Structure and photoluminescence of Mn-activated doubly ordered spinel Mg(Ga/Al)SbO: site-selective Al-to-Ga substitution enabling Mn accumulation, excellent anti-thermal quenching of Mn green emission, and optical thermometry

Mineral structure-stimulated material design has made great success in the development of excellent phosphor materials. Herein, spinel-type oxides Mg 4 Ga 1− y Al y SbO 8 (MGA y SO) with a double 2 : 1 ordering of Mg/(Ga/Al) and Mg/Sb cations in tetrahedral and octahedral sublattices, respectively,...

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Veröffentlicht in:Inorganic chemistry frontiers 2024-03, Vol.11 (6), p.1923-1936
Hauptverfasser: Cheng, Zien, Lu, Guangxiang, Qi, Yuxuan, Huang, Jinmei, Yan, Gonggui, Fang, Leiming, Avdeev, Maxim, Yang, Tao, Jiang, Pengfei
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container_end_page 1936
container_issue 6
container_start_page 1923
container_title Inorganic chemistry frontiers
container_volume 11
creator Cheng, Zien
Lu, Guangxiang
Qi, Yuxuan
Huang, Jinmei
Yan, Gonggui
Fang, Leiming
Avdeev, Maxim
Yang, Tao
Jiang, Pengfei
description Mineral structure-stimulated material design has made great success in the development of excellent phosphor materials. Herein, spinel-type oxides Mg 4 Ga 1− y Al y SbO 8 (MGA y SO) with a double 2 : 1 ordering of Mg/(Ga/Al) and Mg/Sb cations in tetrahedral and octahedral sublattices, respectively, were rationally designed and structurally characterized by combined Rietveld refinements against high-resolution X-ray powder diffraction (XRPD) data and neutron powder diffraction (NPD) data. A joint hybrid density functional theory (DFT) calculation and crystal orbital Hamilton population (COHP) analysis demonstrated that these new spinels are direct semiconductors with band gap values increasing along with the Al 3+ content due to the lift of anti-bonding states from the Sb2-O pairs. Mn-activated MGSO exhibited dual emissions from multiple green-emitting Mn 2+ and red-emitting Mn 4+ activators due to the facile occurrence of Mn 4+ -to-Mn 2+ self-reduction, which is inevitable in Mn-doped spinel-type phosphors. This self-reduction can be effectively inhibited by the site-selective Al 3+ -to-Ga 3+ substitution in MGA y SO:Mn 2+/4+ , thereby resulting in an accumulation of Mn ions in the octahedrally coordinated sites and a tunable emission colour from green to yellow and then to deep-red. Interestingly, Mn 2+ green emissions presented excellent anti-thermal quenching (165.4% at 463 K) in a very wide temperature range (303-463 K), whereas severe thermal quenching was observed for the Mn 4+ red emissions. This distinctive thermal response could be applied in temperature sensing, as demonstrated by a high relative sensitivity ( S r ) of 1.22% K −1 at room temperature (303 K), which is superior to many reported optical thermometry materials. Our findings not only offer structural insight into new doubly ordered spinels, but also provide an effective strategy for regulating the valence states of Mn ions for potential application in light-emitting diodes and temperature sensing. The site-selective Al 3+ -to-Ga 3+ substitution in doubly ordered spinel Mg 4 (Ga/Al)SbO 8 :Mn 2+/4+ can manipulate the Mn distributions, thereby resulting in a tunable emission color and controllable optical thermometry sensitivity.
doi_str_mv 10.1039/d3qi02618c
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Herein, spinel-type oxides Mg 4 Ga 1− y Al y SbO 8 (MGA y SO) with a double 2 : 1 ordering of Mg/(Ga/Al) and Mg/Sb cations in tetrahedral and octahedral sublattices, respectively, were rationally designed and structurally characterized by combined Rietveld refinements against high-resolution X-ray powder diffraction (XRPD) data and neutron powder diffraction (NPD) data. A joint hybrid density functional theory (DFT) calculation and crystal orbital Hamilton population (COHP) analysis demonstrated that these new spinels are direct semiconductors with band gap values increasing along with the Al 3+ content due to the lift of anti-bonding states from the Sb2-O pairs. Mn-activated MGSO exhibited dual emissions from multiple green-emitting Mn 2+ and red-emitting Mn 4+ activators due to the facile occurrence of Mn 4+ -to-Mn 2+ self-reduction, which is inevitable in Mn-doped spinel-type phosphors. This self-reduction can be effectively inhibited by the site-selective Al 3+ -to-Ga 3+ substitution in MGA y SO:Mn 2+/4+ , thereby resulting in an accumulation of Mn ions in the octahedrally coordinated sites and a tunable emission colour from green to yellow and then to deep-red. Interestingly, Mn 2+ green emissions presented excellent anti-thermal quenching (165.4% at 463 K) in a very wide temperature range (303-463 K), whereas severe thermal quenching was observed for the Mn 4+ red emissions. This distinctive thermal response could be applied in temperature sensing, as demonstrated by a high relative sensitivity ( S r ) of 1.22% K −1 at room temperature (303 K), which is superior to many reported optical thermometry materials. Our findings not only offer structural insight into new doubly ordered spinels, but also provide an effective strategy for regulating the valence states of Mn ions for potential application in light-emitting diodes and temperature sensing. The site-selective Al 3+ -to-Ga 3+ substitution in doubly ordered spinel Mg 4 (Ga/Al)SbO 8 :Mn 2+/4+ can manipulate the Mn distributions, thereby resulting in a tunable emission color and controllable optical thermometry sensitivity.