Structural and Electrical Investigation of Cobalt-Doped NiOx/Perovskite Interface for Efficient Inverted Solar Cells

Inorganic hole-transporting materials (HTMs) for stable and cheap inverted perovskite-based solar cells are highly desired. In this context, NiOx, with low synthesis temperature, has been employed. However, the low conductivity and the large number of defects limit the boost of the efficiency. An approach to improve the conductivity is metal doping. In this work, we have synthesized cobalt-doped NiOx nanoparticles containing 0.75, 1, 1.25, 2.5, and 5 mol% cobalt (Co) ions to be used for the inverted planar perovskite solar cells. The best efficiency of the devices utilizing the low temperature-deposited Co-doped NiOx HTM obtained a champion photoconversion efficiency of 16.42%, with 0.75 mol% of doping. Interestingly, we demonstrated that the improvement is not from an increase of the conductivity of the NiOx film, but due to the improvement of the perovskite layer morphology. We observe that the Co-doping raises the interfacial recombination of the device but more importantly improves the perovskite morphology, enlarging grain size and reducing the density of bulk defects and the bulk recombination. In the case of 0.75 mol% of doping, the beneficial effects do not just compensate for the deleterious one but increase performance further. Therefore, 0.75 mol% Co doping results in a significant improvement in the performance of NiOx-based inverted planar perovskite solar cells, and represents a good compromise to synthesize, and deposit, the inorganic material at low temperature, without losing the performance, due to the strong impact on the structural properties of the perovskite. This work highlights the importance of the interface from two different points of view, electrical and structural, recognizing the role of a low doping Co concentration, as a key to improve the inverted perovskite-based solar cells’ performance

Graphene oxide decorated with gold enables efficient biophotovolatic cells incorporating photosystem I

This paper describes the use of reduced graphene oxide decorated with gold nanoparticles as an efficient electron transfer layer for solid-state biophotovoltic cells containing photosystem I as the sole photo-active component. Together with polytyrosine–polyaniline as a hole transfer layer, this device architecture results in an open-circuit voltage of 0.3 V, a fill factor of 38% and a short-circuit current density of 5.6 mA cm(−2) demonstrating good coupling between photosystem I and the electrodes. The best-performing device reached an external power conversion efficiency of 0.64%, the highest for any solid-state photosystem I-based photovoltaic device that has been reported to date. Our results demonstrate that the functionality of photosystem I in the non-natural environment of solid-state biophotovoltaic cells can be improved through the modification of electrodes with efficient charge-transfer layers. The combination of reduced graphene oxide with gold nanoparticles caused tailoring of the electronic structure and alignment of the energy levels while also increasing electrical conductivity. The decoration of graphene electrodes with gold nanoparticles is a generalizable approach for enhancing charge-transfer across interfaces, particularly when adjusting the levels of the active layer is not feasible, as is the case for photosystem I and other biological molecules

Poly(Caprolactone)-Poly(N-Isopropyl Acrylamide)-Fe₃O₄ Magnetic Nanofibrous Structure with Stimuli Responsive Drug Release

Poly(caprolactone; PCL)—poly(N‐isopropylacrylamie; PNIPAAm)—Fe3O4 fiber, that can be magnetically actuated, is reported. Here, a structure is engineered that can be utilized as a smart carrier for the release of chemotherapeutic drug via magneto‐thermal activation, with the aid of magnetic nanoparticles (MNPs). The magnetic measurement of the fibers revealed saturation magnetization values within the range of 1.2–2.2 emu g−1. The magnetic PCL‐PNIPAAm‐Fe3O4 scaffold shows a specific loss power value of 4.19 W g−1 at 20 wt% MNPs. A temperature increase of 40 °C led to a 600% swelling after only 3 h. Doxorubicin (DOX) as a model drug, demonstrates a controllable drug release profile. 39% ± 0.92 of the total drug loaded is released after 96 h at 37 °C, while 25% drug release in 3 h at 40 °C is detected. Cytotoxicity results show no significant difference in cell attachment efficiency between the MNP‐loaded fibers and control while the DOX‐loaded fibers effectively inhibited cell proliferation at 24 h matching the drug release profile. The noncytotoxic effect, coupled with the magneto‐thermal property and controlled drug release, renders excellent potential for these fibers to be used as a smart drug‐release agent for localized cancer therapy

Fullerenes Enhance Self-Assembly and Electron Injection of Photosystem i in Biophotovoltaic Devices

