One-Pot Preparation of Nitro-Functionalized Bimetallic UiO-66(Zr-Hf) with Hierarchical Porosity for Oxidative Desulfurization Performance

被引:6
作者
Shi, Guangming [1 ]
Liang, Yalong [1 ]
Nie, Long [2 ]
Huang, Ruodi [1 ]
Yang, Zhaohan [1 ]
Liu, Xinying [1 ]
Zhou, Jun [1 ]
Zhang, Qiuli [1 ]
Ye, Gan [1 ]
机构
[1] Xian Univ Architecture & Technol, Sch Chem & Chem Engn, Xian 710055, Peoples R China
[2] Shenzhen Univ, Coll Mat Sci & Engn, Shenzhen 518060, Peoples R China
基金
中国国家自然科学基金;
关键词
METAL-ORGANIC FRAMEWORK; BOOSTING CATALYTIC PERFORMANCE; ZR; DEFECTS; GREEN;
D O I
10.1021/acs.inorgchem.4c02959
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Preparation of multifunctional metal-organic frameworks (MOFs) offers new opportunities to obtain ultrahigh synergistic catalytic performance for heterogeneous reactions; however, the application of a one-pot method for preparing multifunctional MOFs remains challenging. Herein, we develop a one-pot green route for synthesizing bimetallic nitro-functionalized UiO-66(Zr-Hf)-NO2 with hierarchical porosity under solvent-free conditions. The optimal UiO-66(Zr-Hf-0.6)-NO2 shows an ultrahigh enhancement of oxidative desulfurization (ODS) efficiency to oxidize sulfur compounds (1000 ppm sulfur) in a model fuel at 40 degrees C within 12 min due to the introduction of more active Hf sites in the nodes, the increased Lewis acidity of Zr/Hf-O nodes by the electron-withdrawing NO2 group, and the enhanced diffusion rates by the mesopores. The turnover frequency (TOF) over UiO-66(Zr-Hf-0.6)-NO2 at 40 or 50 degrees C reaches 145.3 or 217.0 h(-1) that surpasses the TOF of most reported MOF-based catalysts in the ODS reaction. Quenching and electron paramagnetic resonance experiments confirm that the formed Hf-OH on the Zr/Hf-O nodes can easily decompose the oxidant (H2O2) for generating a Hf-OOH-active intermediate and dominate the ODS efficiency. This contribution provides a one-pot solvent-free avenue to synthesize multifunctional MOFs for enhancing their catalytic activities for targeted applications.
引用
收藏
页码:16554 / 16564
页数:11
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