Yang Xusheng, Liu Tianhui, Li Ruoming, Yang Xiaoxin, Lyu Min, Fang Li, Zhang Lei, Wang Kun, Zhu Anquan, Zhang Luyao, Qiu Chenguang, Zhang Yuan-Zhu, Wang Xiao, Peng Lian-Mao, Yang Feng, Li Yan
Department of Chemistry, Southern University of Science and Technology, Shenzhen 518055, China.
Beijing National Laboratory for Molecular Science, Key Laboratory for the Physics and Chemistry of Nanodevices, State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China.
J Am Chem Soc. 2021 Jul 14;143(27):10120-10130. doi: 10.1021/jacs.1c02245. Epub 2021 Jun 9.
Semiconducting single-walled carbon nanotubes (s-SWCNTs) with a diameter of around 1.0-1.5 nm, which present bandgaps comparable to silicon, are highly desired for electronic applications. Therefore, the preparation of s-SWCNTs of such diameters has been attracting great attention. The inner surface of SWCNTs has a suitable curvature and large contacting area, which is attractive in host-guest chemistry triggered by electron transfer. Here we reported a strategy of host-guest molecular interaction between SWCNTs and inner clusters with designed size, thus selectively separating s-SWCNTs of expected diameters. When polyoxometalate clusters of ∼1 nm in size were filled in the inner cavities of SWCNTs, s-SWCNTs with diameters concentrated at ∼1.3-1.4 nm were selectively extracted with the purity of ∼98% by a commercially available polyfluorene derivative. The field-effect transistors built from the sorted s-SWCNTs showed a typical behavior of semiconductors. The sorting mechanisms associated with size-dependent electron transfer from nanotubes to inner polyoxometalate were revealed by the spectroscopic and electron microscopic evidence as well as the theoretical calculation. The polyoxometalates with designable size and redox property enable the flexible regulation of interaction between the nanotubes and the clusters, thus tuning the diameter of sorted s-SWCNTs. The present sorting strategy is simple and should be generally feasible in other SWCNT sorting techniques, bringing both great easiness in dispersant design and improved selectivity.
直径约为1.0 - 1.5纳米的半导体单壁碳纳米管(s-SWCNTs)具有与硅相当的带隙,在电子应用中极具吸引力。因此,制备这种直径的s-SWCNTs一直备受关注。单壁碳纳米管的内表面具有合适的曲率和较大的接触面积,在由电子转移引发的主客体化学中很有吸引力。在此,我们报道了一种单壁碳纳米管与具有特定尺寸的内部簇之间的主客体分子相互作用策略,从而选择性地分离出预期直径的s-SWCNTs。当尺寸约为1纳米的多金属氧酸盐簇填充到单壁碳纳米管的内腔中时,通过一种市售的聚芴衍生物可选择性地提取出直径集中在约1.3 - 1.4纳米的s-SWCNTs,纯度约为98%。由分选后的s-SWCNTs构建的场效应晶体管表现出典型的半导体行为。通过光谱和电子显微镜证据以及理论计算揭示了与从纳米管到内部多金属氧酸盐的尺寸依赖性电子转移相关的分选机制。具有可设计尺寸和氧化还原性质的多金属氧酸盐能够灵活调节纳米管与簇之间的相互作用,从而调整分选后的s-SWCNTs的直径。目前的分选策略简单,在其他单壁碳纳米管分选技术中应该普遍可行,在分散剂设计方面既带来了极大的便利性,又提高了选择性。