocathodes, the PEC water splitting application is reviewed and the properties of each group such as electronic structures, defects, bandgap, and hierarchical structures are critically assessed.

Recent Advances in Plasmonic Perovskite Solar Cells.

Perovskite solar cells (PSCs) have emerged recently as promising candidates for next generation photovoltaics and have reached power conversion efficiencies of 25.2%. Among the various methods to advance solar cell technologies, the implementation of nanoparticles with plasmonic effects is an alternative way for photon and charge carrier management. Surface plasmons at the interfaces or surfaces of sophisticated metal nanostructures are able to interact with electromagnetic radiation. The properties of surface plasmons can be tuned specifically by controlling the shape, size, and dielectric environment of the metal nanostructures. Thus, incorporating metallic nanostructures in solar cells is reported as a possible strategy to explore the enhancement of energy conversion efficiency mainly in semi-transparent solar cells. One particularly interesting option is PSCs with plasmonic structures enable thinner photovoltaic absorber layers without compromising their thickness while maintaining a high light harvest. In this Review, the effects of plasmonic nanostructures in electron transport material, perovskite absorbers, the hole transport material, as well as enhancement of effective refractive index of the medium and the resulting solar cell performance are presented. Aside from providing general considerations and a review of plasmonic nanostructures, the current efforts to introduce these plasmonic structures into semi-transparent solar cells are outlined.

Nanoengineered Advanced Materials for Enabling Hydrogen Economy: Functionalized Graphene-Incorporated Cupric Oxide Catalyst for Efficient Solar Hydrogen Production.

Cupric oxide (CuO) is a promising candidate as a photocathode for visible-light-driven photo-electrochemical (PEC) water splitting. However, the stability of the CuO photocathode against photo-corrosion is crucial for developing CuO-based PEC cells. This study demonstrates a stable and efficient photocathode through the introduction of graphene into CuO film (CuO:G). The CuO:G composite electrodes are prepared using graphene-incorporated CuO sol-gel solution via spin-coating techniques. The graphene is modified with two different types of functional groups, such as amine (-NH2) and carboxylic acid (-COOH). The -COOH-functionalized graphene incorporation into CuO photocathode exhibits better stability and also improves the photocurrent generation compare to control CuO electrode. In addition, -COOH-functionalized graphene reduces the conversion of CuO phase into cuprous oxide (Cu2O) during photo-electrochemical reaction due to effective charge transfer and leads to a more stable photocathode. The reduction of CuO to Cu2O phase is significantly lesser in CuO:G-COOH as compared to CuO and CuO:G-NH2 photocathodes. The photocatalytic degradation of methylene blue (MB) by CuO, CuO:G-NH2 and CuO:G-COOH is also investigated. By integrating CuO:G-COOH photocathode with a sol-gel-deposited TiO2 protecting layer and Au-Pd nanostructure, stable and efficient photocathode are developed for solar hydrogen generation.

Integrating GeSn photodiode on a 200 mm Ge-on-insulator photonics platform with Ge CMOS devices for advanced OEIC operating at 2 µm band.

High-performance GeSn multiple-quantum-well (MQW) photodiode is demonstrated on a 200 mm Ge-on-insulator (GeOI) photonics platform for the first time. Both GeSn MQW active layer stack and Ge layer (top Ge layer of GeOI after bonding) were grown using a single epitaxy step on a standard (001)-oriented Si substrate (donor wafer) using a reduced pressure chemical vapor deposition (RPCVD). Direct wafer bonding and layer transfer technique were then employed to transfer the GeSn MQW device layers and Ge layer to a 200 mm SiO2-terminated Si handle substrate. The surface illuminated GeSn MQW photodiode realized on this platform exhibits an ultra-low leakage current density of 25 mA/cm2 at room temperature and an enhanced photo sensitivity at 2 µm of 30 mA/W as compared to a GeSn MQW photodiode on Si at 2 µm. The underlying GeOI platform enables monolithic integration of a complete suite of photonics devices operating at 2 µm band, including GeOI strip waveguides, grating couplers, micro-ring modulators, Mach-Zehnder interferometer modulators, etc. In addition, Ge CMOS circuits can also be realized on this common platform using a "photonic-first and electronic-last" processing approach. In this work, as prototype demonstration, both Ge p- and n-channel fin field-effect transistors (FinFETs) were realized on GeOI simultaneously with decent static electrical characteristics. Subthreshold swings of 150 and 99 mV/decade at |VD| = 0.1 V and drive currents of 91 and 10.3 µA/µm at |VG-VTH| = 1 V and |VD| = 0.75 V were achieved for p- and n-FinFETs, respectively. This works illustrates the potential of integrating GeSn (as photo detection material) on GeOI platform for Ge-based optoelectronics integrated circuits (OEICs) targeting communication applications at 2 µm band.

