Heuristic Approach to Predict the Performance Degradation of a Solid Oxide Fuel Cell Cathode.

The present work aims to predict the degradation in the performance of a solid oxide fuel cell (SOFC) cathode owing to cation interdiffusion between the electrolyte and cathode and surface segregation. Cation migration in the (La0.60Sr0.40)0.95Co0.20Fe0.80O3-x (LSCF)-Gd0.10Ce0.90O1.95 (GDC) composite cathode is evaluated in relation to time up to 1000 h using scanning transmission electron microscopy (STEM)-energy-dispersive X-ray spectroscopy (EDXS). The resulting insulating phase formed within the GDC interlayer is quantified by means of the volume fraction using a two-dimensional (2D) image analysis technique. For the very first time, the amount of the insulating phase in the GDC interlayer is quantified, and the corresponding performance degradation of the LSCF cathode is predicted. Mathematical relationships are established for the estimation of degradation due to surface segregation of the cathode. The ohmic resistance between the cathode and the GDC interlayer/electrolyte interface and the polarization resistance of the cathode, characterized by electrochemical impedance spectroscopy (EIS), show an excellent match with the predicted results. The combined degradation analysis and modeling for the cathode lifetime prediction provide a systematic understanding of the time-dependent cation migration and segregation behavior.

Improving the durability of cobaltite cathode of solid oxide fuel cells - a review.

Solid oxide fuel cells (SOFCs) are highly efficient, low-emission, and fuel-flexible energy conversion devices. However, their commercialization has lagged due to the lack of long-term durability. Among several performance degradation mechanisms, cathode degradation and elemental inter-diffusion of the electrolyte and cathode has been identified as the predominant factors. In the most common SOFC systems, a cobalt-based perovskite material is used, for example LSC or LSCF. These cobalt-based materials offer mixed conductivity and higher concentration of oxygen vacancies as compared to LSM at lower operating temperature leading to favorable reduction kinetics. However, the presence of cobalt results in higher cost, higher thermal expansion co-efficient (TEC) mismatch and most importantly leads to rapid degradation. Various elements like strontium, cobalt, cerium, chromium, or zirconium accumulate or deposit at the electrode-electrolyte interface, which results in sluggish reaction kinetics of the oxygen reduction reaction (ORR). These elements react to form secondary phases that have lower ionic and electronic conductivity, cover active reaction sites, and eventually lead to cell and system deterioration. Over the past decade, several studies have focused on preventative and protective measures to prolong SOFC lifetime which includes novel fabrication techniques, introduction of new layers, addition of thin films to block the cation transport. Such efforts to prevent the formation of insulating phases and decomposition of the cathode have resulted in a remarkable improvement in long-term stability. In this review paper, current research on leading mechanisms responsible for the degradation of cobaltite cathode of solid oxide fuel cell has been summarized and durability improvement strategies of cobalt-based SOFC cathodes have been discussed.

Bifunctional CuS/Cl-terminated greener MXene electrocatalyst for efficient hydrogen production by water splitting.

Metal sulfides and 2D materials are the propitious candidates for numerous electrochemical applications, due to their superior conductivity and ample active sites. Herein, CuS nanoparticles were fabricated on 2D greener HF-free Cl-terminated MXene (Ti3C2Cl2) sheets by the hydrothermal process as a proficient electrocatalyst for the hydrogen evolution reaction (HER) and overall water splitting. CuS/Ti3C2Cl2 showed an overpotential of 163 mV and a Tafel slope of 77 mV dec-1 at 10 mA cm-2 for the HER. In the case of the OER, CuS/Ti3C2Cl2 exhibited an overpotential of 334 mV at 50 mA cm-2 and a Tafel slope of 42 mV dec-1. Moreover, the assembled CuS/Ti3C2Cl2||CuS/Ti3C2Cl2 electrolyzer delivered current density of 20 mA cm-2 at 1.87 V for overall water splitting. The CuS/Ti3C2Cl2 electrocatalyst showed excellent stability to retain 96% of its initial value for about 48 hours at 100 mA cm-2 current density. The synthesis of CuS/Ti3C2Cl2 enriches the applications of MXene/metal sulfides in efficient bifunctional electrocatalysis for alkaline water splitting.

Development of high-capacity surface-engineered MXene composite for heavy metal Cr (VI) removal from industrial wastewater.

