Soft-Templated Sol–Gel Synthesis of Mesoporous Perovskite-Type Multicomponent Metal Oxide (Bi <sub>0.2</sub> Na <sub>0.2</sub> K <sub>0.2</sub> La <sub>0.2</sub> Sr <sub>0.2</sub> )TiO <sub>3</sub> and Its Enhanced Photocatalytic Activity
The high calcination temperature required for the crystallization of multicomponent metal oxides is a challenge because this treatment significantly reduces their specific surface area while increasing the crystallite size, thereby limiting their photocatalytic performances. In this study, we have addressed this issue for a multicomponent perovskite photocatalyst, (Bi<sub>0.2</sub>Na<sub>0.2</sub>K<sub>0.2</sub>La<sub>0.2</sub>Sr<sub>0.2</sub>)-TiO<sub>3</sub> (BNKLST), by employing a soft-templating sol-gel method using Pluronic F-127. The synthesis process was optimized by adjusting the solution's pH to ensure uniform micelle self-assembly and by determining the optimum calcination temperature for the pore formation. This approach enabled the successful low-temperature synthesis of BNKLST, which retained a high specific surface area of 50.4 m<sup>2</sup> g<sup>-1</sup> at 400 °C. The resulting catalyst exhibited excellent photocatalytic activity, degrading methylene blue under UV irradiation (250-450 nm) at a rate more than six times faster than that obtained using commercial SrTiO<sub>3</sub>. These findings demonstrate that enhancing the specific surface area of multicomponent metal oxides through a soft-templating approach is an effective strategy in photocatalyst design.
Authors
- Go Kawamura
- Andrei Jitianu (ORCID: https://orcid.org/0000-0001-6111-531X)
- Atsunori Matsuda
- Kazuki Inoue
- Wai Kian Tan
- Hanzo Tsubota
- Hiroyuki Muto
Institutions
- The Graduate Center, CUNY (US)
- Toyohashi University of Technology (JP)
- Lehman College (US)
- City University of New York (US)
Publication Details
- Journal
- ACS Omega
- Published
- 2026-01-05
- DOI
- https://doi.org/10.1021/acsomega.5c12465
- Primary Topic
- Advanced Photocatalysis Techniques
- Type
- article
- Field-Weighted Citation Impact
- 0.00