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Today, silicon solar cells (amorphous films and wafer-based) are a main source of green energy. These cells and their components are produced by employing various technologies. Unfortunately, during the production process, chemicals that are harmful for the environment and for human life are used. For example, hydrofluoric acid is used to texture the top electrode to improve light harvesting. In this work, and also in recent ones, we report a way to obtain 3D textures on the top electrode by using zinc oxide nanorods. The efficiency of a textured solar cell structure is compared with the one obtained for a planar zinc oxide/silicon structure. The present results show the possibility to produce efficient solar cells on a relatively thin 50 μm thick silicon substrate. Solar cells with structured top electrodes were examined by numerous measuring techniques. Scanning electron microscopy revealed a grain-like morphology of the magnesium-doped zinc oxide film. The size of the grains is closely related to the structure of the nanorods. The external quantum efficiency of the cells was measured. The obtained solar cell shows response in a wide spectral range from ultraviolet to infrared. Current–voltage and current–voltage–temperature measurements were performed to evaluate basic photovoltaic parameters. At room temperature, the cells efficiency equals to 9.1% for textured structures and 5.4% for planar structures, respectively. The work, therefore, describes an environmentally friendly technology for PV architecture with surface textures increasing the efficiency of PV cells.

In order to effectively utilize the photovoltaic properties of gallium arsenide, its surface/interface needs to be properly prepared. In the experiments described here we examined eight different paths of GaAs surface treatment (cleaning, etching, passivation) which resulted in different external quantum efficiency (EQE) values of the tested photovoltaic (PV) cells. Atomic force microscopy (AFM) and scanning electron microscopy (SEM) examinations were conducted to obtain structural details of the devices. X-ray photoelectron spectroscopy (XPS) with depth profiling was used to examine interface structure and changes in the elemental content and chemical bonds. The photoluminescence (PL) properties and bandgap measurements of the deposited layers were also reported. The highest EQE value was obtained for the samples initially etched with a citric acid-based etchant and, in the last preparation step, either passivated with ammonium sulfide aqueous solution or treated with ammonium hydroxide solution with no final passivation. Subsequent I–V measurements, however, confirmed that from these samples, only the sulfur-passivated ones provided the highest current density. The tested devices were fabricated by using the ALD method.

Atomic layer deposition of HfO2 from TDMAH and water or ammonia water at different temperatures below 400 °C is studied. Growth per cycle (GPC) has been recorded in the range of 1.2–1.6 Å. At low temperatures (≤100 °C), the films grew faster and are structurally more disordered, amorphous and/or polycrystalline with crystal sizes up to 29 nm, compared to the films grown at higher temperatures. At high temperatures of 240 °C, the films are better crystallized with crystal sizes of 38–40 nm but grew slower. GPC, dielectric constant, and crystalline structure are improved by depositing at temperatures above 300 °C. The dielectric constant value and the roughness of the films have been determined for monoclinic HfO2, a mixture of orthorhombic and monoclinic, as well as for amorphous HfO2. Moreover, the present study shows that the increase in the dielectric constant of the films can be achieved by using ammonia water as an oxygen precursor in the ALD growth. The detailed investigations of the relationship between HfO2 properties and growth parameters presented here have not been reported so far, and the possibilities of fine-tuning and controlling the structure and performance of these layers are still being sought.

Hereby the possible applications of oxide nanoparticles in the cancer diagnostics and therapy are presented. Cancer diseases are nowadays one of the most common causes of death in the highly-developed countries. Discussed will be the current clinical cancer detection methods with their shortcomings. The role of nanomedicine in cancer medicine and the potential applications of nanoparticles debated in the literature will be critically evaluated. In the second part, the most common methods for the nanoparticle synthesis will be discussed. Finally, the system for cancer detection based on the enhanced permeation-retention of multimodal high-k oxide nanoparticles doped with lanthanides will be proposed for both for themagnetic resonance imaging (non-gadolinium contrast agents) and for fluorescence guided biopsy and surgery.