This paper describes the fabrication of microfluidic devices with a focus on controlling the orientation of photosystem I (PSI) complexes, which directly affects the performance of biophotovoltaic devices by maximizing the efficiency of the extraction of electron/hole pairs from the complexes. The surface chemistry of the electrode on which the complexes assemble plays a critical role in their orientation. We compared the degree of orientation on self-assembled monolayers of phenyl-C61-butyric acid and a custom peptide on nanostructured gold electrodes. Biophotovoltaic devices fabricated with the C61 fulleroid exhibit significantly improved performance and reproducibility compared to those utilizing the peptide, yielding a 1.6-fold increase in efficiency. In addition, the C61-based devices were more stable under continuous illumination. Our findings show that fulleroids, which are well-known acceptor materials in organic photovoltaic devices, facilitate the extraction of electrons from PSI complexes without sacrificing control over the orientation of the complexes, highlighting this combination of traditional organic semiconductors with biomolecules as a viable approach to coopting natural photosynthetic systems for use in solar cells

Solidification behavior and microstructural features of the cast and HIPed N-bearing Ti–48Al–2Cr–2Nb intermetallic alloys

Copyright © 2023 The Author(s). Effect of N addition (0.5, 1, and 2 at. %) on solidification behavior and microstructural features of the cast and hot isostatically pressed (HIPed) Ti–48Al–2Cr–2Nb (4822) intermetallic alloy was investigated. Alloys were fabricated using vacuum arc re-melting followed by HIPing. The results showed that N addition changes the primary β phase dendrites to α phase. The morphological uniformity of the as-cast microstructures was notably increased by N addition. In addition, N addition beyond its solubility limit led to the formation of primary Ti2AlN precipitates located within lamellar colonies. A possible mechanism for nucleation of the Ti2AlN precipitates is proposed. Furthermore, N addition caused much more microstructure stability during HIPing. Although a duplex structure was formed after HIPing in the 4822 alloy, N addition decreased the formation of this structure. Moreover, highly extended network of secondary Ti2AlN precipitates were formed in almost all of (α2+γ) lamellas interfaces in the N-bearing alloys.Iran National Science Foundation (research project no. 98006118)

Effects of heat treatment on the atomic structure and surface energy of rutile and anatase TiO2 nanoparticles under vacuum and water environments

Nanomaterials have become a widely used group of materials in many chemical engineering applications owing to their ability to provide an enhanced level of functional properties compared to their crystalline and bulk counterparts. Here we report fundamental level advancements on how the anatase and rutile phase of TiO2 nanoparticles chemo-thermally respond between room temperature and the melting temperature under both vacuum and water environments. The current study is based on using molecular dynamics (MD) simulations. We present results on the equilibrium crystal morphology of these phases, structural and surface energy of TiO2 nanoparticles in the size range of 2-6 nm under different temperatures. Thermodynamic and structural properties, in the form of potential energy and Radial Distribution Functions (RDF’s) respectively, are calculated for both forms of TiO2 nanoparticles. The temperature associated with the melting transition increased with an increase in the particle size in both the phases. The potential energy change associated with the melting transition for anatase was seen to be less than that for rutile nanoparticles. Also the temperature at which the RDF’s began to stretch and broaden was observed to be lower for the case of anatase than rutile, suggesting that rutile attains the most thermal stable phase for the nano particle sizes considered in this study. Structural changes in anatase and rutile nanoparticles under different temperatures revealed that non-spherical (rod-like) rutile nanoparticles tend to be thermodynamically more stable. Surface energy influences the shape of TiO2 nanoparticles at different temperatures. The increase in the surface energy of nanoparticles under vacuum when compared with that of water environment is higher for the anatase phase than the rutile phase of nanoparticle sizes studied here. The fundamental level simulation results reported here provide a strong platform for potentially accounting for the effects of atomic-scale phase characteristics of TiO2 nanoparticles and surface energy under different temperature fields in nano processing applications and related multi-scale modelling approaches in future

EBSD characterization of cryogenically rolled type 321 austenitic stainless steel

Electron backscatter diffraction was applied to investigate microstructure evolution during cryogenic rolling of type 321 metastable austenitic stainless steel. As expected, rolling promoted deformation-induced martensitic transformation which developed preferentially in deformation bands. Because a large fraction of the imposed strain was accommodated by deformation banding, grain refinement in the parent austenite phase was minimal. The martensitic transformation was found to follow a general orientation relationship, {111}γ||{0001}ε||{110}α′ and 〈110〉γ||〈11-20〉ε||〈111〉α′, and was characterized by noticeable variant selection

Artificial neural network models for production of nano-grained structure in AISI 304L stainless steel by predicting thermo-mechanical parameters

An artificial neural network (ANN) model is developed for the analysis, simulation, and prediction of the austenite reversion in the thermo-mechanical treatment of 304L austenitic stainless steel. The results of the ANN model are in good agreement with the experimental data. The model is used to predict an appropriate annealing condition for austenite reversion through the martensite to austenite transformation. This model can also be used as a guide for further grain refining and to improve mechanical properties of the AISI 304L stainless steel.Upprättat; 2009; 20160623 (andbra