Anode Substrate Research Articles

Intermittent polarity inversion of stainless-steel paired electrodes for efficient and durable water electrolysis

Designing robust and cost-effective catalysts through straightforward and replicable techniques is crucial for advancing water electrolysis. In this study, we introduce a dynamic polarization control method for the continuous activation of stainless steel (SS) substrates to achieve high water-splitting performance and durability. By applying periodic inverted current density during high-current–density operation (0.5 or 1 A cm−2) on bare SS adopted as both cathode and anode substrates, a NiFe-based oxide structure favorable for the hydrogen evolution reaction is formed at the cathode, while a Fe-incorporated NiOOH structure with high efficacy for the oxygen evolution reaction develops at the anode. Implemented in an anion exchange membrane water electrolysis system, this inverted polarization approach applied for the SS paired electrolyzer system successfully maintains a cell voltage of approximately 1.9 V for 500 h at a current density of 1 A cm−2 using bare SS for both electrodes.

Illustrating the influence of anodic/cathodic second-phases on dissolution mode via Mg–Ca–Sn alloy anodes for primary Mg-air cells

Two second-phases with an opposite potential difference to the α-Mg matrix may affect the discharge mechanism of magnesium (Mg) anodes for primary Mg-air cells through different micro-galvanic behaviors. Herein, using Mg–Ca-xSn alloys anode with Mg2Ca and CaMgSn phases, we investigated their influence on the dissolution mode of Mg-anode during discharge state via in-situ scanning vibrating electrode technique (SVET) technology. Firstly, the peak surface positive potential of Mg–1Ca alloy only containing Mg2Ca phase and Mg–1Ca–1Sn alloy with CaMgSn/Mg2Ca phase increases multiplied by 10 during the discharge process compared to that of OCP, exhibiting accelerated anodic substrate dissolution. Moreover, Mg2Ca-phases can be attacked firstly while promoting the discharge of the α-Mg matrix surrounding them, leading to the preferential dissolution of grain boundaries and “chunk effects (CE)” occurrence. More CaMgSn/α-Mg couples are activated to form dispersed micro-galvanic cell islands, which also boosts the dissolution of the α-Mg matrix but reduces the area of high-intensity dissolution reaction due to CaMgSn acting as a cathode. However, excessive CaMgSn-phase generally fails to discharge effectively to reduce anode efficiency, although it can improve the self-peeling capacity of the film layer through physical detachment; in addition, with Sn content increasing to 3 wt%, the open circuit voltage of Mg–1Ca–3Sn significantly declines. Mg–1Ca-0.2Sn exhibits the highest cell voltage and anodic efficiency by introducing a tiny amount of dispersed short rod-like CaMgSn, due to the adjusted dissolution mode, enhanced electrochemical activity and inhibited CE. Finally, our study provides a universal mechanism for fabricating Mg-anode with high performance via phase composition modulation.

Regulating the Helmholtz plane by trace ionic liquid additive for advanced Al-air battery

Al-air batteries (AABs) are the next generation of alternative energy sources due to their high theoretical energy density, low cost, and environmental friendliness. Researchers have been interested in AABs with stable discharge in alkaline solution, long discharge time, and high conductivity. However, the uncontrolled self-corrosion of the Al anode and the severe hydrogen evolution reaction in alkaline electrolytes have been two major drawbacks hindering the commercial development of AABs. These shortcomings reduce the Al anode's utilization and significantly shorten the battery's service life. Herein, the Helmholtz plane structure was reconstructed using an ionic liquid additive called 1-aminopropyl-3-methylimidazolium bromide (AMIB) to regulate the electrochemical interface between the electrolyte and the Al anode. Electrochemical tests found that when 3 mM AMIB was added, the corrosion inhibition efficiency could reach up to 60 %. Further surface analysis and theoretical calculations showed that AMIB can form a dense and uniform protective layer on the surface of the Al anode substrate, which reduces the anode corrosion, lowers the active centers for hydrogen evolution on the Al surface, and reduces the hydrogen evolution rate. The full-cell studies found that the specific capacity of the cell increased from 1227 to 2564 mAh g−1, the energy density increased from 1546 to 3359 Wh kg−1, and the Al anode utilization increased from 41.2 % to 86.1 % as the AMIB addition to the alkaline electrolyte risen from 0 to 3 mM. This method of electrolyte regulation provides an efficient strategy for the commercial development of AABs.

