Polyaromatic hydrocarbon inner-structured carbon nanodots for interfacial enhancement of carbon fiber composite

It is well known that carbon substances with a polyaromatic hydrocarbon (PAH) inner structure only form at high temperature. In this work, we introduce fabrication of massive and PAH inner-structured carbon nanodots (CNDs) via hydrothermal treatment of glucose aqueous solution in the monolithic methyl silicone hydrogel at 200 °C. During the carbonization process, all the precursor solution is confined in nano-vessels (2-20 nm) of the thermostable methyl silicone hydrogel, thus forming CNDs without aggregation. The resulting CNDs, with a yield of 65%, were separated facilely and characterized using various spectroscopy and microscopy techniques. The glucose-derived CNDs have diameters of 2-5 nm and contain 18.9 wt% carboxyl groups, and their aqueous solubility depends on the pH. The CNDs consist of large PAH clusters, confirmed by solid-state ¹³C NMR, which were different to other reported carbon substances prepared at similar low temperatures. The formation mechanism of the PAH structure in the CNDs probably relates to the high interfacial energy of the prewetted superhydrophobic methyl silicone nano-framework in the hydrogel. Moreover, the tunable fluorescence properties of the CNDs prepared using this method can be attributed to the arene carboxylic groups in the CNDs. Finally, the resultant PAH CNDs with abundant groups were applied as a sizing in carbon fiber (CF) composite fabrication, resulting in an obvious interface enhancement of the CF/epoxy composite.