Toward high-efficiency photovoltaics-assisted electrochemical and photoelectrochemical CO2 reduction: Strategy and challenge.

The realization of a complete techno-economy through a significant carbon dioxide (CO2) reduction in the atmosphere has been explored to promote a low-carbon economy in various ways. CO2 reduction reactions (CO2RRs) can be induced using sustainable energy, including electric and solar energy, using systems such as electrochemical (EC) CO2RR and photoelectrochemical (PEC) systems. This study summarizes various fabrication strategies for non-noble metal, copper-based, and metal-organic framework-based catalysts with excellent Faradaic efficiency (FE) for target carbon compounds, and for noble metals with low overvoltage. Although EC and PEC systems achieve high energy conversion efficiency with excellent catalysts, they still require external power and lack complete bias-free operation. Therefore, photovoltaics, which can overcome the limitations of these systems, have been introduced. The utilization of silicon and perovskite-based solar cells for photovoltaics-assisted EC (PV-EC) and photovoltaics-assisted PEC (PV-PEC) CO2RR systems are cost-efficient, and the III-V semiconductor photoabsorbers achieved high solar-to-carbon efficiency. This work focuses on PV-EC and PV-PEC CO2RR systems and their components and then summarizes the special cell configurations, including the tandem and stacked structures. Additionally, the study discusses current issues, such as low energy conversion, expensive PV, theoretical limits, and industrial scale-up, along with proposed solutions.

Hollow Ni/NiO/C composite derived from metal-organic frameworks as a high-efficiency electrocatalyst for the hydrogen evolution reaction.

Metal-organic frameworks (MOFs) constitute a class of crystalline porous materials employed in storage and energy conversion applications. MOFs possess characteristics that render them ideal in the preparation of electrocatalysts, and exhibit excellent performance for the hydrogen evolution reaction (HER). Herein, H-Ni/NiO/C catalysts were synthesized from a Ni-based MOF hollow structure via a two-step process involving carbonization and oxidation. Interestingly, the performance of the H-Ni/NiO/C catalyst was superior to those of H-Ni/C, H-NiO/C, and NH-Ni/NiO/C catalysts for the HER. Notably, H-Ni/NiO/C exhibited the best electrocatalytic activity for the HER, with a low overpotential of 87 mV for 10 mA cm-2 and a Tafel slope of 91.7 mV dec-1. The high performance is ascribed to the synergistic effect of the metal/metal oxide and hollow architecture, which is favorable for breaking the H-OH bond, forming hydrogen atoms, and enabling charge transport. These results indicate that the employed approach is promising for fabricating cost-effective catalysts for hydrogen production in alkaline media.

Nanostructure and nanoindentation study of pulse electric-current sintered TiB2-SiC-Cf composite.

A carbon-fiber (Cf) doped TiB2-SiC composite was prepared and investigated to determine its densification behavior, micro/nanostructural properties, and mechanical characteristics. TiB2-25 vol% SiC-2 wt% Cf was prepared at 40 MPa and 1800 °C for 7 min using the pulsed electric-current sintering technique, and a relative density of 98.5% was realized. The as-sintered composite was characterized using advanced techniques, e.g., X-ray diffractometry, energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, field-emission scanning electron microscopy, high-resolution transmission electron microscopy, field-emission electron probe micro-analysis, and nanoindentation. The Cf additive could remove the surface oxide layers from the TiB2 and SiC domains, thus transforming them into TiB2 and SiC. According to micro/nanostructural studies, Cf could not retain its initial structure and was eventually converted into graphite nanosheets. In addition, the prepared composite was examined using the nanoindentation technique, and the following results were obtained for the calculated hardness, elastic modulus, and stiffness values: TiB2 > SiC > TiB2/SiC interface.

Transition Metal Ion Doping on ZIF-8 Enhances the Electrochemical CO2 Reduction Reaction.

