Metal–organic framework (MOF) is a powerful material for electrocatalytic applications due to its structural diversity and tunability. Herein, the MOF with an extended organic linker, NiFe(dobpdc), is synthesized and investigated for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). NiFe(dobpdc) features a yarn-ball like structure assembly from 2D nanosheets subunits and high electrocatalytic activity properties. Theoretical calculations suggest the dobpdc⁴⁻ can extract/release charges in the electrocatalytic reaction of (* → OH*) and (OH* → O*), respectively. This bifunctional NiFe(dobpdc) electrocatalyst significantly elevates electrocatalytic performance with a lowest overpotential of 207 mV@10 mA cm⁻² for OER and 113 mV@10 mA cm⁻² for HER, meanwhile, the ultralow overpotentials needed to achieve the high current density of 100 mA cm⁻² for OER (251 mV) and HER (170 mV). This study provides a promising strategy to design MOF electrocatalysts for electrocatalytic applications.

A facile strategy for the synthesis of acidic ionic liquid based UiO-67 type MOFs was developed in this study. Brønsted acids (H₂SO₄, CF₃SO₃H and hifpOSO₃H (hexafluoroisopropyl sulfuric acid)) were introduced into UiO-67–bpy (bpy = 2,2′-bipyridine-5,5′-dicarboxylic acid) frameworks by reacting with bipyridyl nitrogen to introduce the properties of an acidic ionic liquid into the frameworks. The prepared catalysts, denoted as UiO-67–HSO₄, UiO-67–CF₃SO₃ and UiO-67–hifpOSO₃, were characterized by XRD, SEM, FT-IR, EA, TGA and N₂ adsorption–desorption studies. The relatively high surface area was still maintained and acidic active groups were uniformly dispersed in the frameworks. The catalytic performance of UiO-67–HSO₄, UiO-67–CF₃SO₃ and UiO-67–hifpOSO₃ was evaluated by the esterification of acetic acid with isooctyl alcohol. The prepared catalysts showed good catalytic activities in the esterification, of which UiO-67–CF₃SO₃ gave the maximum isooctyl alcohol conversion of 98.6% under optimized conditions. The catalyst could be reused five times without a significant decrease in the conversion of isooctyl alcohol, and almost no active species were leached, indicating the excellent stability and reusability of the catalyst. Our study provides one effective way to synthesize heterogeneous acidic ionic liquid catalysts consisting of isolated, well defined acidic groups that will probably attract interest in acid catalyst chemistry.