Abstract
The hydrogen-bonded organic frameworks (HOFs) as a new type of porous framework materials have been widely studied in various areas. However, the lack of appropriate active sites, low intrinsic conductivity, and poor stability limited their performance in the field of electrocatalysis. Herein, we designed two 2D metal hydrogen-bonded organic frameworks (2D-M-HOF, M = Cu(2+) or Ni(2+)) with coordination compounds based on 2,3,6,7,14,15-hexahydroxyl cyclotricatechylene and transition metal ions (Cu(2+) and Ni(2+)), respectively. The crystal structure of 2D-Cu-HOF is determined by continuous rotation electron diffraction, indicating an undulated 2D hydrogen-bond network with interlayered π-π stacking. The flexible structure of 2D-M-HOF leads to the formation of self-adaption interlayered sites, resulting in superior activity and selectivity in the electrocatalytic conversion of CO(2) to C(2) products, achieving a total Faradaic efficiency exceeding 80% due to the high-efficiency C-C coupling. The experimental results and density functional calculations verify that the undulated 2D-M-HOF enables the energetically favorable formation of *OCCHO intermediate. This work provides a promising strategy for designing HOF catalysts in electrocatalysis and related processes.