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Highlights Dielectric CaCu3Ti4O12 (CCTO) was used as electrolyte in low-temperature solid oxide fuel cells for the first time. A new heterostructure electrolyte was designed based on CCTO and Ni0.8Co0.15Al0.05LiO2−δ (NCAL). Promising ionic conductivity and high fuel cell performance were achieved CCTO–NCAL realized an electrolyte function due to its good dielectric property and a heterojunction effect.

Interfacial solar‐driven water evaporation has shown promising prospects in desalination technology. However, the lower photothermal conversion efficiency caused by the intermittent nature of sunlight and salt accumulation remains a significant challenge for continuous desalination. Herein, the hierarchical design of interfacial solar evaporation is reported, which realizes enhanced photothermal conversion, waste heat storage/release, and effective thermal management for continuous desalination. The solar evaporator is composed of worm‐like SrCoO3 perovskite oxide anchored on super hydrophilic polyurethane (PU) foam succeeded by in situ polymerization of conducting polypyrrole (SrCoO3@PPy). The energy storage system is introduced within polyurethane matrix by a paraffin block followed by a tongue‐and‐groove structure for convective water transportation, and a heat recovery unit largely reduces heat losses. The solar evaporator possesses excellent evaporation rates (2.13 kg m−2 h−1) along with 93% solar‐to‐vapor conversion efficiency under 1 kw m−2 solar irradiation owing to its minimum equivalent evaporation enthalpy and (0.85 kg m−2 h−1) under intermittent solar irradiation as compared to conventional solar evaporators. More importantly, state‐of‐the‐art experimental investigations validate waste heat recovery/release and the salt‐resistant capability of solar evaporators optimized by computational fluid dynamic simulation. This study breaks conventional solar interfacial evaporation's limitations and demonstrates stable desalination under intermittent sunlight.

Drought stress significantly restricts the growth, yield, and quality of peppers. Strigolactone (SL), a relatively new plant hormone, has shown promise in alleviating drought-related symptoms in pepper plants. However, there is limited knowledge on how SL affects the gene expression in peppers when exposed to drought stress (DS) after the foliar application of SL. To explore this, we conducted a thorough physiological and transcriptome analysis investigation to uncover the mechanisms through which SL mitigates the effects of DS on pepper seedlings. DS inhibited the growth of pepper seedlings, altered antioxidant enzyme activity, reduced relative water content (RWC), and caused oxidative damage. On the contrary, the application of SL significantly enhanced RWC, promoted root morphology, and increased leaf pigment content. SL also protected pepper seedlings from drought-induced oxidative damage by reducing MDA and H2O2 levels and maintaining POD, CAT, and SOD activity. Moreover, transcriptomic analysis revealed that differentially expressed genes were enriched in ribosomes, ABC transporters, phenylpropanoid biosynthesis, and Auxin/MAPK signaling pathways in DS and DS + SL treatment. Furthermore, the results of qRT-PCR showed the up-regulation of AGR7, ABI5, BRI1, and PDR4 and down-regulation of SAPK6, NTF4, PYL6, and GPX4 in SL treatment compared with drought-only treatment. In particular, the key gene for SL signal transduction, SMXL6, was down-regulated under drought. These results elucidate the molecular aspects underlying SL-mediated plant DS tolerance, and provide pivotal strategies for effectively achieving pepper drought resilience.

Abstract Since colossal ionic conductivity was detected in the planar heterostructures consisting of fluorite and perovskite, heterostructures have drawn great research interest as potential electrolytes for solid oxide fuel cells (SOFCs). However, so far, the practical uses of such promising material have failed to materialize in SOFCs due to the short circuit risk caused by SrTiO3. In this study, a series of fluorite/perovskite heterostructures made of Sm-doped CeO2 and SrTiO3 (SDC–STO) are developed in a new bulk-heterostructure form and evaluated as electrolytes. The prepared cells exhibit a peak power density of 892 mW cm−2 along with open circuit voltage of 1.1 V at 550 °C for the optimal composition of 4SDC–6STO. Further electrical studies reveal a high ionic conductivity of 0.05–0.14 S cm−1 at 450–550 °C, which shows remarkable enhancement compared to that of simplex SDC. Via AC impedance analysis, it has been shown that the small grain-boundary and electrode polarization resistances play the major roles in resulting in the superior performance. Furthermore, a Schottky junction effect is proposed by considering the work functions and electronic affinities to interpret the avoidance of short circuit in the SDC–STO cell. Our findings thus indicate a new insight to design electrolytes for low-temperature SOFCs.