Electroplating of zinc onto polyelectrolyte complex membranes as anode for aqueous zinc-ion batteries

Conventionally, the anode of a primary Aqueous zinc-ion batteries (ZIBs) is metallic and rigid, which made it difficult to integrate into flexible designs. In this research, a composite polyelectrolyte complex (PEC) with cationic poly(diallyldimethylammonium chloride), anionic poly(sodium-4-styrenesulfonate) and carbon black (CB) as conductive filler (PEC-CB) was developed as an anode substrate for zinc deposition via electroplating technique. The Zinc-electroplated PEC-CB (Zn-PEC-CB) anode was characterized using electron microscopy and X-Ray diffraction analysis to verify the successful zinc coating. The Zn-PEC-CB was then assembled with PEC-CB-MnO cathodes in an ZIB setup. The results demonstrated the potential of PEC-based electrodes as a promising alternative to conventional materials in ZIBs, encouraging further exploration in energy storage applications.

Driving a deficient cathodic environment using anode to control selectivity for CO2 electroreduction

The anode has not been extensively studied in electrochemical CO2 reduction reaction (CO2RR) systems because it is believed to have no significant effect on the catalytic selectivity and activity of the cathode. Herein, we report that the anode can indeed influence the catalytic activity of the CO2RR by regulating the transfer of water and ions in a membrane electrode assembly. Despite employing identical cathode conditions, we observed optimal ethylene production at different current densities for distinct anode substrates: carbon paper (CP) and Ti meshes (TM). TM shows optimal ethylene Faradaic efficiency (31.1 %) in the high current density region, while CP demonstrates optimal ethylene Faradaic efficiency (20 %) in the low current density region. Based on the results of in situ/operando analysis and transparent cell tests, CP creates an environment deficient in water and cations, thereby promoting local pH effects. Consequently, this leads to a higher valence state of Cu during the CO2RR, resulting in increased catalytic activity for ethylene production. However, in the high-current-density region, the catalytic activity of CP degrades due to the uneven distribution of the reaction. Our study contributes to a deeper understanding of the reaction environment for CO2RR and offers insights for optimizing the catalytic activity of CO2RR systems.

Insights into anode substrate optimization in bioelectrochemical systems for efficient cathodic lanthanum recovery during wastewater treatment

Wastewater containing lanthanum (La) is a significant global environmental concern, prompting the development of various treatment technologies. Existing methods are often costly, generate secondary waste streams, and prioritize removal over recovery. This study investigated La recovery in bioelectrochemical systems (BESs) using diverse substrates (acetate, lactate, methanol, and glucose) with anaerobic sludge as the inoculum. The results showed that acetate-fueled BESs achieved the highest power density (439.29 mW/m2), a chemical oxygen demand (COD) reduction efficiency of 96.52 ± 1.56 %, and a coulombic efficiency of 35.18 ± 1.86 %. Acetate and lactate-fed biofilms achieved high La recovery rates (98.96 ± 1.64 % and 98.24 ± 2.16 %, respectively) by the 36th hour. After 48 h, La was undetectable in these systems, surpassing the environmental guidelines. In contrast, methanol and glucose-fed systems yielded lower recoveries (80 ± 0.04 % and 32.8 ± 1.4 %, respectively) after 48 h, with final La concentrations remaining above the guideline levels. Acetate also enhanced the production of extracellular polymeric substances (EPS). Microbial community analysis revealed that Desulfovibrio and Geobacter predominated in acetate-fed microbial fuel cells (MFCs), while Klebsiella and Simplicispira were dominant in glucose and methanol-fed MFCs, respectively. Recovered La deposits, identified as La2O3 and La(OH)3, on the cathodic surfaces were confirmed via SEM-EDX, XRD, and XPS analyses. This study demonstrates the potential of BESs for efficient La recovery from wastewater.

