WO is a known photocatalytic metal oxide frequently studied for its depollution properties. However, it suffers from a high recombination rate of the photogenerated electron/holes pair that is detrimental to its performance. In this paper, we present a new chemical method to decorate WO nanoleaves (NLs) with a complementary metal oxide (ZnWO) in order to improve the photocatalytic performance of the composite material for the abatement of 400 ppb NO under mild UV exposure. Our strategy was to synthesize WO·2HO nanoleaves, then, to expose them, in water-free organic solution, to an organometallic precursor of Zn(Cy). A structural water molecule from WO·2HO spontaneously decomposes Zn(Cy) and induces the formation of the ZnO@WO·HO nanocomposite. The material was characterized by electronic microscopy (SEM, TEM), TGA, XRD, Raman and solid NMR spectroscopies. A simple thermal treatment under air at 500 °C affords the ZnWO@WO nanocomposite. The resulting material, additionally decorated with 1% wt. Au, presents a remarkable increase (+166%) in the photocatalytic abatement of NO under UV compared to the pristine WO NLs. This synthesis method paves the way to the versatile preparation of a wide range of MOx@WO nanocomposites (MOx = metal oxide).
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http://dx.doi.org/10.3390/nano12244360 | DOI Listing |
Sci Rep
December 2024
College of Mining Engineering, Guizhou University of Engineering Science, Bijie, 551700, China.
The Laurani high-sulfidation epithermal deposit, located in the northeastern Altiplano of Bolivia, is a representative gold-polymetallic deposit linked to the late Miocene volcanic rocks that were formed approximately at about 7.5 Ma. At Laurani, four mineralization stages are defined.
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December 2024
Department of Biomedicine, Aarhus University, 8000, Aarhus C, Denmark.
CD163, a macrophage-specific receptor, plays a critical role in scavenging hemoglobin released during hemolysis, protecting against oxidative effects of heme iron. In the bloodstream, hemoglobin is bound by haptoglobin, leading to its immediate endocytosis by CD163. While haptoglobin's structure and function are well understood, CD163's structure and its interaction with the haptoglobin-hemoglobin complex have remained elusive.
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December 2024
Key Laboratory of Special Functional and Smart Polymer Materials of Ministry of Industry and Information Technology, School of Chemistry and Chemical Engineering, Northwestern Polytechnical University, Xi'an, Shaanxi, China.
Coordination complexes are promising candidates for powerful electrocatalytic oxygen evolution reaction but challenges remain in favoring the kinetics behaviors through local coordination regulation. Herein, by refining the synergy of carboxylate anions and multiconjugated benzimidazole ligands, we tailor a series of well-defined and stable coordination complexes with three-dimensional supramolecular/coordinated structures. The coordinated water as potential open coordination sites can directly become intermediates, while the metal center easily achieves re-coordination with water molecules in the pores to resist lattice oxygen dissolution.
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December 2024
Key Laboratory of Urban Pollutant Conversion, Institute of Urban Environment, Chinese Academy of Sciences, Xiamen, China.
The emergence of single-atom catalysts offers exciting prospects for the green production of hydrogen peroxide; however, their optimal local structure and the underlying structure-activity relationships remain unclear. Here we show trace Fe, up to 278 mg/kg and derived from microbial protein, serve as precursors to synthesize a variety of Fe single-atom catalysts containing FeNO (1 ≤ x ≤ 4) moieties through controlled pyrolysis. These moieties resemble the structural features of nonheme Fe-dependent enzymes while being effectively confined on a microbe-derived, electrically conductive carbon support, enabling high-current density electrolysis.
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December 2024
Key Laboratory of UV Light-Emitting Materials and Technology of Ministry of Education, Northeast Normal University, Changchun, 130024, China.
Fast-charging metal-ion batteries are essential for advancing energy storage technologies, but their performance is often limited by the high activation energy (E) required for ion diffusion in solids. Addressing this challenge has been particularly difficult for multivalent ions like Zn. Here, we present an amorphous organic-hybrid vanadium oxide (AOH-VO), featuring one-dimensional chains arranged in a disordered structure with atomic/molecular-level pores for promoting hierarchical ion diffusion pathways and reducing Zn interactions with the solid skeleton.
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