环己烷
催化作用
石墨氮化碳
吸附
材料科学
离解(化学)
选择性
金属
纳米棒
氮化碳
氮化物
光化学
化学工程
纳米技术
无机化学
化学
物理化学
光催化
有机化学
冶金
图层(电子)
工程类
作者
Mingdong Xu,Yongling Yu,Guojun Shi,Panming Jian,Xu Hou,Enxian Yuan
出处
期刊:ACS applied nano materials
[American Chemical Society]
日期:2024-05-09
卷期号:7 (10): 11952-11964
标识
DOI:10.1021/acsanm.4c01538
摘要
Although single metal sites on graphitic carbon nitride (g-C3N4) are extensively employed in the catalysis field, the related study is based on the flat g-C3N4 surface model, which is far beyond the reality of the curved structure involved in g-C3N4. Herein, g-C3N4 nanorods with diameters of 9.0 and 7.0 nm are synthesized via the hard template approach to support single-atom Co for the catalytic oxidation of cyclohexane. Comprehensive characterizations, combined with theoretical calculations, find that the curved structure would broaden the space of g-C3N4 interlayers, modulate the electronic structure, and reduce the coordination number of atomic Co. The mechanism study reveals that compared with Co atoms on a flat g-C3N4 surface, the low-coordinated Co atoms anchored on a curved g-C3N4 surface are capable of enhancing the reactant adsorption and facilitating the oxygen dissociation, thereby boosting the catalytic cyclohexane oxidation. The cyclohexane conversion on resultant Co/g-C3N4-9 nm reaches up to 22.4% at the overall selectivity of above 95% under mild reaction conditions, outperforming state-of-the-art nonprecious metal-based catalysts. The present work not only offers a synthesis strategy of the effective single-atom metal catalysts for the cyclohexane oxidation but also sheds light on the origin of the enhanced catalytic performance of curved g-C3N4-based catalysts.
科研通智能强力驱动
Strongly Powered by AbleSci AI