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J. Korean Ceram. Soc. > Volume 62(5); 2025 > Article
Journal of the Korean Ceramic Society 2025;62(5): 891-903.
doi: https://doi.org/10.1007/s43207-025-00512-2
Spray pyrolysis-based synthesis of self-floating black TiO2-x microspheres for solar-driven interfacial evaporation
Seungheon Han1, Hee Yeon Jeon1, Myeongjun Ji2, Young-In Lee1
1Department of Materials Science and Engineering, Seoul National University of Science and Technology, Seoul, 01811, Republic of Korea
2Department of Mechanical Engineering, University of Nevada, Las Vegas, NV, 89154, USA
Correspondence  Myeongjun Ji ,Email: myeongjun.ji@unlv.edu
Young-In Lee ,Email: youngin@seoultech.ac.kr
Received: December 13, 2024; Revised: March 14, 2025   Accepted: April 20, 2025.  Published online: May 12, 2025.
ABSTRACT
While solar-driven interfacial evaporation (SIE) using self-floating monodispersed photothermal microspheres has emerged as a promising method for eco-friendly and continuous clean water production without performance degradation by contaminant accumulation, few studies have been conducted on self-floating SIE due to the lack of appropriate synthesis methods for the self-floating, large-size photothermal particles. In this study, a facile and versatile spray pyrolysis-based process is demonstrated to synthesize self-floating black TiO2-x microspheres. This process facilitates defect engineering within the bulk region of large-sized metal oxides to enhance photothermal properties, a capability that is challenging to achieve with conventional reduction-based methods. The physicochemical properties as a function of process conditions were systematically investigated. The results demonstrated that high concentrations of oxygen vacancies, which were introduced within the bulk region of the black TiO2-x microspheres, extended the light absorption range, improved absorptivity across a wide spectrum, and enhanced photo-to-heat conversion by promoting non-radiative recombination. Consequently, the synthesized defective TiO2-x microspheres exhibited an outstanding solar-driven interfacial evaporation rate of 0.532 kgm-2 h-1. While floating independently without hydrophilic support, the evaporation performance of the self-floating TiO2-x microspheres is 1.63-fold faster than that of bulk water evaporation under light irradiation with an intensity of 1 kWm-2.
Key words: Solar-driven interfacial evaporation · Self-floating · Photothermal metal oxide · Bulk oxygen vacancy · Ultrasonic spray pyrolysis
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