The substantial quantity of Cr(VI) contaminants in the aqueous atmosphere is a major environmental fear that cannot be overlooked. For the first time, MXene and chitosan-coated polyurethane foam have been employed for wastewater treatment, including heavy metal ions (Cr (VI)) through a fixed-bed column study. It is also the most inexpensive, lightweight, and globally friendly material tested. The Mxene and chitosan-coated polyurethane foam hybrid materials were thoroughly investigated using FTIR (Fourier transform infrared), SEM (scanning electron microscope), XPS (X-ray photoelectron spectroscopy) and XRD (X-ray diffraction). The presence of the rough surface and the pore creation in the Mxene- MX3@CS3@PUF should rise its surface area, which is useful to interact the surface-active assembly of MX3@CS3@PUF and the Cr(VI) contaminations in the aqueous solution. With the help of the ion exchange mechanism and electrostatic contact, negatively charged MXene hexavalent ions were being adsorbed on the surface. MXene and chitosan have been coated on PUF foam in the form of three different layers, which shows the highest adsorption capacity, where up to ∼70% Cr (VI) was removed in the first 10 min and more than 60% elimination after 3 h when the metal ion concentration was 20 ppm. The electrostatic interaction between the negative charge MXene and the positive charge chitosan on the surface of PUF, which was absent in MX@PUF, is accountable for the high removal efficiency. This was done through a sequence of fixed-bed column studies, which took place in the continuous flowing of wastewater.

Correction: Solution processed high performance perovskite solar cells based on a silver nanowire-titanium dioxide hybrid top electrode.

[This corrects the article DOI: 10.1039/D2RA06778A.].

Solution processed high performance perovskite solar cells based on a silver nanowire-titanium dioxide hybrid top electrode.

Longer silver nanowires (AgNWs) > 50 µm and even 90 µm in length have been produced via a polyol method by just changing the stirring speed at a temperature of 130 °C. As-synthesized longer AgNWs are further utilized to construct transparent conductive AgNWs films by a facile drop-casting technique that attained a sheet resistance of 14.5 Ω sq-1 and transmittance over 85%, which is higher than ITO film. The use of a AgNWs/TiO2 hybrid electrode decreases the sheet resistance to 8.3 Ω sq-1, which is attributed to the enhancement of connections between AgNWs by filling the empty spaces between nanowires and TiO2 nanoparticles. Transparent perovskite solar cells (PSCs) on the basis of these AgNWs and AgNWs/TiO2 hybrid top electrodes were made and examined. Due to the light scattering nature of TiO2 nanoparticles, optical transmittance of the AgNWs/TiO2 hybrid electrode enhances to some extent after the coating of a TiO2 layer. Both cell efficiencies and stability of the PSCs are enhanced by using the AgNWs/TiO2 top electrode. A power conversion efficiency (PCE) of 10.65% was attained for perovskite devices based on only the AgNW electrode with a sheet resistance of 14.5 Ω sq-1. A PCE of 14.53% was achieved after coating with TiO2 nanoparticles, indicating the layer effect of TiO2 coating.

Development of Binder-Free Three-Dimensional Honeycomb-like Porous Ternary Layered Double Hydroxide-Embedded MXene Sheets for Bi-Functional Overall Water Splitting Reactions.

In this study, a honeycomb-like porous-structured nickel-iron-cobalt layered double hydroxide/Ti3C2Tx (NiFeCo-LDH@MXene) composite was successfully fabricated on a three-dimensional nickel foam using a simple hydrothermal approach. Owing to their distinguishable characteristics, the fabricated honeycomb porous-structured NiFeCo-LDH@MXene composites exhibited outstanding bifunctional electrocatalytic activity for pair hydrogen and oxygen evolution reactions in alkaline medium. The developed NiFeCo-LDH@MXene electrocatalyst required low overpotentials of 130 and 34 mV to attain a current density of 10 mA cm-2 for OER and HER, respectively. Furthermore, an assembled NiFeCo-LDH@MXene‖NiFeCo-LDH@MXene device exhibited a cell voltage of 1.41 V for overall water splitting with a robust firmness for over 24 h to reach 10 mA cm-2 current density, signifying outstanding performance for water splitting reactions. These results demonstrated the promising potential of the designed 3D porous NiFeCo-LDH@MXene sheets as outstanding candidates to replace future green energy conversion devices.