A Spray-Drying Approach for Highly Active Amorphous NiFe2O4 for AEM Water Electrolysis

Water electrolysis, a key process for hydrogen production, holds immense potential in mitigating carbon dioxide emissions when powered by renewable energy sources, thereby contributing to a sustainable and clean energy future. Commercially available and widely recognized technologies for water electrolysis include the proton exchange membrane water electrolysis (PEMWE) and the traditional alkaline water electrolysis (AWE). In order to use the benefits of both systems, the anion exchange membrane water electrolysis (AEMWE) method is proposed, enabling the utilization of non-noble catalyst materials and achieving high current densities at low cell voltages [1].In the present work, the influence of a spray-drying approach compared to a co-precipitation method on the bimetallic non-noble NiFe2O4 catalysts on the oxygen evolution reaction (OER) activity is systematically investigated. State of the art catalyst for OER is Iridium oxide and so far, the best non-noble catalyst has not been found yet. A widely used non-noble catalyst is NiFe- layered double hydroxide but it suffers from low electric conductivity [2]. Another promising catalyst is the NiFe2O4, which also provides low OER overvoltage. However, amorphous oxides are said to have a higher activity than crystalline [3]. Furthermore, the use of a spray drying approach is highly reproducible, with which the crystallinity can be set very easily [4, 5].The experimental study of the catalysts was carried out in a commercial Baltic-Fuel Cell with a geometrical area of 25 cm² at 60 °C in 1 M KOH electrolyte and a contact pressure of 1.25 MPa. The electrodes were prepared by directly spray coating the desired amount of catalyst onto the anode and cathode substrates. A Bekipor® 2NI 18-0.25 nickel felt was used as the substrate for the anode, while AvCarb MGL370 carbon paper was employed for the cathode. As cathode catalyst Pt/C from Tanaka (TEC10E40E, 37.2 % Pt) was used, while a loading of 0.5 mg cm-2 Pt was targeted during the spraying procedure. On the anode, the NiFe2O4 loading was set to 2 mg cm-2. Both electrodes were separated by a Sustainion® X37-50 Grade T membrane. For determination of relevant catalyst activity data chronopotentiometry (CP) and electrochemical impedance spectroscopy (EIS) were carried out.Figure 1 reveals that the spray-dried NiFe2O4 (amorphous, red curve) has a superior performance compared to the precipitated NiFe2O4 (green curve), which is partly crystalline. With the spray-dried catalyst, a reduction in overvoltage of approx. 60 mV at 1 A cm-2 can be achieved. With a cell voltage of less than 1.7 V at a current density of 1 A cm-2, our recently developed catalyst ranks among the most outstandingly described in the literature to date [6]. These findings can contribute to a further development of amorphous catalysts with even higher activity.[1] Cossar, E., Murphy, F. and Baranova, E.A. (2022), Nickel-based anodes in anion exchange membrane water electrolysis: a review. J Chem Technol Biotechnol, 97: 1611-1624.[2] Jeon, S.S., Lim, J. Kang, P.W., Lee, J.W., Kang, G., Lee, H. (2021), Design Principles of NiFe-Layered Double Hydroxide Anode Catalysts for Anion Exchange Membrane Water Electrolyzers. ACS Appl Mater Interfaces,13 (31): 37179-37186.[3] Shi, G., Arata, C., Tryk, D., Tano, T., Yamaguchi, M., Iiyama, A., Uchia, M., Iida, K., Watanabe, S., Kakinuma, K. (2023), NiFe Alloy Integrated with Amorphous/Crystalline NiFe Oxide as an Electrocatalyst for Alkaline Hydrogen and Oxygen Evolution Reactions. ACS Omega, 8: 13068−13077.[4] Kreitz, B., Arias, A. M., Martin, J., Weber, A. P., Turek, T. (2020), Spray-Dried Ni Catalysts with Tailored Properties for CO2 Methanation, Catalysts, 10 (12): 1410.[5] Arias, A. M., Weber, A. P. (2019), Aerosol synthesis of porous SiO2-cobalt-catalyst with tailored pores and tunable metal particle size for Fischer-Tropsch synthesis (FTS), J Aerosol Sci, 131: 1-12.[6] Du, N., Roy, C. Peach, R., Turnbull, M., Thiele, S. and Bock, C. (2022), Anion-Exchange Membrane Water Electrolyzers. Chem Rev, 122: 11830-11895. Figure 1

Microbial electrochemical enhanced composting of sludge and kitchen waste: Electricity generation, composting efficiency and health risk assessment for land use

