光催化
三聚氰胺
氮化碳
材料科学
三聚氰酸
氮化物
单斜晶系
碳纤维
催化作用
纳米技术
无机化学
晶体结构
化学工程
化学
结晶学
有机化学
复合材料
图层(电子)
复合数
工程类
作者
Shien Guo,Zhao‐Peng Deng,Mingxia Li,Baojiang Jiang,Chungui Tian,Qing‐Jiang Pan,Honggang Fu
标识
DOI:10.1002/ange.201508505
摘要
Abstract Phosphorus‐doped hexagonal tubular carbon nitride (P‐TCN) with the layered stacking structure was obtained from a hexagonal rod‐like single crystal supramolecular precursor (monoclinic, C 2/ m ). The production process of P‐TCN involves two steps: 1) the precursor was prepared by self‐assembly of melamine with cyanuric acid from in situ hydrolysis of melamine under phosphorous acid‐assisted hydrothermal conditions; 2) the pyrolysis was initiated at the center of precursor under heating, thus giving the hexagonal P‐TCN. The tubular structure favors the enhancement of light scattering and active sites. Meanwhile, the introduction of phosphorus leads to a narrow band gap and increased electric conductivity. Thus, the P‐TCN exhibited a high hydrogen evolution rate of 67 μmol h −1 (0.1 g catalyst, λ >420 nm) in the presence of sacrificial agents, and an apparent quantum efficiency of 5.68 % at 420 nm, which is better than most of bulk g‐C 3 N 4 reported.
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