Persistent Luminescence Properties Research Articles

Energy trapping to substitutional and charge compensation defects in persistent luminescent BaAl2O4:Tb3+

The holistic approach of the photoluminescence (PL), thermoluminescence (TL), and persistent luminescence properties at room temperature of BaAl2O4:Tb3+ were investigated in detail using a wide range of techniques. Materials were obtained using a solution combustion synthesis. The x-ray powder diffraction patterns of nondoped and Tb3+ doped BaAl2O4 indicated the hexagonal phase, and a Tb4O7 solid solution was observed at 4 and 5 mol% Tb doped aluminate. X-ray photoelectron spectroscopy revealed that Ba occupied one site and that Tb ions occupied this site as Tb3+ as well as TbIV. PL emission in blue, green, and red was observed under an excitation at 228 nm, that originated from the interconfigurational 4f8–4f75d1 transitions of Tb3+. Time-of-flight secondary ion mass spectroscopy, UV–vis diffuse reflectance, and PL revealed the presence of a Cr3+ impurity. The 0.5 mol% Tb3+ doped BaAl2O4 exhibited a strong TL band at 354, 437 and 598 K, which were attributed to the traps formed by Tb3+ doping and subsequent O2− charge compensation. A persistent luminescence mechanism was constructed for the Tb3+ doped BaAl2O4. After the energy was stored in thermally liberated Tb3+ in the Ba2+ substitution sites and charge compensation defects, the Tb3+ was the source of the continuous luminescence.

Overcoming surface quenching in persistent luminescence nanoparticles with organic ligand coordination: Implications for enhanced optical imaging

Persistent luminescence nanoparticles (PLNPs) have been considered as excellent luminescent tools for sensitive optical imaging. However, the persistent luminescence (PL) properties of PLNPs are usually suppressed due to severe surface quenching caused by nanoscale size. Despite considerable efforts, the understanding of surface quenching mechanisms remains a challenge. Here we report a surface ligand coordination method to enhance the PL properties of ZnGa2O4:Al,Cr (ZGO:AC) PLNPs. ZGO:AC PLNPs coated with organic ligands containing carboxyl groups show enhanced PL intensity and prolonged decay time. Among the six ligands, the phthalic acid (PA) ligands yielded the largest luminescence enhancement effect, on which the PL intensity and decay time increased 3 and 2 times compared with ligand-free ZGO:AC PLNPs, respectively. Density functional theory (DFT) calculations and detailed characterizations demonstrated that surface quenching is suppressed due to the coordination of non-saturated Ga ions and -COO- of ligands. Finally, ZGO:AC@PA PLNPs were applied in autofluorescence-free bioimaging and exhibited high imaging sensitivity and contrast ratio. These findings provide insights into the surface quenching mechanisms of PLNPs and offer a platform for developing highly emissive PLNPs on nanoscale.

Simultaneously enhanced photoluminescence and persistent luminescence in SrLaAlO4: Tb type layered perovskite via Gd3+ codoping

Gd3+ co-doping is effective to enhance the photoluminescence of rare earth activators in various host due to energy transfer, however, it is rarely reported via such strategy to regulate persistent luminescence properties. In this work, Gd3+ was co-doped into the SrLaAlO4: Tb persistent luminescence phosphors, and it is found that the photoluminescence and persistent luminescence of the products can be simultaneously improved. The results indicate that as the doping concentration of Gd3+ increases, the particle diameters increase which contributes the increased luminescence. Additionally, an energy transfer process from Gd3+ to Tb3+ ions was observed, which enhances the emission of Tb3+ ions. Furthermore, the persistent luminescence properties of the synthesized phosphors were improved. When the UV light source is turned off, the persistent luminescence of SrLaAlO4: 0.03Tb3+, xGd3+ (x = 0.00–0.97) can last for more than 2 h, which is 100 % enhanced compared to SrLaAlO4: 0.03Tb3+. The trap distribution of SrLaAlO4: 0.03Tb3+, xGd3+ (x = 0.00–0.97) phosphors was analyzed by thermoluminescence. It is found that after the substitution of La3+ with Gd3+, the trap position shifted towards higher temperatures and the trap concentration increased. The initial intensity of the persistent luminescence was also enhanced after Gd3+ co-doping. Based on the experimental findings, the luminescence and persistent luminescence mechanism of SrLaAlO4: 0.03Tb3+, xGd3+ (x = 0.00–0.97) phosphors were described and discussed.

