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热解石墨化石墨烯结构演变中涉及的原子掺杂剂。

Atomic dopants involved in the structural evolution of thermally graphitized graphene.

机构信息

Department of Energy Science, Sungkyunkwan University, 300 Cheoncheon-dong, Jangan-gu, Suwon, Gyeonggi-do 440-746, Korea.

出版信息

Chemistry. 2012 Oct 15;18(42):13466-72. doi: 10.1002/chem.201201901. Epub 2012 Sep 13.

Abstract

Thermally doped nitrogen atoms on the sp(2)-carbon network of reduced graphene oxide (rGO) enhance its electrical conductivity. Atomic structural information of thermally annealed graphene oxide (GO) provides an understanding on how the heteroatomic doping could affect electronic property of rGO. Herein, the spectroscopic and microscopic variations during thermal graphitization from 573 to 1,373 K are reported in two different rGO sheets, prepared by thermal annealing of GO (rGO(therm)) and post-thermal annealing of chemically nitrogen-doped rGO (post-therm-rGO(N(2)H(4))). The spectroscopic transitions of rGO(N(2)H(4)) in thermal annealing ultimately showed new oxygen-functional groups, such as cyclic edge ethers and new graphitized nitrogen atoms at 1,373 K. During the graphitization process, the microscopic evolution resolved by scanning tunneling microscopy (STM) produced more wrinkled surface morphology with graphitized nanocrystalline domains due to atomic doping of nitrogen on a post-therm-rGO(N(2)H(4)) sheet. As a result, the post-therm-rGO(N(2)H(4))-containing nitrogen showed a less defected sp(2)-carbon network, resulting in enhanced conductivity, whereas the rGO(therm) sheet containing no nitrogen had large topological defects on the basal plane of the sp(2)-carbon network. Thus, our investigation of the structural evolution of original wrinkles on a GO sheet incorporated into the graphitized N-doped rGO helps to explain how the atomic doping can enhance the electrical conductivity.

摘要

在还原氧化石墨烯 (rGO) 的 sp(2)-碳网络上掺杂热氮原子可以提高其电导率。热退火氧化石墨烯 (GO) 的原子结构信息提供了一个理解杂原子掺杂如何影响 rGO 电子性质的途径。在此,我们报告了两种不同 rGO 片(通过热退火 GO 制备的 rGO(therm)和通过化学氮掺杂 rGO 的后热退火制备的 post-therm-rGO(N(2)H(4)))在 573 至 1373 K 之间热石墨化过程中的光谱和微观变化。rGO(N(2)H(4))在热退火过程中的光谱跃迁最终在 1373 K 时显示出新的氧官能团,如环状边缘醚和新的石墨化氮原子。在石墨化过程中,通过扫描隧道显微镜 (STM) 解析的微观演化产生了更褶皱的表面形貌,由于后热-rGO(N(2)H(4))片上氮原子的原子掺杂,出现了石墨化纳米晶畴。因此,后热-rGO(N(2)H(4))-含氮表现出较少缺陷的 sp(2)-碳网络,导致电导率增强,而不含氮的 rGO(therm)片在 sp(2)-碳网络的基面有大的拓扑缺陷。因此,我们对原始 GO 片上的结构演化的研究,将其纳入石墨化氮掺杂 rGO 中,有助于解释原子掺杂如何增强电导率。

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