Aleksandra Seweryn,1 Ariadna Pielok,2 Krystyna Lawniczak-Jablonska,1 Rafal Pietruszka,1 Klaudia Marcinkowska,2 Mateusz Sikora,2 Bartlomiej S Witkowski,1 Marek Godlewski,1 Krzysztof Marycz,2,3 Agnieszka Smieszek2 1Institute of Physics, Polish Academy of Sciences, Warsaw PL-02668, Poland; 2Wroclaw University of Environmental and Life Sciences, Department of Experimental Biology, Wroclaw PL-50375, Poland; 3Cardinal Stefan Wyszynski University, Collegium Medicum, Warsaw PL-01938, PolandCorrespondence: Aleksandra SewerynPolish Academy of Sciences, Aleja Lotnikow 32/46, Warsaw PL-02668, PolandTel +48 22 116 33 99Fax +48 22 843 09 26Email aseweryn@ifpan.edu.plAgnieszka SmieszekWroclaw University of Environmental and Life Sciences, Norwida St. 27 B, Wroclaw PL-50-375, PolandTel +48 71 320 5229Fax +48 22 843 09 26Email agnieszka.smieszek@upwr.edu.plIntroduction: The development of the field of biomaterials engineering is rapid. Various bioactive coatings are created to improve the biocompatibility of substrates used for bone regeneration, which includes formulation of thin zirconia coatings with pro-osteogenic properties. The aim of this study was to assess the biological properties of ZrO2 thin films grown by Atomic Layer Deposition (ALD) technology (ZrO2ALD).Methodology: The cytocompatibility of the obtained layers was analysed using the mice pre-osteoblastic cell line (MC3T3) characterized by decreased expression of microRNA 21-5p (miR-21-5p) in order to evaluate the potential pro-osteogenic properties of the coatings. The in vitro experiments were designed to determine the effect of ZrO2ALD coatings on cell morphology (confocal microscope), proliferative activity (cell cycle analysis) and metabolism, reflected by mitochondrial membrane potential (cytometric-based measurement). Additionally, the influence of layers on the expression of genes associated with cell survival and osteogenesis was studied using RT-qPCR. The following genes were investigated: B-cell lymphoma 2 (Bcl-2), Bcl-2-associated X protein (Bax), p53 and p21, as well as osteogenic markers, i.e. collagen type 1 (Coll-1), osteopontin (Opn), osteocalcin (Ocl) and runt-related transcription factor 2 (Runx-2). The levels of microRNA (miRNA/miR) involved in the regulation of osteogenic genes were determined, including miR-7, miR-21, miR-124 and miR-223.Results: The analysis revealed that the obtained coatings are cytocompatible and may increase the metabolism of pre-osteoblast, which was correlated with increased mitochondrial membrane potential and extensive development of the mitochondrial network. The obtained coatings affected the viability and proliferative status of cells, reducing the population of actively dividing cells. However, in cultures propagated on ZrO2ALD coatings, the up-regulation of genes essential for bone metabolism was noted.Discussion: The data obtained indicate that ZrO2 coatings created using the ALD method may have pro-osteogenic properties and may improve the metabolism of bone precursor cells. Given the above, further development of ZrO2ALD layers is essential in terms of their potential clinical application in bone regenerative medicine.Keywords: ALD, zirconia-based coatings, pro-osteogenic properties, cytocompatibility, osteoblasts precursors

Titanium nitride is a well-known conductive ceramic material that has recently experienced resumed attention because of its plasmonic properties comparable to metallic gold and silver. Thus, TiN is an attractive alternative for modern and future photonic applications that require compatibility with the Complementary Metal-Oxide-Semiconductor (CMOS) technology or improved resistance to temperatures or radiation. This work demonstrates that polycrystalline TiNx films sputtered on silicon at room temperature can exhibit plasmonic properties continuously from 400 nm up to 30 μm. The films’ composition, expressed as nitrogen to titanium ratio x and determined in the Secondary Ion Mass Spectroscopy (SIMS) experiment to be in the range of 0.84 to 1.21, is essential for optimizing the plasmonic properties. In the visible range, the dielectric function renders the interband optical transitions. For wavelengths longer than 800 nm, the optical properties of TiNx are well described by the Drude model modified by an additional Lorentz term, which has to be included for part of the samples. The ab initio calculations support the experimental results both in the visible and infra-red ranges; particularly, the existence of a very low energy optical transition is predicted. Some other minor features in the dielectric function observed for the longest wavelengths are suspected to be of phonon origin.

Two-step synthesis of Y2O3:Eu nanostructures was performed. It includes microwave driven hydrothermal and calcination stages. Performed route results in crystallization of Y4O(OH)9(NO3):Eu crystals initially, then Y2O3:Eu crystals after calcination. Arranged Eu contents in relation to overall cation quantity were set to 2 mol%, 10 mol% and 20 mol%. Varying europium concentrations influence habit of obtained Y4O(OH)9(NO3):Eu crystals from needle-like to plate-like and as a result, also shapes of final Y2O3:Eu nanostructures. Additionally, certain amount of Eu2+ ions was detected in as-grown material using laser spectroscopy and decay kinetics measurements. Obtained material was calcined at 1200 °C in the air, which results in oxidation of Eu2+ ions and crystallization of small number of cubic Eu2O3 nanocrystals. Characterization of obtained materials was performed using XRD, SEM, TEM, EDX, CL, Raman and photoluminescence spectroscopy.

Europium doped hafnium dioxide nanoparticles were crystallized using biologically friendly microwave hydrothermal method and employed in observation of small rodents tissues. Main solvent in synthesis is water, in consequence nanoparticles are found surrounded by thin hydroxide layer. Size of the nanoparticles is controlled by temperature of calcination. 1200 °C heating causes drop of luminescence intensity, explained as damage of high symmetry surface emission centers in the nanocrystals. On the other hand, growth of crystallites increases intensity of X-ray and electron beam excited luminescence. This makes them promising activator in photodynamic therapy.