The militia as an informal pro-government irregular force helps government forces through a range of asymmetric security threats. Since 9/11, the employment of militia forces has been on the rise. Although the informal Pro-Government Militias (PGMs) operate in juxtaposition with the regular land forces, they are loosely aligned with them. Given the nativity of its members to the battlefield, a militia is best suited to comprehend the operational and tactical situation and, making itself a viable option for state-led forces both from the perspective of low-cost force or its flexibility to deal with irregular threats. Most informal PGMs maintain a stronger ideological and political base, they do not often care about the limitation of their sponsoring state's sovereignty and the legitimacy of their actions. They may even develop linkages with the terrorist outfits for their immediate goals. This puts national security in grave danger. Given the risks, weaker states become vulnerable at the hands of their sponsored militants. Still, the state-led forces will remain inclined to exploit such paramilitary forces to let them shoulder the burden of national security against asymmetric threats.

Improving the ionic conductivity and slow oxygen reduction electro-catalytic activity of reactions occurring at low operating temperature would do wonders for the widespread use of low-operating temperature ceramic fuel cells (LT-CFCs; 450–550 °C). In this work, we present a novel semiconductor heterostructure composite made of a spinel-like structure of Co0.6Mn0.4Fe0.4Al1.6O4 (CMFA) and ZnO, which functions as an effective electrolyte membrane for solid oxide fuel cells. For enhanced fuel cell performance at sub-optimal temperatures, the CMFA–ZnO heterostructure composite was developed. We have shown that a button-sized SOFC fueled by H2 and ambient air can provide 835 mW/cm2 of power and 2216 mA/cm2 of current at 550 °C, possibly functioning down to 450 °C. In addition, the oxygen vacancy formation energy and activation energy of the CMFA–ZnO heterostructure composite is lower than those of the individual CMFA and ZnO, facilitating ion transit. The improved ionic conduction of the CMFA–ZnO heterostructure composite was investigated using several transmission and spectroscopic measures, including X-ray diffraction, photoelectron, and UV–visible spectroscopy, and density functional theory (DFT) calculations. These findings suggest that the heterostructure approach is practical for LT-SOFCs.

The challenging research topic for developing low-temperature ceramic fuel cells (LT-CFCs) is to design electrolytes with sufficient ionic conductivity either via doping or composite semiconductors with ionic conductors. Following this challenging topic, we have developed and synthesized a novel semiconductor ionic heterostructure La0.8Sr0.2Co0.8Fe0.2O3-Gd0.1Ce0.9O2 (LSCF-GDC) with different compositions and deployed it as an electrolyte to realize the functionality of the fuel cell. The developed LSCF-GDC electrolyte with mixed conduction of ions and protons possesses high ionic conductivity with only 0.06 Ohm·cm2 of ohmic area-specific resistance for the electrolyte component. The fuel cell using 3LSCF-7GDC as the electrolyte exhibits the best fuel cell performance of 1060 mW·cm−2 and an open circuit voltage (OCV) of 1.11 V at a low operating temperature of 550 °C among individual GDC, LSCF, and different heterostructures of LSCF and GDC. The attained performance and ionic conductivity are specially accredited to constructing heterostructures and massively deficient structures at the interface of the LSCF and GDC. The advanced semiconductor ionic heterostructure of LSCF-GDC provides new insight into designing new electrolytes with high ionic conductivity for LT-CFC applications.

