Cobalt coordinated olefin-linked covalent organic frameworks toward highly efficient photocatalytic hydrogen production

被引:0
|
作者
Cui, Xiaoxia [1 ]
Ji, Xufeng [1 ]
Zhang, Xuan [1 ]
Ding, Xing [1 ]
Chai, Bo [2 ]
Ding, Deng [2 ]
Yang, Yi [1 ]
Zhang, Xiaohu [1 ]
Chen, Hao [1 ]
机构
[1] Huazhong Agr Univ, Coll Chem, Wuhan 430070, Peoples R China
[2] Wuhan Polytech Univ, Sch Chem & Environm Engn, Wuhan 430023, Peoples R China
基金
中国国家自然科学基金;
关键词
Covalent organic frameworks; Photocatalytic H 2 production; Co coordination; Visible light; Highly efficient; WATER;
D O I
10.1016/j.apsusc.2024.161988
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Covalent organic frameworks (COFs) have emerged as a crystalline porous materials for photocatalytic hydrogen production. However, the design of efficient COF-based catalyst for satisfactory solar-to-hydrogen energy conversion is still challenging. Here, cobalt was anchored on the bipyridine moieties in the framework of olefin- linked sp2c-COFdpy by convenient post-metalation (sp2c-COFdpy-Co). Experimental results showed that sp2c- COFdpy-Co exhibited wider visible light absorption region and quicker photogenerated e- /h + separation efficiency than sp2c-COFdpy. Photocatalytic experiments revealed that sp2c-COFdpy-Co was highly efficient for H2 production after photodeposition of Pt co-catalyst (Pt@sp2c-COFdpy-Co). The optimized Pt@sp2c-COFdpy-Co exhibited a high photocatalytic H2 production rate of 324.4 mu mol/h under visible light irradiation in the presence of 1.0 wt% Pt as co-catalyst, which was higher than Pt@sp2c-COFdpy-Fe and Pt@sp2c-COFdpy-Ni, and it was much higher than that of its counterparts and many reported works. This work provides new insights into design of highly efficient COF-based catalyst for photocatalytic H2 production.
引用
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页数:10
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