Electrochemical CO2 reduction reaction provides
a mild
avenue for resource utilization of CO2. Metal–organic
framework (MOF) materials are considered among the promising catalysts
due to unique structural advantages. However, the catalytic performance
of MOFs is hindered by poor conductivity, making it crucial to enhance
the charge transfer for improved efficiency. Herein, a hybrid catalyst
was constructed based on the In-based porphyrin framework (In-TCPP)
and conducting MXene nanosheets for efficient CO2 conversion.
As expected, MXene as a unique conductive support significantly improves
the catalytic performance of the hybrid material, achieving a Faraday
efficiency for HCOO– of 94.0% with a 2.2-fold increase
in the practical current density. Furthermore, a pure formic acid
solution with a concentration of ca. 0.22 M was prepared via execution
in a solid-state electrolyte-mediated MEA (MEA-SSE) device. Theoretical
calculations and in situ ATR-FTIR spectra reveal that the introduction
of MXene not only endows the hybrid material with metallic properties
to facilitate charge transfer but also modulates the electronic structure
to optimize the adsorption of the key intermediate *OCHO. This work
enlightens the rational design of MOF-based electrocatalysts via the
regulation of MXene and demonstrates the promise of the MEA-SSE device
for practical CO2 reduction applications.