CORC  > 金属研究所  > 中国科学院金属研究所
Single Au Anion Can Catalyze Acetylene Hydrochlorination: Tunable Catalytic Performance from Rational Doping
Ali, Sajjad1,2; Olanrele, Samson2,3; Liu, TianFu2,3; Lian, Zan2,3; Si, Chaowei2,3; Yang, Min2,3; Li, Bo2
刊名JOURNAL OF PHYSICAL CHEMISTRY C
2019-12-05
卷号123期号:48页码:29203-29208
ISSN号1932-7447
DOI10.1021/acs.jpcc.9b07557
通讯作者Li, Bo(boli@imr.ac.cn)
英文摘要In this work, for the first time it is demonstrated that supported single Au in either a positive or a negative charge state can catalyze acetylene hydrochlorination competitively with regard to other reported Au catalysts by using first-principle calculations. The nitrogen and boron dopants on the single-walled carbon nanotube (SWCNT) not only behave as stable anchoring positions for the single Au but also effectively adjust the electronic structure of Au. It is revealed that Au becomes positively and negatively charged on nitrogenand boron-doped SWCNT, respectively. The different charge state of Au directly influences the interactions with the reactants C2H2. Moreover, the charge transfer during C2H2 adsorption exhibits an opposite effect for Au cation and anion. Therefore, the dopant on the support is effectively a tool to tune the properties of the supported single Au. The reaction obeys an Eley-Rideal-like mechanism, in which C2H2 binds first, followed by HCI activation and product formation. Detailed reaction pathway analysis reveals that both positively and negatively charged Au are active acetylene hydrochlorination catalysts with comparable reaction barriers. The current work not only broadens the scope of Au catalysts in acetylene hydrochlorination, with the inclusion of negative Au, but also verifies the effectiveness of support doping to tune the catalytic performance.
资助项目NSFC[21573255] ; Natural Science Foundation of LiaoNing Province[20180510014] ; Institute of Metal Research[Y3NBA211A1] ; State Key Laboratory of Catalytic Materials and Reaction Engineering (RIPP, SINOPEC) ; Special Program for Applied Research on Super Computation of the NSFC Guangdong Joint Fund (the second phase)[U1501501]
WOS研究方向Chemistry ; Science & Technology - Other Topics ; Materials Science
语种英语
出版者AMER CHEMICAL SOC
WOS记录号WOS:000501623100014
资助机构NSFC ; Natural Science Foundation of LiaoNing Province ; Institute of Metal Research ; State Key Laboratory of Catalytic Materials and Reaction Engineering (RIPP, SINOPEC) ; Special Program for Applied Research on Super Computation of the NSFC Guangdong Joint Fund (the second phase)
内容类型期刊论文
源URL[http://ir.imr.ac.cn/handle/321006/136230]  
专题金属研究所_中国科学院金属研究所
通讯作者Li, Bo
作者单位1.Univ Chinese Acad Sci, 19A Yuquan Rd, Beijing 100049, Peoples R China
2.Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, 72 Wenhua Rd, Shenyang 110016, Liaoning, Peoples R China
3.Univ Sci & Technol China, Sch Mat Sci & Engn, Shenyang 110016, Liaoning, Peoples R China
推荐引用方式
GB/T 7714
Ali, Sajjad,Olanrele, Samson,Liu, TianFu,et al. Single Au Anion Can Catalyze Acetylene Hydrochlorination: Tunable Catalytic Performance from Rational Doping[J]. JOURNAL OF PHYSICAL CHEMISTRY C,2019,123(48):29203-29208.
APA Ali, Sajjad.,Olanrele, Samson.,Liu, TianFu.,Lian, Zan.,Si, Chaowei.,...&Li, Bo.(2019).Single Au Anion Can Catalyze Acetylene Hydrochlorination: Tunable Catalytic Performance from Rational Doping.JOURNAL OF PHYSICAL CHEMISTRY C,123(48),29203-29208.
MLA Ali, Sajjad,et al."Single Au Anion Can Catalyze Acetylene Hydrochlorination: Tunable Catalytic Performance from Rational Doping".JOURNAL OF PHYSICAL CHEMISTRY C 123.48(2019):29203-29208.
个性服务
查看访问统计
相关权益政策
暂无数据
收藏/分享
所有评论 (0)
暂无评论
 

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。


©版权所有 ©2017 CSpace - Powered by CSpace