Bi2O2(OH)(NO3) as a desirable [Bi2O2](2+) layered photocatalyst: strong intrinsic polarity, rational band structure and {001} active facets co-beneficial for robust photooxidation capability

Developing high-performance photocatalytic materials is of huge significance and highly desirable for fulfilling the pressing need in environmental remediation. In this work, we demonstrate the use of bismuth nitrate Bi2O2(OH)(NO3) as an absorbing photocatalyst, which integrates multiple superiorities, like a [Bi2O2](2+) layered configuration, a non-centrosymmetric (NCS) polar structure and highly reactive {001} facets. Bi2O2(OH)(NO3) nanosheets are obtained by a facile one-pot hydrothermal route using Bi(NO3)(3)center dot 5H(2)O as the sole raw material. Photocatalysis assessment revealed that Bi2O2(OH)(NO3) holds an unprecedented photooxidation ability in contaminant decomposition, far out-performing the well-known photocatalysts BiPO4, Bi2O2CO3, BiOCl and P25 (commercial TiO2). Particularly, it displays a universally powerful catalytic activity against various stubborn industrial contaminants and pharmaceuticals, including phenol, bisphenol A, 2,4-dichlorophenol and tetracycline hydrochloride. In-depth experimental and density functional theory (DFT) investigations co-uncovered that the manifold advantages, such as large polarizability and rational band structure, as well as exposed {001} active facets, induced robust generation of strong oxidating superoxide radicals (center dot O-2(-)) in the conduction band and hydroxyl radicals ((OH)-O-center dot) in the valence band, thus enabling Bi2O2(OH)(NO3) to have a powerful and durable photooxidation capability. Bi2O2(OH)(NO3) also presents high photochemical stability. This work not only rendered a highly active and stable photocatalyst for practical applications, but also laid a solid foundation for future initiatives aimed at designing new photoelectronic materials by manipulating multiple advantageous factors.