</description><identifier>EISSN: 2052-1553</identifier><identifier>DOI: 10.1039/d3qi02618c</identifier><ispartof>Inorganic chemistry frontiers, 2024-03, Vol.11 (6), p.1923-1936</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Cheng, Zien</creatorcontrib><creatorcontrib>Lu, Guangxiang</creatorcontrib><creatorcontrib>Qi, Yuxuan</creatorcontrib><creatorcontrib>Huang, Jinmei</creatorcontrib><creatorcontrib>Yan, Gonggui</creatorcontrib><creatorcontrib>Fang, Leiming</creatorcontrib><creatorcontrib>Avdeev, Maxim</creatorcontrib><creatorcontrib>Yang, Tao</creatorcontrib><creatorcontrib>Jiang, Pengfei</creatorcontrib><title>Structure and photoluminescence of Mn-activated doubly ordered spinel Mg(Ga/Al)SbO: site-selective Al-to-Ga substitution enabling Mn accumulation, excellent anti-thermal quenching of Mn green emission, and optical thermometry</title><title>Inorganic chemistry frontiers</title><description>Mineral structure-stimulated material design has made great success in the development of excellent phosphor materials. Herein, spinel-type oxides Mg 4 Ga 1− y Al y SbO 8 (MGA y SO) with a double 2 : 1 ordering of Mg/(Ga/Al) and Mg/Sb cations in tetrahedral and octahedral sublattices, respectively, were rationally designed and structurally characterized by combined Rietveld refinements against high-resolution X-ray powder diffraction (XRPD) data and neutron powder diffraction (NPD) data. A joint hybrid density functional theory (DFT) calculation and crystal orbital Hamilton population (COHP) analysis demonstrated that these new spinels are direct semiconductors with band gap values increasing along with the Al 3+ content due to the lift of anti-bonding states from the Sb2-O pairs. Mn-activated MGSO exhibited dual emissions from multiple green-emitting Mn 2+ and red-emitting Mn 4+ activators due to the facile occurrence of Mn 4+ -to-Mn 2+ self-reduction, which is inevitable in Mn-doped spinel-type phosphors. This self-reduction can be effectively inhibited by the site-selective Al 3+ -to-Ga 3+ substitution in MGA y SO:Mn 2+/4+ , thereby resulting in an accumulation of Mn ions in the octahedrally coordinated sites and a tunable emission colour from green to yellow and then to deep-red. Interestingly, Mn 2+ green emissions presented excellent anti-thermal quenching (165.4% at 463 K) in a very wide temperature range (303-463 K), whereas severe thermal quenching was observed for the Mn 4+ red emissions. This distinctive thermal response could be applied in temperature sensing, as demonstrated by a high relative sensitivity ( S r ) of 1.22% K −1 at room temperature (303 K), which is superior to many reported optical thermometry materials. Our findings not only offer structural insight into new doubly ordered spinels, but also provide an effective strategy for regulating the valence states of Mn ions for potential application in light-emitting diodes and temperature sensing. 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Herein, spinel-type oxides Mg 4 Ga 1− y Al y SbO 8 (MGA y SO) with a double 2 : 1 ordering of Mg/(Ga/Al) and Mg/Sb cations in tetrahedral and octahedral sublattices, respectively, were rationally designed and structurally characterized by combined Rietveld refinements against high-resolution X-ray powder diffraction (XRPD) data and neutron powder diffraction (NPD) data. A joint hybrid density functional theory (DFT) calculation and crystal orbital Hamilton population (COHP) analysis demonstrated that these new spinels are direct semiconductors with band gap values increasing along with the Al 3+ content due to the lift of anti-bonding states from the Sb2-O pairs. Mn-activated MGSO exhibited dual emissions from multiple green-emitting Mn 2+ and red-emitting Mn 4+ activators due to the facile occurrence of Mn 4+ -to-Mn 2+ self-reduction, which is inevitable in Mn-doped spinel-type phosphors. This self-reduction can be effectively inhibited by the site-selective Al 3+ -to-Ga 3+ substitution in MGA y SO:Mn 2+/4+ , thereby resulting in an accumulation of Mn ions in the octahedrally coordinated sites and a tunable emission colour from green to yellow and then to deep-red. Interestingly, Mn 2+ green emissions presented excellent anti-thermal quenching (165.4% at 463 K) in a very wide temperature range (303-463 K), whereas severe thermal quenching was observed for the Mn 4+ red emissions. This distinctive thermal response could be applied in temperature sensing, as demonstrated by a high relative sensitivity ( S r ) of 1.22% K −1 at room temperature (303 K), which is superior to many reported optical thermometry materials. Our findings not only offer structural insight into new doubly ordered spinels, but also provide an effective strategy for regulating the valence states of Mn ions for potential application in light-emitting diodes and temperature sensing. The site-selective Al 3+ -to-Ga 3+ substitution in doubly ordered spinel Mg 4 (Ga/Al)SbO 8 :Mn 2+/4+ can manipulate the Mn distributions, thereby resulting in a tunable emission color and controllable optical thermometry sensitivity.</abstract><doi>10.1039/d3qi02618c</doi><tpages>14</tpages></addata></record>
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title Structure and photoluminescence of Mn-activated doubly ordered spinel Mg(Ga/Al)SbO: site-selective Al-to-Ga substitution enabling Mn accumulation, excellent anti-thermal quenching of Mn green emission, and optical thermometry
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