Visible Light Driven Heterojunction Photocatalyst of CuO-Cu2O Thin Films for Photocatalytic Degradation of Organic Pollutants.

A high recombination rate and low charge collection are the main limiting factors of copper oxides (cupric and cuprous oxide) for the photocatalytic degradation of organic pollutants. In this paper, a high performance copper oxide photocatalyst was developed by integrating cupric oxide (CuO) and cuprous oxide (Cu2O) thin films, which showed superior performance for the photocatalytic degradation of methylene blue (MB) compared to the control CuO and Cu2O photocatalyst. Our results show that a heterojunction photocatalyst of CuO-Cu2O thin films could significantly increase the charge collection, reduce the recombination rate, and improve the photocatalytic activity.

High-speed photo detection at two-micron-wavelength: technology enablement by GeSn/Ge multiple-quantum-well photodiode on 300 mm Si substrate.

We report high-speed photo detection at two-micron-wavelength achieved by a GeSn/Ge multiple-quantum-well (MQW) p-i-n photodiode, exhibiting a 3-dB bandwidth (f3-dB) above 10 GHz for the first time. The epitaxy of device layer stacks was performed on a standard (001)-oriented 300 mm Si substrate by using reduced pressure chemical vapor deposition (RPCVD). The results showed promise for large-scale manufacturing. To our knowledge, this is also the first photodiodes-on-Si with direct radio-frequency (RF) measurement to quantitatively confirm high-speed functionality with tens of GHz f3-dB at 2 µm, which is considered as a promising candidate for the next data communication window. This work illustrates the potential for using GeSn to extend the utility of Si photonics in 2 µm band integrated optical transceivers for communication applications.

Evaluation of Solar-Driven Photocatalytic Activity of Thermal Treated TiO2 under Various Atmospheres.

In this report, the photocatalytic activity of P25 has been explored and the influence of thermal treatment under various atmospheres (air, vacuum and hydrogen) were discussed. The samples' characteristics were disclosed by means of various instruments including X-ray diffraction (XRD), Electron paramagnetic resonance (EPR), X-ray photoelectron spectroscopy (XPS) and UV⁻vis. This study also accentuates various states of the oxygen vacancy density formed inside the samples as well as the colour turning observed in treated P25 under various atmospheres. Produced coloured TiO2 samples were then exploited for their photocatalytic capability concerning photodegradation of methylene blue (MB) using air mass (AM) 1.5 G solar light irradiation. Our findings revealed that exceptional photocatalytic activity of P25 is related to the thermal treatment. Neither oxygen vacancy formation nor photocatalytic activity enhancement was observed in the air-treated sample. H2-treated samples have shown better photoactivity which even could be further improved by optimizing treatment conditions to achieve the advantages of the positive role of oxygen vacancy (O-vacancy at higher concentration than optimum acts as electron trapping sites). The chemical structure and stability of the samples were also studied. There was no sign of deteriorating of O2-vacancies inside the samples after 6 months. High stability of thermal treated samples in terms of both long and short-term time intervals is another significant feature of the produced photocatalyst.

Preparation of a New Type of Black TiO2 under a Vacuum Atmosphere for Sunlight Photocatalysis.

Black TiO2 as a solar-driven photocatalyst has attracted enormous attention from scientists and engineers in water and wastewater treatment field. Most of the methods used for the preparation of black TiO2 are thermal treatment under a hydrogen atmosphere. Nevertheless, it is well known that working with hydrogen is not safe and needs special maintenance. Here, for the first time, we prepared black TiO2 by sintering P25 pellets at different temperatures (500-800 °C) under a vacuum atmosphere that showed the same performance with the prepared black TiO2 under a hydrogen atmosphere. The samples were characterized by X-ray diffraction, Raman spectra field emission scanning electron microscopy, transmission electron microscopy, electron paramagnetic resonance, X-ray photoelectron spectroscopy, and ultraviolet-visible deep resistivity sounding techniques. The differences between the formation of oxygen vacancy density and color turning in sintered powder and pellet were also studied. The results showed that the color of the P25 powder became darker after sintering but not completely turning to black, whereas the P25 pellets completely turned black after sintering. The resultant black TiO2 was used for the photocatalytic degradation of the acetaminophen (ACE) in aqueous solution under AM 1.5G solar light illumination; it was found that the P25 pellet sintered in 500 °C had the highest photocatalytic performance for ACE degradation under AM 1.5G solar light illumination. The photocatalytic activity of prepared black TiO2 under vacuum and hydrogen atmospheres was also compared together; the results showed that photocatalytic activities of both samples were so close together. The existence of the oxygen vacancy after 6 months and long and short-term stability (by application for photocatalytic degradation of ACE in an aqueous solution) of the black TiO2 pellets was also studied; the results showed that the TiO2 pellets in aqueous phase had acceptable stability.

