1.四川轻化工大学 化学与环境工程学院 自贡 643000
2.东北大学理学院 沈阳 110819
E-mail: xuzhai@suse.edu.cn;; E-mail: yufu@suse.edu.cn
E-mail: yufu@suse.edu.cn
收稿:2026-02-13,
录用:2026-04-21,
网络首发:2026-06-16,
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翟旭, 高兴, 唐海燕, 侯冰洁, 滕凯旋, 张罚, 史伟良, 付昱. 一锅法合成富缺陷的双配体金属有机框架. 高分子学报, doi: 10.11777/j.issn1000-3304.2026.26054.
Zhai, X.; Gao, X.; Tang, H. Y.; Hou, B. J.; Teng, K. X.; Zhang, F.; Shi, W. L.; Fu, Y. One-pot synthesis of a defective dual-ligand metal-organic framework. Acta Polymerica Sinica (in Chinese), doi: 10.11777/j.issn1000-3304.2026.26054.
翟旭, 高兴, 唐海燕, 侯冰洁, 滕凯旋, 张罚, 史伟良, 付昱. 一锅法合成富缺陷的双配体金属有机框架. 高分子学报, doi: 10.11777/j.issn1000-3304.2026.26054. DOI: CSTR: 32057.14.GFZXB.2026.7607.
Zhai, X.; Gao, X.; Tang, H. Y.; Hou, B. J.; Teng, K. X.; Zhang, F.; Shi, W. L.; Fu, Y. One-pot synthesis of a defective dual-ligand metal-organic framework. Acta Polymerica Sinica (in Chinese), doi: 10.11777/j.issn1000-3304.2026.26054. DOI: CSTR: 32057.14.GFZXB.2026.7607.
直接合成稳定的、具有高缺陷的金属有机框架(MOF)材料在材料科学上是一种挑战,本研究通过一锅水热合成法,基于混合配体诱导策略成功制备出富含结构缺陷的双配体MOF材料(UiO-66-NO
2
/50BDC). 热重(TGA)定量分析确认其缺陷数为4.02. 高于原始单配体的1.
86. 在氧化降解芥子气模拟物CEES的催化反应中,该MOF材料展现出优异性能,不仅实现了93.3%的高转化率,更重要的是对无毒亚砜产物(CEESO)的选择性超过99%,兼具高活性与高选择性. 其性能显著优于4种单配体MOF (UiO-66、UiO-66-NO
2
、HKUST-1及MIL-88A). 催化活性的显著提升,主要源于丰富的路易斯酸位点(由结构缺陷产生)、因缺陷导致孔道扩张进而增强的反应物/产物扩散以及较大的比表面积.
The direct synthesis of stable metal-organic frameworks (MOFs) with high defect concentrations remains a challenge in materials science. In this work
we successfully prepared mixed-ligand MOF with structural defects
denoted as UiO-66-NO
2
/50BDC
via
a one-pot hydrothermal synthesis based on a mixed-ligand induction strategy. Quantitative TGA analysis confirmed a defect number of 4.02 per Zr
6
cluster
which was substantially higher than that of the pristine single-ligand MOF (1.86). In the catalytic oxidation degradation of the sulfur mustard simulant CEES
this MOF material exhibited outstanding performance
achieving not only a high conversion rate of 93.3% but also a selectivity exceeding 99% for the non-toxic sulfoxide product (CEESO). Its performance was significantly superior to that of four single-ligand MOFs (UiO-66
UiO-66-NO
2
HKUST-1
and MIL-88A
). The remarkable enhancement in catalytic activity was primarily attributed to the abundant Lewis acid sites (generated by structural defects)
enhanced diffusion of reactants/products resulting from defect-induced pore expansion
and the large specific surface area.
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