Enhancement Of Electrical Conductivity Research Articles

Cubic autocatalysis implementation in blood for non-Newtonian tetra hybrid nanofluid model through bounded artery

Abstract Tetra hybrid nanofluids are significant due to their unique properties like thermal and electrical conductivity enhancement, increased heat transfer, and improved fluid flow characteristics. This attempt proposes a tetra hybrid cross nanofluid model with the implementation of cubic autocatalysis in the context of blood flow passing through a stenosis artery. The model includes the effects of nanofluid, magnetic field, thermal radiation, and the cubic autocatalysis mechanism. This research investigates the innovative application of cubic autocatalysis within the context of blood flow through a tetra hybrid cross nanofluid model, specifically designed to simulate conditions within a stenosis horizontal artery. The equations governing the fluid flow are solved using the bvp5c method, and the numerical solutions are obtained for various parameter values. Specifically, the cubic autocatalysis mechanism profoundly impacts the velocity and concentration profiles of the blood flow. The proposed model and the obtained results provide new insights into the physics of blood flow passing through stenosis arteries. They may have important implications for the diagnosis and treatment of cardiovascular diseases. This article has a unique combination of tetra hybrid cross nanofluid model, cubic autocatalysis, and blood flow passing through the stenosis artery. These facts are not typically studied together in the context of blood flow.

Cu-doped NiO thin film's structural, optical, and electrical properties and its negative absorption behaviour in the Infra-Red region

NiO undoped and Cu-doped thin films on FTO-coated glass (fluorine-doped tin oxide) are prepared by employing the sol-gel spin coating method. The Cu-doping effect was observed in all the characterized reports such as absorption, transmittance, field emission scanning electron microscope (FESEM), Grazing Incidence X-ray Diffraction (GIXRD), photoluminescence (PL), Raman spectra, current-voltage measurement (IV), and X-ray photoelectron spectroscopy (XPS). Enhancement in electrical conductivity due to Cu doping and IR illumination has been found. Band gap can also be tuned by varying doping concentrations. One new phenomenon called negative absorption (NA) has been found while investigating the optical properties in the infrared (IR) region for both undoped and Cu-doped NiO on the FTO substrate, which opens a new door for advanced research. The multifarious properties of NiO thin films offer various applications in many different fields.

PERFORMANCE ENHANCEMENT OF BRASS EDM ELECTRODES WITH CRYOGENIC TREATMENT WHILE MACHINING THE COLD WORK STEEL AISI D2

This study investigates the performance of deep cryogenically treated brass (CuZn25Al5) electrodes in the die-sink EDM process. Two different cryogenic treatment durations, 6 h and 12 h, were applied to 8 mm diameter electrodes, and their effects were compared to untreated electrodes. The machining tests were conducted under moderate and aggressive conditions. In the machining tests, the 6-h cryo-treated electrode exhibited a 16.8% increase in material removal rate (MRR) under moderate conditions and a 19.7% increase under aggressive conditions compared to the reference electrode. The 12-h cryo-treated electrode showed similar MRR values to the reference electrode but improved tool wear resistance by 9.4% under moderate conditions. The kerf angle was minimized, indicating better hole verticality, in the 6-h cryo-treated electrode group. The improvement in machining performance was attributed to the enhancement in electrical conductivity of the electrodes, which increased by 28% for the 6-h cryo-treated electrode and 20% for the 12-h cryo-treated electrode. X-ray diffraction (XRD) analysis revealed shifts in peak positions and possible phase transformations due to cryogenic treatment. Surface roughness measurements showed improved surface conditions in the cryo-treated electrodes under aggressive conditions. The results indicate that cryogenic treatment enhances MRR, reduces tool wear, and improves surface quality in die-sink EDM. These improvements are attributed to increased electrical conductivity and changes in the internal structure of the brass electrode.

