Increase In Electrical Conductivity Research Articles

Electrical conductivity of Ni ferrite nanofluids: An experimental study on the effects of temperature, volume fraction, and base fluid

This study investigates the electrical conductivity of NiFe2O4 nanofluids in water and ethylene glycol (EG) as base fluids, aiming to understand how varying volume fractions (φ= 0 %, 0.1 %, 0.25 %, 0.45 %, 0.7 %, and 1 %) and temperatures (20–70°C) influence electrical conductivity. NiFe2O4 nanoparticles were synthesized using the chemical co-precipitation method and characterized through X-ray Diffraction (XRD), Field Emission Scanning Electron Microscopy (FESEM), and Energy Dispersive Spectroscopy (EDS). The results revealed that at 70°C, the electrical conductivity of NiFe2O4-water nanofluid increased by 1100 % within the volume fraction range of 0–1 %. For NiFe2O4-EG nanofluid, the increase in electrical conductivity was even more significant, reaching 1235 % within the same volume fraction range. Similarly, at a 1 % volume fraction within the temperature range of 20–70°C, the electrical conductivity of NiFe2O4-water nanofluid increased by 136 %, while for NiFe2O4-EG nanofluid, it was 370 %. These findings indicate that both temperature and volume fraction significantly enhance the electrical conductivity of the nanofluids, with a more pronounced effect observed in the NiFe2O4-EG nanofluid compared to the NiFe2O4-water nanofluid. The study validated Shen et al.'s model for electrical conductivity in nanofluids, contrasting with Maxwell's model. The novelty of this work lies in the comprehensive analysis of the electrical conductivity behavior of these nanofluids, which has not been extensively reported in the literature. These findings have potential applications in heat transfer enhancement and magnetic-targeted drug delivery.

Effect of BaTiO3 Filler Modification with Multiwalled Carbon Nanotubes on Electric Properties of Polymer Nanocomposites.

Two ranges of dielectric permittivity (k) increase in polymer composites upon the modification of BaTiO3 filler with multiwalled carbon nanotubes (MWCNTs) are shown for the first time. The first increase in permittivity is observed at low MWCNT content in the composite (approximately 0.07 vol.%) without a considerable increase in dielectric loss tangent and electrical conductivity. This effect is determined by the intensification of filler-polymer interactions caused by the nanotubes, which introduce Brønsted acidic centers on the modified filler surface and thus promote interactions with the cyanoethyl ester of polyvinyl alcohol (CEPVA) polymer binder. Consequently, the structure of the composites becomes more uniform: the permittivity increase is accompanied by a decrease in the lacunarity (nonuniformity) of the structure and an increase in scale invariance, which characterizes the self-similarity of the composite structure. The permittivity of the composites in the first range follows a modified Lichtenecker equation, including the content of Brønsted acidic centers as a parameter. The second permittivity growth range features a drastic increase in the dielectric loss tangent and conductivity corresponding to the percolation effect with the threshold at 0.3 vol.% of MWCNTs.

Seasonal Effects of Wildfires on the Physical and Chemical Properties of Soil in Andean Grassland Ecosystems in Cusco, Peru: Pending Challenges

Soils are a valuable renewable resource on human timescales, and they interact with distinctive grassland ecosystems characterized by unique biodiversity and essential provision of ecosystem services, such as water supply and carbon sequestration. However, knowledge of the effects of wildfires on soil properties and nutrient availability in the Andes remains limited. Andean grasslands are currently one of the ecosystems of the Peruvian Andes most affected by wildfires. Our objective is to analyze the effect of fire activity on the physicochemical properties of soil and analyze its social context in Cusco, in the southern Andes of Peru. Soil samples were collected during five periods, spanning both the dry and rainy seasons, to characterize changes in soil properties and monitor vegetation recovery post-fire in two local communities dedicated to livestock activities. The vegetation restored after the wildfire was measured by the “step transect” method. Post-fire changes in soil properties indicate slight increases in pH, electrical conductivity, organic matter, nitrogen, phosphorus, and potassium during the onset of the rainy season; thereafter, a gradual reduction in these values was observed. This reduction can be attributed to leaching associated with the seasonal rainfall and runoff regime. Our findings indicate that one-year post-fire, the biomass in burned areas is reduced to 30–46% of the biomass in unburned areas. A complete regeneration is likely to occur in up to 4 years; this assertion is supported by the perceptions of the affected population, as expressed in interviews conducted in the two farming communities. These results are significant for decision-makers formulation of policies and regulations regarding grasslands and their seasonal restoration.

