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Journal of Materials Chemistry B · 2014 ·Vol. 2 ·期 38 ·6626-6633 · IF 0

Mn2+-doped NaYF4:Yb/Er upconversion nanoparticles with amplified electrogenerated chemiluminescence for tumor biomarker detection

Min Liu,Yuhang Ye,Cheng Yao,Wenbo Zhao,Xiaohua Huang

Chemiluminescence was used as an excitation light source to construct a universal photoelectrochemical platform based on Mn2+-doped NaYF4:Yb/Er upconversion nanoparticles, which greatly improves the electrochemiluminescence intensity and offers more stable cathodic signals compared to pure NaYF4:Yb/Er NPs. Here, we report for the first time the ECL behaviors of Mn2+-doped NaYF4:Yb/Er NPs, which were synthesized via a facile strategy. Mn2+ doping resulted in a 4-fold ECL intensity enhancement of NaYF4:Yb/Er. The characteristics of Mn2+-doped NaYF4:Yb/Er nanocomposites were obtained using transmission electron microscopy (TEM), energy dispersive X-ray spectrometer (EDS), and fluorescence spectra. After all the results had indicated that NaYF4:Yb/Er upconversion nanoparticles were successfully doped with Mn2+, the electrochemiluminescence platform was built. The as-prepared NaYF4:Yb/Er NPs were rendered water-soluble and then employed as ECL emitters for carcinoembryonic antigen (CEA) determination. The results indicated that the modified electrode can be used to determine CEA without interference from non-specific proteins, with a low detection limit of 5.2 pg mL−1. The biosensor can also be used for quantification of the CEA concentration in real samples.

研究领域: 生物医学工程 · 纳米医学
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CRYSTENGCOMM · 2022 ·Vol. 24 ·期 9 ·1803-1811 · IF 3.756

Hexamethyldisilazane-assisted Mn2+ doping of perovskite nanocrystals under ambient conditions

Kaiwen Hu,Yongfei Hu,Tan Li,Fen Qiao,Yunxia Chen,Jianjun Han,Lee Li,Ghafar Ali,Yi Xie

Doping Mn2+ ions into lead halide perovskite (LHP) nanocrystals (NCs) has attracted great attention in the optoelectronic fields due to the stability enhancement and unique dual-color emission characteristics arising from the energy transfer from the LHP host to the dopants (i.e., Mn2+ ions). Herein, we report a facile and scalable synthetic protocol for Mn2+-doped CsPbCl3 and CsPbBrxCl3−x nanoplates via a one-pot room-temperature (RT) procedure in the presence of hexamethyldisilazane (HMDS). It is noteworthy that both HMDS and Mn2+ ions play a critical role in triggering the crystallization of the Mn-doped LHP NCs under ambient conditions by functioning as a passivation agent with Lewis base groups that coordinate with Pb2+ ions. The optical properties including the emission wavelength and the relative PL intensity of the band-to-band emission and the Mn2+ emission are tuned by changing the amount of HMDS and the precursor ratios Mn : Pb and Br : Cl. It is interesting that the representative Mn-doped CsPbCl3 NCs displayed enhanced thermal stability, which was confirmed by the observation that the emission intensity of the sample annealed below 95 °C for 2 h increases compared with that of the fresh sample. Ion exchanges between not only Cl−, Br− and I− but also Mn2+ and Pb2+ are also investigated.

研究领域: 材料科学 · 光电子学 · 纳米技术
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OPTICS LETTERS · 2024 ·Vol. 49 ·期 9 ·2245-2248 · IF 3.1

Mn2+/Mg2+ co-doped AlON ceramic with ultra-narrowband green emission combining high transparency toward a wide gamut backlight application

Xiaolan Zhou,Xiaolan Zhou,Shengyuan Chen,Shengyuan Chen,Cong Zhang,Cong Zhang,Xu Huang,Xu Huang,Kailei Lu,Kailei Lu,Jianqi Qi,Jianqi Qi,Jianqi Qi,Tiecheng Lu,Tiecheng Lu,Tiecheng Lu,Tiecheng Lu

