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Ti8Zr2O12(COO)16 Cluster: An Ideal Inorganic Building Unit for Photoactive Metal–Organic Frameworks

机译:Ti8ZR2O12(COO)16集群:光活性金属 - 有机框架的理想无机建筑单元

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摘要

Metal–organic frameworks (MOFs) based on Ti-oxo clusters (Ti-MOFs) represent a naturally self-assembled superlattice of TiO2 nanoparticles separated by designable organic linkers as antenna chromophores, epitomizing a promising platform for solar energy conversion. However, despite the vast, diverse, and well-developed Ti-cluster chemistry, only a scarce number of Ti-MOFs have been documented. The synthetic conditions of most Ti-based clusters are incompatible with those required for MOF crystallization, which has severely limited the development of Ti-MOFs. This challenge has been met herein by the discovery of the [Ti8Zr2O12­(COO)16] cluster as a nearly ideal building unit for photoactive MOFs. A family of isoreticular photoactive MOFs were assembled, and their orbital alignments were fine-tuned by rational functionalization of organic linkers under computational guidance. These MOFs demonstrate high porosity, excellent chemical stability, tunable photoresponse, and good activity toward photocatalytic hydrogen evolution reactions. The discovery of the [Ti8Zr2O12­(COO)16] cluster and the facile construction of photoactive MOFs from this cluster shall pave the way for the development of future Ti-MOF-based photocatalysts.
机译:基于Ti-Oxo簇(Ti-Mofs)的金属 - 有机框架(MOF)代表了由可名称的有机接头作为天线发色团分离的天然自组装的TiO2纳米粒子超晶格,展示了太阳能转换的有望平台。然而,尽管有了广阔,多样化,并且发达良好的Ti簇化学,但只记录了稀缺数量的Ti-Mof。大多数基于Ti的簇的合成条件与MOF结晶所需的合成条件不相容,这严重限制了Ti-MOF的发育。本文通过发现[TI8ZR2O12(COO)16]簇作为光活性MOF的近乎理想的构建单元,已经达到了这一挑战。组装了一系列非机构光活性MOF,并通过在计算引导下通过有机接头的合理官能化进行微调。这些MOFS表现出高孔隙率,优异的化学稳定性,可调光响应和良好的光催化氢气进化反应。 [Ti8ZR2O12(COO)16]集群的发现和来自该群集的光活性MOF的嵌入式应为未来TI-MOF基光催化剂的开发铺平道路。

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