Construction of a Nanoporous Highly Crystalline Hexagonal Boron Nitride from an Amorphous Precursor for Catalytic Dehydrogenation

被引:60
作者
Chen, Hao [1 ,2 ,3 ]
Yang, Zhenzhen [2 ,3 ]
Zhang, Zihao [1 ]
Chen, Zitao [5 ]
Chi, Miaofang [5 ]
Wang, Song [4 ]
Fu, Jie [1 ]
Dai, Sheng [2 ,3 ]
机构
[1] Zhejiang Univ, Minist Educ, Coll Chem & Biol Engn, Key Lab Biomass Chem Engn, Hangzhou 310027, Peoples R China
[2] Oak Ridge Natl Lab, Div Chem Sci, Oak Ridge, TN 37831 USA
[3] Univ Tennessee, Dept Chem, Knoxville, TN 37996 USA
[4] Univ Calif Riverside, Dept Chem, Riverside, CA 92521 USA
[5] Oak Ridge Natl Lab, Ctr Nanophase Mat Sci, Oak Ridge, TN 37831 USA
基金
中国国家自然科学基金;
关键词
boron nitride; dehydrogenation; nanosheets; heterogeneous catalysis; magnesium; CARRIERS; GRAPHITIZATION; CARBONS; ENERGY;
D O I
10.1002/anie.201904996
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hexagonal boron nitride (h-BN) is regarded as a graphene analogue and exhibits important characteristics and vast application potentials. However, discovering a facile method for the preparation of nanoporous crystalline h-BN nanosheets (h-BNNS) is still a challenge. Herein, a novel and simple route for the conversion of amorphous h-BN precursors into highly crystalline h-BNNS was achieved through a successive dissolution-precipitation/crystallization process in the presence of magnesium. The h-BNNS has high crystallinity, high porosity with a surface area of 347 m(2) g(-1), high purity, and enhanced thermal stability. Improved catalytic performance of crystalline h-BNNS was evidenced by its much higher catalytic efficiency in the dehydrogenation of dodecahydro-N-ethylcarbazole, compared with its amorphous h-BN precursor, as well as other precious-metal-loaded heterogeneous catalysts.
引用
收藏
页码:10626 / 10630
页数:5
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