There is tremendous potential for both small- and large-scale applications of low-temperature operational ceramic fuel cells (LT-CFCs), which operate between 350 °C and 550 °C. Unfortunately, the low operating temperature of CFCs was hampered by inadequate oxygen reduction electrocatalysts. In this work, the electrochemical characteristics of a semiconductor heterostructure composite based on WO3-CaFe2O4 deposited over porous Ni-foam are investigated. At low working temperatures of 450–500 °C, the developed WO3-CaFe2O4 pasted on porous Ni–foam heterostructure composite cathode exhibits very low area-specific resistance (0.78 Ω cm2) and high oxygen reduction reaction (ORR) activity. For button-sized SOFCs with H2 and atmospheric air fuels, we have demonstrated high-power densities of 508 mW cm−2 running at 550 °C, and even potential operation at 450 °C, using WO3-CaFe2O4 seeded on porous Ni-foam cathode. Moreover, WO3-CaFe2O4 composite heterostructure with Ni foam paste exhibits very low activation energy compared to both WO3 and CaFe2O4 alone, which supports ORR activity. To comprehend the enhanced ORR electrocatalytic activity of WO3-CaFe2O4 pasted on porous Ni-foam heterostructure composite, several spectroscopic tests including X-ray diffraction (XRD), photoelectron spectroscopy (XPS), and electrochemical impedance spectroscopy (EIS) were used. The findings may also aid in the creation of useful cobalt-free electrocatalysts for LT-SOFCs.

Low-temperature solid fuel cells (LT-SOFCs) hold remarkable promise for the cooperative corporation of small- and large-scale applications. However, the meager oxygen-reduction retort of cathode materials mires the low operating temperature conditions of SOFCs. Herein, we have developed a perovskite structured LaFeO3 by the co-doping of Gd and Ce ions, and their electrochemical properties have been studied. The developed LaFe0.8Gd0.1Ce0.1O3-δ cathode exhibits very small-area-specific-resistance and good oxygen-reduction reaction (ORR) activity at low operating temperatures of 450–500 °C. We have demonstrated a high-power density of 0.419 W-cm−2 with a LaFe0.8Gd0.1Ce0.1O3-δ cathode operating at 550 °C with H2 and atmospheric air as fuels. Moreover, LaFe0.8Gd0.1Ce0.1O3-δ exhibits high activation energy as compared to individual LaFeO3, which helps to promote ORR activity. Various spectroscopic measurements such as X-ray diffraction, SEM, EIS, UV-visible, TGA, Ramana, and photoelectron spectroscopy were employed to understand the improved ORR electrocatalytic activity of Gd and Ce co-doped LaFeO3 cathode. The results can further help to develop functional cobalt-free electro-catalysts for LT-SOFCs.

Abstract Recently, semiconductor-ionic materials (SIMs) have emerged as new functional materials, which possessed high ionic conductivity with successful applications as the electrolyte in advanced low-temperature solid oxide fuel cells (LT-SOFCs). In order to reveal the ion-conducting mechanism in SIM, a typical SIM pellet consisted of semiconductor La0.6Sr0.4Co0.2Fe0.8O3-δ (LSCF) and ionic conductor Sm and Ca Co-doped ceria Ce0.8Sm0.05Ca0.15O2-δ (SCDC) are suffered from sintering at different temperatures. It has been found that the performance of LSCF-SCDC electrolyte fuel cell decreases with the sintering temperature, the cell assembled from LSCF-SCDC pellet sintered at 600 °C exhibits a peak power density (P max) of 543 mW/cm2 at 550 °C and also excellent performance of 312 mW/cm2 even at LT (500 °C). On the contrary, devices based on 1000 °C pellet presented a poor P max of 106 mW/cm2. The performance difference may result from the diverse ionic conductivity of SIM pellet through different temperatures sintering. The high-temperature sintering could severely destroy the interface between SCDC and LSCF, which provide fast transport pathways for oxygen ions conduction. Such phenomenon provides direct and strong evidence for the interfacial conduction in LSCF-SCDC SIMs.

In recent years, tuning perovskite and fluorite-based materials and modifying them to ionic conductors has been an interesting but challenging topic for advanced low-temperature ceramic fuel cells (LT-CFCs). In this regard, we prepared a new composite heterostructure, BaCe0.4Zr0.4Y0.1Yb0.1O3-Sm0.2Ce0.8O2 (BCZYYb-SDC), and evaluated it as an electrolyte to realize the fuel cell reaction. The developed electrolyte could be a hybrid ionic conductor, possess a very small ohmic area-specific resistance, and exhibit excellent fuel cell performance of over 1.0 W/cm2 along with higher OCV of more than 1.1 V at a low operating temperature of 550 °C. The attained performance and ionic conductivity are specially accredited to constructing the heterostructure of BCZYYb-SDC. Moreover, various spectroscopy and microscopic analysis methods have been used to investigate the ions’ transportation, while on the other hand suppressing the electronic conduction. The developed composite heterostructure proposes and suggests new insight to design new electrolytes for LT-CFCs.

