用于热催化应用的穿孔单晶 Mn2O3 微立方体的合成†.

IF 2.5 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Santra Merin Saju and Anuj A. Vargeese
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引用次数: 0

摘要

过渡金属氧化物(TMOs)因其随化学环境变化而呈现不同氧化态的趋势,以及通过形态控制提高表面活性的可能性,日益成为催化应用的可行选择。开发高效、低成本的方法来合成具有介观至纳米级形态和更好特性的 TMOs 仍然是一项重大挑战。在此,我们报告了一种无模板合成策略,通过形态保留的前驱体转化方法制备穿孔介孔氧化锰 (III) 微立方体 (PMOM)。扫描电子显微镜(SEM)和透射电子显微镜(TEM)证实了具有立方结构和孔径在 20 纳米范围内的 PMOM 的形成。Mn2O3 样品呈现出瑞士奶酪般的多孔结构,粒径在 0.70 至 1.2 微米之间。此外,还研究了合成的 PMOM 样品对高氯酸铵(AP)(一种用于固体推进剂的氧化剂)热催化分解的催化活性。Mn3+ 到 Mn2+ 氧化态之间的转变促进了电子的转移,使金属表面在水分子氧化过程中充当电子受体。由于表面发生氧化-还原循环,大量电子可用于促进表面反应。因此,PMOM 的(211)表面增强了 AP 的热分解,并提出了这种催化活性的合理机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Synthesis of perforated single-crystalline Mn2O3 microcubes for thermocatalytic applications†

Synthesis of perforated single-crystalline Mn2O3 microcubes for thermocatalytic applications†

Transition metal oxides (TMOs) are increasingly viable choices for catalytic applications because of their tendency to exhibit variable oxidation states depending on the chemical environment and the possibility of enhancing surface activity through morphology control. The development of efficient and cost-effective methods for the synthesis of TMOs with meso-to nanoscale morphologies and improved characteristics remains a significant challenge. Herein, we report a template-free synthesis strategy for the preparation of perforated mesoporous manganese(III) oxide microcubes (PMOM) through a morphology-conserved transformation of the precursor method. The formation of PMOM with cubic structures and pore sizes in the range of 20 nm was confirmed using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The Mn2O3 samples exhibited a Swiss cheese-like porous structure with a particle size of 0.70 to 1.2 μm. Furthermore, the catalytic activity of the synthesized PMOM samples on the thermocatalytic decomposition of ammonium perchlorate (AP), an oxidizer used in solid propellants, was investigated. The transition between Mn3+ to Mn2+ oxidation states facilitates the transfer of electrons, allowing the metal surface to act as an electron acceptor during the oxidation of water molecules. Due to the oxidation–reduction cycle occurring on the surface, a considerable number of electrons are available for promoting surface reactions. Thus, the (211) surface of PMOM enhanced the thermal decomposition of AP, and a plausible mechanism for this catalytic activity was proposed.

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来源期刊
New Journal of Chemistry
New Journal of Chemistry 化学-化学综合
CiteScore
5.30
自引率
6.10%
发文量
1832
审稿时长
2 months
期刊介绍: A journal for new directions in chemistry
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