化学
表面改性
金属有机骨架
连接器
带隙
钛
价(化学)
金属
价带
组合化学
配体(生物化学)
纳米技术
光电子学
有机化学
物理化学
材料科学
吸附
受体
操作系统
生物化学
计算机科学
作者
Christopher H. Hendon,Davide Tiana,Marc Fontecave,Clément Sánchez,Loïc D'Arras,Capucine Sassoye,Laurence Rozes,Caroline Mellot‐Draznieks,Aron Walsh
摘要
Herein we discuss band gap modification of MIL-125, a TiO2/1,4-benzenedicarboxylate (bdc) metal–organic framework (MOF). Through a combination of synthesis and computation, we elucidated the electronic structure of MIL-125 with aminated linkers. The band gap decrease observed when the monoaminated bdc-NH2 linker was used arises from donation of the N 2p electrons to the aromatic linking unit, resulting in a red-shifted band above the valence-band edge of MIL-125. We further explored in silico MIL-125 with the diaminated linker bdc-(NH2)2 and other functional groups (−OH, −CH3, −Cl) as alternative substitutions to control the optical response. The bdc-(NH2)2 linking unit was predicted to lower the band gap of MIL-125 to 1.28 eV, and this was confirmed through the targeted synthesis of the bdc-(NH2)2-based MIL-125. This study illustrates the possibility of tuning the optical response of MOFs through rational functionalization of the linking unit, and the strength of combined synthetic/computational approaches for targeting functionalized hybrid materials.
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