While synthesis methods for pure ZnO nanostructures are well established, an efficient technique for the growth of ZnO-based nanowires or microrods that incorporate any type of quantum structure is yet to be established. Here, we report on the fabrication and optical properties of axial Zn1-xMgxO/ZnO/Zn1-xMgxO quantum wells that were deposited by molecular beam epitaxy on ZnO microrods obtained using a hydrothermal method. Using the emission energy results found in cathodoluminescence measurements and the results of a numerical modeling process, we found the quantum well width to be 4 nm, as intended, at the growth stage. The emission of quantum well-confined excitons persists up to room temperature. We used the fabricated structures to determine the carrier diffusion length (>280 nm) in ZnO using spatially resolved cathodoluminescence. The micro-photoluminescence results suggest an increase in the electron-phonon coupling strength with increasing microrod size.

Core/shell CdSe/(Cd,Mn)S colloidal nanoplatelets containing magnetic Mn2+ ions are investigated by the optically detected magnetic resonance technique, combining 60 GHz microwave excitation and photoluminescence detection. Resonant heating of the Mn spin system is observed. We identify two mechanisms of optical detection, via variation of either the photoluminescence polarization or its intensity in an external magnetic field. The spin-lattice relaxation dynamics of the Mn spin system is measured and used for evaluation of the Mn concentration. In CdSe/(Cd,Zn,Mn)S nanoplatelets the addition of Zn in the shells significantly broadens the magnetic resonance, evidencing local strain.

Atomic layer deposition (ALD) technology has started to attract attention as an efficient method for obtaining bioactive, ultrathin oxide coatings. In this study, using ALD, we have created titanium dioxide (TiO2) layers. The coatings were characterised in terms of physicochemical and biological properties. The chemical composition of coatings, as well as thickness, roughness, wettability, was determined using XPS, XRD, XRR. Cytocompatibillity of ALD TiO2 coatings was accessed applying model of mouse pre-osteoblast cell line MC3T3-E1. The accumulation of transcripts essential for bone metabolism (both mRNA and miRNA) was determined using RT-qPCR. Obtained ALD TiO2 coatings were characterised as amorphous and homogeneous. Cytocompatibility of the layers was expressed by proper morphology and growth pattern of the osteoblasts, as well as their increased viability, proliferative and metabolic activity. Simultaneously, we observed decreased activity of osteoclasts. Obtained coatings promoted expression of Opn, Coll-1, miR-17 and miR-21 in MC3T3-E1 cells. The results are promising in terms of the potential application of TiO2 coatings obtained by ALD in the field of orthopaedics, especially in terms of metabolic- and age-related bone diseases, including osteoporosis.

ZnO nanorods (NRs) were synthesized by the hydrothermal method and coated by HfO2 sell layers by using the atomic layer deposition to form ZnO/HfO2 core/shell NRs arrays. XRD showed the hexagonal wurtzite structure of ZnO NRs and tetragonal phase of HfO2. Scanning electron microscope and atomic force microscopy analysis illustrated vertically well-aligned ZnO/HfO2 core/shell NRs structure. Optical property was studied by PL which revealed that the near band-edge emission of the ZnO NRs improved after coating by HfO2 shells. The band gap energy was estimated about 3.51 eV by UV–Vis. For the first time, the measurements of nonlinear optical (NLO) properties of ZnO/HfO2 core/shell NRs structures have been performed by using a continuous-wave (cw) Nd:YAG laser at 532 nm by the Z-scan technique. A negative nonlinear refractive index and a positive absorption coefficient were calculated equal to 8.6 × 10−6 cm2/W and 1.75 cm/W for ZnO/HfO2 core/shell NRs, respectively. A third-order NLO susceptibility of ZnO/HfO2 core/shell NRs was measured of the order of 10−2 esu which is a large value. The results suggest that ZnO/HfO2 core/shell NRs are promising candidates for NLO applications.

Zinc oxide nanoparticles were synthesized with microwave hydrothermal technique and tested as luminescent contrast for biological imaging. Luminescence was activated by Eu3+ ions embedded in the nanoparticle matrix in the increasing concentrations of 1, 5 and 10 %mol. It was found that europium did not create a separate crystalline phase up to the concentration as high as 5 %mol. However, Eu3+ ions did not substitute Zn2+ in the host lattice, but allocated in the low symmetry environment. It was proposed that europium was locating in the inter-grain space or on the surface of nanoparticles. The luminescence intensity in ZnO:Eu, as well as the size of particles, increased with the Eu ion concentration. Moreover, in 10 %mol Eu sample, the separate phase of Eu-hydroxide was identified with crystals of micrometre length. Interestingly, in vivo study revealed, that contrary to the in silico experiments, following gastric gavage, the brightest nanoparticle-related luminescence signal was observed at 1 %mol. concentration of Eu. Since the alimentary uptake of nanoparticles was related to their size, we concluded that the increase in luminescence at 5 and 10 %mol. Eu concentrations was associated with the largest ZnO:Eu and Eu-hydroxide particles that did not cross the gastrointestinal barrier.

