Photoelectrochemical N<sub>2</sub>-to-NH<sub>3</sub> Fixation with Recorded Yield Rate by Steering Solid-Electrolyte Interphase.
basic_science · Level V
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- Record sourced from PubMed, PMID 41855080.
- Also identified by DOI 10.1002/adma.72853.
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Abstract
Achieving efficiently lithium (Li)-mediated photoelectrochemical (PEC) nitrogen (N<sub>2</sub>)-to-ammonia (NH<sub>3</sub>) fixation at low overpotential under mild conditions remains a highly challenging task due to the complex and sluggish interfacial chemical processes. Here, we report a novel multifunctional electrolyte with ethyl 3,3,3-trifluoropropionate and sodium cation (Na<sup>+</sup>) to form a porous solid-electrolyte interphase (SEI) with optimizing organic/inorganic composition on the photocathode surface, leading to a rapid and stable conversion cycle of Li<sup>+</sup> → Li → lithium nitride (Li<sub>3</sub>N). As a result, the Li-mediated PEC N<sub>2</sub> reduction reaction system realizes a high NH<sub>3</sub> yield rate of ∼93 µg h<sup>-1</sup> cm<sup>-2</sup> with a high faradaic efficiency (FE) of ∼67% at 0.55 V vs. Li redox couple (vs. Li/Li<sup>+</sup>) under 1 sun illumination. When the light intensity is increased to 2 sun, it even achieves a record-breaking submilligram-level NH<sub>3</sub> yield rate, ∼109 µg h<sup>-1</sup> cm<sup>-2</sup>. This work reveals a critical role of SEI for accelerating Li-Li<sup>+</sup> cycle and provides a valuable guidance for building an efficient Li-mediated PEC N<sub>2</sub>-to-NH<sub>3</sub> fixation at ultra-positive potential vs. Li/Li<sup>+</sup>.