Thermophysical properties, crystallization behavior and structure of CaO–SiO2–MgO–Al2O3–TiO2–FeO slag with varying TiO2 contents

This study investigated the effect of TiO2 content on the viscosity, free running temperature, electrical conductivity, crystallization behavior, and structure of high-titanium CaO–SiO2-10 wt% MgO-13 wt%Al2O3–TiO2-4 wt.% FeO slag by experiments and molecular dynamics simulations. The results revealed that increasing TiO2 weakened the overall bonding energy and simplified the slag structure, leading to a decrease in viscosity and an increase in electrical conductivity. Thermodynamic calculations revealed a continuous enrichment of the slag towards the pseudobrookite region with increasing TiO2 content. The precipitation of pseudobrookite phase during cooling resulted in short-slag characteristics and a rising free running temperature. Additionally, the peak intensity of pseudobrookite phase gradually enhanced and its morphology changed from elongated strips to plates with higher TiO2 concentration. Structural analysis demonstrated that the poorly stabilized [TiO6] octahedron was the major form of Ti atoms in the slag, and its proportion progressively increased with increasing TiO2 content.

Highly flexible EMA/Fe3O4@g-C3N4 composite for thermal control and EMI shielding application

Developing advanced EMI shielding materials, possessing robust mechanical properties, and exhibiting efficient thermal conductivity is challenging for contemporary electronic devices. This study involved creating a robust and adaptable polymer composite by combining an EMA (Ethylene Methyl Acrylate Copolymer) polymer matrix with Fe3O4@g-C3N4 (iron oxide decorated on Graphitic carbon nitride) filler utilising a solvent mixing approach. The material showed exceptional electromagnetic interference (EMI) shielding, beneficial thermal conductivity, and mechanical strength. Morphological analysis indicates that the Fe3O4@g-C3N4 particles are evenly dispersed inside the EMA matrix, facilitating a compact spatial network all over the matrix to enable electron hopping. The composites, consisting of Fe3O4@g-C3N4 (15 wt%) conductive filler, demonstrated a notable increase in electrical conductivity, reaching 10−2 S/cm, and an effective EMI SE of −32.4 dB. Additionally, the composite showed a thermal conductivity of 1.3 W.m−1. K−1 and outstanding mechanical strength. The synthesized polymer composite shows great potential for EMI shielding and is well-suited for wearing smart devices.

Effect of functionalized graphene nanoplatelet dispersion on thermal and electrical properties of hybrid carbon fiber reinforced aviation epoxy laminated composite

Carbon fiber reinforced polymers (CFRP) alone cannot meet the increasing requirements of the aerospace industry. Therefore, graphene nanoplatelets (GNPs) dispersed homogeneously in the matrix offer unique advantages. This study aimed to increase the thermal and electrical properties by adding functionalized GNPs (f-GNP) to the aviation epoxy matrix (Araldite LY5052) in CFRP at different rates (neat - 0.5–1–1.5 wt%) for the first time and to provide homogeneous dispersion with surfactant. The results showed that FGNP as an additive achieved significant homogeneity. While the glass transition temperature (Tg) in the neat composite is 121 °C, it is 123 °C, 127 °C and 133 °C in nanocomposites with 0.5–1–1.5 wt% additives, respectively. In addition, the melting point is 366 °C in the neat composite and 368.6 °C, 370 °C, and 370.3 °C in the nanocomposites with 0.5–1–1.5 wt% additives, respectively. The oxygen groups in the additive increased the energy barrier, thus increasing the percolation threshold. There was a 50 % increase in electrical conductivity in the sample with 0.5 wt% doping with bulk current density and an 18 % increase with 1 wt% doping with surface current density. Meanwhile, the π-π bonds formed by the surfactant with GNPs and the hydrogen bonds formed with the matrix served as a bridge by filling the gaps in the interphase, significantly increasing the flow of heat and electricity.

