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A generalized approach to adjust the catalytic activity of borocarbonitride for alkane oxidative dehydrogenation reactions
Zhang, Xuefei1; Dai, Xueya2; Wu, Kuang-Hsu3; Su, Bingjian4; Chen, Jinming4; Qi, Wei2; Xie, Zailai1
通讯作者Qi, Wei(wqi@imr.ac.cn) ; Xie, Zailai(zlxie@fzu.edu.cn)
2022
发表期刊JOURNAL OF CATALYSIS
ISSN0021-9517
卷号405页码:105-115
摘要The borocarbonitrides (BCNs) have exhibited enormous potential as non-metallic catalysts for alkane oxidative dehydrogenation (ODH) reactions. However, the poor electron transportation ability in BCN leads to a low reactivity of oxygen functional groups (-C=O and-B-OH). Herein, we present a generalized strategy to promote the catalytic activity of BCN through in situ encapsulation of transition-metal (Fe, Co, Ni) nanoparticles within BCN nanotubes (BCNNTs). Among them, individual metal particles themselves do not contribute directly on ODH reactions and mainly serve as electron modulators to tune the electron density of-C=O and-B-OH active sites on BCNNTs. As a result, catalytic activities of all metal@BCNNTs catalysts surpass pure BCN in ethylbenzene (EB) ODH reactions, among which Fe@BCNNTs displays a significant activity enhancement with 36 % EB conversion with the styrene (ST) selectivity remaining >98% under gentle reaction conditions. Structural and kinetic analyses proved that the promotion effect originated from the strong interactions between metal nanoparticles and BCNNTs. The theoretical calculations disclosed that the enhanced ODH activity was due to the electron transfer from the encapsulated metal to BCNNTs, which increases the electron transportation ability and electron density of BCNNTs, thus promoting the nucleophilicity of-C=O and-B-OH active sites, leading to the reduced activation energy barrier for-C-H bond dissociation. The present work sets forth the structure function relationship, identifying opportunities for rational design of highly efficient BCN catalysts for ODH reactions. (c) 2021 Elsevier Inc. All rights reserved.
关键词Borocarbonitride catalysts Transition metal encapsulation Strong interactions Alkane oxidative dehydrogenation Heterogeneous catalysis
资助者NSFC of China ; Natural Science Foundation of Fujian Province of China ; Natural Science Foundation of Liaoning Province of China
DOI10.1016/j.jcat.2021.11.036
收录类别SCI
语种英语
资助项目NSFC of China[22072018] ; NSFC of China[22072163] ; NSFC of China[21761132010] ; NSFC of China[91645114] ; Natural Science Foundation of Fujian Province of China[2021J06010] ; Natural Science Foundation of Liaoning Province of China[2020-YQ-02]
WOS研究方向Chemistry ; Engineering
WOS类目Chemistry, Physical ; Engineering, Chemical
WOS记录号WOS:000753137100005
出版者ACADEMIC PRESS INC ELSEVIER SCIENCE
引用统计
被引频次:18[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/321006/173399
专题中国科学院金属研究所
通讯作者Qi, Wei; Xie, Zailai
作者单位1.Fuzhou Univ, Coll Chem, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350016, Peoples R China
2.Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, Shenyang 110016, Peoples R China
3.Univ New South Wales, Sch Chem Engn, Sydney, NSW, Australia
4.Natl Synchrot Radiat Res Ctr, Hsinchu 30076, Taiwan
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Zhang, Xuefei,Dai, Xueya,Wu, Kuang-Hsu,et al. A generalized approach to adjust the catalytic activity of borocarbonitride for alkane oxidative dehydrogenation reactions[J]. JOURNAL OF CATALYSIS,2022,405:105-115.
APA Zhang, Xuefei.,Dai, Xueya.,Wu, Kuang-Hsu.,Su, Bingjian.,Chen, Jinming.,...&Xie, Zailai.(2022).A generalized approach to adjust the catalytic activity of borocarbonitride for alkane oxidative dehydrogenation reactions.JOURNAL OF CATALYSIS,405,105-115.
MLA Zhang, Xuefei,et al."A generalized approach to adjust the catalytic activity of borocarbonitride for alkane oxidative dehydrogenation reactions".JOURNAL OF CATALYSIS 405(2022):105-115.
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