Zinc oxide, a direct band gap semiconductor of ≥3.30 eV, is prevalent in potential requests for energy devices. The early-stage demonstration of ZnO provides a new method of developing high ionic conductivity in multifunctional semiconductors for electrolyte applications in ceramic fuel cells (CFCs). In the present work, we successfully synthesized Na-doped ZnO nanorods by a hydrothermal method and employed them as an electrolyte in CFCs. The synthesized Na-doped-ZnO nanorods showed an effective ionic conductivity of 8.75 × 10−2 S cm−1 along with an excellent power density of 609 mWcm−2 ± 5% when the fuel cell was operating at 550 °C. The enhanced ionic conductivity could be due to Na+ doping into Zn2+ and the high ionic radius of Na ions producing bulk oxygen vacancies in the ZnO structure to conduct oxygen ions or protons. Furthermore, we used experimental analysis, such as X-ray diffraction (XRD), high-resolution transmission electron microscopy (HR-TEM), scanning electron microscopy (SEM), ultraviolet–visible (UV–visible), X-ray photoelectron spectroscopy (XPS), and electrochemical impedance spectroscopy (EIS), to evaluate the change in structural properties and mechanism of ionic transport in ZnO nanorods with sodium doping. The presented work provides insight into a novel approach of developing the high ionic conductivity of electrolytes in a low-cost ZnO semiconductor material.

Lately, ceramic fuel cells (CFCs) have held exceptional promise for joint small- and large-scale applications. However, the low-oxygen reduction response of cathode materials has hindered the low operating temperature of CFCs. Herein, we have developed a semiconductor based on La and Ce co-doped SrCoO3 and embedded them in porous Ni-foam to study their electrochemical properties. The porous Ni-foam-pasted La0.2Sr0.8Co0.8Ce0.2O3‒δ cathode displays small-area-specific resistance and excellent ORR (oxygen reduction reaction) activity at low operating temperatures (LT) of 450–500 °C. The proposed device has delivered an impressive fuel cell performance of 440 mW-cm−2, using La0.2Sr0.8Co0.8Ce0.2O3−δ embedded on porous Ni-foam substrate cathode operation at 550 °C with H2 fuel and atmospheric air. It even can function well at a lower temperature of 450 °C. Moreover, La0.2Sr0.8Co0.8Ce0.2O3−δ embedded on porous Ni-foam shows very good activation energy compared to individual SrCoO3 and La0.1Sr0.9Co0.9Ce0.1O3−δ embedded on porous Ni-foam, which help to promote ORR activity. Different characterization has been deployed, likewise: X-ray diffraction, photoelectron-spectroscopy, and electrochemical impedance spectroscopy for a better understanding of improved ORR electrocatalytic activity of prepared La0.2Sr0.8Co0.8Ce0.2O3−δ embedded on porous Ni-foam substrate. These results can further help to develop functional cobalt-free electrocatalysts for LT-SOFCs.

Environmental variations caused by global climate change significantly affect plant yield and productivity. Because water scarcity is one of the most significant risks to agriculture’s future, improving the performance of plants to cope with water stress is critical. Our research scrutinized the impact of melatonin application on the photosynthetic machinery, photosynthetic physiology, root system, osmoprotectant accumulation, and oxidative stress in tomato plants during drought. The results showed that melatonin-treated tomato plants had remarkably higher water levels, gas exchange activities, root system morphological parameters (average diameter, root activity, root forks, projected area, root crossings, root volume, root surface area, root length, root tips, and root numbers), osmoprotectant (proline, trehalose, fructose, sucrose, and GB) accumulation, and transcript levels of the photosynthetic genes SlPsb28, SlPetF, SlPsbP, SlPsbQ, SlPetE, and SlPsbW. In addition, melatonin effectively maintained the plants’ photosynthetic physiology. Moreover, melatonin treatment maintained the soluble protein content and antioxidant capacity during drought. Melatonin application also resulted in membrane stability, evidenced by less electrolyte leakage and lower H2O2, MDA, and O2− levels in the drought-stress environment. Additionally, melatonin application enhanced the antioxidant defense enzymes and antioxidant-stress-resistance-related gene (SlCAT1, SlAPX, SlGR, SlDHAR, SlPOD, and SOD) transcript levels in plants. These outcomes imply that the impacts of melatonin treatment on improving drought resistance could be ascribed to the mitigation of photosynthetic function inhibition, the enhancement of the water status, and the alleviation of oxidative stress in tomato plants. Our study findings reveal new and incredible aspects of the response of melatonin-treated tomato plants to drought stress and provide a list of candidate targets for increasing plant tolerance to the drought-stress environment.