Incorporation of Ni in Cu2SnSe3: An insight into the reduction in electrical resistivity

In the present study, Cu2SnSe3/x% Ni (x = 0, 1, 2 and 3 wt%) composite thermoelectric were synthesized using solid-state reaction followed by sintering in the mid-temperature range 300–570 K. XRD studies revealed that the samples have a diamond cubic structure with the F4¯3m space group. Scanning Electron Microscopy indicates that the synthesized samples possess homogeneous surfaces with fewer pores. The sample with 3% Ni exhibits an approximately eight-fold increase in electrical conductivity than the pure sample at 307 K. However, the addition of Ni decreased the Seebeck coefficient, resulting in a lower overall power factor (PF) for the composites. The highest PF of ∼420 μW/mK2, was observed in the pristine sample at 570 K. Although Ni addition improves electrical properties, it negatively impacts the overall thermoelectric performance due to the significant reduction in Seebeck coefficient, thereby lowering the overall power factor.

Enhancing Effect of Fullerene Guest and Counterion on the Structural Stability and Electrical Conductivity of Octahedral Metallo‐Supramolecular Cages

Metallo‐supramolecular cages have garnered tremendous attention for their diverse yet molecular‐level precision structures. However, physical properties of these supramolecular ensembles, which are of potential significance in molecular electronics, remain largely unexplored. We herein constructed a series of octahedral metallo‐cages and cage‐fullerene complexes with notably enhanced structural stability. As such, we could systematically evaluate the electrical conductivity of these ensembles at both single‐molecule level and aggregated bulk state (as well‐defined films). Our findings reveal that counteranions and fullerene guests play a pivotal role in determining the electrical conductivity of aggregated state, while such effects are less significant for single‐molecule conductance. Both counteranions and fullerenes effectively tune the electronic structures and packing density of metallo‐supramolecular assemblies, and facilitate efficient charge transfer between the cage hosts and fullerenes, resulting in a notable one order of magnitude increase in electrical conductivity of the aggregated state.

Photoconductivity of explosive percolation in conductive polymer/graphene oxide nanocomposite films

AbstractIn this study, we explored the behavior of protonated polyaniline/graphene oxide (PANI‐CSA/GO) nanocomposite films with varying GO concentrations, focusing on the novel phenomenon of explosive percolation. We observed a significant increase in electrical conductivity at the explosive percolation threshold, attributed to the emergence of a percolating metallic pathway. This discovery positions PANI‐CSA/GO films as promising materials for various electronic and electrical engineering applications. Additionally, the films demonstrated consistent and repeatable photoconductivity, showing potential for use in high‐performance UV‐photodetectors, photoactive layers in solar cells, light‐emitting diodes, and energy storage devices. Structural analyses using fourier transform infrared spectroscopy (FTIR) and x‐ray diffraction (XRD) confirmed successful GO incorporation within the PANI‐CSA matrix. Different morphological features were observed depending on the GO volume fraction, with increased GO enhancing thermal stability in the conductive zone. Our findings highlight the immense potential of PANI‐CSA/GO nanocomposite films in advanced electronic applications, emphasizing their novel conductive and photoconductive properties and improved thermal stability.