GeSn lateral p-i-n photodetector on insulating substrate.

We report the first experimental demonstration of germanium-tin (GeSn) lateral p-i-n photodetector on a novel GeSn-on-insulator (GeSnOI) substrate. The GeSnOI is formed by direct wafer bonding and layer transfer technique, which is promising for large-scale integration of nano-electronics and photonics devices. The fabricated GeSnOI photodetector shows well-behaved diode characteristics with high Ion/Ioff ratio of ~4 orders of magnitude (at ± 1 V) at room temperature. A cutoff detection beyond 2 µm with photo responsivity (Rop) of 0.016 A/W was achieved at the wavelength (λ) of 2004 nm.

Stable and Efficient CuO Based Photocathode through Oxygen-Rich Composition and Au-Pd Nanostructure Incorporation for Solar-Hydrogen Production.

Enhancing stability against photocorrosion and improving photocurrent response are the main challenges toward the development of cupric oxide (CuO) based photocathodes for solar-driven hydrogen production. In this paper, stable and efficient CuO-photocathodes have been developed using in situ materials engineering and through gold-palladium (Au-Pd) nanoparticles deposition on the CuO surface. The CuO photocathode exhibits a photocurrent generation of ∼3 mA/cm2 at 0 V v/s RHE. Time-of-flight secondary ion mass spectrometry (TOF-SIMS) analysis and X-ray spectroscopy (XPS) confirm the formation of oxygen-rich (O-rich) CuO film which demonstrates a highly stable photocathode with retained photocurrent of ∼90% for 20 min. The influence of chemical composition on the photocathode performance and stability has been discussed in detail. In addition, O-rich CuO photocathodes deposited with Au-Pd nanostructures have shown enhanced photoelectrochemical performance. Linear scan voltammetry characteristic shows ∼25% enhancement in photocurrent after Au-Pd deposition and reaches ∼4 mA/cm2 at "0" V v/s RHE. Hydrogen evolution rate significantly depends on the elemental composition of CuO and metal nanostructure. The present work has demonstrated a stable photocathode with high photocurrent for visible-light-driven water splitting and hydrogen production.

Impact of molybdenum out diffusion and interface quality on the performance of sputter grown CZTS based solar cells.

We have investigated the impact of Cu2ZnSnS4-Molybdenum (Mo) interface quality on the performance of sputter-grown Cu2ZnSnS4 (CZTS) solar cell. Thin film CZTS was deposited by sputter deposition technique using stoichiometry quaternary CZTS target. Formation of molybdenum sulphide (MoSx) interfacial layer is observed in sputter grown CZTS films after sulphurization. Thickness of MoSx layer is found ~142 nm when CZTS layer (550 nm thick) is sulphurized at 600 °C. Thickness of MoSx layer significantly increased to ~240 nm in case of thicker CZTS layer (650 nm) under similar sulphurization condition. We also observe that high temperature (600 °C) annealing suppress the elemental impurities (Cu, Zn, Sn) at interfacial layer. The amount of out-diffused Mo significantly varies with the change in sulphurization temperature. The out-diffused Mo into CZTS layer and reconstructed interfacial layer remarkably decreases series resistance and increases shunt resistance of the solar cell. The overall efficiency of the solar cell is improved by nearly five times when 600 °C sulphurized CZTS layer is applied in place of 500 °C sulphurized layer. Molybdenum and sulphur diffusion reconstruct the interface layer during heat treatment and play the major role in charge carrier dynamics of a photovoltaic device.

Color tunable low cost transparent heat reflector using copper and titanium oxide for energy saving application.