Surfactant assisted tuning of electrical conductivity, electromagnetic interference shielding effectiveness, wetting properties of poly(lactic acid)-expanded graphite-magnetite nanocube hybrid bio-nanocomposites

The study aimed at demonstrating polyvinylpyrrolidone (PVP) amount is critical for tuning electrical conductivity and electromagnetic interference shielding effectiveness (EMI SE) of poly(lactic acid)-expanded graphite (ExGr)-magnetite (Fe3O4) nanocube hybrid nanocomposites. An optimum loading of PVP (1 wt.%) was found to disperse the nanofillers resulting in enhanced electrical conductivity and EMI SE in the X-band dominated by the absorption mechanism. The electrical conductivity enhancement in hybrid nanocomposites was not only attributed to the network formation between fillers but also to the thickness of the coated surfactant layer. The inter-junction capacitance and real part of relative permittivity of the hybrid nanocomposites were also enhanced at 1 wt.% PVP addition in comparison to 0 wt.% and 2 wt.% surfactant loading. The water contact angle was found to depend on the surface roughness of the film, which varied with both PVP and ExGr loadings. These PLA-based hybrid nanocomposites can be used as microwave-absorbing material.

Enhancement of thermoelectric performance of thienoisoindigo based D‐A conjugated polymers through the incorporation of 3,4‐ethylenedioxythiophene as donor unit

AbstractWith the good planarity of conjugated backbone and high charge carrier mobilities, thienoisoindigo (TIIG)‐based polymers show great potential in organic electronic devices. In this work, two TIIG‐based D‐A conjugated polymers (PTIIG‐3T and PTIIG‐2T‐EDOT) were designed and synthesized, which exhibit high lying highest occupied molecular orbital (HOMO) energy level and can be facilely doped by FeCl3. Compared with PTIIG‐3T, one thiophene unit in the donor building block is replaced by 3,4‐ethylenedioxythiophene (EDOT) in PTIIG‐2T‐EDOT, and PTIIG‐2T‐EDOT shows a higher HOMO level with slightly higher coplanarity than PTIIG‐3T, which induce an enhancement in electrical conductivity after oxidation doping. After proper doping, doped PTIIG‐2T‐EDOT film achieved a higher TE power factor of 17.9 μW m−1 K−2 than that of PTIIG‐3T due to its higher conductivity. The results indicate that TIIG unit is a promising building block for future high‐performance conjugated polymers for thermoelectric applications, and incorporation of the EDOT unit into D‐A conjugated polymers could be an effective way to develop high performance thermoelectric polymers.

Metal oxide-based nanocomposites as advanced electrode materials for enhancing electrochemical performance of Supercapacitors: A comprehensive review

In recent years, the escalating use of nonrenewable fossil fuels has emerged as a significant threat to global sustainability, prompting the need for renewable, cost-effective, and eco-friendly energy storage solutions. Supercapacitors (SCs) are notable for their high power density (PD), cycle stability, and swift charge/discharge rates, although they fall short in energy density (ED) compared to traditional batteries. The performance of SCs is greatly influenced by the electrode materials used, highlighting the importance of material innovation in tackling the challenges posed by increasing fossil fuel consumption. Transition metal oxides (TMOs), known for their redox activity in energy storage, have been thoroughly investigated for their exceptional specific capacitance, which ranges from 100 to 2000F g−1, surpassing that of electrical double-layer capacitors (EDLCs). TMOs such as ruthenium oxide (RuO2), manganese oxide (MnO2), nickel oxide (NiO), cobalt oxide (Co3O4), tin oxide (SnO2), zinc oxide (ZnO), tungsten oxide (WO3), and vanadium pentoxide (V2O5) are widely researched for their high theoretical capacitance, affordability, and longevity. This review emphasizes the groundbreaking potential of metal oxide nanocomposites (NCs) formed by combining them with graphene, carbon nanotubes (CNTs), and polymers, leading to synergistic enhancements in electrical conductivity, surface area, and charge storage capacity. This thorough review not only presents an in-depth analysis of current research but also sheds light on potential future developments, contributing to the ongoing progress in the field of advanced electrode materials for energy storage.

