光催化
水溶液
二苯并噻吩
共轭体系
接受者
聚合物
噻吩
光化学
材料科学
剥脱关节
化学
高分子化学
催化作用
有机化学
纳米技术
凝聚态物理
物理
石墨烯
作者
Yuxiang Liu,Jun Wu,Feng Wang
标识
DOI:10.1016/j.apcatb.2022.121144
摘要
Molecular engineering in donor–acceptor conjugated polymers is currently one of the most successful and popular strategy to prepare high performance photocatalysts for hydrogen evolution. In this contribution, we have designed and synthesized two novel conjugated polymers with tailored donor–acceptor structures based on dibenzothiophene-S,S-dioxide and thiophene derivatives, which exhibited tunable band gaps and adjustable charge separation efficiencies. As a result, PDBTSO-T showed an outstanding hydrogen evolution rate (HER) of 1.47 mmol h−1 by DMF exfoliation under UV−vis region with Pt cocatalyst in ascorbic acid aqueous solution at 10 mg level, which is among the top performance for photocatalysis conversion reported so far. Very excitingly, when the photocatalysis tests were subjected to natural sunlight irradiation, an impressive HER of ~27 mL (107 mmol g−1 h−1) was achieved after 0.5 h of illumination (12:30 pm − 13:00 pm) on a consistently sunny day under identical reaction conditions.
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