Narrowband green-emission, combined with superior physicochemical stability and thermal performance, is regarded as a common pursuit in backlight display applications. However, mainstream phosphor-converted materials composed of resin or silicone resin easily encounter the dilemma of thermal decomposition and chemical corrosion for practical use. To overcome this problem, in this work, Mn2+/Mg2+ co-doped AlON ceramic is successfully realized with ultra-narrowband green-emission and high transparency. The luminescent property of AlON: Mn2+–Mg2+ ceramic exhibits narrowband green emission centered at 509 nm with a full width at half maximum of 36 nm, which is smaller than the corresponding powder counterpart (44 nm). Moreover, AlON: Mn2+–Mg2+ ceramic presents a wide color gamut (103.6%) and high color purity (74%). Concurrently, high transmittance of this ceramic, at 82%, unveils a potential innovation in the display technology field. This work may facilitate the development of narrowband green light-emitting converters based on AlON: Mn2+–Mg2+ transparent ceramics in large color gamut backlight display applications.

研究领域: 材料科学 · 光学工程 · 显示技术
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ACS Applied Materials & Interfaces · 2018 · IF 8.097

Confining Mn2+-Doped Lead Halide Perovskite in Zeolite-Y as Ultrastable Orange-Red Phosphor Composites for White Light-Emitting Diodes

Shi Ye,Jia-Yi Sun,Yu-Hong Han,Ya-Yun Zhou,Qin-Yuan Zhang

CsPbX3 (X = Cl, Br, I) perovskite quantum dots (QDs) have emerged as competitive candidate luminescent materials in the photoelectric fields due to their superior luminescence properties. However, the major drawback such as poor resistance to temperature, moisture, and irradiation of light, especially for the red QDs with I–, hinders their practical applications. Herein, we synthesized Mn2+-doped CsPbCl3 embedded in the cage of zeolite-Y as a new orange-red phosphor for the white light-emitting diode (WLED). The composites have significantly improved resistance to both elevated temperature and water over the bare Mn2+-doped QDs. The former exhibits little degradation whereas the latter shows apparent decline upon the irradiation of lights in the orange LED devices, which are fabricated by employing each material as a color-conversion phosphor coated on a 365 nm UV chip. A WLED is also achieved with a 365 nm UV chip coated with a CsPb(Cl0.5,Br0.5)3–Y blue phosphor and a CsPb0.75Mn0.25Cl3–Y orange phosphor. The device possesses a Commission Internationale de l’Éclairage coordinate of (0.34, 0.36), a correlated color temperature of 5336 K and a color rendering index of 81.

研究领域: 材料科学 · 光电领域
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OPTICS EXPRESS · 2023 ·Vol. 31 ·期 6 ·10191-10200 · IF 3.8

Modulating the afterglow time of Mn2+ doped double perovskites by size tuning and its applications in dynamic information display

Peng Wang,Ying Wang,Wei Guan,Hongzhou Dong,Lina Sui,Zhixing Gan,Zhixing Gan,Lifeng Dong,Lifeng Dong,Liyan Yu,Liyan Yu

Mn2+ doped lead-free double perovskites are emerging afterglow materials that can avoid the usage of rare earth ions. However, the regulation of the afterglow time is still a challenge. In this work, the Mn doped Cs2Na0.2Ag0.8InCl6 crystals with afterglow emission at about 600 nm are synthesized by a solvothermal method. Then, the Mn2+ doped double perovskite crystals are crushed into different sizes. As the size decreases from 1.7 mm to 0.075 mm, the afterglow time decreases from 2070 s to 196 s. Steady-state photoluminescence (PL) spectra, time resolved PL, thermoluminescence (TL) reveal the afterglow time monotonously decreases due to the enhanced nonradiative surface trapping. The modulation on afterglow time will greatly promote their applications in various fields, such as bioimaging, sensing, encryption, and anti-counterfeiting. As a proof of concept, dynamic display of information is realized based on different afterglow times.

