期刊
JOURNAL OF MATERIALS SCIENCE
卷 56, 期 21, 页码 12285-12314出版社
SPRINGER
DOI: 10.1007/s10853-021-06001-1
关键词
-
资金
- Kondo Memorial Foundation in Japan
Graphene nanoribbons (GNR) with adjustable band gap have attracted attention for their properties. The introduction of sp(3)C-H on GNR edges can alter the peak positions of sp(2)C-H on the aromatic edges.
Graphene nanoribbon (GNR) has attracted attention because of the adjustable band gap, depending on the width and functional groups. The introduction of sp(3)C-H on edges is one of the choices to reduce the agglomeration between GNRs and to change their various properties. Infrared spectroscopy is among the powerful tools to analyze the edge structures of carbon materials, but the number of detailed reports is almost nonexistent for sp(3)C-H in carbon materials. In this work, the influence of the presence of sp(3)C-H on the peak position of sp(2)C-H on zigzag and armchair edges of GNR was revealed by comparing experimental and computational infrared spectra of aromatic compounds. The introduction of methylene and methyl groups next to sp(2)C-H affected peak positions of in-plane stretching and out-of-plane bending vibration of sp(2)C-H. The peak position of sp(2)C-H was further shifted by introducing methylene and methyl groups on both sides of sp(2)C-H. The presence of either methylene or methyl groups can be clearly distinguished from the difference in coupled vibration of out-of-plane vibration of sp(2)C-H and quadrant stretching vibration of C=C because the presence of methylene groups affects the conjugated system significantly, whereas methyl groups did not affect the conjugated system.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据