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       Material synthesis. In a typical procedure for synthesis of OH-GQDs, pyrene (2 g, TCI, purity 498%) was nitrated into trinitropyrene in hot HNO3 (160ml) at 80 C under refluxing and stirring for 12 h. After cooled to room temperature, the mixture was diluted with deionized (DI) water (1 l) and filtered through a 0.22 mm microporous membrane to remove the acid. The resultant yellow 1,3,6-trinitropyrene (3.0 g, yield of 90%) was dispersed in an NaOH solution of DI water (0.6 l, 0.2M) by ultrasonication (500W, 40 kHz) for 2 h. The suspension was transferred to a poly(tetrafluoroethylene) (Teflon)-lined autoclave (1 l) and heated at 200 C for 10 h. After cooled to room temperature, the product containing water-soluble GQDs was filtered through a 0.22 mm microporous membrane to remove insoluble carbon product, and further dialysed in a dialysis bag (retained molecular weight: 3,500Da) for 2 days to remove sodium salt and unfused small molecules. The purified black OH-GQDs were dried at 80 C for structural characterization and property measurement.
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