To realize the energy and resource utilization from organic solid waste, a two-phase microbial desalination cell (TPMDC) was constructed using dewatered sludge and kitchen waste as the anode substrate. The performance of electricity generation and composting efficacy was investigated, along with a comprehensive assessment of the potential health risks associated with the land use of the resulting mixed compost products. Experimental outcomes revealed a maximum open-circuit voltage of 0.893 ± 0.005 V and a maximum volumetric power density of 0.797 ± 0.009 W/m³. After 90 days of composting enhanced by microbial electrochemistry, a significant organic matter removal rate of 31.13 ± 0.44 % was obtained, and the anode substrate electric conductivity was reduced by 30.02 ± 0.04 % based on the anode desalination. Simultaneously, there was an increase in the content of available nitrogen, phosphorus, and potassium, as well as an improvement in the seed germination index. The forms of heavy metals shifted from bioavailable to stable residual states. The non-carcinogenic hazard index (HI) values for heavy metals and polycyclic aromatic hydrocarbons (PAHs) during the land use of compost products were less than 1, and the total carcinogenic risk (TCR) values for heavy metals and PAHs were below the acceptable threshold of 10−4. The occupational population risk of infection from five pathogens was higher than that of the general public, with all risk values ranging from 8.67 × 10−8 to 1, where the highest risk was attributed to occupational exposure to Legionella. These outcomes demonstrated that the mixture of dewatered sludge and kitchen waste was an appropriate anode substrate to enhance TPMDC stability for electricity generation, and its compost products have promising land use suitability and acceptable land use risk, which will provide important guidance for the safe treatment and disposal of organic solid waste.

Optimizing luminous efficiency in polymer light-emitting diodes through anode oxygen-plasma treatment under diverse pressure conditions

This study investigates the impact of oxygen-plasma (O2-plasma) treatment on the microscale electrical properties of indium tin oxide (ITO) surfaces for enhancement of the luminous efficiency of polymer light-emitting diodes (PLEDs). Significant effects on conductivity distribution were observed when treatment was performed at pressures exceeding 0.4 Torr. ITO-6, the ITO treated with O2-plasma at 0.6 Torr, emerged as the preferred anode substrate for PLEDs, displaying a 72.5 % coverage of stable-conductive regions. When utilized as the anode in PLED, it exhibited a remarkable 209 % increase in average current efficiency and a 184 % enhancement in electroluminescent intensity compared to the reference PLED. These findings provide valuable insights for optimizing PLEDs through surface modification of ITO.

Insight into electricity production performance from dried waste activated sludge in dual chamber microbial fuel cells: Influencing factors, neural network modelling and microbial community analysis

Directly deriving electrical energy from waste activated sludge (WAS) by using microbial fuel cell (MFC) is one of the most promising alternatives to resource utilization of WAS. However, obtaining high MFC performance is still a great challenge for the full-scale implementation of MFC. Therefore, this study aimed to quantify and model the effect of different operating parameters on the performance of MFC fed with dried WAS as anode substrate. The results indicated that MFC exhibited a fast start-up time of 3 days at the inoculated anaerobic sludge: dry WAS mass ratio of 1:5. Moreover, the output voltage and power density of MFC were highly dependent of anolyte pH and temperature, WAS concentration, which was well simulated and predicted by the BPANN model. It was revealed that MFC fed with dry WAS exhibited good performance at 55ºC, pH 9.0 and WAS concentration of 16 g/L, while the stable output voltage and power density were 0.705 V and 5.248 W/m3, respectively. The anolyte temperature significantly affected microbial communities of the anode biofilm. At the phylum level, Synergistota and Proteobacteria dominated the anode biofilm at 35ºC, while Firmicutes was absolutely enriched in the anode biofilm at 55ºC. At the genus level, the predominant Advenella is detected in the anode biofilm at 35ºC, whereas the preponderant MBA03 is identified in the anode biofilm at 35ºC. The findings herein may provide a route for efficiently driving power energy from WAS, which can facilitate the fulfillment of full-scale MFC for the resource utilization of WAS.

Redox Stability Optimization in Anode-Supported Solid Oxide Fuel Cells.