Spin coated ultrathin PEDOT:PSS/SWCNT film with high electronic conductivity

Conductive Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) has been extensively used as non-metallic electrodes. However, the relatively low electrical conductivity of pristine PEDOT:PSS film restricts its further application. Although doping high content conductive filler or increasing the film thickness are effective for enhancing the electrical property, the transparency is sacrificed, which limits the application of PEDOT:PSS films. In this study, preparing PEDOT:PSS composite film with highly conductive and transparent property was the primary purpose. To achieve this goal, single-walled carbon nanotubes (SWCNTs) and dimethyl sulfoxide (DMSO) was chosen to composite with PEDOT:PSS. The spin-coated SWCNT/PEDOT:PSS composite film exhibited excellent electrical conductivity and transparency. The electrical conductivity of composite film with desired transmittance property (78%) reached the highest value (1060.96 S cm−1) at the SWCNTs content was 6 wt%. Under the modification process applied in this work, the non-conductive PSS was partially removed by incorporated DMSO and SWCNTs. Then, the molecular chains of PEDOT stretched and adsorbed onto the surface of SWCNTs, forming a highly efficient three-dimensional conductive structure, which contributed to the enhancement of electrical conductivity and transparency. Additionally, the spin-coating process allowed for the reduction of film thickness, ensuring better transparency. This research contributed to expanding the further applications of PEDOT:PSS films in high-performance transparent film electrodes.

Chemically functionalized AlN quantum dots for effective sensing and removal of methanol, ethanol, and formaldehyde: A first principle study

In this study, we delve into the structural and electronic intricacies of 2D aluminum nitride quantum dots (AlN-QDs) and their derivatives. Through detailed analysis, we uncover notable variations in bond lengths upon passivation with elements such as fluorine (F) and hydroxyl (OH) groups, with the latter exhibiting a particularly intriguing stability profile with a binding energy of 5.171 eV. Our investigation reveals a substantial energy gap of ∼5 eV in AlN-QDs, indicating enhanced electron confinement and optimal conditions for semiconductor applications. Furthermore, we elucidate the electron donation properties of nitrogen atoms and electron acceptance tendencies of aluminum atoms within AlN-QDs, shedding light on their unique electronic structure. Quantum stability assessments unveil charge distribution asymmetries and variations in electronegativity, contributing to a deeper understanding of AlN-QDs' robustness. We also demonstrate a significant enhancement in electrical conductivity, notably with AlN-QDs-surf-2CO exhibiting remarkable performance. Additionally, our study showcases AlN-QDs-OH's exceptional adsorption capabilities, evidenced by significantly higher adsorption energies for small organic compounds, highlighting their potential as highly effective sensors. Optical investigations further reinforce these findings, revealing distinct shifts in absorption spectra upon adsorption, which underscore the substantial impact of adsorbates on AlN-QDs' optical properties

Selective Cu electroplating enabled by surface patterning and enhanced conductivity of carbon fiber reinforced polymers upon air plasma etching

We demonstrate a sustainable post-processing of carbon fiber reinforced epoxy polymer (CFRP) composites by air plasma etching that permits regular electroconductive surface patterning through direct Cu galvanic metallization, in contrast to the untreated composite. Our study reveals a significant property dependence of the composite with respect to the position to the fiber/matrix composite surface and treatment. The enhancement in electrical conductivity was not compromised by the lower structural integrity of the composite, as the embedded carbon fibers remained unaffected by the air plasma etching process. The metallized Cu domains on the composite exhibit good hardness and excellent solderability potential. Thus, the electroconductive surface patterning of the composite, preceding galvanic metallization, facilitates the selective deposition of Cu layer domains. This step by step process, relying on the creation of selective electroconductive areas on the composite by plasma etching, enables galvanic metallization. Consequently, it enhances the potential for multifunctional composite applications. The feasibility of galvanic metallization brings new perspectives in selective metallization of composites by allowing the tailoring of the metal layer thickness, microstructure and selection of the metal.

Simultaneous Enhancement of Electrical Conductivity and Porosity of a Metal–Organic Framework Toward Thermoelectric Applications

AbstractMetal–organic frameworks (MOFs) exhibit large surface areas and low thermal conductivity, making them promising for thermoelectric generation. However, their limited electrical conductivity poses a significant hurdle to be practically useful. Traditionally, enhancing the electrical conductivity of MOFs typically comes at the cost of reducing surface area, thereby increasing thermal conductivity. This study introduces an approach to simultaneously boost the electrical conductivity and porosity of a MOF‐based material while maintaining remarkably low thermal conductivity. The electrically conductive poly(3,4‐ethylenedioxythiophene)‐poly(styrenesulfonate) (PEDOT:PSS) is deployed to nucleate the growth of Cu3(BTC)2 (or simply CuBTC, where BTC = benzene‐1,3,5‐tricarboxylic acid), resulting in the synthesis of composites labeled CPP‐y (where y denotes wt% PEDOT:PSS). Predictably, the CPP‐y composites are more electrically conductive than pure CuBTC, achieving an electrical conductivity exceeding 1.40 S cm−1 at room temperature. Furthermore, the CPP‐y composites exhibit consistently high Brunauer–Emmett–Teller (BET) surface areas of ≈1600 m2 g−1, comparable to pristine CuBTC, while maintaining thermal conductivities below 0.04 W m−1 K−1 at room temperature. With a high Seebeck coefficient in the range 180–373 µV K−1, CPP‐15 and CPP‐23 demonstrate a figure‐of‐merit (zT) of 0.25 and 0.11, respectively, at 285 K, marking a substantial achievement for MOF‐based materials.