Fabrication of ionic liquid stabilized MXene interface for electrochemical dopamine detection.

Development of MXene (Ti3C2Cl2)-based sensing platforms by exploiting their inherent active electrochemistry is highly challenging due to their characteristic poor stability in air and water. Herein, we report a cost-effective methodology to deposit MXene on a conductive graphitic pencil electrode (GPE). MXenes can provide active surface area due to their clever morphology of accordion-like sheets; however, the disposition to stack together limits their potential applications. A task-specific ionic liquid (1-methyl imidazolium acetate) is utilized as a multiplex host material to engineer MXene interface via π-π interactions as well as to act as a selective binding site for biomolecules. The resulting IL-MXene/GPE interface proved to be a highly stable interface owing to good interactions between MXene and IL that inhibited electrode leaching and boosted electron transfer at the electrode-electrolyte interface. It resulted in robust dopamine (DA) oxidation with amplified faradaic response and enhanced sensitivity (9.61 µA µM-1 cm-2) for DA detection. This fabricated sensor demonstrated large linear range (10 µM - 2000 µM), low detection limit (702 nM), high reproducibility, and good selectivity. We anticipate that such platform will pave the way for the development of stable and economically viable MXene-based sensors without sacrificing their inherent properties. Scheme 1 Schematic illustration of the IL-MXene/GPE fabrication and oxidative process towards non-enzymatic dopamine sensor.

Reutilizing Methane Reforming Spent Catalysts as Efficient Overall Water-Splitting Electrocatalysts.

It is extremely prudent and highly challenging to design a greener bifunctional electrocatalyst that shows effective electrocatalytic activity and high stability toward electrochemical water splitting. As several hundred tons of catalysts are annually deactivated by deposition of carbon, herein, we came up with a strategy to reutilize spent methane reforming catalysts that were deactivated by the formation of graphitic carbon (GC) and carbon nanofibers (CNF). An electrocatalyst was successfully synthesized by in situ deposition of noble metal-free MoS2 over spent catalysts via a hydrothermal method that showed exceptional performance regarding the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER). At 25 mA cm-2, phenomenal OER overpotentials (η25) of 128 and 154 mV and modest HER overpotentials of 186 and 207 mV were achieved for MoS2@CNF and MoS2@GC, respectively. Moreover, OER Tafel slopes of 41 and 71 mV dec-1 and HER Tafel slopes of 99 and 107 mV dec-1 were obtained for MoS2@CNF and MoS2@GC, respectively. Furthermore, the synthesized catalysts exhibited good long-term durability for about 18 h at 100 µA cm-2 with unnoticeable changes in the linear sweep voltammetry (LSV) curve of the HER after 1000 cycles. The carbon on the spent catalyst increased the conductivity, while MoS2 enhanced the electrocatalytic activity; hence, the synergistic effect of both materials resulted in enhanced electrocatalysts for overall water splitting. This work of synthesizing enhanced nanostructured electrocatalysts with minimal usage of inexpensive MoS2 gives a rationale for engineering potent greener electrocatalysts.

Applications of artificial intelligence in COVID-19 pandemic: A comprehensive review.

During the current global public health emergency caused by novel coronavirus disease 19 (COVID-19), researchers and medical experts started working day and night to search for new technologies to mitigate the COVID-19 pandemic. Recent studies have shown that artificial intelligence (AI) has been successfully employed in the health sector for various healthcare procedures. This study comprehensively reviewed the research and development on state-of-the-art applications of artificial intelligence for combating the COVID-19 pandemic. In the process of literature retrieval, the relevant literature from citation databases including ScienceDirect, Google Scholar, and Preprints from arXiv, medRxiv, and bioRxiv was selected. Recent advances in the field of AI-based technologies are critically reviewed and summarized. Various challenges associated with the use of these technologies are highlighted and based on updated studies and critical analysis, research gaps and future recommendations are identified and discussed. The comparison between various machine learning (ML) and deep learning (DL) methods, the dominant AI-based technique, mostly used ML and DL methods for COVID-19 detection, diagnosis, screening, classification, drug repurposing, prediction, and forecasting, and insights about where the current research is heading are highlighted. Recent research and development in the field of artificial intelligence has greatly improved the COVID-19 screening, diagnostics, and prediction and results in better scale-up, timely response, most reliable, and efficient outcomes, and sometimes outperforms humans in certain healthcare tasks. This review article will help researchers, healthcare institutes and organizations, government officials, and policymakers with new insights into how AI can control the COVID-19 pandemic and drive more research and studies for mitigating the COVID-19 outbreak.