In recent years, a series of investigations has been devoted to a possibility of using crystals based on CdTe with addition of magnesium (Mg) for X and gamma radiation detectors. Since we have had wide technological possibilities of preparing crystals and investigating their properties, we performed crystallizations of the crystals mentioned above. Thereafter, we investigated selected properties of the obtained materials. The crystallization processes were performed by using the Low Pressure Bridgman (LPB) method. The elements used: Cd, Te, Mg were of the highest purity available at present. In order to obtain reliable conclusions the crystallization processes were carried out at identical technological conditions. The details of our technological method and the results of the investigation of physical properties of the samples are presented below.

In this paper we present luminescence results of nitrogen doped and undoped ZnO layers grown at 100 °C by atomic layer deposition and post grown annealed. A comprehensive analysis of the excitonic peaks as well as the controversial band at ~3.32 eV is presented. Based on temperature dependent luminescence analysis we identified PL peaks originating from donor and acceptor bound excitons D°X and A°X. It has been found that two acceptor-related PL peaks observed between 3.30 and 3.32 eV reveal different temperature behavior. The emission at 3.302 eV has been assigned to donor-acceptor pairs (DAP), whereas the emission at 3.318 eV to free electrons to acceptor transition. Activation of an acceptor as a result of high temperature annealing is reflected in PL spectra as an appreciable increase of the DAP emission. The binding energies of existing donors and acceptors have been also calculated and the possible origin of the donors and acceptors in ZnO and ZnO:N layers grown at low temperature was proposed. Furthermore, the planar cathodoluminescence images discover that acceptor related emission comes from whole grains area.

Zinc oxide is nowadays widely investigated in many different science areas. In particular, this wide band gap semiconductor is valued due to its possible use in transparent electronics as TCO (Transparent Conductive Oxide) and/or as ARC (Antireflective Coating). In other applications, ZnO can also play active role in light source devices, UV detectors, solar cells, etc. In this experiment we focused on zinc oxide applicability assessment in solar cell devices. ZnO as well as its Al-doped form AZO (Aluminum doped Zinc Oxide) were examined in view of their use both as TCO and the n-type partner for the p-type gallium arsenide (GaAs) substrate, that resulted in creation of the p-n heterojunction-based photovoltaic device. In order to deposit both ZnO as well as AZO layers, the ALD (Atomic Layer Deposition) method was applied.

Well-aligned ZnO nano/micro-rods with identical crystallographic orientation were synthesized on a c-plane GaN template, using a microwave-assisted hydrothermal method at 50 °C for duration of 2 min. The ZnO nanorods exhibited true epitaxial growth, in contrast to most of the previously reported methods, which involve nucleation on a ZnO buffer layer pre-deposited on the substrate. Homogeneous in-plane alignment as well as the c-axis orientation were confirmed by X-ray diffraction measurements and TEM analysis. More importantly, in the photoluminescence spectra of the nanorods a strong, narrow excitonic emission and an extremely weak deep level emission were observed, indicating high optical quality. The diameter was controlled by adjusting pH of the solution used in the growth process. The main achievement of the research was the opportunity to obtain oriented, high quality ZnO nano/microrods, using a surprisingly quick, cheap, and safe growth process, without the use of toxic substances or ultra-high purity compounds.

In recent years, a series of investigations has been devoted to a possibility of using crystals based on CdTe with addition of magnesium (Mg), selenium (Se), or manganese (Mn) for X and gamma radiation detectors. In the literature there are contradictory data with respect to the segregation of Mg in (Cd,Mg)Te and Se in Cd(Te,Se) and to the possibility of obtaining materials with a homogeneous composition without grains and twins. We have wide technological possibilities of preparing crystals and investigating some of their properties. Thus, we performed crystallizations of (Cd,Mg)Te, Cd(Te,Se), (Cd,Mn)(Te,Se), and (Cd,Mn)Te compounds. The aim of our studies was to check whether any of the investigated materials may be easily obtained by the Low Pressure Bridgman (LPB) method in the form of large, homogeneous, high resistivity single crystals with as few as possible twins, subgrains, and tellurium inclusions. The crystallization processes were performed by using the LPB method. The elements used: Cd, Te, Mn, Mg, and Se were of the highest purity available at that time. In order to obtain reliable conclusions the crystallization processes were carried out under identical technological conditions. The details of our technological method and the results of the investigation of physical properties of the samples are presented below.

The thin layers of ZnO and ZnO: Al (Al doped zinc oxide—AZO) were deposited by the atomic deposition layer (ALD) method on silicon and glass substrates. The structures were deposited using diethylzinc (DEZ) and deionized water as zinc and oxygen precursors. A precursor of trimethylaluminum (TMA) was used to introduce the aluminum dopant. The present study of ALD-deposited ZnO and AZO films was motivated by their applications in photovoltaics. We attempted to expose several properties of such films. Structural, optical (including ellipsometric measurements) and electrical investigations were performed. We discussed the relations between samples doped with different Al fractions and their properties.