Assessing the Impact of Brackish Water on Soil Salinization with Time-Lapse Inversion of Electromagnetic Induction Data

Over the last decade, electromagnetic induction (EMI) measurements have been increasingly used for investigating soil salinization caused by the use of brackish or saline water as an irrigation source. EMI measurements proved to be a powerful tool for providing spatial information on the investigated soil because of the correlation between the output geophysical parameter, i.e., the electrical conductivity, to soil moisture and salinity. In addition, their non-invasive nature and their capability to collect a high amount of data over broad areas and in a relatively short time makes these measurements attractive for monitoring flow and transport dynamics, which are otherwise undetectable with conventional measurements. In an experimental field, EMI measurements were collected during the growth season of tomatoes and irrigated with three different irrigation strategies. Time-lapse data were collected over three months in order to visualize changes in electrical conductivity associated with soil salinity. A rigorous time-lapse inversion procedure was set for modeling the soil salinization induced by brackish irrigation water. A clear soil response in terms of an increase in electrical conductivity (EC) in the upper soil layer confirmed the reliability of the geophysical tool to predict soil salinization trends.

Changes in the Properties of Soils Contaminated with Oil Production Water Before and Af ter Treatment with CaO

In the Mexican southeast, hydrocarbon spills and their residues af fect various agricultural sites. A specific case is spills of oil production or congenital waters that cause soil salinization. When soil is contaminated, restorations are regularly carried out based on regulatory limits, but many regions still do not consider the pedological classification, so restorations are not entirely ef fective and, in the case of agricultural soils, reduce your productivity. For these reasons, this study evaluated the cation exchange with CaO applied to four soils contaminated with congenital waters and determined if there are dif ferences in the treatment behavior according to the properties of each soil. It will be found that sandy soils require less treatment time, but have greater ef fects on their properties compared to clay soils, mainly in field capacity, pH, and porosity. Furthermore, it was found that contaminant removal times vary with respect to the type of soil and that this could be related to the amount and type of clay. In the case of congenital water spills, clay soils show a greater increase in electrical conductivity (EC) compared to sandy soils. When remediated with CaO, clay soils needed longer treatment times to reduce EC, but presented fewer changes in their physical and chemical properties. In addition, it was found that, although washing with drinking water is carried out, the treatment with CaO adds alkalinity to the soils, so they must be managed according to the crop to be developed. It is concluded that soils have dif ferent physical and chemical properties, this influences the response they have to an external agent, both when contaminated and when remediated.

Defect and dopant complex mediated high power factor in transparent selenium-doped copper iodide thin films

Copper iodide (CuI) is a promising p-type transparent thermoelectric material for near-room temperature energy harvesting. We report a high-power factor for selenium (Se)-doped CuI films. Ion beam-sputtered CuI films were doped using 30 keV 80Se+ implantation with Se concentration varying between 0.50% and 6.50%. Hall effect measurements showed a ∼34% increase in electrical conductivity (σ ≈ 36.1 Ω−1cm−1) due to a ∼54% increase in carrier density (pH ≈ 5.4 × 1019 cm−3) in the p-type γ-CuI film implanted with 5.0 × 1014 Se.cm−2. A high Seebeck coefficient, α ≈ 388.9 μVK−1−1, and moderate electrical conductivity, σ ≈ 29.1 Ω−1cm−1, yield a nearly 85% increase in the power factor, α2σ ≈ 439.7 μWm−1K−2, for a 1.0 × 1015 Se.cm−2 implanted film compared to the unimplanted film (α2σ ≈ 236.4 μWm−1K−2). Monte Carlo simulation and ab initio density functional theory calculations revealed that the increased displacement per atom values and the {SeI−VCu} defect complex-induced shallow acceptor could be attributed to the observed increase in hole density. Our results highlight that native defects and defect complexes are beneficial for enhancing the power factor in transparent CuI for thermoelectric applications.

