摘要
A heterocycle 2,5-bis(2-pyridyl)-1,3,4-thiadiazole (bptd) as a polydentate reacts with CoCl 2 ∙6H 2 O and NiCl 2 · 6H 2 O to form two novel monomeric complexes, [Co(bptd) 2 Cl 2 ]∙4H 2 O ( 1 ) and [Ni(bptd) 2 Cl 2 ]∙4H 2 O ( 2 ). The complex 1 can act as electron cocatalyst to improve the rate of hydrogen evolution of CdS NRs under visible light irradiation . After the introduction of cobalt lactate complex as a hole cocatalyst, this noble-metal-free system exhibited a hydrogen evolution rate of 1123 μmol h −1 , which is 12.2 times higher than that of pure CdS NRs. This system could work for 50 h with a TON of 7490, and the average AQY is 17% at 420 nm. Based on the results of experiments, the synergistic effect of complex 1 and cobalt lactate complex is proved and a possible mechanism for hydrogen production is proposed. This work may provide a reference for remedying the defects of faster carrier recombination and photocorrosion of CdS in heterogeneous environment.
危险品化学品经营许可证(带存储)