Decisive role of electrostatic interaction in rheological evolution of graphene oxide under ultrasonic fragmentation.

The aqueous dispersibility and processability of graphene oxide (GO) are pivotal for various applications, including the fluid assembly of macroscopic materials and nanofluidic systems. Despite the widespread utilization of ultrasonic treatment to achieve homogeneous dispersions, the rheological changes of GO during sonication have remained relatively unexplored, leading to conflicting research findings. In this study, we demonstrate that the viscoelastic evolution of GO can significantly differ under ultrasonic fragmentation depending on the balance between repulsion force and attraction force at the initial state before fragmentation. When electrostatic repulsion is in delicate equilibrium with attractive forces, gelation occurs under ultrasonic fragmentation, leading to increased viscosity under sonication. Conversely, when electrostatic repulsion predominates, viscosity decreases during sonication. This study reconciles conflicting observations on the rheological evolution of GO dispersions under ultrasonic fragmentation and provides valuable guidance and insights for the rheological engineering of GO colloidal systems.

Humidity-tolerant porous polymer coating for passive daytime radiative cooling.

Coating building envelopes with a passive daytime radiative cooling (PDRC) material has attracted enormous attention as an alternative cooling technique with minimal energy consumption and carbon footprint. Despite the exceptional performance and scalability of porous polymer coating (PPC), achieving consistent performance over a wide range of drying environments remains a major challenge for its commercialization as a radiative cooling paint. Herein, we demonstrate the humidity vulnerability of PPC during the drying process and propose a simple strategy to greatly mitigate the issue. Specifically, we find that the solar reflectance of the PPC rapidly decreases with increasing humidity from 30% RH, and the PPC completely losses its PDRC ability at 45% RH and even become a solar-heating material at higher humidity. However, by adding a small amount of polymer reinforcement to the PPC, it maintains its PDRC performance up to 60% RH, resulting in a 950% increase in estimated areal coverage compared to PPC in the United States. This study sheds light on a crucial consistency issue that has thus far been rarely addressed, and offers engineering guidance to handle this fundamental threat to the development of dependable PDRC paint for industrial applications.

Effective single web-structured electrode for high membrane electrode assembly performance in polymer electrolyte membrane fuel cell.

To achieve a sustainable society, CO2 emissions must be reduced and efficiency of energy systems must be enhanced. The polymer electrolyte membrane fuel cell (PEMFC) has zero CO2 emissions and high effectiveness for various applications. A well-designed membrane electrolyte assembly (MEA) composed of electrode layers of effective materials and structure can alter the performance and durability of PEMFC. We demonstrate an efficient electrode deposition method through a well-designed carbon single web with a porous 3D web structure that can be commercially adopted. To achieve excellent electrochemical properties, active Pt nanoparticles are controlled by a nanoglue effect on a highly graphitized carbon surface. The developed MEA exhibits a notable maximum power density of 1082 mW/cm2 at 80°C, H2/air, 50% RH, and 1.8 atm; low cathode loading of 0.1 mgPt/cm2; and catalytic performance decays of only 23.18 and 13.42% under commercial-based durability protocols, respectively, thereby achieving all desirables for commercial applications.

Harnessing Strong Metal-Support Interaction to Proliferate the Dry Reforming of Methane Performance by In Situ Reduction.

The strong bonding at the interface between the metal and the support, which can inhibit the undesirable aggregation of metal nanoparticles and carbon deposition from reforming of hydrocarbon, is well known as the classical strong metal-support interaction (SMSI). SMSI of nanocatalysts was significantly affected by heat treatment and reducing conditions during catalyst preparation.the heat treatment and reduction conditions during catalyst preparation. SMSI can be weakened by the decrement of metal-doped sites in the supporting oxide and can often deactivate catalysts by the encapsulation of active sites through these processes. To retain SMSI near the active sites and to enhance the catalytic activity of the nanocatalyst, it is essential to increase the number of surficial metal-doped sites between nanometal and the support. Herein, we propose a mild reduction process using dry methane (CH4/CO2) gas that suppresses the aggregation of nanoparticles and increases the exposed interface between the metal and support, Ni and cerium oxide. The effects of mild reduction on the chemical state of Ni-cerium oxide nanocatalysts were specifically investigated in this study. As a result, mild reduction led to form large amounts of the Ni3+ phase at the catalyst surface of which SMSI was significantly enhanced. It can be easily fabricated while the dry reforming of methane (DRM) reaction is on stream. The superior performance of the catalyst achieved a considerably high CH4 conversion rate of approximately 60% and stable operation up to 550 h at a low temperature, 600 °C.

Effects of boron nitride nanotube content on waterborne polyurethane-acrylate composite coating materials.