Zinc oxide (ZnO), a direct wide band gap semiconductor (≥3.30 eV), has widespread potential for applications in energy devices and related industries. The initial physical demonstration of ZnO in ceramic fuel cells (CFCs) gave a new view of developing high ionic conductivity for multifunctional semiconductor technology. However, in the present work, we successfully synthesized highly textured nanoparticles of ZnO using a hydrothermal method followed by sintering in a reducing atmosphere. The resultant ZnO materials as electrolytes showed efficient ionic conductivity (5.28 × 10−2 S cm−1) and an excellent power density of 520 mW cm−2 ± 5% at 550 °C for low-temperature ceramic fuel cells (LT-CFCs). The achievement of enhanced ionic conductivity without any external ions or cation doping in the CFC was anticipated, since there was a rare possibility of vacancies in the bulk ZnO structure to conduct oxygen ions or protons. Therefore, we found that laterally the surfaces of the ZnO nanoparticles could be textured to become oxygen-deficient when sintered in an H2 atmosphere, which suggests a special mechanism for effective ionic transport. Furthermore, experimental analyses such as SEM, XPS, UV–visible, and EIS methods were performed to analyze the changes in the structural properties and mechanism of ionic transport in ZnO nanoparticles. The presented work provides insights into a novel approach for developing high ionic conductivity in electrolytes in low-cost semiconductor oxides such as ZnO for energy storage and conversion devices.

Water scarcity has emerged as an intense global threat to humanity and needs prompt attention from the scientific community. Solar-driven interfacial evaporation and seawater desalination are promising strategies to resolve the primitive water shortage issue using renewable resources. However, the fragile solar thermal devices, complex fabricating techniques, and high cost greatly hinder extensive solar energy utilization in remote locations. Herein, we report the facile fabrication of a cost-effective solar-driven interfacial evaporator and seawater desalination system composed of carbon cloth (CC)-wrapped polyurethane foam (CC@PU). The developed solar evaporator had outstanding photo-thermal conversion efficiency (90%) with a high evaporation rate (1.71 kg m−2 h−1). The interfacial layer of black CC induced multiple incident rays on the surface allowing the excellent solar absorption (92%) and intensifying heat localization (67.37 °C) under 1 kW m−2 with spatially defined hydrophilicity to facilitate the easy vapor escape and validate the efficacious evaporation structure using extensive solar energy exploitation for practical application. More importantly, the long-term evaporation experiments with minimum discrepancy under seawater conditions endowed excellent mass change (15.24 kg m−2 in consecutive 8 h under 1 kW m−2 solar irradiations) and promoted its operational sustainability for multi-media rejection and self-dissolving potential (3.5 g NaCl rejected from CC@PU surface in 210 min). Hence, the low-cost and facile fabrication of CC@PU-based interfacial evaporation structure showcases the potential for enhanced solar-driven interfacial heat accumulation for freshwater production with simultaneous salt rejection.

