Efficient photocatalytic NO oxidation over novel NiAl layered double hydroxide/BiTiO Z-scheme heterojunctions with boosted charge separation and O activation

Suffering from inefficient carrier migration and the lack of active sites, the effective photocatalytic removal of low-concentration NO is still a formidable challenge. In this work, a NiAl-LDH/Bi 4 Ti 3 O 12 Z-scheme heterojunction photocatalyst was prepared successfully through a facile two-step hydrothermal procedure. In this, the Fermi-level difference at the interface of Bi 4 Ti 3 O 12 and NiAl-LDH results in the formation of a strong built-in electric field (BIEF). The strong BIEF enables the formation of a Z-scheme heterojunction, offering a novel charge transfer pathway that promotes the efficient migration of photogenerated electrons and holes while retaining their strong redox capability. Additionally, the unique NiAlLDH-modified sheet-like stacked nano-flower structure has a large specific surface area, which is beneficial for semiconductor absorption of sufficient photons to increase the concentration of charge carriers, and providing more reaction sites for the adsorption and activation of oxygen, thereby generating more reactive oxygen species. As a result, the optimized NiAl-LDH/Bi 4 Ti 3 O 12 catalyst exhibits enhanced photocatalytic NO removal efficiency (75.51%), which significantly surpasses that of pristine Bi 4 Ti 3 O 12 (62.35%) and NiAl-LDH (5.12%). The findings of this research offer insights into the rational development of Bi 4 Ti 3 O 12 -based heterostructure photocatalysts for air purification. The novel NiAl-LDH/Bi 4 Ti 3 O 12 Z-scheme heterojunction exhibits excellent NO oxidation performance with low toxic NO 2 generation. The enhanced activity can be attributed to the boosted charge separation and optimized oxygen activation capability.