In Situ Generation of Pseudorutile Oxide as the Cathode for Direct Electrolysis of CO2

The conversion of CO2 into CO in high-temperature solid oxide electrolysis cells (SOECs) is an attractive route for the CO2 utilization using the intermittent renewables. The low-cost and highly catalytic cathode is important for the direct electrolysis of pure CO2. In this study, non-perovskite Fe0.5Mg0.25+0.5xTi0.25-0.5xNb1-xMoxO4 oxides (denoted as Mo-x when x is equal to 0, 0.1, and 0.2) are evaluated as the cathode of an SOEC for the direct electrolysis of CO2. Mo6+ doping converted the wolframite Mo-0 into an a-PbO2-type with cation disordering, while further doping to Mo-0.2 showed a wolframite with cation ordering again. The SOEC with Mo-0.2 as the cathode exhibits the best electrochemical performance for the direct electrolysis of CO2 as a large portion of the oxide converted into oxygen-deficient pseudorutile-type oxide with a nominal formula of M5O9 (M = cation). The pseudorutile, a crystallographic shear phase of rutile, can be obtained after 60 h of direct electrolysis in CO2 at a 1.3 V bias rather than a reduction under 5% H-2. The SOEC with Mo-0.2 as the cathode imparted a stable current density of 0.45 A cm(-2), which could be related to the production of pseudorutile decorated with nanoparticles of MoO2. These results show that molybdenum doping is an effective strategy for developing oxygen-deficient rutile (pseudorutile) for the electrolysis of CO2.

Automated summary

This study evaluates non-perovskite oxides as cathodes for CO2 electrolysis and finds that molybdenum doping can enhance the electrochemical performance by forming oxygen-deficient rutile phase.