Persistent ultraviolet luminescence and photocatalytic properties of SiO2-Zn2SiO4:Ga,Pb nanoparticles

Persistent phosphors possess unique afterglow optical properties. In this paper, a class of ultra-violet (UV) persistent luminescence nanoparticles were developed for catalytic photodegradation applications. UV persistent luminescence nanoparticles of SiO2-Zn2SiO4:Ga and SiO2-Zn2SiO4:Ga,Pb were successfully synthesized by using a mesoporous template method. The UV persistent luminescence intensity of SiO2-Zn2SiO4:Ga at 405 nm was enhanced up to ca. 3.5 times by co-doping with Pb2+ (396 nm), along with longer persistent luminescence duration. The photodegradation results indicate that it is useful to introduce UV persistent luminescence property into SiO2-Zn2SiO4:Ga,Pb to obtain enhanced catalytic activity of SiO2-Zn2SiO4 with a bigger catalytic oxidation reaction kinetic constant (up to ∼4 times). This kind of UV persistent catalysis strategy may become a potential feasible method for better catalytic photodegradation activity. The UV persistent photocatalyst has potential applications in the photooxidation of organic molecules in high chroma and/or turbidity aqueous systems.

Persistent Luminescent Nanoparticle-Loaded Filaments for Identification of Fabrics in the Visible and Infrared.

Persistent luminescent materials are those which can store an amount of energy locally and release it slowly in the form of light. In this work, persistent luminescent nanoparticles (PLNPs) were synthesized and incorporated into polypropylene (PP) filaments at various loading percentages. We investigated the optical properties of both the as-prepared PLNPs and the PLNP-loaded filaments, focusing on any changes resulting from the integration into the filaments. Specifically, visible and near-infrared spectroscopy were used to analyze the emission, excitation, and persistent luminescence of the PLNPs and PLNP-loaded filaments. The tensile properties of the extruded filaments were also investigated through breaking tenacity, elongation at break, Young's modulus, and secant modulus. All PLNP-loaded filaments were shown to exhibit persistent luminescence when exposed to ultraviolet light. While there were no significant changes in the elongation at break or Young's modulus for the loading percentages tested, there was a slight increase in breaking tenacity and a decrease in the secant modulus. Finally, the filaments were shown to maintain their optical properties and persistent luminescence even after abrasion testing used to simulate the normal wear and tear that fabric experiences during use. These results show that PLNPs can be successfully incorporated into filaments which can be used in fabrics and will maintain the persistent luminescent properties.

Biodegradable Persistent Luminescence Nanoparticles as Pyroptosis Inducer for High-Efficiency Tumor Immunotherapy.

Pyroptosis possesses potent antitumor immune activity, making pyroptosis inducer development a promising direction for tumor immunotherapy. Persistent luminescence nanoparticles (PLNPs) are highly sensitive optical probes extensively employed in tumor diagnosis and therapy. However, a pyroptosis inducer based on PLNPs has not been reported yet. Herein, polyethylene glycol-poly lactic acid-co-glycolic acid (PEG-PLGA: PP) modified biodegradable CaS:Eu2+ (CSE@PP) PLNPs are synthesized as a pyroptosis inducer for tumor immunotherapy for the first time. The synthesized CSE@PP possesses biowindow persistent luminescence (PersL) and pH-responsive degradation properties, allowing it to remain stable under neutral pH but degrade when exposed to weak acid (pH< 6.5). During degradation within the tumor, CSE@PP constantly releases H2S and Ca2+ while its PersL gradually fades away. Thus, the PersL signal can self-monitor H2S and Ca2+ release. Furthermore, the released H2S and Ca2+ result in mitochondrial dysfunction and the inactivation of reactive oxygen species scavenging enzymes, synergistic facilitating intracellular oxidative stress, which induces caspase-1/GSDM-D dependent pyroptosis and subsequent antitumor immune responses. In a word, it is confirmed that CSE@PP can self-monitor H2S and Ca2+ release and pyroptosis-mediated tumor Immunotherapy. This work will facilitate biomedical applications of PLNPs and inspire pyroptosis-induced tumor immunotherapy.