For Ni-YSZ anode-supported solid oxide fuel cells (SOFCs), the main drawback is that they are susceptible to reducing and oxidizing atmosphere changes because of the Ni/NiO volume variation. The anode expansion upon oxidation can cause significant stresses in the cell, eventually leading to failure. In order to improve the redox stability, an analytical model is developed to study the effect of anode structure on redox stability. Compared with the SOFC without AFL, the tensile stresses in the electrolyte and cathode of SOFC with an anode functional layer (AFL) after anode oxidation are increased by 27.07% and 20.77%, respectively. The thickness of the anode structure has a great influence on the structure's stability. Therefore, the influence of anode thickness and AFL thickness on the stress in these two structures after oxidation is also discussed. The thickness of the anode substrate plays a more important role in the SOFC without AFL than in the SOFC with AFL. By increasing the thickness of the anode substrate, the stresses in the electrolyte and cathode decrease. This method provides a theoretical basis for the design of a reliable SOFC in the redox condition and will be more reliable with more experimental proofs in the future.

Mxene-based capacitive enzyme-free biofuel cell Self-Powered sensor for lead ion detection in human plasma

In response to the health risks posed by heavy metal lead, we have developed a self-powered sensor specifically designed for detection of lead ions in this work. This sensor is designed based on an enzyme-free biofuel cell as a self-powered source. The biofuel cell utilizes two-dimensional lamellar Au NPs-Ti3C2Tx heterostructures as the capacitive anode substrate material. The Ti3C2Tx MXene with the excellent charge storage capacity and fast discharge characteristics, provides a large instantaneous current for signal amplification. Furthermore, the DNA walker technique was combined to regulate the loading of ultra-small Au NPs exhibiting glucose oxidase-like properties. Meanwhile, Co, Mn nitrogen-doped carbon-based nanosheets were designed as the cathode with outstanding oxygen reduction reaction catalytic activity. As a result, the constructed enzyme-free biofuel cell has been used to detect Pb2+ with a wide linear range (0.01–7500 nM) and a low detection limit (0.43 pM). It has been successfully applied to the determination of Pb2+ in human plasma, achieving excellent recovery rates (94.0–110.5 %). The developed capacitive anodes not only significantly optimized the performance of the biofuel cell self-powered sensors, but also provided important insights for the future design and construction of biofuel cells.

Gas Permeation through V2O5 Nanoribbons‐Based Membrane

AbstractMembrane separation processes play a crucial role in gas separation applications, with the need for ongoing development to fulfill new needs for today's challenges. For this purpose, novel 2D nanomaterials are progressively showing promise over conventional polymer‐based membrane material, exhibiting excellent molecular transport properties. Beyond the 2D materials already studied in this field, this article presents the first gas separation performances of vanadium pentoxide membrane. Brand new in gas separation topic, 2D van der Waals nanoribbons of V2O5 are successfully synthesized and layered on an anodic aluminum oxide substrate. Gas permeation analysis of He, N2, and CO2 are performed on various membranes made from different quantities of the nanomaterial. Gas permeance results suggest a deviation from an expected Knudsen diffusion mechanism of the V2O5‐based membrane for He separation. The ideal selectivities of He/N2 and He/CO2 are compared to Robeson's upper bound for polymeric membranes. V2O5 membranes, prepared with the highest V2O5 quantity, exceeded the upper bound from 2008 for He/N2 and 2019 (the most recent) for He/CO2, demonstrating the interesting potential of V2O5 2D materials for gas separation.

First-Principles Study of Discharge Products and Their Stability for Lithium-Nitrogen Batteries.

Li-N2 batteries present a relatively novel approach to N2 immobilization, and an advanced N2/Li3N cycling method is introduced in this study. The low operating overpotential of metal-air batteries is quite favorable to their stable cycling performance, providing a prospect for the development of a new type of battery with extreme voltage. The battery system of Li-N2 uses N2 as the positive electrode, lithium metal as the negative electrode, and a conductive medium containing soluble lithium salts as the electrolyte. In accordance with its voltage-distribution trend, a variety of lithium-nitrogen molecule intermediates are produced during the discharge process. There is a lack of theoretical description of material changes at the microscopic level during the discharge process. In this paper, the first-principles approach is used to simulate and analyze possible material changes during the discharge process of Li-N2 batteries. The discharge process is simulated on a 4N-graphene anode substrate model, and simulations of its electrostatic potential, Density of States (DOS), HOMO (Highest Occupied Molecular Orbital) and LUMO (Lowest Unoccupied Molecular Orbital) aspects confirm that the experimentally found Li3N becomes the final stabilized product of the Li-N2 battery. It can also be seen in the density of states that graphene with adsorption of 4N transforms from semiconducting to metallic properties. In addition, the differential charge also indicates that the Li-N2 material has a strong adsorption effect on the substrate, which can play the dual role of electricity storage and nitrogen fixation.