研究领域: 材料科学 · 光学
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Advanced Science · 2023 · IF 15.1

Pressure-Induced Remarkable Spectral Red-Shift in Mn2+-Activated NaY9(SiO4)6O2 Red-Emitting Phosphors for High-Sensitive Optical Manometry

Qifeng Zeng,Marcin Runowski,Junpeng Xue,Laihui Luo,Lukasz Marciniak,Víctor Lavín,Peng Du

To settle the low sensitivity of luminescent manometers, the Mn 2+ -activated NaY 9 (SiO 4 ) 6 O 2 red-emitting phosphors with splendid pressure sensing performances are developed. Excited by 408 nm, the resulting products emit bright red emission originating from 4 T 1 ( 4 G) → 6 A 1 transition of Mn 2+ , in which the optimal concentration of the activator ion is ≈1 mol%. Moreover, the admirable thermal stability of the developed phosphors is studied and confirmed by the temperature-dependent emission spectra, based on which the activation energy is derived to be 0.275 eV. By analyzing the pressure-dependent Raman spectra, the structural stability of the synthesized compounds at extreme conditions is verified. Furthermore, the designed phosphors exhibit remarkable spectral red-shift at elevated pressure. Especially, as pressure increases from 0.75 to 7.16 GPa, the emission band centroid shifts from 617.2 to 663.4 nm, resulting in a high sensitivity (d λ /d P ) of 7.00 nm GPa −1 , whereas the full width at half maximum (FWHM) increases from 83.0 to 110.6 nm, leading to the ultra-high sensitivity (dFWHM/d P ) of 10.13 nm GPa −1 . These achievements manifest that the designed red-emitting phosphors are appropriate for ultrasensitive optical manometry. More importantly, the developed manometer is a current global leader in sensitivity, when operating in the band-width mode, that is, FWHM.

研究领域: 材料科学 · 光学工程
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CERAMICS INTERNATIONAL · 2025 · IF 5.6

Quantitative reduction of Eu3+ to Eu2+ by a convenient method using (NH4)2HPO4 for enhancing Mn2+ luminescence in P2O5-B2O3-ZnO-KBr glass

Changyuan Xu,Fengjiao Zhao,Yan Ding,Haizhen Song,Qun Wang,Hongming Yin

In this study, we propose a novel strategy to reduce Eu 2 O 3 to Eu 2+ in the 34.88P 2 O 5 -13.57B 2 O 3 -34.88ZnO-16.67KBr (PBZB) glass system by introducing (NH 4 ) 2 HPO 4 as a reducing phosphorus source. Photoluminescence (PL), photoluminescence excitation (PLE) spectral and UV–Vis absorption spectral analyses revealed that the emission peak at 325 nm excitation originates from the 4f 6 5d 1 → 4f 7 transition of Eu 2+ , confirming the reduction efficacy of (NH 4 ) 2 HPO 4 . Furthermore, incorporating 7.14 % Mn 2+ into PBZB glass and adjusting the concentration of Eu 2 O 3 demonstrated that Eu 2+ doping significantly enhances the red emission of Mn 2+ at 630 nm. Specifically, when the Eu 2 O 3 concentration is 0.12 mol%, the Mn 2+ emission intensity reaches its peak, with a 32.6 % increase in photoluminescence quantum yield (PLQY). However, further increasing the Eu 2 O 3 concentration leads to a decrease in Mn 2+ emission intensity and the appearance of Eu 3+ emission peaks, indicating a limited reduction capacity. Emission spectrum analysis showed a Eu 3+ reduction rate of 76.09 %. The effective energy transfer mechanism from Eu 2+ to Mn 2+ was verified through spectral overlap and decay curve analysis, with calculated energy transfer efficiency being similar to the PLQY increment. This study simplifies the Eu 3+ reduction process and provides a new method for optimizing Mn 2+ red emission in glass.