Metavalently bonded tellurides: the essence of improved thermoelectric performance in elemental Te

Elemental Te is important for semiconductor applications including thermoelectric energy conversion. Introducing dopants such as As, Sb, and Bi has been proven critical for improving its thermoelectric performance. However, the remarkably low solubility of these elements in Te raises questions about the mechanism with which these dopants can improve the thermoelectric properties. Indeed, these dopants overwhelmingly form precipitates rather than dissolve in the Te lattice. To distinguish the role of doping and precipitation on the properties, we have developed a correlative method to locally determine the structure-property relationship for an individual matrix or precipitate. We reveal that the conspicuous enhancement of electrical conductivity and power factor of bulk Te stems from the dopant-induced metavalently bonded telluride precipitates. These precipitates form electrically beneficial interfaces with the Te matrix. A quantum-mechanical-derived map uncovers more candidates for advancing Te thermoelectrics. This unconventional doping scenario adds another recipe to the design options for thermoelectrics and opens interesting pathways for microstructure design.

Chemical modification and doping of poly(p-phenylenes): A theoretical study.

Conjugated polymers (CPs) have been recognized as promising materials for the manufacture of electronic devices. However, further studies are still needed to enhance the electrical conductivity of these type of organic materials. The two main strategies for achieving this improvement are the doping process and chemical modification of the polymer chain. Therefore, in this article, we conduct a theoretical investigation, employing DFT calculations to evaluate the structural, energetic, and electronic properties of pristine and push-pull-derived poly(p-phenylene) oligomers (PPPs), as well as the analysis at the molecular level of the polymer doping process. As a primary conclusion, we determined that the PPP oligomer substituted with the push-pull group 4-EtN/CNPhNO2 exhibited the smallest HOMO-LUMO gap (Eg) among the studied oligomers. Moreover, we observed that the doping process, whether through electron removal or the introduction of the dopant anion ClO4-, led to a substantial reduction in the Eg of the PPP, indicating an enhancement in the polymer's electrical conductivity. DFT calculations were conducted using the PBE0 functional along with the Pople's split valence 6-31G(d,p) basis set, which includes polarization functions on all atoms (B97D/6-31G(d,p)).

Enhancing thermoelectric behavior of Bismuth Selenide crystal via substitution of Sulfur and Tellurium

Sulfur and Tellurium substituted Bismuth Selenide (Bi2Se3-x-ySxTey, x = y = 0, 0.1, 0.15, 0.2) quaternary alloy crystals were synthesized by using vertical Bridgman technique. Energy dispersive analysis of X-rays confirmed elemental composition and purity of the grown crystals. Field emission scanning electron microscopy showed that the growth of crystals has occurred by layer growth mechanism. Rhombohedral crystal structure is validated through analysis of powder X-ray diffraction pattern. Thermoelectric parameters such as electrical conductivity, Seebeck coefficient and thermal conductivity were calculated from 303 K to 773 K and from that power factor as well as figure of merit have been determined for all grown crystals. Electrical conductivity significantly increased due to Sulfur and Tellurium incorporation and maximum value obtained is 147.72 S/cm at 503 K for Bi2Se2.6S0.2Te0.2. Seebeck coefficient and thermal conductivity showed decrement with incorporation of Sulfur and Tellurium. Reduction in thermal conductivity and enhancement in electrical conductivity resulted in the improvement of figure of merit. Sulfur and Tellurium substitution showed considerable improvement in ZT from 0.31 (533 K) for pristine Bi2Se3 to 1.28 (523 K) for Bi2Se2.6S0.2Te0.2.

