Wu Changzheng, Guo Qixun, Yin Ping, Li Tanwei, Yang Qing, Xie Yi
Nanomaterials and Nano-chemistry, Hefei National Laboratory for Physical Sciences at Microscale, University of Science & Technology of China, Hefei, Anhui 230026, China.
J Phys Chem B. 2005 Feb 24;109(7):2597-604. doi: 10.1021/jp045530m.
Nitrogen-doped carbon nanostructures including particles, whiskers, square frameworks, lamellar layers, hollow spheres, and tubular structures have been successfully synthesized by designed direct chemical reactions of small molecule carbon halides (such as CCl4, C2Cl6) and nitridation reagent NaN3 in the absence of any templates and catalysts. The N/C ratios of the as-prepared CNx nanostructures (0.01 approximately 0.33) are strongly and systematically related to the reaction temperatures and the choice of carbon sources, as well as the presence or absence of the solvent. The Raman spectra indicate that the approaching graphitization process has occurred as the reaction temperature increases. The possible reaction mechanisms for the formation of the hollow structures are tentatively discussed according to the experimental results. This strategy provides an alternative route to synthesize nitrogen-doped carbon nanostructures and is expected to open up a new route for the synthesis of carbon nitrides.
通过小分子碳卤化物(如CCl4、C2Cl6)与氮化试剂NaN3在无任何模板和催化剂的情况下进行设计好的直接化学反应,已成功合成了包括颗粒、晶须、方形框架、层状层、空心球和管状结构在内的氮掺杂碳纳米结构。所制备的CNx纳米结构的N/C比(约0.01至0.33)与反应温度、碳源的选择以及溶剂的有无密切且系统地相关。拉曼光谱表明,随着反应温度升高,已发生接近石墨化的过程。根据实验结果初步讨论了形成空心结构的可能反应机理。该策略为合成氮掺杂碳纳米结构提供了一条替代途径,并有望为碳氮化物的合成开辟一条新途径。