介孔材料
光催化
金属有机骨架
配体(生物化学)
材料科学
纳米技术
催化作用
吸附
化学
有机化学
生物化学
受体
作者
Shaghayegh Naghdi,Alexey Cherevan,Ariane Giesriegl,Rémy Guillet‐Nicolas,Santu Biswas,Tushar Gupta,Jia Wang,Thomas Haunold,Bernhard C. Bayer,Günther Rupprechter,Maytal Caspary Toroker,Freddy Kleitz,Dominik Eder
标识
DOI:10.1038/s41467-021-27775-7
摘要
Metal-organic frameworks (MOFs) are commended as photocatalysts for H2 evolution and CO2 reduction as they combine light-harvesting and catalytic functions with excellent reactant adsorption capabilities. For dynamic processes in liquid phase, the accessibility of active sites becomes a critical parameter as reactant diffusion is limited by the inherently small micropores. Our strategy is to introduce additional mesopores by selectively removing one ligand in mixed-ligand MOFs via thermolysis. Here we report photoactive MOFs of the MIL-125-Ti family with two distinct mesopore architectures resembling either large cavities or branching fractures. The ligand removal is highly selective and follows a 2-step process tunable by temperature and time. The introduction of mesopores and the associated formation of new active sites have improved the HER rates of the MOFs by up to 500%. We envision that this strategy will allow the purposeful engineering of hierarchical MOFs and advance their applicability in environmental and energy technologies.
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