Waterborne polyurethane-acrylate (WPUA) is a promising eco-friendly material for adhesives and coatings such as paints and inks on substrates including fibers, leather, paper, rubber, and wood. Recently, WPUA and its composites have been studied to overcome severe problems such as poor water resistance, mechanical properties, chemical resistance, and thermal stability. In this study, composite films consisting of WPUA and rod-type boron nitride nanotubes (BNNTs), which have excellent intrinsic properties including high mechanical strength and chemical stability, were investigated. Specifically, BNNT/WPUA composite films were synthesized by mixing aqueous solutions of BNNT and WPUA via facile mechanical agitation without any organic solvents or additives, and the optimal content of BNNTs was determined. For the 2.5 wt% BNNT/WPUA composite, the BNNTs were found to be well distributed in the WPUA matrix and this material showed the overall best performance in terms of water resistance, thermal conductivity, and corrosion resistance. Owing to these advantageous properties and their environmentally friendly nature, BNNT/WPUA composite coating materials are expected to be applicable in a wide variety of industries.

Transparent Bendable Secondary Zinc-Air Batteries by Controlled Void Ionic Separators.

First ever transparent bendable secondary zinc-air batteries were fabricated. Transparent stainless-steel mesh was utilized as the current collector for the electrodes due to its reliable mechanical stability and electrical conductivity. After which separate methods were used to apply the active redox species. For the preparation of the anode, zinc was loaded by an electroplating process to the mesh. For the cathode, catalyst ink solution was spray coated with an airbrush for desired dimensions. An alkaline gel electrolyte layer was used for the electrolyte. Microscale domain control of the materials becomes a crucial factor for fabricating transparent batteries. As for the presented cell, anionic exchange polymer layer has been uniquely incorporated on to the cathode mesh as the separator which becomes a key procedure in the fabrication process for obtaining the desired optical properties of the battery. The ionic resin is applied in a fashion where controlled voids exist between the openings of the grid which facilitates light passage while guaranteeing electrical insulation between the electrodes. Further analysis correlates the electrode dimensions to the transparency of the system. Recorded average light transmittance is 48.8% in the visible light region and exhibited a maximum power density of 9.77 mW/cm2. The produced battery shows both transparent and flexible properties while maintaining a stable discharge/charge operation.

Effects of dispersed copper nanoparticles on Ni-ceria based dry methanol fuelled low temperature solid oxide fuel cells.

Methanol is an attractive energy source due to its portability and thermodynamic coke resistance by its oxygen content. In order to operate dry methanol fuel low temperature solid oxide fuel cells (LT-SOFCs), it is important to solve the problems of carbon formation and its low performance. In this study, copper impregnation was selected to decrease the carbon deposition and enhance the performance at low temperature. The interaction of copper, ceria and nickel improves CO oxidation capacity which improves coke tolerance and nano-sized nickel copper alloys improved durability and catalytic performance under methanol feed. It markedly amplified the performance about 0.4 W cm-2 at 550 °C with the durable operation at 1.4 A cm-2 over 50 h. Loading copper nanoparticles is promising method for Ni-ceria based LT-SOFC using methanol fuel with high performance and stable operation.

Synthesis and application of hexagonal perovskite BaNiO3 with quadrivalent nickel under atmospheric and low-temperature conditions.

A hexagonal perovskite BaNiO3 with unusually high-valence nickel(iv) was synthesized under atmospheric and low-temperature conditions by an ethylenediamine-derived wet-chemical route. Secondary phases disappeared with increase in the pH value, and the single-phase BaNiO3 was successfully synthesized at pH 10. The specific surface area was ∼32 m(2) g(-1), which is significantly enhanced compared to the BaNiO3 (0.3 m(2) g(-1)) synthesized by flux-mediated crystal growth. The BaNiO3 was used as an oxygen-evolution reaction (OER) catalyst, and the specific mass activity was ∼5 times higher than that of the BaNiO3 synthesized by flux-mediated crystal growth. As a result, the ethylenediamine-derived sol-gel synthesis could be a simple technique to prepare crystalline compounds such as perovskites and spinels, with unusually high-valence transition metals.

A New Family of Perovskite Catalysts for Oxygen-Evolution Reaction in Alkaline Media: BaNiO3 and BaNi(0.83)O(2.5).

Establishment of a sustainable energy society has been strong driving force to develop cost-effective and highly active catalysts for energy conversion and storage devices such as metal-air batteries and electrochemical water splitting systems. This is because the oxygen evolution reaction (OER), a vital reaction for the operation, is substantially sluggish even with precious metals-based catalysts. Here, we show for the first time that a hexagonal perovskite, BaNiO3, can be a highly functional catalyst for OER in alkaline media. We demonstrate that the BaNiO3 performs OER activity at least an order of magnitude higher than an IrO2 catalyst. Using integrated density functional theory calculations and experimental validations, we unveil that the underlying mechanism originates from structural transformation from BaNiO3 to BaNi(0.83)O(2.5) (Ba6Ni5O15) over the OER cycling process.