Demonstrates improved nitrogen incorporation in perovskites using guanidinium carbonate, suggesting novel synthesis methods.
An ammonia-free solid-state nitridation strategy employing guanidinium carbonate (GdmC) as a carbon–nitrogen precursor is demonstrated using BaTaO 2 N as a model oxynitride perovskite. While BaTaO 2 N is a well-established compound, the present study focuses on the reaction chemistry enabled by GdmC under flowing N 2 . Systematic comparison with other nitrogen-containing reagents reveals that GdmC provides a unique balance between nitridation capability and reducing character, enabling phase-pure BaTaO 2 N formation within a short dwell time of 0.5 h. Thermal and structural analyses suggest the transient formation of carbon–nitrogen intermediates, including BaNCN species, which facilitate nitrogen incorporation into the perovskite lattice under ammonia-free conditions. Furthermore, partial La-substitution suppresses anion nonstoichiometry–related defects, leading to optical absorption characteristics comparable to those of ammonolyzed samples. These results highlight carbon–nitrogen solid-state chemistry as an effective approach for controlled nitrogen incorporation in complex oxynitride compounds.
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Choi et al. (2026) studied this question.
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