超小MoC-MoO2异质结耦合氮掺杂还原石墨烯促进燃料油深度氧化脱硫

IF 3.9 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Yefeng Liu*, , , Fuyan Zhao, , , Zhilin Fang, , , Chuan Li, , , Yu Wang, , , Jiajin Wu, , , Shuangyang Zhang, , , Xu Cai, , , Ruichen Li, , , Yanbo Sun, , and , Peng Zuo*, 
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引用次数: 0

摘要

在本研究中,合成了一种由二维氮掺杂还原氧化石墨烯(NCrGO)和超小碳化钼-二氧化钼(MoC-MoO2)异质结组成的MoC-MoO2@NCrGO-900复合催化剂。优化后的催化剂具有良好的氧化脱硫性能。具体而言,含硫量为4000 ppm的模拟油在30分钟内完全脱硫,连续6次循环后脱硫效率达到98.1%。此外,该催化剂在广泛的硫浓度范围内(1000 - 5000ppm)具有广泛的适用性。MoC-MoO2@NCrGO-900之所以具有优异的催化活性,主要归功于MoC-MoO2异质结结构内部的协同作用、NCrGO载体的强给电子特性以及均匀分散的Mo活性位点。通过自由基清除实验和电子顺磁共振波谱的机理研究表明,羟基自由基(·OH)在氧化过程中起主导作用,载体和活性中心之间的电子转移进一步提高了催化效率。总之,本研究为构建碳负载异质结提供了一种通用的、可扩展的原位封装策略,在ODS的实际应用中具有广阔的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ultrasmall MoC-MoO2 Heterojunction Coupled with Nitrogen-Doped Reduced Graphene for Boosting the Deep Oxidative Desulfurization of Fuel Oils

Ultrasmall MoC-MoO2 Heterojunction Coupled with Nitrogen-Doped Reduced Graphene for Boosting the Deep Oxidative Desulfurization of Fuel Oils

Ultrasmall MoC-MoO2 Heterojunction Coupled with Nitrogen-Doped Reduced Graphene for Boosting the Deep Oxidative Desulfurization of Fuel Oils

In this study, a MoC-MoO2@NCrGO-900 composite catalyst comprising two-dimensional nitrogen-doped reduced graphene oxide (NCrGO) and ultrasmall molybdenum carbide-molybdenum dioxide (MoC-MoO2) heterojunctions was synthesized. The optimized catalyst exhibited an outstanding oxidative desulfurization (ODS) performance. Specifically, a model oil containing 4000 ppm sulfur was completely desulfurized within 30 min, with a desulfurization efficiency of 98.1% being recorded after six consecutive cycles. Moreover, the catalyst demonstrated a broad applicability over a wide range of sulfur concentrations (1000–5000 ppm). The excellent catalytic activity of MoC-MoO2@NCrGO-900 was attributed to synergy within the MoC-MoO2 heterojunction structure, the strong electron-donating properties of the NCrGO support, and the uniformly dispersed Mo active sites. Mechanistic studies using radical scavenging experiments and electron paramagnetic resonance spectroscopy revealed that hydroxyl radicals (·OH) play a dominant role in the oxidation process, with electron transfer between the support and the active centers further enhancing the catalytic efficiency. Overall, this study provides a general and scalable in situ encapsulation strategy for constructing carbon-supported heterojunctions that offer promising prospects for use in practical ODS applications.

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来源期刊
Langmuir
Langmuir 化学-材料科学:综合
CiteScore
6.50
自引率
10.30%
发文量
1464
审稿时长
2.1 months
期刊介绍: Langmuir is an interdisciplinary journal publishing articles in the following subject categories: Colloids: surfactants and self-assembly, dispersions, emulsions, foams Interfaces: adsorption, reactions, films, forces Biological Interfaces: biocolloids, biomolecular and biomimetic materials Materials: nano- and mesostructured materials, polymers, gels, liquid crystals Electrochemistry: interfacial charge transfer, charge transport, electrocatalysis, electrokinetic phenomena, bioelectrochemistry Devices and Applications: sensors, fluidics, patterning, catalysis, photonic crystals However, when high-impact, original work is submitted that does not fit within the above categories, decisions to accept or decline such papers will be based on one criteria: What Would Irving Do? Langmuir ranks #2 in citations out of 136 journals in the category of Physical Chemistry with 113,157 total citations. The journal received an Impact Factor of 4.384*. This journal is also indexed in the categories of Materials Science (ranked #1) and Multidisciplinary Chemistry (ranked #5).
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