Demonstration scale chemical–physical treatment and agricultural reuse of highly saline textile wastewater

AbstractThis study aimed to develop an energy‐efficient process for treating highly saline textile wastewater (TWW) in a 10 m3/day pilot plant and evaluate forage sorghum irrigation with treated wastewater in terms of crop production and soil and irrigation device performance. The TWW treatment pilot plant, consisting of a coagulation/flocculation unit followed by a sand filter and an anion exchange resin column, produced treated effluent that complied with the permissible limits specified in the ISO 16075‐2:2020 standard for Category C irrigation water. The corresponding average energy consumption was 1.77 kWh/m3. Reusing treated TWW for forage sorghum irrigation over a 13‐week cycle yielded crop performances comparable with freshwater irrigation, with no negative impact on the irrigation system. Although soil profiles were similar between treated TWW and freshwater irrigation, both soils featured an increase in electrical conductivity, which may reversibly or irreversibly affect soil quality and damage salt‐sensitive crops. These findings demonstrate the effective treatment and reuse of saline TWW for irrigating salt‐tolerant crops, offering significant implications for industrial wastewater management and cropping patterns in arid and semi‐arid regions.

SODIUM, MONOETHANOLAMMONIUM AND POLYETHYLENE POLYAMMONIUM CITRATES AQUEOUS SOLUTIONS ELECTROCHEMICAL PROPERTIES

pH and conductometric study of aqueous (0.1 ÷ 9.0)⋅10-3 mol/l solutions of sodium (Na3Cit), monoethanolammonium (H3Cit⋅3MEA) and polyethylenepolyammonium (kH3Cit⋅3PEPA) citrates was carried out. Features of the electrochemical behavior of monoethanolamine and polyethylenepolamine ammonium citrates aqueous solutions were revealed in comparison with Na3Cit. As the temperature increases from 293 to 303 K, the pH values and Na3Cit solutions molar electrical conductivity increase. Due to hydrolytic processes, when diluting H3Cit⋅3MEA solutions, a change in pH is observed from slightly acidic to slightly alkaline, in contrast to Na3Cit. An increase in temperature (in the region of 293–308 K) leads to an increase in the medium acidity, in contrast to sodium citrate solutions, which is accompanied by an atypical decrease in molar electrical conductivity at the same H3Cit⋅3MEA content. It has been shown that an increase in temperature in the range of 293-308 K leads to a decrease in H3Cit⋅3MEA aqueous solutions pH, in contrast to Na3Cit and kH3Cit⋅3PEPA solutions, which is accompanied by an atypical decrease in molar electrical conductivity at the same H3Cit⋅3MEA content. The component composition of Na3Cit, H3Cit⋅3MEA and kH3Cit⋅3PEPA aqueous solutions was calculated. The probability of the existence of negatively charged ion-molecular complexes in H3Cit⋅3MEA and kH3Cit⋅3PEPA aqueous solutions is shown. The concentration and temperature dependence of citrate ions hydrolysis constant was obtained. The concentration and temperature dependence of these complexes was assessed. The atypical negative effect of heating on H3Cit⋅3MEA aqueous solutions molar electrical conductivity is associated with a change in the radius of the ion-molecular complex and its stability. The value of the limiting molar electrical conductivity of sodium, monoethanolammonium and polyethylenepolyammonium citrates aqueous solutions in the range of 293–313 K was estimated. Correlations were revealed between the values of the limiting electrical conductivity and ion-molecular complexes formation constants in H3Cit⋅PEPA aqueous solutions. The values of energy, enthalpy and entropy of activation of molar electrical conductivities of aqueous solutions were calculated. For the solutions studied, compensation effects were noted in the activation parameters of molar electrical conductivity.

