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具有源自金属有机框架前驱体氧化蚀刻的多种活性区域的纳米片态钴锰氧化物用于甲苯的催化燃烧

Nanosheet-state cobalt-manganese oxide with multifarious active regions derived from oxidation-etching of metal organic framework precursor for catalytic combustion of toluene.

作者信息

Zhao Jinggang, Wang Peifen, Liu Changlin, Zhao Qiang, Wang Junli, Shi Lei, Xu Guangwen, Abudula Abuliti, Guan Guoqing

机构信息

Graduate School of Science and Technology, Hirosaki University, 1-Bunkyocho, Hirosaki 036-8560, Japan.

Graduate School of Science and Technology, Hirosaki University, 1-Bunkyocho, Hirosaki 036-8560, Japan; Department of Environmental Science and Engineering, Taiyuan University of Technology, Taiyuan 030024, P. R. China.

出版信息

J Colloid Interface Sci. 2023 Jan;629(Pt A):706-722. doi: 10.1016/j.jcis.2022.08.187. Epub 2022 Sep 5.

Abstract

For the first time, a nanosheet-state CoMnx mixed oxide with multifarious active regions was synthesized by oxidation-etching assembly of metal organic framework (MOF) precursor and applied for catalytic combustion of toluene at low temperatures. The obtained optimum catalyst denoted as CoMn6 showed excellent performance, which achieved 90% conversion of 1,000 ppm toluene under a weight hourly space velocity (WHSV) of 60,000 mL/(g·h) at 219 °C. While, it also exhibited long-term stability with strong water resistance property. The characterizations of physicochemical properties indicated that the oxidation-etching assembly process built an abundant mesoporous structure in the CoMnx catalyst, which greatly increased the specific surface area (SSA). Especially, potassium permanganate as oxidant and manganese source led to uniform dispersion and assembling of cobalt atoms, which caused the generation of low-crystallinity CoMnx mixed oxide with abundant dislocations, vacancies, phase interfaces and amorphous structures, resulting in excellent low-temperature reducibility, outstanding lattice oxygen mobility and abundant active species such as Mn, Co and adsorbed oxygen species. Density functional theory (DFT) calculations demonstrated that gaseous oxygen with the longer bond length (1.406 Å) and stronger adsorption energy (-4.443 eV) could be adsorbed and activated well on the MnCoO (311) plane, which is beneficial for the toluene oxidation. In situ diffuse reflectance infrared spectroscopy (DRIFTS) technique was applied to track the intermediates of toluene combustion under different atmospheres, which further deduced the contributions of different active regions and oxidation mechanism over the CoMnx catalyst. The present facile strategy of oxidation-etching assembly of the MOF precursor for the creating of novel catalyst with high performance could be applied in a wide variety of materials besides VOC combustion catalysts.

摘要

首次通过金属有机框架(MOF)前驱体的氧化蚀刻组装合成了具有多种活性区域的纳米片态CoMnx混合氧化物,并将其应用于甲苯的低温催化燃烧。所获得的最佳催化剂CoMn6表现出优异的性能,在219℃、重量空速(WHSV)为60,000 mL/(g·h)的条件下,1000 ppm甲苯的转化率达到90%。同时,它还表现出长期稳定性和很强的耐水性。物理化学性质表征表明,氧化蚀刻组装过程在CoMnx催化剂中构建了丰富的介孔结构,大大增加了比表面积(SSA)。特别是,高锰酸钾作为氧化剂和锰源导致钴原子均匀分散和组装,从而生成具有大量位错、空位、相界面和非晶结构的低结晶度CoMnx混合氧化物,具有优异的低温还原性、出色的晶格氧迁移率以及丰富的活性物种,如Mn、Co和吸附氧物种。密度泛函理论(DFT)计算表明,键长较长(1.406 Å)且吸附能较强(-4.443 eV)的气态氧能够在MnCoO(311)平面上被良好地吸附和活化,这有利于甲苯氧化。原位漫反射红外光谱(DRIFTS)技术用于跟踪不同气氛下甲苯燃烧的中间体,进一步推导了CoMnx催化剂上不同活性区域的贡献和氧化机理。这种通过MOF前驱体氧化蚀刻组装制备高性能新型催化剂的简便策略,除了VOC燃烧催化剂外,还可应用于多种材料。

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