Enhancing Strategy of the Small-Polaron Conductivity in LaCrO3: First-Principles Calculations and Experimental Validation.

LaCrO3 (LCO) has promising applications as a p-type conductive material in the fields of transparent conducting oxes, high-temperature sensors, and magnetohydrodynamic power generators. However, the easy volatility of the Cr element, along with the issues of low electrical conductivity caused by the small-polaron conduction mechanism and wide band gap, has hindered the widespread application of LCO. In this work, based on band engineering and defect engineering, we screened doping schemes through first-principles calculations that can reduce Cr volatility by enhancing the Cr-O bond energy. We also aimed to promote small-polaron hopping and improve the electrical conductivity by introducing impurity levels. Additionally, we conducted a thorough analysis of the small-polaron conductivity mechanism. Through the solid-state method, we successfully prepared codoped LCO with Ca and Zn. The Zn dopants effectively enhanced the Cr-O bond strength, suppressed the Cr volatility, and improved high-temperature stability. The Zn dopants introduced additional impurity energy levels within the band gap, significantly changing the mobility of small polarons. Through optimal doping concentration, the La0.7Ca0.3Cr0.95Zn0.05O3 sample demonstrated a significant enhancement in electrical conductivity compared to La0.7Ca0.3CrO3, increasing from 7 to 60 at 1000 K. Additionally, the impurity energy levels enhanced the asymmetry near the Fermi level, resulting in an increased Seebeck coefficient (S). This is beneficial for the production of high-temperature sensors. The output voltage of an LCO thermocouple module reaches up to 58 mV at 2170 K, indicating that the performance optimization strategy employed in this work has significant implications for the regulation and application of oxide electrical materials.

Regulating the aspect ratio of bulk few-layer graphene to improve the field emission performance

Owing to its excellent electrical conductivity and local electric field enhancement capability from abundant electron tunneling edges, graphene is a promising material for field emission. However, graphene thin-film emitters mostly emit in planar structures, and due to the flexibility of the thin film, it is commonly challenging to achieve vertical structure emission with large aspect ratios. Therefore, the emission performance of current graphene field emitters is difficult to meet the requirements of high current applications. In the present investigation, bulk few-layer graphene cathodes are formed by cold pressing to achieve upright structural field emission, and the emission performance is enhanced by appropriately adjusting the aspect ratio. The obtained bulk few-layer graphene emitters exhibit a higher conductivity of 2498 S/cm and tensile strength of 6.02 MPa. The turn-on electric field (at 1 mA/cm2) and threshold electric field (at 10 mA/cm2) in order are determined to be 1.78 V/μm and 2.66 V/μm, with a maximum current density of 986 mA/cm2 (at 6.65 V/μm) and a maximum field enhancement factor of 14,891. Excellent emission stability is achieved over a continuous period of 110 h at 5 mA @ 526 mA/cm2. With the increase of emission current, the bulk few-layer graphene with large aspect ratios exhibits better emission stability. This work provides valuable insights into the application of graphene-based field emitters at high currents.

Enhancement of electrical conductivity of biopolymer by sulfur nanoparticle dispersion technique

AbstractPresent work reports the investigation of the effect of different percentages of nanosized elemental sulfur particle grown in a biopolymer matrix. Sulfur is known for treatment against bacterial infections as an antimicrobial agent from ages as elemental sulfur and sulfur‐rich compounds interact with biological systems. In‐situ growth of sulfur nanoparticles is processed by the passage of environment friendly hydrogen sulfide gas in hydrated solution of gum acacia biopolymer. Gum acacia is ion conducting, plant derived natural polymer. In this work, structural and morphological studies are examined by x‐ray diffraction and scanning electron microscopy. It is found that with increasing concentration of sulfur nanoparticles the spheroidal shaped nanostructures grow in size and approaches the micron realm. Electrical characterization of the nanostructure synthesized biopolymer is observed by varying frequency over a broad‐spectrum range. Direct current electrical conductivity is found to be enhanced by 40 times higher over pure specimen.

