化学
光激发
沸石咪唑盐骨架
光催化
激发态
咪唑酯
超快激光光谱学
光化学
金属有机骨架
化学物理
纳米技术
催化作用
光谱学
物理化学
无机化学
有机化学
原子物理学
吸附
材料科学
物理
量子力学
作者
Brian Pattengale,Sizhuo Yang,John Ludwig,Zhuangqun Huang,Xiaoyi Zhang,Jier Huang
摘要
Zeolitic imidazolate frameworks (ZIFs) have emerged as a novel class of porous metal–organic frameworks (MOFs) for catalysis application because of their exceptional thermal and chemical stability. Inspired by the broad absorption of ZIF-67 in UV–vis-near IR region, we explored its excited state and charge separation dynamics, properties essential for photocatalytic applications, using optical (OTA) and X-ray transient absorption (XTA) spectroscopy. OTA results show that an exceptionally long-lived excited state is formed after photoexcitation. This long-lived excited state was confirmed to be the charge-separated (CS) state with ligand-to-metal charge-transfer character using XTA. The surprisingly long-lived CS state, together with its intrinsic hybrid nature, all point to its potential application in heterogeneous photocatalysis and energy conversion.
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