Electromagnetic wave absorption value of iron-rich steel slag for application in foam concrete

In this study, iron-rich steel slag (IRSS) and carbon fiber (CF) were incorporated into foam concrete to maximize the economic benefits of composites and multifunctional integration while improving the overall performance of foam concrete. The study found that the optimal IRSS content for maximizing foam concrete’s compressive strength was 15 %, which increased by 18.59 % compared to the control. Additionally, S15 specimens showed a 37.87 % increase in electrical conductivity compared to the control. In addition, the average value of the fundamental part of the dielectric constant of the S15 specimen was 7.409, the average value of the imaginary part was 3.057, and the angular tangent of the electrical loss (tanδε) value and the reflection loss were both improved, which indicated that the S15 specimen material had a better ability to absorb electromagnetic waves and had an excellent performance of electromagnetic loss.

Photoluminescent ionic liquid-poly(vinylidene fluoride) hybrid materials for UV-Vis filter applications

Smart multifunctional materials have been increasingly applied in different fields of knowledge. In particular, photoluminescent materials have been explored for displays, radiation detection, lamps or anti-counterfeiting applications, among others. This work reports the development of photoluminescent materials based on poly(vinylidene fluoride) (PVDF) polymer incorporating different contents (0, 5, 10, and 20 % w/w) of the luminescent ionic liquid (IL) 1-butyl-3-methylimidazolium tetrakis(thenoyltrifluoroacetonato)europate(III) ([Bmim][Eu(tta)4]). The inclusion of the IL induced an increase of roughness and a slightly porous structure. No changes occur in the PVDF chemical structure and thermal behaviour. A decrease in the Young Modulus was observed, from 1.75×103 ± 1.56×102 to 5.09×102 ± 2.07×102 MPa for the sample incorporating 20 % w/w of IL which acted as a plasticizer. Further, the presence of ionic charges promoted an increase in electrical conductivity. The influence of IL content on the luminance was evaluated and a proof of concept demonstrating the potential of the composites as a UV–vis filter converter is provided.

Investigating the properties of nanoparticles from heveabrasiliensis shell for coolant application in PEMFCs

Extensive consumption of petroleum-based products, which has resulted in energy depletion, prompted a need to seek alternative and renewable means of transportation. PEMFCs can achieve high power density, low operating temperatures, rapid start-up, and clean energy, making them ideal for transportation. Several studies have demonstrated that conventional cooling agents, such as water or water with ethylene glycol, do not dissipate heat efficiently in PEMFCs, resulting in deteriorating performance and a shortened operational lifespan over time. The incorporation of bio-sourced nanofluids as an alternative coolant for Proton Exchange Membrane (PEM) fuel cells is the newest venture to take over PEM fuel cell development. Utilizing bio-sourced nanofluids is being evaluated for elevating the heat conduction and decreasing the electrical conductivity of proton exchange membrane fuel cells (PEMFCs). The objective of this article is to investigate Hevea brasiliensis Shell (HBS)-based nanofluids dispersed in water and Ethylene glycol (EG) at varying concentrations of 0.1 vol%, 0.3 vol%, and 0.5 vol% by paying attention to improving heat transfer, extracting high electrical output, reducing pump loss, and increasing the longevity of cells. As an adverse effect, incorporating HBS at a 0.5 % volume concentration within an 80:20 mixture of water and ethylene glycol (W:EG) resulted in an 8 % improvement in heat transfer and a 77 % increase in electrical conductivity when compared to W:EG (80:20), which is promising as a pertinent cooling technique for PEMFC stacks.