Dual co-doping strategy for prolonged luminescence in laser-sintered BaAl2O4:Eu2+, RE3+ ceramics

This work reports on the influence of co-doping on the luminescence and persistent luminescence properties of BaAl2O4 (BaO·Al2O3) laser-sintered ceramics. The samples were doped with Eu and doubly co-doped with different rare earths (Dy, Er, Nd, Pr, and Tm) followed by laser-sintering without an atmospheric control, at a power density of 1.6 W/mm2. All sintered ceramics contained the hexagonal BaAl2O4 phase and had a homogeneous microstructure. A photoluminescence emission band centered at 495 nm was observed, which was due to the 4f65 d1 → 4f7 Eu2+ transition in the BaAl2O4 matrix. The persistent luminescence emission was monitored for 15 min after charging at 345 nm for 3 min. The combination of Nd and Dy co-doping led to substantial improvements in decay time and persistent luminescence intensity compared to individual co-doping. These results suggested that the two co-dopants interacted by modifying the trap configurations in the BaAl2O4 matrix.

Chromium-doped zinc gallate: Impact of Sn4+ co-doping on the persistent luminescence properties at the nanoscale applied to bio-imaging

Persistent luminescence (PersL) nanoparticles emit a signal that lasts long after the excitation has ended, enabling highly sensitive bioimaging without background noise. By using UV light as the excitation source prior to injection, a strong PersL signal can be detected in vivo before disappearing within a few hours. For long-term imaging, we have shown in the past that visible LED can be used to re-excite ZnGa1.995Cr0.005O4 (ZGO:Cr3+) nanoparticles in vivo, producing a signal intensity that is, however, much lower compared to the signal obtained after the UV pre-excitation method. This lower signal intensity of the nanoprobe when using a visible LED may prevent its detection in some cases. Herein, we report an improvement in visible LED excitation efficiency using PersL Zn1.33Ga1.335Cr0.005Sn0.33O4 (ZGSO:Cr3+) nanoparticles. We fully compared ZGSO:Cr3+ and the original ZGO:Cr nanoparticles in terms of structure, optical properties and bio-imaging potential. Co-doping with tin strongly increases persistent luminescence, even at the nanoscale. In vivo imaging results showed that ZGSO:Cr3+ exhibited an approximately 3-fold signal enhancement over ZGO:Cr3+ using UV pre-excitation. More interestingly, when using LED excitation, the signal intensity of ZGSO: Cr3+ is more than 10 times higher than that of ZGO:Cr3+, making ZGSO nanoparticles much easier to detect. ZGSO:Cr nanoparticles can be surface-modified with PEG to produce nanoprobes with much longer residence time in blood. This unique comparison between the two compositions makes ZGSO:Cr3+ a more effective imaging diagnostic probe than the original ZGO:Cr3+ nanoparticles, opening up new applications for in vivo diagnostics.

Pr3+-Doped Lithium Niobate and Sodium Niobate with Persistent Luminescence and Mechano-Luminescence Properties

In this research, a comprehensive series of Pr3+-doped lithium niobate and sodium niobate materials were obtained at different temperatures via solid-state sintering, and their structures and properties were compared. NaNbO3: 0.75% Pr3+ phosphors were synthesized by sintering at 1150 °C for 2 h and emitted red persistent luminescence for more than 1200 s, peaking at 612 nm under UV excitation, which was a typical long persistent luminescence phenomenon. Furthermore, the sample glowed when pressurized, and a red bright luminescence which lasted for several seconds was visible to the naked eye. This was a typical mechanical luminescence phenomenon of samples under mechanical stress, directly converting mechanical energy into light energy. It was determined that NaNbO3:Pr3+ and LiNbO3:Pr3+ both possess multimode luminescence. Owing to their red long persistent luminescence (LPL) and mechano-luminescence (ML) properties, Pr3+ phosphors can be employed in fields, such as display technologies, stress sensing, structural damage detection, and other complex applications.

Chemical tuning of photo- and persistent luminescence of Cr3+-activated β-Ga2O3 by alloying with Al2O3 and In2O3

An effect of alloying of the monoclinic β-Ga2O3 with Al2O3 and In2O3 on the photoluminescent, thermoluminescent and persistent luminescent properties of Cr3+ ions has been comprehensively investigated. For this purpose, various series of Cr3+ and Ca2+ co-doped microcrystalline phosphors were synthesized by the solution combustion method, including pseudobinary compounds like (Ga-Al)2O3 with up to 20 % Al and (Ga-In)2O3 with up to 50 % In as well as pseudoternary compounds (Ga-Al-In)2O3 with balanced proportion of Al, Ga and In. The phase composition and crystal structure of the obtained materials were examined by X-ray powder diffraction technique. Detailed luminescence studies were conducted for the (Ga-Al)2O3 and (Ga-In)2O3 compounds which exhibited a single-phase monoclinic structure. Low-temperature and time-resolved photoluminescence investigations of the Cr-doped pseudobinary compounds unveiled several types of Cr3+ centres, attributed to the Al-, Ga- and In-centred octahedra in the studied alloys. The obtained results underscore the benefit of bandgap engineering through alteration in the host lattice chemical composition for efficient tuning of the thermoluminescent and persistent luminescent properties of the near-infrared-emitting β-Ga2O3:Cr based phosphors. Furthermore, it was demonstrated that modification of the chemical composition of the host lattice also adjusts the thermometric performance of the studied phosphors. Indeed, the specific sensitivity of the β-Ga2O3:Cr3+ decay time luminescence thermometer showed nearly twofold enhancement when the host lattice was alloyed with 30 % of In2O3.

