陆安慧

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教授

博士生导师

硕士生导师

主要任职:校长助理

其他任职:精细化工国家重点实验室副主任,辽宁省低碳资源高值化利用重点实验室主任

性别:男

毕业院校:中科院山西煤化所

学位:博士

所在单位:化工学院

学科:工业催化. 化学工艺. 能源化工

办公地点:大连市凌工路2号大连理工大学西部校区化工楼,邮编:116024

联系方式:0411-84986112

电子邮箱:anhuilu@dlut.edu.cn

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A Mechanochemical-Assisted Synthesis of Boron, Nitrogen Co-Doped Porous Carbons as Metal-Free Catalysts

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论文类型:期刊论文

发表时间:2020-02-11

发表刊物:CHEMISTRY-A EUROPEAN JOURNAL

收录刊物:PubMed、EI、SCIE

卷号:26

期号:9

页面范围:2041-2050

ISSN号:0947-6539

关键字:B; N co-doped carbon; cooperative effects; mechanochemical methods; metal-free catalysis; solid-state synthesis

摘要:A green and convenient solid-state method assisted by mechanical energy is employed for the synthesis of boron (B) and nitrogen (N) co-doped porous carbons (B,N-Cs). Glutamic acid (Glu) and boric acid (H3BO3) are used as the N-containing carbon precursor and boron source, respectively. This method is easy to perform and proved to be efficient towards co-doping B and N into the carbon matrix with high contents of B (7 atom %) and N (10 atom %). By adjusting the molar ratio of H3BO3 to Glu, the surface chemical states of B and N could be readily modulated. When increasing H3BO3 dosage, the pore size of B,N-Cs could be tuned ranging from micropores to mesopores with a Brunauer-Emmett-Teller (BET) surface area up to 940 m(2) g(-1). Finally, the B,N-Cs were applied as metal-free catalysts for the cycloaddition of CO2 to epoxides, which outperform the N-doped carbon catalyst (NC-900) and the physically mixed catalyst of NC-900/B4C. The enhanced activity is attributed to the cooperative effect between B and N sites. X-ray photoelectron spectroscopy (XPS) analysis reveals that BN3 in the B,N-Cs serves as a critical active site for the cooperative catalysis.