异质结
带材弯曲
材料科学
X射线光电子能谱
光电子学
波段图
半导体
带隙
光催化
氮化物
带偏移量
氮化碳
宽禁带半导体
纳米技术
价带
化学工程
化学
催化作用
图层(电子)
工程类
生物化学
作者
Giulia E. M. Schukraft,Benjamin Moss,Andreas Kafizas,Camille Petit
标识
DOI:10.1021/acsami.2c00335
摘要
Semiconductor/metal-organic framework (MOF) heterojunctions have demonstrated promising performance for the photoconversion of CO2 into value-added chemicals. To further improve performance, we must understand better the factors which govern charge transfer across the heterojunction interface. However, the effects of interfacial electric fields, which can drive or hinder electron flow, are not commonly investigated in MOF-based heterojunctions. In this study, we highlight the importance of interfacial band bending using two carbon nitride/MOF heterojunctions with either Co-ZIF-L or Ti-MIL-125-NH2. Direct measurement of the electronic structures using X-ray photoelectron spectroscopy (XPS), work function, valence band, and band gap measurements led to the construction of a simple band model at the heterojunction interface. This model, based on the heterojunction components and band bending, enabled us to rationalize the photocatalytic enhancements and losses observed in MOF-based heterojunctions. Using the insight gained from a promising band bending diagram, we developed a Type II carbon nitride/MOF heterojunction with a 2-fold enhanced CO2 photoreduction activity compared to the physical mixture.
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