RESUMEN

The deployment of Li-S batteries in the commercial sector faces obstacles due to their low electrical conductivity, slow redox reactions, quick fading of capacity, and reduced coulombic efficiency. These issues stem from the "shuttle effect" associated with lithium polysulfides (LiPSs). In this work, a haystack-like CeO2 derived from a cerium-based metal-organic framework (Ce-MOF) is obtained for the modification of a polypropylene separator. The carbon framework and CeO2 coexist in this haystack-like structure and contribute to a synergistic effect on the restriction of LiPSs shuttling. The carbon network enhances electron transfer in the conversion of LiPSs, improving the rate performance of the battery. Moreover, CeO2 enhances the redox kinetics of LiPSs, effectively reducing the "shuttle effect" in Li-S batteries. The Li-S battery with the optimized CeO2 modified separator shows an initial discharge capacity of 870.7 mAh/g at 2 C, maintaining excellent capacity over 500 cycles. This research offers insights into designing functional separators to mitigate the "shuttle effect" in Li-S batteries.

RESUMEN

Lead is the most widely used X-ray-shielding material, but it is heavy (density ≈ 11.34 g/cm3) and toxic. Therefore, the replacement of Pb with lightweight, ecofriendly materials would be beneficial, and such materials would have applications in medicine, electronics, and aerospace engineering. However, the shielding ability of Pb-free materials is significantly lower than that of Pb itself. To maximize the radiation attenuation of non-Pb-based shielding materials, a high-attenuation cross-section, normal to the incoming X-ray direction, must be achieved. In this study, we developed efficient X-ray-shielding materials composed of sulfated cerium oxide (S-CeO2) and bismuth halides. Crucially, the materials are lightweight and mechanically flexible because of the absence of heavy metals (for example, Pb and W). Further, by pre-forming the doped metal oxide as a porous sponge matrix, and then incorporating the bismuth halides into the porous matrix, uniform, compact, and intimate composites with a high-attenuation cross-section were achieved. Owing to the synergetic effect of the doped metal oxide and bismuth halides, the resultant thin (approximately 3 mm) and lightweight (0.85 g·cm-3) composite achieved an excellent X-ray-shielding rate of approximately 92% at 60 kV, one of the highest values reported for non-heavy-metal shielding materials.

RESUMEN

Platinum group metal (PGM)-free catalysts represented by nitrogen and iron co-doped carbon (Fe-N-C) catalysts are desirable and critical for metal-air batteries, but challenges still exist in performance and stability. Here, cerium oxides (CeOx) are incorporated into a two-dimensional Fe-N-C catalyst (FeNC-Ce-950) via a host-guest strategy. The Ce4+/Ce3+ redox system creates a large number of oxygen vacancies for rapid O2 adsorption to accelerate the kinetics of oxygen reduction reaction (ORR). Consequently, the as-synthesized FeNC-Ce-950 catalyst exhibits a half-wave potential (E1/2) of 0.921 V and negligible decay (<2 mV for ΔE1/2) after 5,000 accelerated durability cycles, significantly outperforming most of ORR catalysts reported in recent years and precious metal counterparts. When applied in a zinc-air battery, it demonstrates a peak power density of 175 mW cm-2 and a specific capacity of 757 mAh gZn-1. This study also provides a reference for the exploration of Fe-N-C catalysts decorated with variable valence metal oxides.

RESUMEN

In this study, we prepared a three-dimensional self-supported electrocatalyst based on a thin layer of cerium oxide nanocrystals doped with cobalt heteroatoms (CeO2-Co) and then uniformly shelled over one-dimensional tin oxide (SnO2) nanorods supported by carbon cloth substrate. The material was used as a binder-free sensor that could nonenzymatically detect xanthine (XA) with an excellent sensitivity of 3.56 µA µM-1, wide linear range of 25 nM to 55 µM, low detection limit of 58 nM, and good selectivity. A screen-printed electrode based on the material accurately detected XA in food samples as well. The achievements were resulted from synergistic effects coming from the unique core@shell formation and Co-doping strategy, which efficiently modified electronic structure of the material to expose more electroactive site numbers/types and fast charge transfer, thereby producing intrinsic catalytic properties for XA oxidation. These results suggested that the SnO2@CeO2-Co is potential for developing efficient sensor to detect XA with good sensitivity and accuracy in food-quality monitoring.

