Molecular engineering of polymeric carbon nitride for highly efficient photocatalytic oxytetracycline degradation and H2O2 production

Molecular engineering of polymeric carbon nitride for highly efficient photocatalytic oxytetracycline degradation and H2O2 production
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聚合氮化碳的分子工程用于高效光催化土霉素降解和 H2O2 生产

DOI:
10.1016/j.apcatb.2020.118970
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发表时间:
2020-09
影响因子:
22.1
通讯作者:
Zhou Yin
Zhou Yin
中科院分区:
化学1区
文献类型:
--
作者:
Yang Yang;Zeng Guangming;Huang Danlian(黄丹莲;通讯作者);Zhang Chen;He Donghui;Zhou Chengyun;Wang Wenjun;Xiong Weiping;Li Xiaopei;Li Bisheng;Dong Wanyue;Zhou Yin

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开发高效的光催化剂降解难降解污染物和生产过氧化氢(H2 O2)是解决环境污染和能源危机的理想策略。为了解决这些问题,我们采用简单的酮-烯醇原位环化法合成了一种新型的2-羟基-4,6-二甲基嘧啶接枝的高分子氮化碳光催化剂(ACN)。光生电子和空穴分别迁移到H2 O2和Heptazine基团。CN和ACN-10光生电荷的平均衰变寿命从(222 +/- 23)ps增加到(289 +/- 38)ps。由于电子迁移的可控性和分子内电荷分离的加速性,ACN光催化剂在可见光驱动下对土霉素的降解和H2 O2的产生具有良好的上级光催化活性.本研究为研究氰化物分子内电荷动力学提供了新的思路,为土霉素的降解和H2 O2的产生提供了新的途径。
Developing highly efficient photocatalysts for refractory pollutants degradation and hydrogen peroxide (H2O2) production is an ideal strategy to tackle environmental pollution and energy crisis. Herein, we synthesize a novel 2-hydroxy-4,6-dimethylpyrimidine (HDMP) grafted polymeric carbon nitride (CN) photocatalyst (ACN) by a facile in situ keto-enol cyclization method for addressing these issues. The photogenerated electrons and holes are migrated to HDMP and heptazine moiety, respectively. And the average decay lifetime of photogenerated charges of CN and ACN-10 is increased form (222 +/- 23) to (289 +/- 38) ps. Benefiting from the controllable electronic migration and accelerated intramolecular charge separation, the ACN photocatalyst exhibits a superior visible-light-driven photocatalytic activity for oxytetracycline degradation and H2O2 production. This work makes an insight into the intramolecular charge dynamics in CN, and presents a promising approach to the oxytetracycline degradation and H2O2 production.
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