98%
921
2 minutes
20
Investigating the distribution of different Zn species on Zn-containing zeolite catalysts is crucial for identifying the active sites and establishing the relationship between the catalyst's structure and its activity in the process of ethylene aromatization. By utilizing X-ray absorption near edge spectra (XANES) of various reference samples, this study employed linear combination fitting (LCF) analysis on XANES spectra of real samples to accurately measure the changes in the distribution of Zn species in Zn-containing HZSM-5 zeolites under different Zn sources and loadings. The results showed that ZnOH, ZnO clusters, and ZnO crystalline structures coexist in Zn/HZSM-5 catalysts prepared through physical mixing and incipient wet impregnation methods. A similar trend was observed for catalysts prepared using different methods, with an increase in Zn content resulting in a decrease in the proportion of ZnOH and a significant increase in the amount of larger ZnO crystals. Furthermore, ZnO clusters were confined within the zeolite pores. The findings of this study established a direct correlation between the amount of ZnOH determined through LCF analysis and both the rate of hydrogen production and the rate of aromatics formation, providing strong evidence for the catalytic role of ZnOH as an active center for dehydrogenation, which plays a key role in promoting the formation of aromatics. The method of LCF analysis on XANES spectra allows for the determination of the local structure of Zn species, facilitating a more precise analysis based on the distribution of these species. This method not only provides detailed information about the Zn species but also enhances the accuracy of the overall analysis.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10856302 | PMC |
http://dx.doi.org/10.3390/molecules29030631 | DOI Listing |
ACS Appl Mater Interfaces
August 2025
Faculty of Materials Science and Engineering, Kunming University of Science and Technology, Kunming 650093, China.
The insufficient d-electron density in V metal atoms limits O dissociation, constraining the kinetics and activity of the oxygen reduction reaction and the oxygen evolution reaction in VN-based catalysts. Herein, Co dopant was employed to modulate the electronic characteristics of the d-orbitals and associated free energy of VN, thereby further enhancing its catalytic activity. XPS and XANES spectra revealed that Co atoms replaced V and strongly bonded with neighboring N atoms, effectively regulating the local electronic structure.
View Article and Find Full Text PDFPhys Chem Chem Phys
August 2025
Carl von Ossietzky Universität Oldenburg, Institute of Physics, 26129 Oldenburg, Germany.
Multi-alkali antimonides (MAAs) are promising materials for vacuum electron sources. While sodium-based MAAs have demonstrated superior characteristics for ultrabright electron sources, their synthesis remains challenging, often resulting in mixed stoichiometries and polycrystalline domains. To address this complexity and guide the characterization of experimentally grown photocathodes, we present a comprehensive theoretical study of the X-ray near-edge spectroscopy (XANES) of four ternary MAAs: cubic NaKSb and hexagonal NaKSb, representing the experimentally known phase of each stoichiometry, as well as hexagonal NaKSb and cubic NaKSb, two computationally predicted polymorphs.
View Article and Find Full Text PDFActa Crystallogr C Struct Chem
September 2025
School of Food Technology and Natural Sciences, Massey University, Riddet Road, Palmerston North, 4410, New Zealand.
The extraction and separation of rare earth elements (lanthanides) can be difficult due to their chemical similarities. Biological processes can have very selective activity towards different elements. We investigated the use of microalgae for this purpose by looking at the interaction of Ce, Gd and Yb with the microalga Chlamydomonas reinhardtii, which has been induced to form polyphosphate granules.
View Article and Find Full Text PDFThe evolution of Er clusters in CaF crystals has not been fully understood, making the underlying mechanism for regulating the upconversion luminescence color of Er:CaF crystals remains unclear. In this work, the first-principles calculation is combined with the synchrotron X-ray absorption near-edge structure (XANES) and extended X-ray absorption fine structure (EXAFS), as well as the dielectric spectra and absorption spectra to study the Er-doped CaF crystals. The spectral analysis reveals the potential mechanism underlying the red-to-green (R/G) ratio transformation; specifically, the cross-relaxation rates of different clusters differed significantly.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
School of Materials Science and Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore, 639798, Singapore.
A rationally designed, bifunctional ammonia-oxidation catalyst spatially decouples NH activation and *OH adsorption to overcome the intrinsic trade-off of single-component systems. Atomically dispersed Zn single atoms in an N,O-doped carbon support (Zn/NOC) serve as dedicated *OH-adsorption sites, while Ir-modulated Pt(100) nanocubes selectively activate NH. Comprehensive structural characterization (AC HAADF-STEM, XPS, XANES, EXAFS) confirms Zn-NO coordination and atomically isolated Zn centers.
View Article and Find Full Text PDF