Precisely Tuning Band Gaps of Hexabenzocoronene‐Based MOFs Toward Enhanced Photocatalysis
Hao Zhang, Cha Li, Feifan Lang, Mei Li, Haoyu Liu, Di‐Chang Zhong, Jun‐Sheng Qin, Zhengyi Di, Danhong Wang, Le Zeng, Jiandong Pang, Xian‐He Bu, Xian‐He Bu
Abstract
Abstract Precise adjusting the band gaps in metal–organic frameworks (MOFs) is crucial for improving their visible‐light absorption capacity during photocatalysis, presenting both a formidable challenge and a charming opportunity. This present study employed a symmetry‐reduction strategy to pre‐design six novel 4‐connected ligands with systematic substituents (−NO 2 , ‐H, ‐ t Bu, ‐OCH 3 , ‐OH and ‐NH 2 ) and synthesized the corresponding pillared‐layer Zr‐MOFs (NKM‐668) retaining the hexaphenylbenzene fragment. Subsequently, the NKM‐668 MOFs were transformed into large‐π‐conjugated hexabenzocoronene‐based MOFs (pNKM‐668) via the Scholl reaction. These twelve MOFs exhibited broad and tunable band gaps over 1.41 eV (ranging from 3.25 eV to 1.84 eV), and the photocatalytic CO 2 conversion rate raised by 33.2‐fold. This study not only enriches the type of hexaphenylbenzene‐based MOFs, but also paves the way for nanographene‐containing MOFs in the further application of photocatalysis.