期刊
ADVANCED FUNCTIONAL MATERIALS
卷 31, 期 52, 页码 -出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202106120
关键词
covalent organic frameworks; hydrogen peroxide production; mass transfer; photocatalysis; triphase interfaces
类别
资金
- Guangdong Basic and Applied Basic Research Foundation [2019B1515120058]
- National Natural Science Foundation of China [51902357]
- Natural Science Foundation of Guangdong Province, China [2019A1515012143]
- Start-up Funds for High-Level Talents of Sun Yat-sen University [38000-18841209]
- Fundamental Research Funds for the Central Universities [19lgpy153]
- Research Grants Council of Hong Kong Special Administrative Region [14308018]
- Hong Kong Ph.D. Fellowship Scheme [PF17-10186]
This study introduces a COF-based photocatalyst that can efficiently reduce O-2 to H2O2 in pure water under visible-light irradiation, overcoming the mass-transfer limitation of oxygen in water. By loading this catalyst onto a porous substrate to create a triphase interface, the production rate of H2O2 is significantly increased.
Solar-driven photocatalytic oxygen reduction is a potentially sustainable route for the production of hydrogen peroxide (H2O2). However, this approach suffers from the limited solubility and slow diffusion of oxygen in water. Another problem is that most photocatalytic oxygen reduction systems do not work well with just water. They often require the addition of sacrificial agents such as alcohols. Here, a covalent organic framework (COF)-based photocatalyst that can reduce O-2 to H2O2 efficiently in pure water under visible-light irradiation is reported. A solar-to-chemical conversion of 0.76% is achieved for H2O2 generation. More importantly, the hydrophobic and mesoporous properties of triphenylbenzene-dimethoxyterephthaldehyde-COF allow the formation of a triphase interface (gas-liquid-solid) when loading this catalyst onto a porous substrate. The H2O2 production rate reaches approximate to 2.9 mmol g(cat)(-1) h(-1) at the triphase interface by overcoming the mass-transfer limitation of O-2 in water. Notably, this rate is 15 times higher than that in a diphase system (liquid-solid). The photoelectrochemical tests reveal that the increase in yield is closely related to the enhanced mass-transfer rate and the higher interfacial O-2 concentration. Furthermore, the triphenylbenzene part is identified as the reactive site based on theoretical calculations.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据