Trap engineering in LiInSi2O6:Cr,Pr by excess cristobalite silica for X-ray activated near-infrared persistent luminescence imaging in vivo

Chromium-doped persistent luminescence nanoparticles (PLNPs) have promising biomedical applications in X-ray charged near-infrared (NIR) luminous imaging. The persistent luminescence (PersL) property was usually adjusted by co-doping with other ions. Impurity phases were thought to be adverse to the PersL. In this study, a composite material, LiInSi2O6:Cr,Pr·2SiO2 (LICP-S), was synthesized with a PersL peak at 800 nm after being charged by 1 Gy X-ray while LiInSi2O6:Cr (LIC) and LiInSi2O6:Cr,Pr (LICP) possessed no or very weak PersL. Distinctively, excess metastable cristobalite silica was found essential for the much more intense PersL of LICP-S than LICP and LIC. Thermostimulated luminescence spectra studies indicated that cristobalite adjusted the Pr-related traps from deep traps to shallow ones, which facilitated the room temperature PersL. The low dose X-ray charged PersL of LICP-S was applied to demonstrate the luminous labeling of a medical silicone prosthesis that was supposed to be imbedded in body for years via X-ray activated PersL imaging in vitro and in vivo. This work not only provides a kind of PLNPs with 800 nm emission suitable for low dose X-ray activation, but also an unusual strategy for trap engineering in PersL materials by designing multi-phase composites.

Study on preparation, optical properties and mechanism of Zn2SnO4:Cr3+ with high NIR luminescence intensity

In this work, Zn2SnO4:xCr3+ with high near-infrared luminescence intensity (broad emission centered at 800 nm and sharp emission at 703 nm) were successfully prepared by high temperature solid state method. Measurements indicated that the samples exhibited obvious photoluminescence as well as persistent luminescence properties. The results of X-ray diffraction indicated that high temperature facilitated the entry of Cr3+ into the Zn2SnO4 crystal lattice and formed replacement doping and promoted the luminescence efficiency of the samples. And, under the condition of 1450 °C and 0.002 at% Cr3+ concentration, sample with optimum NIR fluorescence properties was prepared. In the high-temperature sintering process, many defects of Zn2SnO4 were generated, which effectively promoted the formation of vacancies. The energy levels of these lattice defects (trap energy levels) facilitated the sub-stable trapping of electrons and produce afterglow properties. Analysis of luminescence mechanism reveals that the broad emission band centered at 800 nm and the sharp emission peak at 703 nm were derived from the energy level transitions of 4T2(4F)→4A2 and 2E→4A2 of Cr3+, respectively. Though, the long afterglow luminescence duration of Zn2SnO4:Cr3+ needs to be further improved compared with gallate-based NIR phosphors, Zn2SnO4:Cr3+ do have a promising application in bio-imaging due to its special NIR emission range.

Persistent luminescence of commercial TLD-100 dosimeter: Using shallow traps for radiation dosimetry

This work reports the persistent luminescence (PersL) properties of the commercial LiF:Mg,Ti (TLD-100) dosimeter and its performance in dosimetry applications. The thermoluminescence (TL) glow curve of the TLD-100 exhibits a peak at 96 °C that rapidly vanishes at room temperature, enabling the PersL phenomenon. The TLD-100 was exposed to beta particle irradiation within in the range of 0.22–32 Gy. The resulting PersL intensity was measured and found to increase as the irradiation dose increased. Notably, there was no saturation of the PersL intensity within this dose range with linear dependence from 0.55 to up 32 Gy. The TLD-100 showed good repeatability with a deviation of 0.1% after seven irradiation-readout cycles for twenty irradiations. The calculated lower detection limit was 2 mGy. Our results indicate that the TLD-100 can be used as a PersL and TL dosimeter for dosimetry applications, with the advantages of fast post-irradiation measurements.