Perylene diimide/MXene-modified graphitic pencil electrode-based electrochemical sensor for dopamine detection.

The synthesis of novel architecture comprising perylene diimide (PDI)-MXene (Ti3C2TX)-integrated graphitic pencil electrode for electrochemical detection of dopamine (DA) is reported. The good electron passage between PDI-MXene resulted in an unprecedented nano-adduct bearing enhanced electrocatalytic activity with low-energy electronic transitions. The anionic groups of PDI corroborated enhanced active surface area for selective binding and robust oxidation of DA, thereby decreasing the applied potential. Meanwhile, the MXene layers acted as functional conducive support for PDI absorption via strong H-bonding. The considerable conductivity of MXene enhanced electron transportation thus increasing the sensitivity of sensing interface. The inclusively engineered nano-adduct resulted in robust DA oxidation with ultra-sensitivity (38.1 µAµM-1cm-2), and low detection limit (240 nM) at very low oxidation potential (-0.135 V). Moreover, it selectively signaled DA in the presence of physiological interferents with wide linearity (100-1000 µM). The developed transducing interface performed well in human serum samples with RSD (0.1 to 0.4%) and recovery (98.6 to 100.2%) corroborating the viability of the practical implementation of this integrated system. Graphical abstract Schematic illustration of the oxidative process involved on constructed sensing interface for the development of a non-enzymatic dopamine sensor.

Two-dimensional transition metal carbide (Ti3C2Tx) as an efficient adsorbent to remove cesium (Cs+).

Industrial utilization of nuclear resources greatly depends on the effective treatment of nuclear waste. The efficient removal of radioactive nuclides from liquid effluents by using different adsorbents has thus become crucial. Herein, for the first time, two-dimensional transition metal carbides (MXenes) are investigated as scavengers of cesium (Cs+) from contaminated water. Due to the combined advantages of the layered structure and the presence of heterogeneous sites (hydroxyl, oxygen and fluorine groups), the adsorbent reached the steady state within 1 min with the maximum Cs+ adsorption capacity of 25.4 mg g-1 at room temperature. The kinetics studies of the Cs+ scavenging process demonstrated that the adsorption of Cs+ followed the pseudo-second-order model whereas the adsorption equilibrium data obeyed the Freundlich model. Thermodynamic studies revealed that the adsorption process was endothermic. The adsorbent showed an excellent Cs+ removal efficiency in neutral to slightly alkaline solutions. Moreover, it can retain Cs+ even in the presence of a high concentration of competing cations (Li+, Na+, K+, Mg2+ and Sr2+). The Cs+ loaded adsorbent was regenerated with a 0.2 M HCl solution and reused at least five times for over 91% removal of contaminants.

MAPbI3 microneedle-arrays for perovskite photovoltaic application.

Methyl-ammonium lead iodide perovskite (MAPbI3) was synthesized in the form of micro-needles via a hydrothermal route at a low temperature of 100 °C in a two-step procedure for the first time. The results exhibit that the amount of the surfactant is crucial for the synthesis of the MAPbI3 nanostructures with well-controlled morphologies. In contrast to bulk MAPbI3, the one-dimensional (1-D) micro-needle perovskite with a diameter of 200 nm showed an improved hole injection from the perovskite to the hole transporting layer (HTL), providing a unique platform at the perovskite/HTL interface. The best performing device employing MAPbI3 perovskite micro-needles yielded stable and hysteresis-free devices with a best power conversion efficiency of (PCEbest) of 17.98%. The current findings highlight the potential of perovskite micro-needles as novel absorber systems and lay the basis for future commercialization.

Co-axial electrospray: a versatile tool to fabricate hybrid electron transporting materials for high efficiency and stable perovskite photovoltaics.

