烟气脱硫
催化作用
异质结
硫黄
石墨烯
钼
光催化
化学工程
化学
激进的
氧化物
材料科学
电子顺磁共振
无机化学
光化学
纳米技术
有机化学
工程类
物理
光电子学
核磁共振
作者
Yefeng Liu,Fuyan Zhao,Zhilin Fang,Chuan Li,Yu Wang,Jiajin Wu,Shudong Zhang,Xu Cai,Ruichen Li,Yanbo Sun,Peng Zuo
出处
期刊:Langmuir
[American Chemical Society]
日期:2025-09-09
标识
DOI:10.1021/acs.langmuir.5c03587
摘要
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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