热致晶体
芯(光纤)
石墨烯
材料科学
液晶
纳米技术
结晶学
化学
光电子学
液晶
复合材料
作者
Jun Hu,Zhen Yu,Yong Yang,Jiaxiang Huang,Zhiyang Liu,Shuai Huang,Meng Wang,Hong Yang
标识
DOI:10.1002/ange.202501161
摘要
Graphene nanoribbons (GNRs) with hierarchical and well‐ordered structures are believed to deliver superior performance in semiconductor device applications. Despite this potential, traditional alignment techniques for GNRs often fall short in producing defect‐free and precisely defined molecular architectures. Here, we introduce a strategy for the fabrication of highly‐ordered GNRs by empowering them with thermotropic liquid crystallinity, utilizing a bottom‐up solution synthesis approach. The resulting GNR liquid crystal (GNR‐LC) molecule can self‐assemble into a hexagonal columnar phase. The homeotropic alignment of GNR‐LC is enabled by the intrinsic self‐assembly capabilities of the thermotropic liquid crystalline state, thereby forming one‐dimensional charge transport pathways. Devices incorporating GNR‐LC have demonstrated significantly enhanced hole mobility, reaching up to 2.4 cm2 V‐1 s‐1, underscoring their viability as organic semiconductors for optoelectronic applications.
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