Solar-driven evaporation is a promising technology for desalinating seawater and wastewater without mechanical or electrical energy. The approaches to obtaining fresh water with higher evaporation efficiency are essential to address the water-scarcity issue in remote sensing areas. Herein, we report a highly efficient solar evaporator derived from the nanocomposite of anatase TiO2/activated carbon (TiO2/AC), which was coated on washable cotton fabric using the dip-dry technique for solar water evaporation. The ultra-black fabric offers enhanced solar absorption (93.03%), hydrophilic water transport, and an efficient evaporation rate of 1.65 kg/m2h under 1 kW m−2 or one sun solar intensity. More importantly, the sideways water channels and centralized thermal insulation of the designed TiO2/AC solar evaporator accumulated photothermal heat at the liquid and air interface along with an enhanced surface temperature of 40.98 °C under one sun. The fabricated solar evaporator desalinated seawater (3.5 wt%) without affecting the evaporation rates, and the collected condensed water met the standard of drinking water set by the World Health Organization (WHO). This approach eventually enabled the engineering design groups to develop the technology pathways as well as optimum conditions for low-cost, scalable, efficient, and sustainable solar-driven steam generators to cope with global water scarcity.

Auxin/indole-3-acetic acid (Aux/IAA) is a transcriptional repressor in the auxin signaling pathway that plays a role in several plant growth and development as well as fruit and embryo development. However, it is unclear what role they play in Japanese apricot (Prunus mume) fruit development and maturity. To investigate the role of Aux/IAA genes in fruit texture, development, and maturity, we comprehensively identified and expressed 19 PmIAA genes, and demonstrated their conserved domains and homology across species. The majority of PmIAA genes are highly responsive and expressed in different hormone treatments. PmIAA2, PmIAA5, PmIAA7, PmIAA10, PmIAA13, PmIAA18, and PmIAA19 showed a substantial increase in expression, suggesting that these genes are involved in fruit growth and maturity. During fruit maturation, alteration in the expression of PmIAA genes in response to 1-Methylcyclopropene (1-MCP) treatment revealed an interaction between auxin and ethylene. The current study investigated the response of Aux/IAA development regulators to auxin during fruit ripening, with the goal of better understanding their potential application in functional genomics.

The current research empirically investigated whether total quality management (TQM) as a multidimensional construct (organic and mechanistic) has a better explanatory power toward innovation performance dimensions with the mediating effect of business innovation capability (BIC) and moderating effect of business innovation culture. After an in-depth examination of the literature, a holistic TQM–BIC–innovation performance framework is being developed based on theoretical knowledge as well as empirical justification. This would help scholars and practitioners to comprehend ways through which quality and innovation are integrated. To this end, structural equation modeling–partial least squares (SEM-PLS) is used for analyzing the data. It has been found that both soft and hard TQM trigger innovation performance and firm BIC mediates this relationship. Lastly, the role of business innovation culture in enhancing firm’s radical innovation performance was empirically established. Thus, developing BIC and business innovation culture in a TQM-based firm could trigger innovating performance.

Environmental stresses negatively affect the growth and development of plants. Several previous studies have elucidated the response mechanisms of plants to drought and heat applied separately; however, these two abiotic stresses often coincide in environmental conditions. The global climate change pattern has projected that combined drought and heat stresses will tend to increase in the near future. In this study, we down-regulated the expression of a cytokinin receptor gene SlHK2 using RNAi and investigated the role of this gene in regulating plant responses to individual drought, heat, and combined stresses (drought + heat) in tomato. Compared to the wild-type (WT), SlHK2 RNAi plants exhibited fewer stress symptoms in response to individual and combined stress treatments. The enhanced abiotic stress tolerance of SlHK2 RNAi plants can be associated with increased membrane stability, osmoprotectant accumulation, and antioxidant enzyme activities. Furthermore, photosynthesis machinery was also protected in SlHK2 RNAi plants. Collectively, our results show that down-regulation of the cytokinin receptor gene SlHK2, and consequently cytokinin signaling, can improve plant tolerance to drought, heat, and combined stress.

