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Dazzling cool white light emission from Ce3+/Sm3+ activated LBZ glasses for W-LED applications

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Abstract We synthesized a batch of co-doped (Ce3++Sm3+): LBZ glass specimens by melt quenching process and their structural and radiation properties were studied by employing XRD, FE-SEM, optical absorption, photoluminescence… Click to show full abstract

Abstract We synthesized a batch of co-doped (Ce3++Sm3+): LBZ glass specimens by melt quenching process and their structural and radiation properties were studied by employing XRD, FE-SEM, optical absorption, photoluminescence and lifetime measurements. UV–Vis–NIR absorption studies of the co-doped (Ce3++Sm3+): LBZ glassy matrix displays pertinent bands of both Ce3+ and Sm3+ ions. Individually doped Sm3+: LBZ glass exhibit bright orange emission at 603 nm (4G5/2 → 6H7/2) under the excitation of 403 nm. Nevertheless, the luminescence intensities pertaining to Sm3+ were extraordinarily increased by co-doping with Ce3+ ions to Sm3+: LBZ glassy matrices because of energy transfer from Ce3+ to Sm3+. The fluorescence spectra of co-doped (Ce3++Sm3+): LBZ exhibits characteristic emission bands of Ce3+ (441 nm, blue) and Sm3+ (603 nm, reddish orange) under the excitation of 362 nm. Decay curves of Ce3+ and Sm3+ ions in co-doped glass has been fitted to double exponential nature. The decreasing lifetime of donor ion and rising lifetime of acceptor ion in double doped glass could support the energy transfer from Ce3+ to Sm3+ ions in the host matrix. The CIE coordinates and CCT values were calculated for all the obtained co-doped glassy samples from their luminescence spectra. By adding Ce3+ ions to individually doped Sm3+: LBZ glass matrix, the emitting color changes from reddish orange to white light which resembles the energy transfer from Ce3+ to Sm3+ ions. These studies, perhaps implied that attained co-doped (Ce3++Sm3+): LBZ glassy samples are potential materials for white lighting appliances.

Keywords: glass; ce3 sm3; sm3 lbz; sm3; emission

Journal Title: Ceramics International
Year Published: 2018

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