光催化
三聚氰胺
石墨氮化碳
氮化碳
降级(电信)
材料科学
氨
氮化物
双酚A
化学工程
比表面积
光化学
化学
催化作用
纳米技术
有机化学
复合材料
环氧树脂
工程类
电信
图层(电子)
计算机科学
作者
Fanpeng Meng,Wenjie Tian,Zhihao Tian,Xiaoyao Tan,Huayang Zhang,Shaobin Wang
标识
DOI:10.1016/j.scitotenv.2022.158360
摘要
Post thermal treatment of bulk graphitic carbon nitride (g-C3N4) by ammonia gas acts as a significant structure regulation approach, while pure ammonia-assisted g-C3N4 synthesis from precursors like melamine is rarely investigated. Here we prove the synthesis of N-defects abundant carbon nitride nanosheets (ACN) through a one-pot thermal polymerization of melamine in pure ammonia gas, for photocatalytic organic pollutant removal in water and H2 evolution applications. Compared to bulk g-C3N4 (BCN), ACN-550 (ACN prepared at 550 °C) exhibited thin-layered porous morphology with higher surface area and abundant N defects, resulting in wider distribution of active sites. Moreover, the abundant N defects in the heptazine heterocycle structure could change the electronic structure of g-C3N4, leading to more efficient transport of photogenerated charge carriers and enhanced photoreduction potential, which gives rise to notable improvement activities in photocatalytic reaction. With superoxide ion radical and photoinduced holes as the predominant reactive species, ACN-550 realized efficient photocatalytic bisphenol A (BPA) degradation, which is 1.6- and 4.7-fold high over commercial TiO2 (P25) and BCN, respectively. ACN-550 exhibited excellent reusability and stability in five consecutive photocatalytic BPA degradation tests. In photo-reductive H2 production system by ACN-550, 761.8 ± 4.3 μmol/h/g H2 was produced, which was 11.6-fold as high as that by BCN.
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