Structural, electrical and photoluminescence properties of Er3+-doped SrBi4Ti4O15--Bi4Ti3O12 inter-growth ceramics

Fang LIU , Xiangping JIANG , Chao CHEN , Xin NIE , Xiaokun HUANG , Yunjing CHEN , Hao HU , Chunyang SU

Front. Mater. Sci. ›› 2019, Vol. 13 ›› Issue (1) : 99 -106.

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Front. Mater. Sci. ›› 2019, Vol. 13 ›› Issue (1) : 99 -106. DOI: 10.1007/s11706-019-0454-3
RESEARCH ARTICLE
RESEARCH ARTICLE

Structural, electrical and photoluminescence properties of Er3+-doped SrBi4Ti4O15--Bi4Ti3O12 inter-growth ceramics

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Abstract

Er3+-doped SrBi4Ti4O15–Bi4Ti3O12 (SBT–BIT–xEr3+, x = 0.00, 0.05, 0.10, 0.15 and 0.20) inter-growth ceramics were synthesized by the solid-state reaction method. Structural, electrical and up-conversion properties of SBT–BIT–xEr3+ were investigated. All samples showed a single phase of the orthorhombic structure. Raman spectroscopy indicated that the Er3+ substitution for Bi3+ at A sites of the pseudo-perovskite layer increases the lattice distortion of SBT–BIT–xEr3+ ceramics. The substitution of Bi3+ by Er3+ leads to a decrease of dielectric loss tanδ and an increase of conductivity activation energy. Piezoelectric constant d33 was slightly improved, but dielectric constant was decreased with the Er3+ doping. The SBT–BIT–xEr3+ ceramic with x = 0.15 exhibits the optimized electrical behavior (d33 ~17 pC/N, tanδ ~0.83%). Moreover, two bright green (532 and 548 nm) and one red (670 nm) emission bands were observed under the 980 nm excitation. Optimized emission intensity was also obtained when x = 0.15 for the SBT–BIT–xEr3+ ceramic. Therefore, this kind of ceramics ought to be promising candidates for multifunctional optoelectronic applications.

Keywords

inter-growth structure / electrical property / multifunctional optoelectronic material / photoluminescence

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Fang LIU, Xiangping JIANG, Chao CHEN, Xin NIE, Xiaokun HUANG, Yunjing CHEN, Hao HU, Chunyang SU. Structural, electrical and photoluminescence properties of Er3+-doped SrBi4Ti4O15--Bi4Ti3O12 inter-growth ceramics. Front. Mater. Sci., 2019, 13(1): 99-106 DOI:10.1007/s11706-019-0454-3

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