We report a cost-effective and simple co-axial electrospray technique to fabricate a hybrid electron transporting material (ETM) consisting of a nanocomposite of hierarchically structured TiO2 nanobeads (NBs) blended with ZnO nanofibers (NFs), namely ZnO NFs + TiO2 NBs, for the first time ever. Owing to its large surface area, highly porous nature and fast electron transport, the hybrid ETM is further used in methylammonium lead iodide (CH3NH3PbI3)-based perovskite solar cells (PSCs). The optimized cells utilizing the hybrid ETM exhibit a maximum power conversion efficiency (PCEmax) of 20.27%, the highest efficiency reported thus far for hybrid ETMs. Moreover, negligible hysteresis and highly reproducible values of PCE are observed for such cells. The PCE of devices based on the ZnO NF + TiO2 NB hybrid ETM is found to be far superior to that of only ZnO NF and hierarchically structured TiO2 NB-based ETMs. Light-induced transient measurement shows that the significantly rapid electron diffusion and longer electron lifetime of the ZnO NF + TiO2 NB hybrid ETM than of only ZnO NF and hierarchically structured TiO2 NB-based ETMs contribute to the enhanced efficiency in PSCs.

Enhanced efficiency and stability of perovskite solar cells using polymer-coated bilayer zinc oxide nanocrystals as the multifunctional electron-transporting layer.

A novel polymer-coated ZnO based bilayer electron transporting material is investigated for highly efficiency perovskite solar cells. The bilayer ETM consisting of an upper-layer of ZnO nanosheets and a lower-layer of ZnO nanoparticles demonstrates the averaged power conversion efficiency of 13.11% and a maximum power conversion efficiency of 15.13%, compared to single-layers of nanosheets (power conversion efficiency = 11.73%) and nanoparticles (power conversion efficiency = 11.08%) films. A conformal coating of a polymer such as polyethylenimine on the surface of bilayered film leading to a significant boost in power conversion efficiency upto 16.39%, thanks to the reduced work function, rapid electron transport and better perovskite infiltration into the bilayer electron transporting material.

Low-temperature electrospray-processed SnO2 nanosheets as an electron transporting layer for stable and high-efficiency perovskite solar cells.

Semiconducting metal oxide electron transporting layers (ETLs) with distinct morphologies have the ability to produce the less-hysteric and high efficiency perovskite solar cells (PSCs). Here, for the first time we introduce a viable electrospraying route for one-step deposition of highly mesoporous SnO2 nanosheets, as the ETLs in PSCs with reduces hysteresis, high charge collection efficiency and improved ambient stability. Furthermore, optimization of the interfacial properties between the SnO2 nanosheets and the perovskite absorber layer by the employment of a C60 interlayer consequences in decreasing the charge recombination, better energy level alignment, and significantly improved power conversion efficiency (PCE). Consequently, the efficient PSCs based on C60-modified SnO2 nanosheets ETLs have almost hysteresis-free behavior, with a best PCE of 20.2% thanks to the highly porous nature of nanosheets and better perovskite infiltration. This study reveals that hierarchical SnO2 is a possible ETL for producing low-cost and efficient PSCs with long-term stability.

Electrosprayed Polymer-Hybridized Multidoped ZnO Mesoscopic Nanocrystals Yield Highly Efficient and Stable Perovskite Solar Cells.

Solid-state perovskite solar cells have been expeditiously developed since the past few years. However, there are a number of open questions and issues related to the perovskite devices, such as their long-term ambient stability and hysteresis in current density-voltage curves. We developed highly efficient and hysteresis-less perovskite devices by changing the frequently used TiO2 mesoscopic layer with polymer-hybridized multidoped ZnO nanocrystals in a common n-i-p structure for the first time. The gradual adjustment of ZnO conduction band position using single- and multidopant atoms will likely enhance the power conversion efficiency (PCE) from 8.26 to 13.54%, with PCEmax = 15.09%. The highest PCEavg of 13.54% was demonstrated by 2 atom % boron and 6 atom % fluorine co-doped (B, F:ZnO) nanolayers (using optimized film thickness of 160 nm) owing to their highest conductivity, carrier concentration, optical transmittance, and band-gap energy compared to other doped films. We also successfully apply a fine polyethylenimine thin layer on the doped ZnO nanolayers, causing the reduction in work function and overall demonstrating the enhancement in PCE from ∼10.86% up to 16.20%. A polymer-mixed electron-transporting layer demonstrates the remarkable PCEmax of 20.74% by decreasing the trap sites in the oxide layer that probably reduces the chances of carrier interfacial recombination originated from traps and thus improves the device performance. Particularly, we produce these electron-rich multidoped ZnO nanolayers via electrospray technique, which is highly suitable for the future development of perovskite solar cells.