Modeling analysis of SOFC supported on anode employing straight channel fabricated by phase-inversion method

A model of an anode supported solid oxide fuel cell prepared using the phase inversion is developed and validated by the experiment data tested at 800°C. The electrochemical properties are analyzed and compared with cells utilizing different anode support substrates. At 0.7 V, the power density of the cell employing a straight anode channel is 23%–40% higher than cells utilizing traditional anode substrates with porosities of 30% or 60%, respectively. Removing the sponge layer increased the power density to 3.1 W cm−2, just 3.3% higher than the straight channel cell. These results demonstrate that the straight channel anode improves gas transport, while removing the sponge layer has minimal impact on the cell's performance.

Nanoplastics Detected in Commercial Sea Salt.

People of all ages consume salt every day, but is it really just salt? Plastic nanoparticles [nanoplastics (NPs)] pose an increasing environmental threat and have begun to contaminate everyday salt in consumer goods. Herein, we developed a combined surface enhanced Raman scattering (SERS) and stimulated Raman scattering (SRS) approach that can realize the filtration, enrichment, and detection of NPs in commercial salt. The Au-loaded (50 nm) anodic alumina oxide substrate was used as the SERS substrate to explore the potential types of NP contaminants in salts. SRS was used to conduct imaging and quantify the presence of the NPs. SRS detection was successfully established through standard plastics, and NPs were identified through the match of the hydrocarbon group of the nanoparticles. Simultaneously, the NPs were quantified based on the high spatial resolution and rapid imaging of the SRS imaging platform. NPs in sea salts produced in Asia, Australasia, Europe, and the Atlantic were studied. We estimate that, depending on the location, an average person could be ingesting as many as 6 million NPs per year through the consumption of sea salt alone. The potential health hazards associated with NP ingestion should not be underestimated.

Electrophoretic deposition of ceramic coatings from modified suspensions of microsized powders of doped BaCeO3 and BaCeO3–BaZrO3 proton-conducting electrolytes

This work investigates the influence of molecular iodine introduced as a charging agent into the suspensions based on the BaCe0.8Sm0.19Cu0·01O3 (BCSCuO), BaCe0·5Zr0·3Y0.1Yb0.1O3-δ (BCZYYbO) and BaCe0.89Gd0.1Cu0·01O3-δ (BCGCuO) proton-conducting electrolytes at concentrations up to 1.0 g/L on their electrokinetic properties. The peculiarities of changes in zeta potential, pH, conductivity of the suspensions, the thickness and morphology of the coatings depending on the amount of iodine added are determined. It has been established that when the iodine concentration increases to 1 g/L, the electrical charge of the particles and the sign of the zeta potential undergo a reversal. Additionally, there is a natural decrease in the pH value towards the acidic side and a corresponding increase in the suspension conductivity. The research has demonstrated that in the suspension with a high iodine content (1 g/L), cathodic and anodic deposition can occur simultaneously under electrophoretic deposition (EPD) conditions at low voltage values (below 8 V). However, as the voltage increases, only cathodic deposition occurs. Therefore, the impact of altering the type of the EPD is threshold in nature relative to the magnitude of the EPD voltage. It has been shown that in order to practically implement EPD of ceramic coatings from modified suspensions of microsized powders of doped BaCeO3 and BaCeO3–BaZrO3 proton-conducting electrolytes, it is necessary to select a small amount of added iodine (0.1–0.2 g/L) to initiate a stable deposition process and to ensure continuity and uniformity of the coatings. This article discusses possible mechanisms of zeta potential inversion, electrophoretic mobility, and the EPD nature under conditions of high concentrations of iodide ions in the suspension bulk. The experiments have demonstrated the viability of the EPD process for the formation of a uniform BCSCuO coating (∼10 μm) on a supporting NiO–BCSCuO anode substrate using an iodine-modified suspension. This coating was subsequently sintered into a dense ceramic film at 1450 °C. In addition to the fundamental significance, the study results have implications for the practical use to improve and simplify the thin-film SOFC technology.

