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Photothermal CO2 methanation reaction represents a promising strategy for addressing CO2‐related environmental issues. The presence of efficient tandem catalytic sites with a localized high‐temperature is an effective pathway to enhance the performance of CO2 methanation. Here the bimetallic RuCo nanoparticles anchored on ZrO2 fiber cotton (RuCo/ZrO2) as a photothermal catalyst for CO2 methanation are prepared. A significant photothermal CO2 methanation performance with optimal CH4 selectivity (99%) and rate (169.93 mmol gcat−1 h−1) is achieved. The photothermal energy of the RuCo bimetallic nanoparticles, confined by the infrared insulation and low thermal conductivity of the ZrO2 fiber cotton (ZrO2 FC), provides a localized high‐temperature. In situ spectroscopic experiments on RuCo/ZrO2, Ru/ZrO2, and Co/ZrO2 indicate that the construction of tandem catalytic sites, where the Co site favors CO2 conversion to CO while incorporating Ru enhances CO* adsorption for subsequent hydrogenation, results in a higher selectivity toward CH4. This work opens a new insight into designing tandem catalysts with a photothermal confinement effect in CO2 methanation reaction. [ABSTRACT FROM AUTHOR]

Catalytic conversion of CO2 to valuable formate provides a pathway to carbon neutrality. Indium (In), as a promising catalyst, exhibits high selectivity toward formate due to its suitable bonding ability of *OCHO intermediates. However, it still suffers from the CO2 activation and the protonation steps, leading to low activity and productivity. Here, an oxygen‐pinned stabilization AgIn single‐atom alloy (Op‐Ag1In) is presented for efficiently converting CO2 into formate (≈92.03% Faradaic efficiency) with a partial current density of 13 mA cm−2 at −0.95 V vs RHE by using standard H‐type reactor. The Op‐Ag1In electrocatalyst is more effective in converting CO2 to formate because the activated In sites of Op‐Ag1In catalyst regulate CO2 activation and protonation step of CO2RR and formation of sufficient amounts of *OCHO, which are confirmed by in situ spectroscopic and theoretical calculations. The continuous production of formate is showcased at 70 mA cm–2 for 24 h by utilizing a flow cell and Op‐Ag1In. [ABSTRACT FROM AUTHOR]

Dry reforming of methane (DRM) is a highly endothermic process, with its development hindered by the harsh thermocatalytic conditions required. We propose an innovative DRM approach utilizing a 16 W pulsed laser in combination with a cost-effective Mo2C catalyst, enabling DRM under milder conditions. The pulsed laser serves a dual function by inducing localized high temperatures and generating *CH plasma on the Mo2C surface. This activates CH4 and CO2, significantly accelerating the DRM reaction. Notably, the laser directly generates *CH plasma from CH4 through thermionic emission and cascade ionization, bypassing the traditional step-by-step dehydrogenation process and eliminating the rate-limiting step of methane cracking. This method maintains a carbon-oxygen balanced environment, thus preventing the deactivation of the Mo2C catalyst due to CO2 oxidation. The laser-catalytic DRM achieves high yields of H2 (14300.8 mmol h−1 g−1) and CO (14949.9 mmol h−1 g−1) with satisfactory energy efficiency (0.98 mmol kJ−1), providing a promising alternative for high-energy-consuming catalytic systems. Dry reforming of methane (DRM) is a highly endothermic process, often limited by the severe thermocatalytic conditions it demands. Here the authors introduce a novel DRM method that employs a 16 W pulsed laser along with a cost-effective Mo2C catalyst, allowing DRM to proceed under milder conditions. [ABSTRACT FROM AUTHOR]

The blending of 2D materials and polymers promote the heterosis in flexible electronics, including senses, computing, memory and logic circuits. [ABSTRACT FROM AUTHOR]

Zn‐based catalytic batteries, recognized as eco‐friendly alternatives, are attracting significant research interest for their applications in energy storage, conversion, pollutant degradation, and ammonia synthesis. This review compiles the latest developments in Zn‐nitrogen oxides (NOx) batteries, covering various types including Zn‐nitrate, Zn‐nitric oxide, and Zn‐nitrite batteries. This study explores the electrode reactions and structural evolutions of these batteries, emphasizing the different challenges posed by cathodic reactions. Advanced design strategies for cathode materials, such as inhibiting hydrogen production, utilizing tandem sites, and enhancing reactant enrichment, are presented and evaluated. These strategies have markedly improved NOx reduction performance and have driven significant progress in Zn‐NOx battery. The future directions for research are outlined, highlighting the need for more efficient NOx reduction catalysts, optimization of Zn anodes, development of alternative metal anodes, battery structure improvements, and exploration of charging reactions. Addressing these challenges is crucial for advancing the development of eco‐friendly and high‐energy‐density Zn‐NOx batteries. [ABSTRACT FROM AUTHOR]

