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A simple hollow-structured “artificial catalyst” in situ formed from CdTe QDs and CoCl2·6H2O in aqueous ascorbic acid solution has shown exceptional activity and stability for photocatalytic H2 evolution (25 μmol h−1 mg−1, 219 100 mol H2 per mol QDs or 59 600 mol H2 per mol Co turnovers, respectively) under visible light irradiation for 70 h.
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Li et al. (2012) studied this question.
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