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Ni–Fe–La(Sr)Fe(Mn)O 3 as a New Active Cermet Cathode for Intermediate‐Temperature CO 2 Electrolysis Using a LaGaO 3 ‐Based Electrolyte
Author(s) -
Wang Shijing,
Tsuruta Hidekazu,
Asanuma Minoru,
Ishihara Tatsumi
Publication year - 2015
Publication title -
advanced energy materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.08
H-Index - 220
eISSN - 1614-6840
pISSN - 1614-6832
DOI - 10.1002/aenm.201401003
Subject(s) - electrolysis , materials science , cermet , electrolyte , oxide , cathode , inorganic chemistry , analytical chemistry (journal) , metallurgy , electrode , chemistry , chromatography , ceramic
Various additives to Ni–Fe systems are studied as cermet cathodes for CO 2 electrolysis (973–1173 K) using a La 0.9 Sr 0.1 Ga 0.8 Mg 0.2 O 3 (LSGM) electrolyte, which is one of the most promising oxide‐ion conductors for intermediate‐temperature solid‐oxide electrolysis cells in terms of ionic‐transport number and conductivity. It is found that Ni–Fe–La 0.6 Sr 0.4 Fe 0.8 Mn 0.2 O 3 (Ni–Fe–LSFM) exhibits a remarkable performance with a current density of 2.32 A cm −2 at 1.6 V and 1073 K. The cathodic overpotential is significantly decreased by mixing the LSFM powder with Ni–Fe, which is related to the increase in the number of reaction sites for CO 2 reduction. For Ni–Fe–LSFM, much smaller particles (<200 nm) are sustained under CO 2 electrolysis conditions at high temperatures than for Ni–Fe. X‐ray diffraction analysis suggests that the main phases of Ni–Fe–LSFM are Ni and LaFeO 3 ; thus, the oxide phase of LaFeO 3 is also maintained during CO 2 electrolysis. Analysis of the gaseous products indicates that only CO is formed, and the rate of CO formation agrees well with that of a four‐electron reduction process, suggesting that the reduction of CO 2 to CO proceeds selectively. It is also confirmed that almost no coke is deposited on the Ni–Fe–LSFM cathode after CO 2 electrolysis.