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金纳米粒子角部和边缘原子的催化活性差异:氢同位素交换反应。

Difference in the Catalytic Activity of Atoms in the Corners and at the Edges of Gold Nanoparticles: Hydrogen Isotope Exchange Reaction.

机构信息

A.N. Frumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Science, Leninsky pr. 31-4, 119071 Moscow, Russia.

出版信息

Int J Mol Sci. 2024 Nov 8;25(22):12022. doi: 10.3390/ijms252212022.

DOI:10.3390/ijms252212022
PMID:39596091
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11594137/
Abstract

The goal of this work is to investigate the catalytic activities of low-coordination atoms located in gold nanoparticles. Gold nanoparticles with sizes from 0.7 to 40 nm deposited on γ-AlO were used as a catalyst. Synthesized gold nanoparticles and prepared catalysts were characterized by HRTEM, SEM, XRD, DLS, and UV-Vis spectroscopy. The specific activity of gold nanoparticles towards the isotope exchange reaction at 77 K was studied as a function of nanoparticle size. The catalytic activity increases significantly when the particle size is less than 3 nm. The activities of low-coordination gold atoms located at the edges and in the corners are markedly different. Corner atoms (CN = 6) are more than 40 times more active in the reaction of hydrogen isotope exchange than edge atoms (CN = 7). TOF for atoms with coordination numbers CN = 6 and CN = 7 are 0.258 ± 0.020 and 0.006 ± 0.001 molecules site s, respectively. An equation was proposed for the dependence of the catalytic activity of the reaction on the particle size, the number of atoms on the surface, and their activity.

摘要

这项工作的目的是研究位于金纳米粒子中低配位原子的催化活性。将尺寸为 0.7 至 40nm 的金纳米粒子沉积在 γ-AlO 上作为催化剂。通过高分辨透射电子显微镜(HRTEM)、扫描电子显微镜(SEM)、X 射线衍射(XRD)、动态光散射(DLS)和紫外可见光谱(UV-Vis 光谱)对合成的金纳米粒子和制备的催化剂进行了表征。研究了金纳米粒子在 77K 下同位素交换反应的比活性作为纳米粒子尺寸的函数。当粒径小于 3nm 时,催化活性显著增加。位于边缘和角上的低配位金原子的活性明显不同。角原子(配位数 CN = 6)在氢同位素交换反应中的活性比边缘原子(配位数 CN = 7)高 40 多倍。配位数 CN = 6 和 CN = 7 的原子的 TOF 分别为 0.258±0.020 和 0.006±0.001 分子位 s。提出了一个关于反应的催化活性与颗粒尺寸、表面原子数量及其活性之间关系的方程。

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