High ionic conductivity in low-cost semiconductor oxides is essential to develop electrochemical energy devices for practical applications. These materials exhibit fast protonic or oxygen-ion transport in oxide materials by structural doping, but their application to solid oxide fuel cells (SOFCs) has remained a significant challenge. In this work, we have successfully synthesized nanostructured monoclinic WO3 through three steps: co-precipitation, hydrothermal, and dry freezing methods. The resulting WO3 exhibited good ionic conductivity of 6.12 × 10−2 S cm−1 and reached an excellent power density of 418 mW cm−2 at 550 °C using as an electrolyte in SOFC. To achieve such a high ionic conductivity and fuel cell performance without any doping contents was surprising, as there should not be any possibility of oxygen vacancies through the bulk structure for the ionic transport. Therefore, laterally we found that the surface layer of WO3 is reduced to oxygen-deficient when exposed to a reducing atmosphere and form WO3−δ/WO3 heterostructure, which reveals a unique ionic transport mechanism. Different microscopic and spectroscopic methods such as HR-TEM, SEM, EIS, Raman, UV-visible, XPS, and ESR spectroscopy were applied to investigate the structural, morphological, and electrochemical properties of WO3 electrolyte. The structural stability of the WO3 is explained by less dispersion between the valence and conduction bands of WO3−δ/WO3, which in turn could prevent current leakage in the fuel cell that is essential to reach high performance. This work provides some new insights for designing high-ion conducting electrolyte materials for energy storage and conversion devices.

Recently, appreciable ionic conduction has been frequently observed in multifunctional semiconductors, pointing out an unconventional way to develop electrolytes for solid oxide fuel cells (SOFCs). Among them, ZnO and Li-doped ZnO (LZO) have shown great potential. In this study, to further improve the electrolyte capability of LZO, a typical ionic conductor Sm0.2Ce0.8O1.9 (SDC) is introduced to form semiconductor-ionic composites with LZO. The designed LZO-SDC composites with various mass ratios are successfully demonstrated in SOFCs at low operating temperatures, exhibiting a peak power density of 713 mW cm−2 and high open circuit voltages (OCVs) of 1.04 V at 550 °C by the best-performing sample 5LZO-5SDC, which is superior to that of simplex LZO electrolyte SOFC. Our electrochemical and electrical analysis reveals that the composite samples have attained enhanced ionic conduction as compared to pure LZO and SDC, reaching a remarkable ionic conductivity of 0.16 S cm−1 at 550 °C, and shows hybrid H+/O2− conducting capability with predominant H+ conduction. Further investigation in terms of interface inspection manifests that oxygen vacancies are enriched at the hetero-interface between LZO and SDC, which gives rise to the high ionic conductivity of 5LZO-5SDC. Our study thus suggests the tremendous potentials of semiconductor ionic materials and indicates an effective way to develop fast ionic transport in electrolytes for low-temperature SOFCs.

Highly catalytic active anode materials are one of the scorching zones in recent solid oxide fuel cells (SOFCs). In order to develop high performance SOFCs compatible anode materials are extremely required. In this work, Ni _0.5 Zn _0.5−x Ce _x -oxides (NZC-oxide) nanocomposite anode material is synthesized by employing facile, low cost wet chemical technique. The phase structure before and after CH _4 environment is studied by x-ray diffraction (XRD) and Raman spectroscopy. However, no significant structural phase change is observed in Ni _0.5 Zn _0.3 Ce _0.2 -oxides after CH _4 treatment. Additional characterizations are investigated by UV-visible spectroscopy, Fourier transform infrared spectroscopy and Scanning electron microscopy (SEM). The dc electrical conductivities are measure by four probe method. The ideal and suitable Ni _0.5 Zn _0.3 Ce _0 . _2 -oxides among all nanocomposites using as anode in fuel cell devices, show maximum power density of 500 mWcm ^−2 with open circuit voltage (OCV) of 1.0 V at 600 °C. By empowering enhanced catalytic assets of Ni _0.5 Zn _0.3 Ce _0.2 -oxides nanocomposite anode may be useful for fuel cell applications.

The purpose of the study is to investigate the impact of capital structure, firm size, and profitability on tax avoidance and to examine the tax planning strategies implied in the oil and gas industry of Pakistan. Owing to its rapid expansion and enormous profits, the oil industry is a symbol of blue-chip businesses. One way it supports the economy is by increasing the nation's tax income. An analysis of the tax planning techniques suggested in this industry is essential for efficient legislation and departmental evaluation. In this research, the explanatory research method is implied, and only firm-specific factors are considered for analysis. The effect of capital structure, firm size, and profitability on corporate tax avoidance is examined by the Ordinary least squares (OLS) regression model. As per the results, capital structure has a negative association whereas firm size and profitability have a positive association with tax avoidance. [ABSTRACT FROM AUTHOR]