Simultaneous enhancement of strength and conductivity via self-assembled lamellar architecture

Simultaneous improvement of strength and conductivity is urgently demanded but challenging for bimetallic materials. Here we show by creating a self-assembled lamellar (SAL) architecture in W-Cu system, enhancement in strength and electrical conductivity is able to be achieved at the same time. The SAL architecture features alternately stacked Cu layers and W lamellae containing high-density dislocations. This unique layout not only enables predominant stress partitioning in the W phase, but also promotes hetero-deformation induced strengthening. In addition, the SAL architecture possesses strong crack-buffering effect and damage tolerance. Meanwhile, it provides continuous conducting channels for electrons and reduces interface scattering. As a result, a yield strength that doubles the value of the counterpart, an increased electrical conductivity, and a large plasticity were achieved simultaneously in the SAL W-Cu composite. This study proposes a flexible strategy of architecture design and an effective method for manufacturing bimetallic composites with excellent integrated properties.

Heterogeneous diamond–TiC composites with high fracture toughness and electrical conductivity

The concurrent enhancement of toughness, electrical conductivity, and thermal stability in polycrystalline diamond composites represents a formidable challenge. Here, a novel diamond-TiC composites (referred to as DTC) with high fracture toughness and conductivity were synthesized through a high-temperature and high-pressure reaction sintering process utilizing two precursors: diamond mixtures containing TiH2 and Ti-coated diamonds. On the one hand, the inherent bonding and encasing of TiC onto the diamond matrix form a heterogeneous structure, providing high strength and excellent fracture toughness up to 11.6 MPa·m1/2. On the other hand, the established oxygen barrier and current pathway offer a thermal stability of 765 °C and high conductivity up to 837 S·m−1. Remarkably, this rare combination of mechanical, electrical, and thermal properties has been realized within a single material under relatively moderate sintering conditions, thus positioning diamond-TiC composites as a promising ceramic for electrical applications in high-stress environments.

Enhancement of gas adsorption on transition metal ion-modified graphene using DFT calculations.

Graphene-based nanomaterial was widely used in gas sensors, detection, and separation. However, weak adsorption and low selectivity of the pristine graphene used for gas sensors are major problems. Here, using density functional theory (DFT) calculations, we reported the significant increase of four gas molecules (N2, CO2, C2H2, and C2H4) adsorption on the transition metal ion (Fe3+, Co2+, Ni2+)-modified graphene complex (Fe3+/Co2+/Ni2+-G) comparing to be absorbed on the pristine graphene (G). Moreover, the Co2+-G is suitable for the selective separation of C2H4/C2H2 due to the larger adsorption energy difference (8.5kcal/mol) between them. The addition of transition metal ions also decreased the HOMO-LUMO gap of the systems, which benefits the enhancement of electrical conductivity. This suggests that the transition metal ion-modified graphene can be used to distinguish the different gas molecule's adsorption, facilitating the design of graphene-based gas sensors and selective separation. All the density functional theory (DFT) calculations were performed by B3LYP with the GD3 dispersion method using Gaussian 16 software. The basis set 6-31G(d) was used for C, H, O, and N atoms, and Lanl2DZ was used for transition metal ions (Fe3+, Co2+, Ni2+). The DOS analysis and energy decomposition analysis were performed using the Multiwfn program.

Metal‐organic Frameworks in Semiconductor Devices

AbstractMetal‐organic frameworks (MOFs) are a specific class of hybrid, crystalline, nano‐porous materials made of metal‐ion‐based ‘nodes’ and organic linkers. Most of the studies on MOFs largely focused on porosity, chemical and structural diversity, gas sorption, sensing, drug delivery, catalysis, and separation applications. In contrast, much less reports paid attention to understanding and tuning the electrical properties of MOFs. Poor electrical conductivity of MOFs (~10−7–10−10 S cm−1), reported in earlier studies, impeded their applications in electronics, optoelectronics, and renewable energy storage. To overcome this drawback, the MOF community has adopted several intriguing strategies for electronic applications. The present review focuses on creatively designed bulk MOFs and surface‐anchored MOFs (SURMOFs) with different metal nodes (from transition metals to lanthanides), ligand functionalities, and doping entities, allowing tuning and enhancement of electrical conductivity. Diverse platforms for MOFs‐based electronic device fabrications, conductivity measurements, and underlying charge transport mechanisms are also addressed. Overall, the review highlights the pros and cons of MOFs‐based electronics (MOFtronics), followed by an analysis of the future directions of research, including optimization of the MOF compositions, heterostructures, electrical contacts, device stacking, and further relevant options which can be of interest for MOF researchers and result in improved devices performance.