Demonstrates enhanced diffraction efficiency in photopolymerizable glass using optimized BODIPY dyes, indicating significant potential for holographic applications.
The photoinitiating system (PIS) is a key component of holographic materials which needs to be carefully selected and optimized to achieve efficient photopolymerization and, as a result, highly efficient holographic structures. Recently, boron dipyrromethene (BODIPY) dyes have been introduced as a new class of photosensitizers for holographic materials, including photopolymerizable glass, which is characterized by excellent environmental stability. Here, we present a study of the holographic recording capability of a photopolymerizable glass, where PIS was optimized using two approaches: (1) adding a second co‐initiator, diphenyl iodonium hexafluorophosphate (DPIHFP) and (2) exploring a range of BODIPY structures, such as anthracene‐ and pyrene‐BODIPYs. The performance of a novel pyrene‐BODIPY dyad was compared with commercially available Erythrosine B, used as a reference. Remarkably, a 9‐fold increase in the diffraction efficiency and refractive index modulation (RIM) was achieved by replacing Erythrosine B with pyrene‐BODIPY dyads, indicating enhanced photopolymerization kinetics with BODIPY sensitization. In addition, incorporating a second co‐initiator, DPIHFP, further increases the exposure sensitivity by a factor of three. These results demonstrate the high efficiency of BODIPY‐based PIS formulations and underscore photopolymerizable glass as a promising platform for developing highly efficient holographic optical elements.
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Mikulchyk et al. (2026) studied this question.
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