The electrochemical reduction of CO2  to diverse value-added chemicals is a unique, environmentally friendly approach for curbing greenhouse gas emissions while addressing sluggish catalytic activity and low Faradaic efficiency (FE) of electrocatalysts. Here, zeolite-imidazolate-frameworks-8 (ZIF-8) containing various transition metal ions-Ni, Fe, and Cu-at varying concentrations upon doping are fabricated for the electrocatalytic CO2 reduction reaction (CO2 RR) to carbon monoxide (CO) without further processing. Atom coordination environments and theoretical electrocatalytic performance are scrutinized via X-ray absorption spectroscopy (XAS) and density functional theory (DFT) calculations. Upon optimized Cu doping on ZIF-8, Cu0.5 Zn0.5 /ZIF-8 achieves a high partial current density of 11.57 mA cm-2 and maximum FE for CO of 88.5% at -1.0 V (versus RHE) with a stable catalytic activity over 6 h. Furthermore, the electron-rich sp2 C atom facilitates COOH* promotion after Cu doping of ZIF-8, leading to a local effect between the zinc-nitrogen (Zn-N4 ) and copper-nitrogen (Cu-N4 ) moieties. Additionally, the advanced CO2 RR pathway is illustrated from various perspectives, including the pre-H-covered state under the CO2 RR. The findings expand the pool of efficient metal-organic framework (MOF)-based CO2 RR catalysts, deeming them viable alternatives to conventional catalysts.

Microstructural and nanoindentation study of TaN incorporated ZrB2 and ZrB2-SiC ceramics.

This study assessed the sinterability and microstructure of ZrB2-SiC-TaN and ZrB2-TaN ceramics. Spark plasma sintering at 2000 °C and 30 MPa for 5 min produced both ceramics. The relative density of ZrB2 ceramic containing TaN was 95.3%; the addition of SiC increased this value to 98.1%. SiC's contribution to the elimination of ZrB2 surface oxides was the primary factor in the advancement of densification. The in situ formation of hexagonal boron nitride at the interface of TaN and ZrB2 was confirmed by high-resolution transmission electron microscopy, field emission-electron probe microanalyzer, X-ray diffractometry, and field emission scanning electron microscopy. Moreover, the in situ graphite might be produced as a byproduct of the SiC-SiO2 process, hence boosting the reduction of oxide compounds in the ternary system. The SiC compound had the highest hardness (29 ± 3 GPa), while the ZrB2/TaN interface exhibited the greatest values of elastic modulus (473 ± 26 GPa) and stiffness (0.76 ± 0.13 mN/nm).

Metal-Organic-Framework- and MXene-Based Taste Sensors and Glucose Detection.

Taste sensors can identify various tastes, including saltiness, bitterness, sweetness, sourness, and umami, and have been useful in the food and beverage industry. Metal-organic frameworks (MOFs) and MXenes have recently received considerable attention for the fabrication of high-performance biosensors owing to their large surface area, high ion transfer ability, adjustable chemical structure. Notably, MOFs with large surface areas, tunable chemical structures, and high stability have been explored in various applications, whereas MXenes with good conductivity, excellent ion-transport characteristics, and ease of modification have exhibited great potential in biochemical sensing. This review first outlines the importance of taste sensors, their operation mechanism, and measuring methods in sensing utilization. Then, recent studies focusing on MOFs and MXenes for the detection of different tastes are discussed. Finally, future directions for biomimetic tongues based on MOFs and MXenes are discussed.

WS2-WC-WO3 nano-hollow spheres as an efficient and durable catalyst for hydrogen evolution reaction.

Transition metal dichalcogenides (TMDs), transition metal carbides (TMCs), and transition metal oxides (TMOs) have been widely investigated for electrocatalytic applications owing to their abundant active sites, high stability, good conductivity, and various other fascinating properties. Therefore, the synthesis of composites of TMDs, TMCs, and TMOs is a new avenue for the preparation of efficient electrocatalysts. Herein, we propose a novel low-cost and facile method to prepare TMD-TMC-TMO nano-hollow spheres (WS2-WC-WO3 NH) as an efficient catalyst for the hydrogen evolution reaction (HER). The crystallinity, morphology, chemical bonding, and composition of the composite material were comprehensively investigated using X-ray diffraction, Raman spectroscopy, field emission scanning electron microscopy, and X-ray photoelectron spectroscopy. The results confirmed the successful synthesis of the WS2-WC-WO3 NH spheres. Interestingly, the presence of nitrogen significantly enhanced the electrical conductivity of the hybrid material, facilitating electron transfer during the catalytic process. As a result, the WS2-WC-WO3 NH hybrid exhibited better HER performance than the pure WS2 nanoflowers, which can be attributed to the synergistic effect of the W-S, W-C, and W-O bonding in the composite. Remarkably, the Tafel slope of the WS2-WC-WO3 NH spheres was 59 mV dec-1, which is significantly lower than that of the pure WS2 NFs (82 mV dec-1). The results also confirmed the unprecedented stability and superior electrocatalytic performance of the WS2-WC-WO3 NH spheres toward the HER, which opens new avenues for the preparation of low-cost and highly effective materials for energy conversion and storage applications.