Nanoplated lanthanum-substituted bismuth titanate (Bi_3.25La_0.75Ti₃O₁₂, BLTO) microspheres constructed with tens of BLTO nanoplates were synthesized by a sol–gel hydrothermal method. Using nanoplated BLTO microspheres, a novel third-generation H₂O₂ biosensor was fabricated with loading of myoglobin (Mb) and chitosan (Chi). Scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and X-ray diffraction (XRD) measurements reveal that partial Bi ions of bismuth titanate (BTO, Bi₄Ti₃O₁₂) are successfully substituted with La ions by the sol–gel hydrothermal method. UV-visible (UV-vis) and Fourier-transform infrared (FTIR) spectra show that Mb encapsulated in the Mb–Chi–BLTO film can retain its bioactivity well. Comparative experiments witness that the Mb–Chi–BLTO biosensor, compared with the Mb–Chi–BTO biosensor, not only has enhanced direct electron-transfer capacity (e.g., stronger redox peak currents (approximately 3-fold) and a larger heterogeneous electron-transfer rate constant of 12.8 ± 3.3 s⁻¹), but also exhibits a wider linear response to H₂O₂ in the concentration range of 2–490 μM, higher sensitivity (88 mA cm⁻² M⁻¹), a lower Michaelis–Menten constant (0.55 mM) and detection limit (0.14 μM), a shorter response time (2.8 s), and better reproducibility and stability. These results imply that La doping greatly improves electrochemical and electrocatalytic properties of the Mb–Chi–BLTO biosensor, which will open up a new idea for the design of third-generation electrochemical biosensors, and the BLTO-based biosensors are also expected to find potential applications in many areas such as clinical diagnosis and food and environmental detection.

Bi₄Ti₃O_12−x nanosheet photocatalysts with abundant oxygen vacancies are fabricated by a facile solid-state chemical reduction method for the first time. This method is simple in operation, has short reaction time, and can be conducted at mild temperatures (300~400 °C). The electron paramagnetic resonance, thermogravimetric analysis, X-ray photoelectron spectrometer, and positron annihilation lifetime spectra results indicate that oxygen vacancies are produced in Bi₄Ti₃O_12−x, and they can be adjusted by tuning the reduction reaction conditions. Control experiments show that the reduction time and temperature have great influences on the photocatalytic activities of Bi₄Ti₃O_12−x. The optimal Bi₄Ti₃O_12−x is the sample undergoing the reduction treatment at 350 °C for 60 min and it affords a hydrogen evolution rate of 129 μmol·g⁻¹·h⁻¹ under visible-light irradiation, which is about 3.4 times that of the pristine Bi₄Ti₃O₁₂. The Bi₄Ti₃O_12−x photocatalysts have good reusability and storage stability and can be used to decompose formaldehyde and formic acid for hydrogen production. The surface oxygen vacancies states result in the broadening of the valence band and the narrowing of the band gap. Such energy level structure variation helps promote the separation of photo-generated electron-hole pairs thus leading to enhancement in the visible-light photocatalytic hydrogen evolution. Meanwhile, the narrowing of the band gap leads to a broader visible light absorption of Bi₄Ti₃O_12−x.