The use of nanoparticles in medicine is a rapidly growing research field with numerous potential applications, especially in the field of cancer diagnosis and therapy. Nanoparticles can be intrinsically diagnostic of therapeutic, or they can be conjugated with diagnostic or therapeutic compounds. Nanoparticles may also passively or actively target tumor cells specifically using the enhanced permeation and retention (EPR) effect, or the addition of targeting ligands to their surface. This may provide a diagnostic or/and therapeutic tools to target primary as well as metastatic tumors. The transport, distribution and toxicity of nanoparticles depends greatly on their size and composition, thus every new formulation needs to be extensively researched. This work was focused on the development of Tb-doped ZrO2 nanoparticles (NPs) for application in cancer imaging. Obtained nanoparticles were below 10 nm with very low influence of Tb concentration on size. Terbium stabilization of ZrO2 had influence on the luminescence properties of obtained material. Partially stabilized zirconium dioxide exhibited broad host related emission peaking at 500 nm, disappearing with the terbium content. We confirmed alimentary absorption and wide distribution of luminescent ZrO2:Tb nanoparticles in mice with their gradual accumulation in the experimentally induced mammary cancers. Furthermore, a high concentration of NPs was found within the lung metastases as opposed to healthy lung tissue, where no NPs-related signal was observed.

Epitaxial ZnO films implanted with ytterbium have been studied by combination of channeling Rutherford backscattering spectrometry and Hall measurements. This approach is able to shed more light onto the difficult problem of optical activation of Yb implanted into the ZnO lattice. ZnO films grown by atomic layer deposition on a GaN/Al 2 O 3 substrate were implanted with Yb + ions to the fluences of 5 × 10 14 , 1 × 10 15 and 5 × 10 15 at./cm 2 . RBS/c spectra show that for as implanted samples the fraction of implanted Yb ions occupying substitutional lattice positions amounts to 72%, 54% and 22%, respectively. Annealing under an ambient atmosphere at 800 °C leads to a partial recovery of the crystal lattice but also substantially reduces substitutional fraction of Yb atoms. Photoluminescence studies on the as-implanted samples revealed a very weak luminescent peak in the near-infrared region, which slightly increases with a fluence. The annealing process leads to optical activation of Yb 3 + ions and significantly increases the previously observed the near-infrared inter-ionic emission. The results obtained from Hall measurements indicate that after implantation Yb ions are mainly in the 2 + state and are transformed to the optically active 3 + state as a result of annealing. It suggests that the process of optical activation via annealing is related not only to lattice recovery, but also to Yb diffusion from substitutional to interstitial positions, where Yb ions are in the optically active 3 + state.

Currently, the first generation of silicon solar cells is dominating the photovoltaic market. Silicon cells are produced by various methods, which employ either crystalline or multi-crystalline substrates. However, both these manufacturing processes are expensive and potentially harmful to the environment and health. One example of this is that the surface is given its texture in a highly corrosive water solution of nitric and hydrofluoric acid. Additionally, both the diffusion and manufacturing of p-n junction and of metal contacts are associated with very high temperatures. This prompted us in our search for cheaper and more environmental friendly technologies. In this work, we discuss the possibility of producing components of photovoltaic cells by employing atomic layer deposition and hydrothermal technologies. This does not require the use of hazardous chemicals and high temperatures. The maximum efficiency of zinc oxide/silicon solar cells is 14% and 10% for textured and planar structures, respectively. A environmentally-friendly and simple procedure is thus being proposed, which, together with its relative efficiency, makes it an attractive alternative to the present procedure.

Scratches and constant abrasive wear can result in zinc oxide (ZnO) and aluminum doped zinc oxide (ZnO:Al) layers that render many devices impracticable to use. Currently, the ZnO and ZnO:Al layers are widely used as transparent conductivity oxide (TCO). The top and/or bottom electrodes based on ZnO and ZnO:Al were used in organic light-emitting diodes (OLED), organic and perovskite solar cells in order to replace expensive indium tin oxide (ITO). Consequently, knowledge of the frictional properties of the ZnO layer is a necessity for many scientists. In this study, the tribological properties of zinc oxide that was formed by the Low Temperature Atomic Layer Deposition (LT ALD) method were investigated. ALD-layers (ZnO and ZnO:Al) were deposited on a glass substrates in pre-selected conditions in order to achieve films appropriate for the application of photovoltaics. The results indicate a good adhesion of the films to the substrate. The layers were abraded during friction with Al 2 O 3 ball and their wear intensity depend on hardness of the film/substrate system. The friction coefficient of ZnO film reached value 0.1 and was higher than friction coefficient of ZnO:Al film equal 0.08. The tribological properties of these films are compared with those reported for bulk ZnO and those films deposited by sputtering.

