Gibbons Bradley, Johnson Eric M, Javed Mohammad Khurram, Yang Xiaozhou, Morris Amanda J
Department of Chemistry, Virginia Tech, Blacksburg, Virginia 24061, United States.
ACS Appl Mater Interfaces. 2024 Oct 2;16(39):52703-52711. doi: 10.1021/acsami.4c11928. Epub 2024 Sep 18.
Zirconium-based metal-organic frameworks (MOFs) have become one of the most promising materials for the adsorption and destruction of chemical warfare agents. While numerous studies have shown differences in reactivity based on MOF topology and postsynthetic modification, the understanding of how modifying MOF macromorphology is less understood. MOF xerogels demonstrate modified defect levels and larger porosity, which increase the number of and access to potential active sites. Indeed, UiO-66 and NU-901 xerogels display reaction rates 2 and 3 times higher, respectively, for the hydrolysis of DMNP relative to their powder morphologies. Upon recycling, MOF-808 xerogel outperforms MOF-808 powder, previously noted as the fastest Zr MOF for hydrolysis of organophosphate nerve agents. The increase in reactivity is largely driven by a higher external surface area and the introduction of mesoporosity to previously microporous materials.
锆基金属有机框架材料(MOFs)已成为用于吸附和销毁化学战剂的最具前景的材料之一。虽然众多研究表明基于MOF拓扑结构和后合成修饰的反应活性存在差异,但对于如何改变MOF宏观形态的理解却较少。MOF干凝胶表现出改变的缺陷水平和更大的孔隙率,这增加了潜在活性位点的数量并提高了对其的可及性。实际上,相对于其粉末形态,UiO - 66和NU - 901干凝胶对DMNP水解的反应速率分别高出2倍和3倍。在循环使用时,MOF - 808干凝胶的性能优于MOF - 808粉末,MOF - 808粉末此前被认为是水解有机磷酸酯神经毒剂最快的锆基MOF。反应活性的提高很大程度上是由更高的外比表面积以及向先前的微孔材料中引入介孔性所驱动的。