研究领域: 材料科学 · 光学
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CHEMOSPHERE · 2022 · IF 8.943

Improved performance of an opposite-flow low-pressure ultrafiltration membrane system in the treatment of groundwater containing Fe2+, Mn2+, and NH4+

Xuesong Ye,Zhencheng Ge,Qiliang Xiao,Bohan Liu,Meng Chen,Fangmin Wu,Jun Nan

In remote areas, low-pressure ultrafiltration membrane (LPM) systems can be applied in decentralized water supplies for the treatment of groundwater containing Fe 2+ , Mn 2+ , and NH 4 + . However, improving the performance of the LPM systems, such as the stable flux and removal capacity, presents a challenge. In this study, a novel opposite-flow low-pressure ultrafiltration membrane (O-LPM) system was applied, and its performance was evaluated. Experimental results showed that after 46 days of operation, the steady flux of the O-LPM systems were 1.87-fold and 1.74-fold higher than that of the conventional D-LPM systems under Mn 2+ concentration of 0.3 mg L −1 and 1.5 mg L −1 , respectively. With a mixed pollutant system containing Fe 2+ (0.5 mg L −1 ), Mn 2+ (0.3 mg L −1 ), and NH 4 + (1.0 mg L −1 ), the O-LPM-ripening period for Mn 2+ removal was shortened from 16 days to 8 days, and the NH 4 + removal efficiency was increased from 61.46% to 80.97%. The bio-cake layer in the O-LPM systems was thinner and had a higher uniformity than in the D-LPM systems, resulting in a larger stable flux range. The relative abundance of functional bacteria (MnOB, IOB, and NOB) was generally higher in O-LPM systems than in the D-LPM systems. Overall, these results are of high relevance for groundwater treatment in remote areas, providing guidance for the widespread application of the O-LPM system in decentralized water supplies.

研究领域: 环境工程 · 微生物学
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ACS Applied Materials & Interfaces · 2023 · IF 9.5

Enhancing Luminescence in Hue-Tunable White-Light Emitting K4CdCl6:Sb3+,Mn2+ All-Inorganic Halide Perovskites: Insights from Defect Engineering and Energy Transfer

Zhichao Liu,Yuexiao Pan,Chengdong Peng,Yihong Ding,Hongzhou Lian,Jun Lin,Liyi Li

All-inorganic halide perovskites (AIHPs) have emerged as highly promising optoelectronic materials owing to their remarkable properties, such as high-optical absorption coefficients, photoluminescence efficiencies, and dopant tolerance. Here, we investigate the AIHPs K4CdCl6:Sb3+,Mn2+ that demonstrate hue-tunable white-light emission with an exceptional photoluminescence quantum yield of up to 97%. Through a detailed investigation, we reveal that efficient energy transfer from Sb3+ to Mn2+ plays a dominant role in the photoluminescence of Mn2+, instead of the conventional 4T1g → 6A1g transition of Mn2+. Thermodynamic analysis highlights the crucial role of a Cl-rich environment in obtaining the K4CdCl6 phase, while transformation from K4CdCl6 to KCdCl3 can be achieved under Cl-poor and K-poor conditions. The theoretical analysis reveals that defect Cli is more readily formed compared to defect VK, corroborating experimental findings that the K4CdCl6:Sb3+ phase is exclusively obtained when the solution contains HCl concentrations higher than 4 mol L–1. Our work provides valuable insights into the photoluminescence mechanism of Sb3+, defect engineering through heterovalent doping, and efficient energy transfer between Sb3+ and Mn2+ in K–Cd–Cl-based perovskites, which offers a new perspective for the design and development of novel AIHPs with superior optoelectronic performance.

