共轭体系
齿合度
金属
钥匙(锁)
材料科学
化学
纳米技术
业务
有机化学
计算机科学
聚合物
计算机安全
作者
Long Chen,Pei Chen,Mingxuan Liu,Rui Li,Xi Su,Guolong Xing,Xiao‐Rui Ren,Dong Wang,Jian Zhang
标识
DOI:10.26434/chemrxiv-2025-xcl2h
摘要
Two-dimensional conjugated metal-organic frameworks (2D c-MOFs) represent an emerging class of crystalline porous materials with promising electrochemical applications. The design of novel organic ligands for constructing 2D c-MOFs remains a crucial research frontier. While the incorporation of macrocycle blocks into 2D c-MOFs can introduce intrinsic cavities with advantageous properties, most existing reports are limited to coordinating with only one equivalent metal ion per macrocyclic cavity. In this work, we developed triangular-shaped Salphen macrocycle-based 2D c-MOFs (SM-MOF-Cu) featuring multidentate internal coordination sites. SM-MOF-Cu exhibits high crystallinity, permanent porosity, and abundant accessible metal sites. Remarkably, this material demonstrates exceptional performance in the electrocatalytic hydrogenation of acetylene to ethylene (E-HAE), achieving a Faradic efficiency of 96.6% for ethylene production at –0.85 V versus the reversible hydrogen electrode under continuous pure acetylene feed. This study not only broaden the family of macrocycle-based 2D c-MOFs but also provides new insights into their potential for advanced electrocatalysis.
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