Exploring the luminescence of tin‐incorporated nickel‐sensitized lithium gallate short‐wave‐infrared phosphors

AbstractA series of Ni2+‐sensitized LiGa5O8 nanocrystals doped with varying amounts of Sn4+ were synthesized via a high‐temperature solid‐state method. X‐ray diffraction and scanning electron microscopy were employed to investigate the microstructure of the LiGa5O8 host, and optical spectroscopy was used to examine the effects of Sn4+ addition on the emission spectra and persistent luminescence (PersL) properties, which indicated a homogeneous distribution of the constituent elements in the phosphor. The Sn4+ incorporation led to an approximately sixfold enhancement of photoluminescence intensity at room temperature and decrease in the energy transition of Ni2+(3T2(3F)→3A2(3F)), which resulted in ∼65 nm bathochromic shift in the photoluminescence emission maxima. However, the addition of Sn4+ dopant led to a decrease in the quantum yield of luminescence compared to that of the original phosphor. Temperature‐dependent thermoluminescence measurements revealed that doping of LiGa5O8 with Sn4+ interfered with the Ni2+ trap centers. Moreover, Ni2+‐sensitized Sn4+‐doped LiGa5O8 nanocrystals exhibited an afterglow effect that persisted for up to 300 s.

Color-tunable persistent luminescence phosphor for multimode dynamic anti-counterfeiting

Using a solid-state approach, the persistent luminescence property in sodium yttrium silicate which was single-doped or co-doped by europium or cerium was studied. The orthorhombic structure with the space group P212121 could be indexed to all samples, according to X-ray powder diffraction. The luminescence characteristics of these phosphors, including photoluminescence, luminescence degradation, and temperature-dependent emission, were systematically investigated. Under UV (∼365 nm) irradiation, blue/green emissions with broad bands peaking at 450/510 nm attributed to the characteristic 5d→4f/4f65d→4f7 transitions of Ce3+/Eu2+ could be observed in Na3LuSi3O9:Ce3+ and Na3LuSi3O9:Eu2+, respectively. Moreover, blue and green persistent luminescence was also observed in Ce3+ or Eu2+ single-doped samples. Thermoluminescence curve of Na3LuSi3O9:Eu2+, Ce3+ reveals that Na3LuSi3O9:Ce3+ and Na3LuSi3O9:Eu2+ have similar trap distribution. Tunable persistent luminescence can be realized via ratio control of Ce3+ and Eu2+. A possible afterglow mechanism was presented and discussed. The prepared materials have the potential of multimode dynamic luminescence, because they are highly sensitive to the composition, the excitation wavelength, and the detecting time. The outstanding abilities of Na3LuSi3O9:Ce3+, Eu2+ demonstrate the practical capability of this material for fingerprint identification and anti-counterfeiting.

Optical Bioimaging and Therapy

Optical Bioimaging and Therapy

Polychromatic long persistent luminescence of CaAlSiN3:Ln (Ln=Eu, Ce, Dy, Pr, Tb, Gd, Sm, Tm, Nd) phosphors prepared by combustion synthesis

Although the phosphors based on CaAlSiN3 (e.g. CaAlSiN3:Eu2+, CaAlSiN3:Ce3+) have been extensively studied in phosphor-converted white light emitting diodes (w-LEDs) due to its outstanding luminescent properties, there have been rare literatures on the persistent luminescence of CaAlSiN3 except for the red afterglow emission of CaAlSiN3:Eu2+. In our work, a series of CaAlSiN3:Ln (Ln=Eu, Ce, Dy, Pr, Tb, Gd, Sm, Tm, Nd) phosphors have been successfully prepared by combustion synthesis and their polychromatic visible afterglow emissions were observed. The long persistent luminescent properties of the phosphors were studied systematically, among which, CaAlSiN3:Eu2+ and CaAlSiN3:Ce3+ show the best red and yellow long persistent luminescence with persistent time of 4980 s and 4860 s at the 0.32 mcd/m2 threshold value, respectively, and other phosphors show relatively weak persistent luminescence performance with other afterglow emission colors. Moreover, Eu2+, Ce3+ co-doped CaAlSiN3 were synthesized to enhance the red long persistent luminescence performance, whose persistent time has reached 6300 s due to a more appropriate trap depth distribution of 0.83–0.9 eV compared with Eu2+ and Ce3+ singly doped CaAlSiN3. We believe that this work is of significance for extending the studies of CaAlSiN3 system to a host material for polychromatic long persistent luminescence.

