Chloroplast-Mimicking Interfaces on In Situ Derived La-Ni Based Perovskite for Solar-Driven CO<sub>2</sub> Reduction to CH<sub>4</sub>.
basic_science · Level V
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- Also identified by DOI 10.1002/adma.74829.
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Abstract
Artificial photosynthesis technology holds great promise for sustainable energy conversion and value-added chemical synthesis, yet integrating efficient light absorption with high product selectivity remains a major challenge. This study constructs an Ni-La<sub>2</sub>O<sub>3</sub>/La<sub>2</sub>NiO<sub>4</sub> catalyst through in situ perovskite derivation that mechanistically and functionally mimics the chloroplast for artificial photosynthesis by coupling photo and photothermal catalysis with the integration of broad-spectrum light harvesting, directional charge transfer, as well as CO<sub>2</sub> adsorption and hydrogenation. Three functional interfaces are formed: La<sub>2</sub>O<sub>3</sub>-La<sub>2</sub>NiO<sub>4</sub> (Z-scheme), Ni-La<sub>2</sub>NiO<sub>4</sub> (Schottky junction), and La<sub>2</sub>O<sub>3</sub>(adsorption)-Ni(activation). The two heterojunctions facilitate electron transfer to metallic Ni nanoparticles, which activates H<sup>+</sup> to form an NADPH-like surface Ni-H species by enabling the collection of photo and photothermal generated electrons. Meanwhile, the Lewis-basic La<sub>2</sub>O<sub>3</sub> captures CO<sub>2</sub> and promotes its activation at the La<sub>2</sub>O<sub>3</sub>-Ni interface. In CO<sub>2</sub>-to-CH<sub>4</sub> conversion, Ni-La<sub>2</sub>O<sub>3</sub>/La<sub>2</sub>NiO<sub>4</sub> demonstrates an exceptional CH<sub>4</sub> production rate of 9.96 µmol h<sup>-1</sup> g<sup>-1</sup> and a selectivity of 92.5% under natural conditions (i.e., AM 1.5 irradiation, ambient temperature, and atmospheric pressure) without external assistance, which outperforms pure La<sub>2</sub>NiO<sub>4</sub> by 10.2 and 4.6 times, respectively. This work advances a new strategy for efficient solar-to-fuel conversion.