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Chinese Academy of Sciences Institutional Repositories Grid
Theoretical Views on Activation of Methane Catalyzed by Hf2+ and Oxidation of CO (x(1)Sigma(+)) by N2O (x(1)Sigma(+)) Catalyzed by HfO2+ and TaO2+

文献类型:期刊论文

作者Nian JY(念敬妍)1; Tie L(铁璐)1; Wang B(王奔)1,2; Guo ZG(郭志光)1,2; Guo ZG(郭志光)
刊名The Journal of Physical Chemistry A
出版日期2013
卷号117期号:36页码:8843-8854
ISSN号1089-5639
通讯作者郭志光
英文摘要The mechanisms of activation of CH4 catalyzed by 1/3Hf 2+ and oxidation of CO by N2O catalyzed by 1/3HfO2+ or 2/4TaO2+ have been investigated using B3LYP level of theory. For the activation of methane, TSR (Two-state reactivity) mechanism has been certified through spin-orbit coupling (SOC) calculation and Landau-Zener-type model. In the vicinity of minimum energy crossing point (MECP), SOC equals 900.23 cm-1 and probability of inter-system crossing is approximately 0.62. Spin inversion makes the activation barrier decline from 1.63 to 0.57 eV. NBO analysis demonstrates that empty 6s and 5d orbitals of Hf atom play the major role for the activation of C-H bonds. Finally, CH4 dehydrogenates to produce Hf-CH22+. For oxidation of CO by N2O catalyzed by HfO2+ or TaO2+, the covalent bonds between transition metal atoms and oxygen atom restrict the freedom of valence electrons. Therefore, they are all SSR (Single-state reactivity). Oxygen atom is directly extracted during the course of oxygen transfer, and its microscopic essence has been discussed. The detailed kinetic information of two catalytic cycles has been calculated by referencing “energetic span (δE)” model. Finally, TOF (HfO2+) / TOF (TaO2+) = 2.7 at 298.15 K, which has a good consistency with experimental result.
学科主题材料科学与物理化学
收录类别SCI
资助信息the National Nature Science Foundation of China (Nos. 31070155;11172301;21203217);the “Funds for Distinguished Young Scientists” of Hubei Province (2012FFA002), the cojoint scientific fieldproject, the “Western Light Talent Culture” Project;the “Top Hundred Talents” Program of Chinese Academy of Sciences
语种英语
WOS记录号WOS:000330145400037
公开日期2013-12-02
源URL[http://210.77.64.217/handle/362003/4223]  
专题兰州化学物理研究所_固体润滑国家重点实验室
通讯作者Guo ZG(郭志光)
作者单位1.Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Solid Lubricat, Lanzhou 730000, Peoples R China
2.Hubei Univ, Key Lab Green Preparat & Applicat Funct Mat, Minist Educ, Wuhan 430062, Peoples R China
推荐引用方式
GB/T 7714
Nian JY,Tie L,Wang B,et al. Theoretical Views on Activation of Methane Catalyzed by Hf2+ and Oxidation of CO (x(1)Sigma(+)) by N2O (x(1)Sigma(+)) Catalyzed by HfO2+ and TaO2+[J]. The Journal of Physical Chemistry A,2013,117(36):8843-8854.
APA Nian JY,Tie L,Wang B,Guo ZG,&郭志光.(2013).Theoretical Views on Activation of Methane Catalyzed by Hf2+ and Oxidation of CO (x(1)Sigma(+)) by N2O (x(1)Sigma(+)) Catalyzed by HfO2+ and TaO2+.The Journal of Physical Chemistry A,117(36),8843-8854.
MLA Nian JY,et al."Theoretical Views on Activation of Methane Catalyzed by Hf2+ and Oxidation of CO (x(1)Sigma(+)) by N2O (x(1)Sigma(+)) Catalyzed by HfO2+ and TaO2+".The Journal of Physical Chemistry A 117.36(2013):8843-8854.

入库方式: OAI收割

来源:兰州化学物理研究所

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