研究领域: 材料科学 · 光学
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ACS Applied Electronic Materials · 2021 · IF 3.314

Unraveling the Ultrafast Self-assembly and Photoluminescence in Zero-Dimensional Mn2+-Based Halides with Narrow-Band Green Emissions

Guojun Zhou,Qiqiong Ren,Maxim S. Molokeev,Yayun Zhou,Jian Zhang,Xian-Ming Zhang

The discovery of narrow-band luminescent materials remains an immense challenge to optimize the performance of white light-emitting diodes (LEDs). So far, the zero-dimensional (0D) Mn2+-based halides with near-unity narrow-band emissions have emerged as a class of promising phosphors in solid-state displays, but the related large-scale synthesis strategies have not been proposed and evaluated. Herein, we report an in situ synthetic process of 0D Mn2+-based halides and utilize (C20H20P)2MnBr4 as a case to investigate the photoluminescence characteristics and the structural essence of ultrafast self-assembly. The bright green emission peak at 523 nm with a full width at half maximum of 48 nm for (C20H20P)2MnBr4 is attributed to the d–d transition (4T1–6A1) of tetrahedrally coordinated [MnBr4]2– centers, and the fabricated white LED device shows a wide color gamut of 103.7% National Television System Committee (NTSC) standard. Remarkably, the experimental and theoretical results indicate that there are hydrogen bonding of C–H···Br and weak van der Waals interactions between [C20H20P]+ and [MnBr4]2–, resulting in the root for the realization of ultrafast self-assembly in 0D Mn2+-based halides. This work reveals a feasible and general synthesis method for preparing 0D Mn2+-based halides, thereby providing a possibility for their industrial application in solid-state displays.

研究领域: 材料科学 · 光学
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JOURNAL OF THE EUROPEAN CERAMIC SOCIETY · 2025 · IF 6.2

Eu2+ co-doped MgAl2O4: Mn2+ green phosphor ceramics: Anti-thermal quenching emission via trap engineering strategy

Junwei Zhang,Hui Lin,Shuo Zhu,Yuetong Zhen,Ruijin Hong,Zhaoxia Han,Dawei Zhang

The rapid advancement of high-power solid-state lighting highlights the importance of developing phosphor ceramics with high resistance to thermal quenching of its luminescence. Herein, a series of Eu 2+ co-doping MgAl 2 O 4 : Mn 2+ phosphor ceramics were synthesized by spark plasma sintering. The significant green light enhancement at 516   nm is attributed to Eu 2+ -Mn 2+ energy transfer. The introduction of Eu 2+ increases the concentration of electron trap levels and improve the luminescence intensity at 423   K from 80% to 110%, compared with the counterparts at room temperature. The strong correlation between trap levels and oxygen vacancies was demonstrated by the X-ray photoelectron spectroscopy and electron paramagnetic resonance analysis. Finally, the application demonstration of the optimized sample was explored through its integration with a 400   nm LED chip. This study proposes a strategy of leveraging trap levels to induce anti-thermal quenching behavior, providing some insights for the development of highly thermally stable phosphor ceramics.

研究领域: 材料科学 · 发光材料 · 固态照明 · 陶瓷学 · 光电子学
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JOURNAL OF ALLOYS AND COMPOUNDS · 2018 · IF 3.779

A novel Ce3+/Mn2+/Eu3+ tri-doped GdF3 nanocrystals for optical temperature sensor and anti-counterfeiting

Han Xia,Lei Lei,Wanqing Hong,Shiqing Xu

Non-contact optical thermometry based on fluorescence intensity ratio (FIR) exhibits potential application in strong electromagnetic and corrosive environment. However, most of the reported systems exhibit high temperature sensitivity only at a narrow temperature range, which limit their practical application. In this work, a novel Ce 3+ /Mn 2+ /Eu 3+ tri-doped GdF 3 nano-thermometry based on different thermal behaviours between Eu 3+ and Mn 2+ ions is constructed. The calculated relative sensitivity in the whole measured temperature range are beyond 1.08% K −1 and the maximum S a is about 0.078 K −1 for the 50Ce/8Mn/2Eu: GdF 3 NCs , which are superior to several other inorganic nano-thermometry at the same temperature. In addition, these colorimetric temperature sensing materials exhibit potential application in anti-counterfeiting field as well.

CAS / MDL: 12125-01-8
研究领域: 材料科学 · 光学
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