{"title":"Surface phosphatization of cerium-lanthanum oxides for catalytically inert white pigments","authors":"Hiroaki Onoda , Takuma Wada , Thitirat Charoonsuk , Phieraya Pulphol , Rangson Muanghlua , Naratip Vittayakorn","doi":"10.1016/j.jphotochem.2025.116522","DOIUrl":null,"url":null,"abstract":"<div><div>Cerium dioxide (CeO<sub>2</sub>) is a UV-scattering agent commonly employed in sunscreens but suffers from oxidative catalytic activity, raising concerns for dermal applications. To address this issue, surface passivation via phosphatization has been explored, although prior attempts with CeO<sub>2</sub> alone failed to eliminate its intrinsic yellow hue due to low reactivity with phosphoric acid. In this study, we introduce a novel white pigment synthesized via the phosphoric acid-mediated treatment of CeO<sub>2</sub>–La<sub>2</sub>O<sub>3</sub> mixtures. By co-utilizing lanthanum oxide, which readily forms lanthanum phosphate—a white, inert compound—we achieved enhanced suppression of oxidative activity alongside improved whiteness. The composite materials were systematically characterized via X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), particle size analysis, colorimetry (L<em>a</em>b*), and catalytic activity assays. The results reveal that phosphatization preferentially proceeds at lanthanum sites, forming phosphate-rich surface layers that diminish redox activity while maintaining favorable dispersion and smoothness properties. The pigment shows high acid resistance and negligible photocatalytic activity, indicating its potential as a safe, non-reactive alternative for cosmetic formulations. This work advances the development of rare-earth-based functional pigments via a scalable, low-temperature route.</div></div>","PeriodicalId":16782,"journal":{"name":"Journal of Photochemistry and Photobiology A-chemistry","volume":"468 ","pages":"Article 116522"},"PeriodicalIF":4.1000,"publicationDate":"2025-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Photochemistry and Photobiology A-chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S101060302500262X","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Cerium dioxide (CeO2) is a UV-scattering agent commonly employed in sunscreens but suffers from oxidative catalytic activity, raising concerns for dermal applications. To address this issue, surface passivation via phosphatization has been explored, although prior attempts with CeO2 alone failed to eliminate its intrinsic yellow hue due to low reactivity with phosphoric acid. In this study, we introduce a novel white pigment synthesized via the phosphoric acid-mediated treatment of CeO2–La2O3 mixtures. By co-utilizing lanthanum oxide, which readily forms lanthanum phosphate—a white, inert compound—we achieved enhanced suppression of oxidative activity alongside improved whiteness. The composite materials were systematically characterized via X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), particle size analysis, colorimetry (Lab*), and catalytic activity assays. The results reveal that phosphatization preferentially proceeds at lanthanum sites, forming phosphate-rich surface layers that diminish redox activity while maintaining favorable dispersion and smoothness properties. The pigment shows high acid resistance and negligible photocatalytic activity, indicating its potential as a safe, non-reactive alternative for cosmetic formulations. This work advances the development of rare-earth-based functional pigments via a scalable, low-temperature route.
期刊介绍:
JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds.
All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor).
The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.