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氨基辅助的NH-UiO-66锚定在多孔g-CN上用于增强可见光驱动的CO还原

Amino-Assisted NH-UiO-66 Anchored on Porous g-CN for Enhanced Visible-Light-Driven CO Reduction.

作者信息

Wang Yanan, Guo Lina, Zeng Yiqing, Guo Haiwei, Wan Shipeng, Ou Man, Zhang Shule, Zhong Qin

机构信息

School of Chemical Engineering , Nanjing University of Science and Technology , Nanjing 210094 , P. R. China.

School of Civil Engineering and Architecture , Anhui University of Technology , Maanshan , Anhui 243000 , P. R. China.

出版信息

ACS Appl Mater Interfaces. 2019 Aug 28;11(34):30673-30681. doi: 10.1021/acsami.9b04302. Epub 2019 Aug 19.

Abstract

Constructing heterostructured photocatalysts is an efficient method to improve photocatalytic carbon dioxide (CO) reduction. Herein, holey g-CN (HGN) with rich amino groups (-NH) was hybridized with NH-UiO-66 (NUZ) via a facile in situ growth method. NUZ nanocrystals were anchored on HGN via NHx-Zr-O chemical bonding, leading to the uniform dispersion and avoiding the leaching of NUZ, thus showing excellent stability in photocatalysis. The chemically bonded interfacial charge transfer effect originated from the NHx-Zr-O formation efficiently accelerated the separation and migration of charge carriers, improving the photoactivity. Benefiting from the NHx-Zr-O formation, the optimized NUZ/HGN-35% heterojunctions exhibited outstanding activity in the photoreduction of CO to CO (31.6 μmol g h), which was about 2 and 3 times higher than that of pure NUZ and HGN under visible-light irradiation. This study is expected to provide useful insights for constructing composites with strong interaction for CO reduction, H production, and N reduction.

摘要

构建异质结构光催化剂是提高光催化二氧化碳(CO₂)还原效率的有效方法。在此,通过简便的原位生长方法,将富含氨基(-NH₂)的多孔g-C₃N₄(HGN)与NH₂-UiO-66(NUZ)进行杂交。NUZ纳米晶体通过NHₓ-Zr-O化学键锚定在HGN上,实现了均匀分散并避免了NUZ的浸出,从而在光催化中表现出优异的稳定性。源于NHₓ-Zr-O形成的化学键合界面电荷转移效应有效地加速了电荷载流子的分离和迁移,提高了光活性。受益于NHₓ-Zr-O的形成,优化后的NUZ/HGN-35%异质结在将CO₂光还原为CO方面表现出出色的活性(31.6 μmol g⁻¹ h⁻¹),在可见光照射下,这分别比纯NUZ和HGN高出约2倍和3倍。该研究有望为构建具有强相互作用的复合材料用于CO₂还原、H₂生成和N₂还原提供有益的见解。

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