Bismuth (Bi) has attracted widespread attention for sodium storage due to its high electronic/ionic conductivity, suitable reaction potential, and theoretical capacity (386 mAh g−1). However, Bi electrodes have a relatively high volumetric expansion ratio, which constrains their high capacity and affects the battery's cycle performance. Herein, a highly dispersed Bi atomic cluster is controllably prepared anchored on a porous TiO2 substrate through in situ segregation from Bi4Ti3O12 (TiO2/BiAC). The highly dispersed Bi clusters can serve as an “Ionic sponge” and accommodate more Na+ without causing excessive stress. Additionally, it aids in the decomposition of NaPF6, leading to the formation of a durable solid‐electrolyte interphase (SEI) layer rich in inorganic components. As expected, TiO2/BiAC exhibits excellent sodium storage performance in terms of cycling stability (346 mAh g−1 after 1000 cycles@ 1A g−1) and rate capability (231 mAh g−1 @ 100 A g−1). The pouch cell is further assembled and exhibits a specific capacity of 1.2 Ah after 200 cycles. This discovery presents a new method for developing efficient anode materials and is essential for steering the advancement of anode materials with fast charge–discharge capabilities. [ABSTRACT FROM AUTHOR]

Ammonia is emerging as a liquefied and renewable‐energy carrier of global interest in the future. The electrochemical reduction of nitrate is widely acknowledged as an alternative to the traditional Haber–Bosch process for ammonia production. However, it is observed that certain catalysts can undergo spontaneous oxidation–reduction reactions with nitrate to some extent, leading to the calculated ammonia Faradaic efficiency exceeding 100%. However, there is a lack of accurate experimental validation as well as effective solutions. To address these problems, it is verified that the spontaneous reaction between the catalyst and nitrate impacts on the calculation of electrocatalytic nitrate reduction performance. Meanwhile, an updated and optimized experimental strategy is proposed to address the interference caused by the spontaneous reaction. This work will significantly contribute to more accurate and reliable electrocatalytic nitrate reduction research. [ABSTRACT FROM AUTHOR]

Settling the structure stacking of graphene (G) nanosheets to maintain the high dispersity has been an intense issue to facilitate their practical application in the microelectronics-related devices. Herein, the co-doping of the highest electronegative fluorine (F) and large atomic radius chlorine (Cl) into G via a one-step electrochemical exfoliation protocol is engineered to actualize the ultralong cycling stability for flexible micro-supercapacitors (MSCs). Density functional theoretical calculations unveiled that the F into G can form the "ionic" C─F bond to increase the repulsive force between nanosheets, and the introduction of Cl can enlarge the layer spacing of G as well as increase active sites by accumulating the charge on pore defects. The co-doping of F and Cl generates the strong synergy to achieve high reversible capacitance and sturdy structure stability for G. The as-constructed aqueous gel-based MSC exhibited the superb cycling stability for 500,000 cycles with no capacitance loss and structure stacking. Furthermore, the ionic liquid gel-based MSC demonstrated a high energy density of 113.9 mW h cm -3 under high voltage of up to 3.5 V. The current work enlightens deep insights into the design and scalable preparation of high-performance co-doped G electrode candidate in the field of flexible microelectronics., (© 2024 The Authors. Advanced Science published by Wiley‐VCH GmbH.)

Photothermal CO 2 methanation reaction represents a promising strategy for addressing CO 2 -related environmental issues. The presence of efficient tandem catalytic sites with a localized high-temperature is an effective pathway to enhance the performance of CO 2 methanation. Here the bimetallic RuCo nanoparticles anchored on ZrO 2 fiber cotton (RuCo/ZrO 2 ) as a photothermal catalyst for CO 2 methanation are prepared. A significant photothermal CO 2 methanation performance with optimal CH 4 selectivity (99%) and rate (169.93 mmol g cat -1 h -1 ) is achieved. The photothermal energy of the RuCo bimetallic nanoparticles, confined by the infrared insulation and low thermal conductivity of the ZrO 2 fiber cotton (ZrO 2 FC), provides a localized high-temperature. In situ spectroscopic experiments on RuCo/ZrO 2 , Ru/ZrO 2 , and Co/ZrO 2 indicate that the construction of tandem catalytic sites, where the Co site favors CO 2 conversion to CO while incorporating Ru enhances CO * adsorption for subsequent hydrogenation, results in a higher selectivity toward CH 4 . This work opens a new insight into designing tandem catalysts with a photothermal confinement effect in CO 2 methanation reaction., (© 2024 The Author(s). Advanced Science published by Wiley‐VCH GmbH.)

Successful bone regeneration requires close cooperation between bone marrow mesenchymal stem cells (BMSCs) and macrophages, but the low osteogenic differentiation efficiency of stem cells and the excessive inflammatory response of immune cells hinder the development of bone repair. It is necessary to develop a strategy that simultaneously regulates the osteogenic differentiation of BMSCs and the anti-inflammatory polarization of macrophages for accelerating the bone regeneration. Herein, calcium-chlorogenic acid nanoparticles (Ca-CGA NPs) are synthesized by combining the small molecules of chlorogenic acid (CGA) with Ca 2+ . Ca-CGA NPs internalized by cells can be dissolved to release free CGA and Ca 2+ under low pH conditions in lysosomes. In vitro results demonstrate that Ca-CGA NPs can not only enhance the osteogenic differentiation of BMSCs but also promote the phenotype transformation of macrophages from M1 to M2. Furthermore, in vivo experiments confirm that Ca-CGA NPs treatment facilitates the recovery of rat skull defect model through both osteoinduction and immunomodulation. This study develops a new Ca-CGA NPs-based strategy to induce the differentiation of BMSCs into osteoblasts and the polarization of macrophages into M2 phenotype, which is promising for accelerating bone repair., (© 2024 Wiley‐VCH GmbH.)