A series of zinc coordination compounds showing persistent luminescence and reversible photochromic properties via charge transfer

Long persistent luminescence materials have wide application prospects in the fields of optical communication, sensors, and anticounterfeiting. Recently, some researchers have proved the feasibility of charge transfer effect in the construction of visible light excited room temperature phosphorescence (RTP) materials. However, materials with electronic effects require elaborate design to exhibit long-lived phosphorescence. Herein, a series of coordination compounds based on viologen ligand HL⋅Cl (4-carboxybenzyl)-4,4′-bipyridinium chloride) and Zn2+ with benzoic acid derivatives (o-, m-, p-phthalic acid) were reported. They exhibit not only reversible photochromic properties, but also long-lived persistent phosphorescence. Three complexes possess different structures through different auxiliary ligands with different optical physical properties. Complex 1 exhibits dynamic phosphorescence emission at low temperatures. Interestingly, we synthesized the first viologen complex (complex 2) with excitation wavelength dependent fluorescence, and the emission color gradually changed from blue to red with the increase of excitation wavelength. In addition, the applications of three complexes in data encryption and anticounterfeiting are further demonstrated. This work not only presents coordination compounds with dynamic afterglow materials, excitation wavelength- and time-dependent emission properties, but also provides a new strategy for the charge transfer effect in visible light-excited RTP materials.

A new insight into the mechanism of persistent luminescence phosphors SrS: Eu2+, Pr3+

The red persistent luminescence phosphors SrS: , (x = 0∼0.001, y = 0∼0.003) were synthesized by the solid-state reaction method in a weak reducing atmosphere of active carbon. The synthetic parameters, photoluminescence characteristics, and dynamic properties of thermoluminescence of the phosphors were studied systematically. According to the results of photoluminescence spectra of SrS: , , the energy level scheme of the phosphors was confirmed quantitatively. Based on the studies of the scanning electron microscope (SEM), UV-Visible absorbance spectra, afterglow decay curves, thermoluminescence(TL) spectra, and X-ray photoelectron spectroscopy (XPS) spectra, we found that the SrS: , (SSEP) phosphor presented the best persistent luminescence property, which mainly resulted from its outstanding absorbance characteristic, deeper depth of () defects, and fewer defect concentration belonging to the higher-order kinetics. Those comprehensive results deduced that a complex defect ()- should present in the Eu2+ doping phosphors, and the Pr3+ doping will produce defects, which can suppress the formation of () defects and increase their energy depth.

Persistent Luminescence Zn2GeO4:Mn2+ Nanoparticles Functionalized with Polyacrylic Acid: One-Pot Synthesis and Biosensing Applications.

Zinc germanate doped with Mn2+ (Zn2GeO4:Mn2+) is known to be a persistent luminescence green phosphor with potential applications in biosensing and bioimaging. Such applications demand nanoparticulated phosphors with a uniform shape and size, good dispersibility in aqueous media, high chemical stability, and surface-functionalization. These characteristics could be major bottlenecks and hence limit their practical applications. This work describes a one-pot, microwave-assisted hydrothermal method to synthesize highly uniform Zn2GeO4:Mn2+ nanoparticles (NPs) using polyacrylic acid (PAA) as an additive. A thorough characterization of the NPs showed that the PAA molecules were essential to realizing uniform NPs as they were responsible for the ordered aggregation of their building blocks. In addition, PAA remained attached to the NPs surface, which conferred high colloidal stability to the NPs through electrostatic and steric interactions, and provided carboxylate groups that can act as anchor sites for the eventual conjugation of biomolecules to the surface. In addition, it was demonstrated that the as-synthesized NPs were chemically stable for, at least, 1 week in phosphate buffer saline (pH range = 6.0-7.4). The luminescence properties of Zn2GeO4 NPs doped with different contents of Mn2+ (0.25-3.00 mol %) were evaluated to find the optimum doping level for the highest photoluminescence (2.50% Mn) and the longest persistent luminescence (0.50% Mn). The NPs with the best persistent luminescence properties were photostable for at least 1 week. Finally, taking advantage of such properties and the presence of surface carboxylate groups, the Zn2GeO4:0.50%Mn2+ sample was successfully used to develop a persistent luminescence-based sandwich immunoassay for the autofluorescence-free detection of interleukin-6 in undiluted human serum and undiluted human plasma samples. This study demonstrates that our persistent Mn-doped Zn2GeO4 nanophosphors are ideal candidates for biosensing applications.