Multilayer coating structure comprising a copper (Cu) layer sandwiched between titanium dioxide (TiO2) were demonstrated as a transparent heat reflecting (THR) coating on glass for energy-saving window application. The main highlight is the utilization of Cu, a low-cost material, in-lieu of silver which is widely used in current commercial heat reflecting coating on glass. Color tunable transparent heat reflecting coating was realized through the design of multilayer structure and process optimization. The impact of thermal treatment on the overall performance of sputter deposited TiO2/Cu/TiO2 multilayer thin film on glass substrate is investigated in detail. Significant enhancement of transmittance in the visible range and reflectance in the infra-red (IR) region has been observed after thermal treatment of TiO2/Cu/TiO2 multilayer thin film at 500 °C due to the improvement of crystal quality of TiO2. Highest visible transmittance of 90% and IR reflectance of 85% at a wavelength of 1200 nm are demonstrated for the TiO2/Cu/TiO2 multilayer thin film after annealing at 500 °C. Performance of TiO2/Cu/TiO2 heat reflector coating decreases after thermal treatment at 600 °C. The wear performance of the TiO2/Cu/TiO2 multilayer structure has been evaluated through scratch hardness test. The present work shows promising characteristics of Cu-based THR coating for energy-saving building industry.

Nanocrystal Engineering of Sputter-Grown CuO Photocathode for Visible-Light-Driven Electrochemical Water Splitting.

Cupric oxide (CuO) thin film was sputtered onto fluorine-doped tin oxide (FTO) coated glass substrate and incorporated into a photoelectrochemical (PEC) cell as a photocathode. Through in situ nanocrystal engineering, sputtered CuO film shows an improvement in its stability and photocurrent generation capability. For the same CuO film thickness (150 nm), films deposited at a sputtering power of 300 W exhibit a photocurrent of ∼0.92 mAcm(-2) (0 V vs RHE), which is significantly higher than those deposited at 30 W (∼0.58 mAcm(-2)). By increasing the film thickness to 500 nm, the photocurrent is further enhanced to 2.5 mAcm(-2), which represents a photocurrent conversion efficiency of 3.1%. Systematic characterization using Raman, XRD, and HR-TEM reveals that the high sputtering power results in an improvement in CuO film crystallinity, which enhances its charge transport property and, hence, its photocurrent generation capabilities.

Current Status and Future Prospects of Copper Oxide Heterojunction Solar Cells.

The current state of thin film heterojunction solar cells based on cuprous oxide (Cu2O), cupric oxide (CuO) and copper (III) oxide (Cu4O3) is reviewed. These p-type semiconducting oxides prepared by Cu oxidation, sputtering or electrochemical deposition are non-toxic, sustainable photovoltaic materials with application potential for solar electricity. However, defects at the copper oxide heterojunction and film quality are still major constraining factors for achieving high power conversion efficiency, η. Amongst the Cu2O heterojunction devices, a maximum η of 6.1% has been obtained by using pulsed laser deposition (PLD) of AlxGa1-xO onto thermal Cu2O doped with Na. The performance of CuO/n-Si heterojunction solar cells formed by magnetron sputtering of CuO is presently limited by both native oxide and Cu rich copper oxide layers at the heterointerface. These interfacial layers can be reduced by using a two-step sputtering process. A high η of 2.88% for CuO heterojunction solar cells has been achieved by incorporation of mixed phase CuO/Cu2O nanopowder. CuO/Cu2O heterojunction solar cells fabricated by electrodeposition and electrochemical doping has a maximum efficiency of 0.64% after surface defect passivation and annealing. Finally, early stage study of Cu4O3/GaN deposited on sapphire substrate has shown a photovoltaic effect and an η of ~10-2%.

Aluminium alloyed iron-silicide/silicon solar cells: A simple approach for low cost environmental-friendly photovoltaic technology.

This work demonstrates the fabrication of silicide/silicon based solar cell towards the development of low cost and environmental friendly photovoltaic technology. A heterostructure solar cells using metallic alpha phase (α-phase) aluminum alloyed iron silicide (FeSi(Al)) on n-type silicon is fabricated with an efficiency of 0.8%. The fabricated device has an open circuit voltage and fill-factor of 240 mV and 60%, respectively. Performance of the device was improved by about 7 fold to 5.1% through the interface engineering. The α-phase FeSi(Al)/silicon solar cell devices have promising photovoltaic characteristic with an open circuit voltage, short-circuit current and a fill factor (FF) of 425 mV, 18.5 mA/cm(2), and 64%, respectively. The significant improvement of α-phase FeSi(Al)/n-Si solar cells is due to the formation p(+-)n homojunction through the formation of re-grown crystalline silicon layer (~5-10 nm) at the silicide/silicon interface. Thickness of the regrown silicon layer is crucial for the silicide/silicon based photovoltaic devices. Performance of the α-FeSi(Al)/n-Si solar cells significantly depends on the thickness of α-FeSi(Al) layer and process temperature during the device fabrication. This study will open up new opportunities for the Si based photovoltaic technology using a simple, sustainable, and los cost method.