Asymmetric ZnO/ZnMgO double quantum well (QW) structures grown on non-polar m-plane ZnO bulk substrates are investigated. Pairs of 2 and 5 nm wide ZnO QWs were grown on ZnMgO buffer/barrier layers with Mg concentrations over 20%. The QWs are separated with 7 nm or 20 nm ZnMgO barriers. Temperature dependent photoluminescence (PL) and low temperature cross-sectional cathodoluminescence allowed to identify the origin of the observed spectral lines. Well resolved and narrow luminescence lines due to localized and free excitons are observed, confirming excellent quality of the structures. The results of luminescence studies suggest that at the barrier width of 7 nm coupling between the wells enhances excitonic emission in 5 nm well via tunneling of charge carriers from 2 nm to 5 nm QW. No trace of inter-well coupling in a structure with a 20 nm thick barrier is observed. It is found that the binding energies of excitons in 2 and 5 nm wells are 52 and 101 meV, respectively. Such large enhancement of the binding energies is due to the quantum confinement in the wells.

Electric measurements were performed on solar cells composed of n-type ZnO nanorods grown by the hydrothermal method on p-type silicon substrate. The nanorods were covered with silver nanoparticles of sizes 20–30 nm and 50–60 nm. The diameters and density of the nanorods and nanoparticles were determined from scanning electron microscopy (SEM) and atomic force microscopy (AFM) images. On top of the structures the ZnO:Al (AZO) layer was deposited as a transparent electrode using the atomic layer deposition (ALD) method. The efficiency of the cells was found to be ∼3.4%, however the sample with larger nanoparticles exhibit better performance. The analysis of the current-voltage (I-V) measurements vs illumination intensity let us conclude that the surface recombination deteriorates their performance. The measurements of capacitance-voltage (C-V) characteristics allowed us to determine the concentration of donors in ZnO and built-in voltage at the ZnO/Si interface. The deep level transient spectroscopy (DLTS) measurements confirmed the presence of defects at the surface as well as deeper in the ZnO nanorods. Obtained results compared with the data reported elsewhere let us conclude that the defect density is much less than in the case of similar heterojunction ZnO/Si solar cells made by other technological methods.

In this work we discuss a method of preparation of a highly sensitive light detector based on ZnO nanorods. A photoresistor constructed by us is based on a heterojunction between high quality ZnO nanorods and high resistivity p-type Si used as a substrate for nanorods’ deposition. ZnO nanorods are grown by a modified version of a microwave assisted hydrothermal method which allows for growth of high quality ZnO nanorods in a few minutes. The obtained photoresistor responds to a wide spectral range of light starting from near infrared (IR) to ultraviolet (UV). Properties of the detector are evaluated. We propose the use of the detector as an optical switch.

ZnO:Al-hydroquinone (AZO-HQ) films were grown on poly(ethylene terephthalate) (PET) substrates by atomic and molecular layer deposition (ALD/MLD). Organic contents in the films varied from 0 to ≈4 vol%. Structural and electrical investigations of the films were carried out. Electrical measurements were performed under film bending. The piezoresistive effect in the films with different organic contents was observed and described. Critical bend radius, critical strain, and piezoresistive coefficient values were related to the film microstructure. The piezoresistivity was found to be enhanced for the deformations of ZnO crystallites along the a-axis whereas higher critical strain was influenced by long crystallites oriented in the deformation direction. AZO-HQ films having 2 vol% of the organic content are characterized by the lowest critical bend radius and the highest critical strain among the films under study. Keywords: Zinc oxide, Molecular layer deposition, Electrical properties, Piezoresistive effect

Iron is the crucial element for living organisms and its deficiency is described as the most common nutritional disorder all over the world. Nowadays, more effective and safe iron supplementation strategies for both humans and animals become one of the most important challenges in the therapy of nutritional deficiencies. Our previous in vivo studies confirmed safety and biodegradability of in-house manufactured zinc oxide-based nanoparticles and their rapid distribution to majority of organs and tissues in the body. In vitro examinations performed on Caco-2 cell line, a model of epithelial cells of the gastrointestinal tract, revealed a low toxicity of studied nanomaterials. In the current study, we investigated biodegradable zinc oxide nanoparticles doped with Fe(III) as a perspective supplementation strategy for iron deficiency. Biodegradable ZnO:Fe nanoparticles were intra-gastrically administered to adult mice and following 24 h, animals were sacrificed with collection of internal organs for further analyses. The iron concentration measured with atomic absorption spectrometry and histological staining (Perl’s method) showed a rapid distribution of iron-doped nanoparticles to tissues specifically related with iron homeostasis. Accumulation of iron was also visible within hepatocytes and around blood vessels within the spleen, which might indicate the transfer of Fe-doped nanoparticles from the bloodstream into the tissue. Reassuming, preliminary results obtained in the current study suggest that biodegradable ZnO nanoparticles doped with Fe might be a good carriers of exogenous iron in the living body. Therefore, subsequent investigations focus on determination an exact mechanisms related with an iron deposition in the tissue and influence of nanoparticle carriers on iron metabolism are required.

