Oxidative dehydrogenation reaction of short alkanes on nanostructured carbon catalysts: a computational account

IMR OpenIR

	Oxidative dehydrogenation reaction of short alkanes on nanostructured carbon catalysts: a computational account
	Sun, XY; Han, P; Li, B; Mao, SJ; Liu, TF; Ali, S; Lian, Z; Su, DS; Su, DS (reprint author), Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, 72 Wenhua Rd, Shenyang 110016, Liaoning, Peoples R China.
	2018-01-25
发表期刊	CHEMICAL COMMUNICATIONS
ISSN	1359-7345
卷号	54 期号:8 页码:864-875
摘要	Recent progress from first principles computational studies is presented for catalytic properties of nanostructured carbon catalysts in the oxidative dehydrogenation (ODH) reaction of short alkanes. Firstly, a brief introduction is given on the development of carbon catalysts in ODH since 1970. Oxygen functional groups have pivotal importance for ODH on nanostructured carbon catalysts. We discuss the oxidation process by HNO3 on pristine and defective carbon materials. The interactions between the oxygen molecule (oxidant) and the nanostructured carbon catalysts are quantitatively calibrated. Moreover the different nucleophilic abilities of oxygen functional groups are carefully compared and the strongest nucleophilic sites are proposed. The active sites and detailed reaction pathway are revealed from several computational studies. Diketone/quinone groups are generally considered to be the active centers in ODH. A reaction pathway via radical formation is considered as the favorable path. Furthermore, single ketone and carbon sites are verified to be active in ODH from the analysis of aromaticity. Heteroatom doping effects in ODH are examined. Nitrogen doping is found to be very reactive towards oxygen molecule activation. Other dopants such as boron, phosphorous and sulfur also have positive effects on the reactivity of ODH. Extensive calculations suggest that the BEP relation is applicable for the doped nanostructured carbon catalysts. In the end, an outlook for the future direction of the computational study is supplied.; Recent progress from first principles computational studies is presented for catalytic properties of nanostructured carbon catalysts in the oxidative dehydrogenation (ODH) reaction of short alkanes. Firstly, a brief introduction is given on the development of carbon catalysts in ODH since 1970. Oxygen functional groups have pivotal importance for ODH on nanostructured carbon catalysts. We discuss the oxidation process by HNO3 on pristine and defective carbon materials. The interactions between the oxygen molecule (oxidant) and the nanostructured carbon catalysts are quantitatively calibrated. Moreover the different nucleophilic abilities of oxygen functional groups are carefully compared and the strongest nucleophilic sites are proposed. The active sites and detailed reaction pathway are revealed from several computational studies. Diketone/quinone groups are generally considered to be the active centers in ODH. A reaction pathway via radical formation is considered as the favorable path. Furthermore, single ketone and carbon sites are verified to be active in ODH from the analysis of aromaticity. Heteroatom doping effects in ODH are examined. Nitrogen doping is found to be very reactive towards oxygen molecule activation. Other dopants such as boron, phosphorous and sulfur also have positive effects on the reactivity of ODH. Extensive calculations suggest that the BEP relation is applicable for the doped nanostructured carbon catalysts. In the end, an outlook for the future direction of the computational study is supplied.
部门归属	[sun, xiaoying ; han, peng] shenyang normal univ, inst catalysis energy & environm, coll chem & chem engn, shenyang 110034, liaoning, peoples r china ; [li, bo ; mao, shanjun ; liu, tianfu ; ali, sajjad ; lian, zan ; su, dangsheng] chinese acad sci, inst met res, shenyang natl lab mat sci, 72 wenhua rd, shenyang 110016, liaoning, peoples r china ; [liu, tianfu ; lian, zan] univ sci & technol china, sch mat sci & engn, shenyang 110016, liaoning, peoples r china ; [ali, sajjad] univ chinese acad sci, beijing 100049, peoples r china
关键词	h Bond Activation Initio Molecular-dynamics Density-functional Theory Vanadium-oxide Catalysts Metal-free Catalysts Nitric-acid Mediated Catalysis Oxygen-adsorption Styrene Synthesis 1st Principles
学科领域	Chemistry, Multidisciplinary
资助者	NSFC [21573255, 51521091]; Chinese Academy of Sciences [XDA09030103]; LiaoNing Natural Science Foundation [201602676]; Special Program for Applied Research on Super Computation of the NSFC Guangdong Joint Fund [U1501501]
收录类别	SCI
语种	英语
WOS记录号	WOS:000423464900001
引用统计	被引频次：32[WOS] [WOS记录] [WOS相关记录]
文献类型	期刊论文
条目标识符	http://ir.imr.ac.cn/handle/321006/79565
专题	中国科学院金属研究所
通讯作者	Li, B; Su, DS (reprint author), Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, 72 Wenhua Rd, Shenyang 110016, Liaoning, Peoples R China.
推荐引用方式 GB/T 7714	Sun, XY,Han, P,Li, B,et al. Oxidative dehydrogenation reaction of short alkanes on nanostructured carbon catalysts: a computational account[J]. CHEMICAL COMMUNICATIONS,2018,54(8):864-875.
APA	Sun, XY.,Han, P.,Li, B.,Mao, SJ.,Liu, TF.,...&Su, DS .(2018).Oxidative dehydrogenation reaction of short alkanes on nanostructured carbon catalysts: a computational account.CHEMICAL COMMUNICATIONS,54(8),864-875.
MLA	Sun, XY,et al."Oxidative dehydrogenation reaction of short alkanes on nanostructured carbon catalysts: a computational account".CHEMICAL COMMUNICATIONS 54.8(2018):864-875.