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RESUMEN

Strong metal-support interaction of supported metal catalysts is an important concept to describe the effect of metal-support interactions on the structures and catalytic performances of supported metal particles. By using an example of CeOx adlayers supported on Ag nanocrystals, herein a concept of electronic oxide-metal strong interaction (EOMSI) is put forward; this interaction significantly affects the electronic structures of oxide adlayers through metal-to-oxide charge transfer. The EOMSI can stabilize oxide adlayers in a low oxidation state under ambient conditions, which individually are not stable; moreover, the oxide adlayers experiencing the EOMSI are resistant to high-temperature oxidation in air to a certain extent. Such an EOMSI concept helps to generalize the strong influence of oxide-metal interactions on the structures and catalytic performance of oxide/metal inverse catalysts, which have been attracting increasing attention.

RESUMEN

In this paper, the syntheses of a set of cerium-bismuth mixed oxides with the formula Ce1-xBixO2-x/2, where the range of x is 0.0 to 1.0 in 10 mol% steps, via co-precipitation methods is described. Two synthesis routes are tested: The "normal" and the so called "reverse strike" (RS) co-precipitation route. The syntheses are performed with an automated synthesis robot. The activity for Diesel soot oxidation is measured by temperature programmed oxidation with an automated, serial thermogravimetric and differential scanning calorimetry system (TGA/DSC). P90 is used as a model soot. An automated and reproducible tight contact between soot and catalyst is used. The synthesized catalysts are characterized in terms of the specific surface area according to Brunauer, Emmett and Teller (SBET), as well as the dynamic oxygen storage capacity (OSCdyn). The crystalline phases of the catalysts are analysed by powder X-ray diffraction (PXRD) and Raman spectroscopy. The elemental mass fraction of the synthesized catalysts is verified by X-ray fluorescence (XRF) analysis. A correlation between the T50 values, OSCdyn and SBET has been discovered. The best catalytic performance is exhibited by the catalyst with the formula RS-Ce0.8Bi0.2Ox which is synthesized by the reverse strike co-precipitation route. Here, a correlation between activity, OSCdyn, and SBET can be confirmed based on structural properties.

RESUMEN

For air pollution control in confined space such as submarine and spacecraft, copper-manganese-cerium ternary oxide catalysts coupled with KOH sorbent were synthesized through the wet impregnation method, solid-state impregnation method A and B, and wet/solid-state impregnation method. The samples were tested for CO and CO2 removal dynamically and isothermally from 30 °C to 150 °C using two fixed bed reactors, and then characterized by XRD, nitrogen adsorption and desorption, and FE-SEM/EDS. The results showed that all the coupled CuMnCe/KOHs were able to catalyze CO and capture the produced CO2 in situ. While the coupling treatments affected the CO oxidation and CO2 absorption performance of the samples significantly and differently. Among all samples, CuMnCe/KOH-WSI with the large KOH bulk phase exhibited the outstanding CO catalytic activity and CO2 sorption efficiency, higher than the uncoupled CuMnCe/KOH. While for CuMnCe/KOH-WI and CuMnCe/KOH-SI-I samples demonstrating high-dispersed KOH species in the catalyst, the addition of the sorbent could inhibit the catalyst activity due to the occupation of the surface site and pore structure. Furtherly, the effect of the temperature was varied for CO conversion and CO2 capture performances of the sample, while they achieved an optimization balance at 150 °C for CuMnCe/KOH-WSI.

RESUMEN

Condensate microdrop self-propelling (CMDSP) surfaces have attracted intensive interest. However, it is still challenging to form metal-based CMDSP surfaces. We design and fabricate a type of copper-based CMDSP porous nanoparticle film. An electrodeposition method based on control over the preferential crystal growth of isotropic nanoparticles and synergistic utilization of tiny hydrogen bubbles as pore-making templates is adopted for the in situ growth of cerium oxide porous nanoparticle films on copper surfaces. After characterizing their microscopic morphology, crystal structure and surface chemistry, we explore their CMDSP properties. The nanostructure can realize the efficient ejection of condensate microdrops with sizes below 50 µm.

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