文献类型：期刊文献

英文题名：Rational Design of Single-Atom-Doped Ga2O3 Catalysts for Propane Dehydrogenation: Breaking through Volcano Plot by Lewis Acid-Base Interactions

作者：Chang, Qing-Yu[1];Wang, Kai-Qi[1];Sui, Zhi-Jun[1];Zhou, Xing-Gui[1];Chen, De[2];Yuan, Wei-Kang[1];Zhu, Yi-An[1]

机构：[1]East China Univ Sci & Technol, UNILAB, State Key Lab Chem Engn, Sch Chem Engn, Shanghai 200237, Peoples R China;[2]Norwegian Univ Sci & Technol, Dept Chem Engn, N-7491 Trondheim, Norway

年份：2021

卷号：11

期号：9

起止页码：5135

外文期刊名：ACS CATALYSIS

收录：;EI(收录号：20211910312766);WOS:【SCI-EXPANDED(收录号:WOS:000649106200021)】；

基金：This work is supported by the Natural Science Foundation of China (91645122 and 22073027), the Natural Science Foundation of Shanghai (20ZR1415800), the National Key Research and Development Program of China (2018YFB0604700), and the Fundamental Research Funds for the Central Universities (222201718003). The computational time provided by the Notur project is highly acknowledged. Q.-Y.C. would like to acknowledge financial support from the China Scholarship Council (202006745008).

语种：英文

外文关键词：propane dehydrogenation; single-atom catalysis; Ir-1-Ga2O3; DFT; microkinetic modeling

摘要：Volcano curves have proven to be particularly useful in new catalyst design in the field of heterogeneous catalysis. On the other hand, the further enhancement of the performance of the optimal catalyst for a given reaction is inherently limited by the Sabatier principle. In this work, microkinetic analysis has been carried out to examine the adsorption and catalytic behaviors of single-atom-doped Ga2O3 catalysts in propane dehydrogenation (PDH), which shows that the volcano-shaped activity plot can be broken through by Lewis acid-base interactions, making it possible to achieve better catalytic performance than that of the most active catalyst lying near the summit of the volcano. The reasoning behind this finding is that the presence of the Lewis acid-base interaction over metal-oxide surfaces may strengthen the coadsorption of a pair of amphoteric species at the M-O site, resulting in distinctly different chemisorption energy and transition state energy scaling relations. As a result, the formation energies of H&H coadsorption at the M-O site and H adsorption on top of O are identified as two different reactivity descriptors in the presence and absence of the Lewis acid-base interaction, respectively, with the resulting activity plots exhibiting a straight-line and a volcano-curve pattern. Further experiments verify that the theoretically predicted catalyst candidate Ir-1-Ga2O3 is more effective than the previously reported trace-Pt-promoted Ga2O3 catalyst, which opens up a new way to the rational design of metal-oxide catalysts for the PDH process.