Low temperature (at 100 °C and below) growth of ZnO thin films by atomic layer deposition (ALD) is demonstrated. Properties of the layers grown with two different oxygen reagents: ozone and water are compared. Diethylzinc (DEZ) was used as metal precursor. Electrical and structural properties of films obtained at several different growth temperatures, ranging from 50 °C to 250 °C were analyzed. It turned out that the film grown in the water-based process at 250 °C and all films grown with ozone have more ordered crystallographic structure with the privileged growth direction (001) perpendicular to the substrate than water-based samples grown in temperatures 100−200 °C. Higher free electron concentration at room temperature was observed for ozone-based samples grown at 100 °C and 150 °C in comparison to water-based samples obtained at the same growth temperature. Low value of resistivity in case of ozone-based samples grown at 100 °C is a promising result, however lower electron mobility requires further optimization.

The use of plasmonic inclusions in heterojunction solar cells promises increase of solar-to-electric energy conversion efficiency. Recently, solar cells with ZnO nanorods attracted a lot of attention due to improved efficiency provided by highly scattering ZnO nanostructures on silicon or perovskite. N-type ZnO nanorods are grown on p-Si monocrystalline 180 μm thick substrates among others by means of a hydrothermal technique which requires prior seeding by deposition of thin film of ZnO or noble metals. In the latter case, naturally formed metal islands can also act as plasmonic nanoparticles (NPs). Excitation of plasmonic resonance on the NPs leads to directional scattering of light towards Si layer and electromagnetic field enhancement at their vicinity, close to the ZnO-Si junction, what results in improved energy absorption in the semiconductor layer and thus energy conversion efficiency. In this study, we investigate optimal conditions at which plasmonic phenomenon further improves light trapping in the Si-ZnO solar cells. In simulations performed by means of 3D FDTD method, we calculate light absorption enhancement in the system due to plasmonic NPs used as a seed layer at the ZnO/Si. In the calculations Ag, and Al NPs of different size and geometry close to that achievable in the experiment are analyzed. Finally, numerical results taking into account the granulometry of metal NPs achieved in the experiment are compared with the efficiency of fabricated cells.

Vertical structures based on Pd Schottky contacts to a ZnO/AZO bilayer have been realized and electrically characterized. Following a preliminary annealing study on the separated ZnO and AZO layers the ZnO/AZO bilayer was first annealed at 450 °C for 30 min to reduce the carrier concentration and then functionalized with a H2O2 dip prior to Pd deposition. On the basis of Atomic Force Microscopy, Transmission electron Microscopy and Capacitance vs Voltage measurements it has been found that the H2O2 treatment lowers the surface roughness and creates a ~ 200 nm thick layer formed by ZnO crystallites with grain size ≲ 10 nm embedded into an amorphous matrix with reduced carrier concentration. However, contrary to what previously reported no formation of ZnO2 has been observed. The obtained Schottky contacts showed a rectification ratio ≳ 10 2 at −2 V/+2 V with a detailed analysis based on the differential approach pointing to field enhanced emission from defective channels as the main leaking mechanisms.

The Finite-Difference Time-Domain (FDTD) numerical simulation method has been applied to interpret cathodoluminecence patterns observed for ZnO nanorods grown by a hydrothermal method. The 3D FDTD simulation reproduced the radial electromagnetic field pattern in the hexagonal resonator, corresponding to the CL emission maps of real ZnO microrods. The simulation result for the H z (TE) polarization—the intense field distribution along edges of the structure, in particular in the corners, but weak in the centre—matched the CL pattern particularly well. Since the experiment was not polarization sensitive, we suppose that polarisation sensitive transmission of electromagnetic field through the ZnO/air interface leads to such an observation. The results of the simulation show also that the lack of axial Fabry-Pérot-like resonances in the CL experiments is caused by leaking of the electromagnetic field from the ZnO resonator into the GaN substrate.

The Effect of Synthesis Pressure on Properties of Eu-Doped ZnO Nanopowders Prepared by Microwave Hydrothermal Method J. Rosowska, J. Kaszewskia,∗, B. Witkowski, Ł. Wachnicki and M. Godlewski Institute of Physics, Polish Academy of Sciences, Aleja Lotnikow 32/46, PL–02668 Warsaw, Poland Dept. of Mathematics and Natural Sciences College of Science, Cardinal S. Wyszynski University, Dewajtis 5, 01-815 Warsaw, Poland

Europium doped ZnO nanopowders made by microwave hydrothermal method are investigated. As zinc oxide precursor zinc nitrate(V) hexahydrate (Zn(NO3)2·6H2O) was used. Two types of nanopowder samples are examined: as grown and annealed at 750 °C in air atmosphere. We investigate the structural, morphological and optical prosperities of europium doped ZnO. Results of scanning electron microscopy, X-ray diffraction, photo- and cathodoluminescence investigations and also CIE1961 chromaticity diagram are presented.

Microwave hydrothermal growth of Y2O3 crystallites results in needle-shaped aggregates of μm length. Thermal treatment has little influence on the material microstructure, but significant impact on the nanometric level. Nanoparticles doped with europium show an intense red luminescence, related to the 5D0 → 7F2 transition of Eu3+ ions. The luminescence intensity increases with the calcination temperature and is accompanied by increasing size of Y2O3:Eu crystallites. EPR studies show the absence of Eu2+ related signals in the material. Y2O3:Eu nanoparticles crystallized via a microwave hydrothermal method were employed as luminescent biomarkers in mice. The initial tests confirmed their applicability as biological markers. Persorption of the Y2O3:Eu nanoparticles after IG in the adult mouse duodenum, brain and liver is reported.

