光催化
材料科学
石墨氮化碳
制氢
化学工程
氮化碳
比表面积
氮化物
带隙
分解水
无机化学
氢
催化作用
纳米技术
化学
光电子学
有机化学
图层(电子)
工程类
作者
Yanting Gao,Feng Hou,Shan Hu,Baogang Wu,Baojiang Jiang
标识
DOI:10.1016/j.apsusc.2019.03.194
摘要
Reaction active surface area and energy band structure determine the visible-light photocatalytic property of semiconductor catalyst such as graphitic carbon nitride (CN). Herein, synchronization iodine surface modified and doped porous carbon nitride (CNI) was prepared. The self-assembly precursors from urea and ammonium iodide were firstly obtained by liquid nitrogen-assisted rapid re-crystallization and lyophilization technology. After the heat treatment of above precursors, CNI was easily synthesized. Compared with bulk CN, CNI shows large specific surface area (57.59 m2 g−1), due to freeze-drying treatment and thermal decomposition of ammonium iodide. As electron donors, iodine species can enrich the electron density in the carbon nitride network and tune the electronic band structure. It is important the surface iodine modification can bound the positive charge holes to inhibit the recombination of photogenerated carriers. As a result, CNI exhibits prompted photocatalytic hydrogen evolution rate of 114.0 μmol h−1 under visible-light irradiation (λ > 420 nm), better than that of bulk CN. This work may provide a promising rapid method for designing another porous and effective semiconductor photocatalysts.
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