Unravelling the impact of microclimatic changes on coastal aquifer of multiple land use through integrated techniques: A comparative study using two decadal data

Regional climatic changes reflect the microclimatic variations and these affect the water resources of a region. Urbanization and population growth significantly influence microclimates, impacting groundwater resources and Land Surface Temperature (LST). The climatic variables (rainfall and temperature) interplay with geospatial parameters such as Land Use Land Cover (LULC), LST influence the quality and quantity of groundwater. Hence, this current approach employs geospatial techniques to explore the interrelationship between these variables by studying the long-term variation for a period of 20 years (1997–2018) to assess the microclimate variation and its impact on groundwater resources of a coastal aquifers with complex lithology. Results reveal a notable increase in minimum and maximum temperatures, with an average annual rise of 0.5°C predominantly along the western part. Spatial rainfall variation for the study period was higher in the northern region influenced by urban heat islands. The change in LULC reflected a 12% increase in agricultural areas and a 1.7% expansion in habitation, accompanied by a decline in surface water bodies in 2018. Maximum increase in electrical conductivity(EC) is observed along the southern coastal region, indicating rise in ionic concentration due contamination from sea water, urban and agricultural sources, witnessed by the isotopic signatures. Comparison of the depth to groundwater between the different study periods indicate a maximum depletion of 49m in northeastern and western regions due to extraction for domestic water supply, agriculture and mining. Further, a maximum rise of 14m in the regions adjacent to the reservoirs was observed, during 2018. The current study reveals the relationship between microclimate and groundwater (quality and the quantity) is predominantly observed in the northern and western parts of the study area. Our findings suggest that managing groundwater extraction and improving land use practices are essential for sustainable development, primarily through policy and governance.

MXenes with ordered triatomic-layer borate polyanion terminations.

Surface terminations profoundly influence the intrinsic properties of MXenes, but existing terminations are limited to monoatomic layers or simple groups, showing disordered arrangements and inferior stability. Here we present the synthesis of MXenes with triatomic-layer borate polyanion terminations (OBO terminations) through a flux-assisted eutectic molten etching approach. During the synthesis, Lewis acidic salts act as the etching agent to obtain the MXene backbone, while borax generates BO2- species, which cap the MXene surface with an O-B-O configuration. In contrast to conventional chlorine/oxygen-terminated Nb2C with localized charge transport, OBO-terminated Nb2C features band transport described by the Drude model, exhibiting a 15-fold increase in electrical conductivity and a 10-fold improvement in charge mobility at the d.c. limit. This transition is attributed to surface ordering that effectively mitigates charge carrier backscattering and trapping. Additionally, OBO terminations provide Ti3C2 MXene with substantially enriched Li+-hosting sites and thereby a large charge-storage capacity of 420 mAh g-1. Our findings illustrate the potential of intricate termination configurations in MXenes and their applications for (opto)electronics and energy storage.

Microporous Zr-metal-organic frameworks based-nanocomposites for thermoelectric applications

In the area of energy storage and conversion, Metal-Organic Frameworks (MOFs) are receiving more and more attention. They combine organic nature with long-range order and low thermal conductivity, giving them qualities to be potentially attractive for thermoelectric applications. To make the framework electrically conductive so far, thermoelectricity in this class of materials requires infiltration by outside conductive guest molecules. In this study, an in-situ polymerization of conductive polyaniline inside the porous structure of MOF-801 was conducted to synthesize PANi@MOF-801 nanocomposites for thermoelectrical applications. The growth of polyaniline chains of different loadings inside the host MOF matrix generally enhanced bulk electrical conductivity by about 6 orders of magnitude, leading to Seebeck coefficient value of -141 µVK−1 and improved thermal stability. The unusual increase in electrical conductivity was attributed to the formation of highly oriented conductive PANi chains inside the MOF pores, besides host–guest physical interaction, while the Seebeck coefficient enhancement was because of the energy filtering effect of the developed structure. Modulating the composition of PANi@MOF-801 composites by varying the aniline: MOF-801 ratio in the synthesis bath from 2:1 and 1:1 to 1:2 leads to a change in the semiconductor properties from p-type semiconductor to n-type. Among the examined composites with n-type semiconducting properties exhibited the highest ZT value, 0.015, and lowest thermal conductivity, 0.24 Wm−1 K−1. The synthesized composites have better performance than those recently reported for a similar category of thermoelectric materials related to MOF-based composites.