Thermally induced crystallization of cubic Eu2O3 obtained with the microwave hydrothermal method has been investigated. The starting material crystallized in the form of needle-shaped agglomerates of nanocrystalline hexagonal Eu(OH)3. Thermal treatment up to 800 °C induced the crystallization of cubic Eu2O3, after further calcination at 1200 °C in the air a monoclinic phase appeared. The phase transformation caused abnormal reduction of Eu3+ ions, related to the oxygen vacancy creation during sintering of the oxide crystallites. The crystallization process of cubic Eu2O3 occurred within the agglomerates without change of their shapes. The cubic form exhibited bright emission of Eu3+ related luminescence with intensity increasing with the size of crystallites.

Our studies focus on test structures for photovoltaic applications based on zinc oxide nanorods grown using a low-temperature hydrothermal method on a p-type silicon substrate. The nanorods were covered with silver nanoparticles of two diameters – 20–30 nm and 50–60 nm – using a sputtering method. Scanning electron microscopy (SEM) micrographs showed that the deposited nanoparticles had the same diameters. The densities of the nanorods were obtained by means of atomic force microscope (AFM) images. SEM images and Raman spectroscopy confirmed the hexagonal wurtzite structure of the nanorods. Photoluminescence measurements proved the good quality of the samples. Afterwards an atomic layer deposition (ALD) method was used to grow ZnO:Al (AZO) layer on top of the nanorods as a transparent electrode and ohmic Au contacts were deposited onto the silicon substrate. For the solar cells prepared in that manner the current-voltage (I-V) characteristics before and after the illumination were measured and their basic performance parameters were determined. It was found that the spectral characteristics of a quantum efficiency exhibit an increase for short wavelengths and this behavior has been linked with the plasmonic effect.

In this paper a new generation of non-toxic nanoparticles based on the zirconium oxide doped with 0.5%Tb and co-doped by the range of 0–70% with Y was evaluated for the use as a fluorescent biomarker of neuronal trafficking. The ZrO 2 :Tb nanoparticles were created by microwave driven hydrothermal method. Influence of the yttrium content and thermal processing on the Tb 3+ related luminescence emission was discussed. The higher intensities were achieved, when host was cubic and for the nanoparticles with 33 nm. Presence of yttrium was associated with the energy coupling of the host and dopant, wide excitation band is present at 309 and 322 nm before and after calcination respectively. For the experiment on living primary neurons, nanoparticles doped with 0.5%Tb and 7%Y were chosen based on their luminescence emission intensity. Recently transfer of the nanoparticles through the barriers in the organism including blood–brain barrier following their alimentary absorption was confirmed (Godlewski and Godlewski, 2012). This raised the possibility of the nanoparticle application as a tool in the neuroscience, and the question of potential mechanisms of nanoparticle turnover in neurons. Concentration of 0.001 mg/ml of ZrO 2 :0.5%Tb 7%Y in growth medium was added to the primary murine culture medium, and the intracellular trafficking of nanoparticles was observed following 15 min pre-incubation period. ZrO 2 :0.5%Tb 7%Y nanoparticles were dynamically absorbed by the neurons and the dynamic passage of transport vesicles containing ZrO 2 :0.5%Tb 7%Y nanoparticles was observed along the neuronal processes and in between two neighbouring neurons. Reassuming, the ZrO 2 :0.5%Tb 7%Y nanoparticles proved to be biocompatible and a valid tool to assess intracellular trafficking dynamics in the neurobiology.

While doping with rare earth ions is used for emission activation, doping with transition metal ions is often used to get specific magnetic properties of a given host material. Recently investigations of transition metal doped materials focused on chances of achieving a room temperature ferromagnetic response. This is because carrier mediated room temperature ferromagnetic order was theoretically predicted for ZnO doped with Mn or Co ions. Such order is required for some of spintronics applications. To realize RT FM both Mn and Co should stay in 2+ charge state, expected when Mn/Co substitute zinc in ZnO. Both ZnMnO and ZnCoO alloys show a strong absorption band, which appears below ZnO band gap transitions. The origin of this absorption in ZnCoO is discussed in the present work. We show based on the results of photoluminescence and photo-ESR investigations that the broad absorption band is related to Co photo-ionization.

Terbium doped yttrium oxide was prepared with the microwave hydrothermal method. The Y 2 O 3 :Tb nanomaterial crystallized as needle-like grains. Bright luminescence in the green region was observed. Significant luminescence intensity increase was obtained after thermal treatment. Reduction of terbium ions was observed after heating in the air atmosphere. Tb 4+ ions were found to be stabilized by crystal impurities. Hydroxyl species were found to have impact on vacancies elimination. The terbium ions were used as optical and magnetic indicator of the material properties.