A novel protonic ceramic fuel cell with SrSn0.8Sc0.2O3-δ electrolyte

The recent discovery of SrSn0.8Sc0.2O3-δ (SSS) perovskite oxide as a promising proton-conducting material has generated interest in its potential application in electrochemical devices as PCFCs. This study assesses the feasibility of SSS in PCFCs by its stability, density, chemical compatibility, and electrochemical performance. The study demonstrated the favorable stability of SSS even after reduction at 800 °C under H2 for 24 h as well as immersion in boiling water for 5 h. The relative density of SSS could easily exceed 94% after sintering with NiO aid at 1400 °C. The chemical compatibility and electrochemical performance of SSS were investigated with various electrode materials. The BaCo0.4Fe0.4Zr0.1Y0.1O3-δ exhibited relatively better electrochemical performance with SSS. The electrolyte was co-sintered with a Ni-based anode substrate and densified to high density at 1450 °C without sintering aids. The fuel cell utilizing an anode-supported Ni-SSS|SSS|BCFZY-SSS configuration exhibited a peak power density of 432.1 mW cm−2 at 800 °C.

Highly permeable and shelf-stable aquaporin biomimetic membrane based on an anodic aluminum oxide substrate

Aquaporin (AQP) biomimetic membranes are a coming-of-age technology for water purification. Although several studies have reported aquaporin biomimetic membrane fabrication to date, these membranes show low water flux mainly due to the low porosity and inherently dense structure of the polymeric substrate materials. Herein, we report a ceramic-based aquaporin biomimetic membrane based on anodic aluminum oxide (AAO) as a substrate, which has a uniform porous structure with a high aspect ratio and pore density compared to conventional polymer substrates and exhibits a high water flux of 27.6 ± 3.6 LMH (L m−2 h−1) and superior membrane selectivity of 0.11 g L−1. Briefly, the AAO substrate was functionalized with amino-silane followed by polydopamine coating, then the AQP vesicles were immobilized on the functionalized AAO substrate surface using an electrokinetic method, and the water rejection performance of the membrane was analyzed in a forward osmosis system. Furthermore, a simple cryodesiccation method is introduced to improve the storage stability and easy transportation of aquaporin membranes, which does not require special environmental conditions to transport or store them.

A Thin‐Layer, Li+ Compensation, Moisture‐Tolerant Interfacial Modification of Cu Substrate Toward the Anode‐Less, Energy/Power Dense Li Metallic Batteries

AbstractThe unregulated metallic deposition and continuous cracking of the fragile solid electrolyte interphase are considered the critical barriers that compromise the cyclability of lithium metal batteries (LMB), especially under low N/P ratio (<3) pairing modes. Herein, an ultra‐thin (5 µm), lightweight (0.25 mg cm−2), and moisture‐proof interfacial layer composed of the high‐entropy alloys (denoted as HEAs) and interweaved carbon nanotubes (CNTs) scaffold is constructed to modify the current collector, moreover, the thermally‐induced Li22Si5 alloy blended with the hydrophobic ethylene‐vinyl acetate copolymer (EVA) is infiltrated into the scaffold pores as the moisture‐proof cation reservoir. The HEA@CNT/Li22Si5@EVA interfacial layer not only maximizes the Li‐utilization degree with minimal voltage divergence in symmetric cells but also compensates for irreversible Li depletion in the pouch‐format anode‐less models. As the HEA@CNT/Li22Si5@EVA‐Cu substrate paired with the LiNi0.8Mn0.1Co0.1O2 cathode in a 200 mAh prototype, the phase evolution of oxide cathode and efficient Li utilization at the anode substrate can be real‐time monitored by the transmission‐mode operando X‐ray diffraction. This interfacial layer strategy affords multifunctionality to enable the LMB prototyping without excessive Li abuse. Consequently, cycling endurance and the balanced energy densities (420.1 Wh kg−1) are obtained on the whole cell.