Emission Of Nanoparticles Research Articles

Solid nanoparticle and gaseous emissions of a diesel engine with a diesel particulate filter and use of a high-sulphur diesel fuel and a medium-sulphur diesel fuel

High-sulphur and medium-sulphur diesel fuels are still used in several countries. Although diesel particulate filter technology for on-road diesel engines has existed since 1989, the availability of high-sulphur and medium-sulphur diesel fuels in the market causes delays in the use of catalysed filter technologies. However, the situation in places such as Tehran is considered unhealthy because of particles and black carbon, and full distribution of ultra-low-sulphur diesel is awaited eagerly. The purpose of this study is to investigate the effect of the sulphur content in fuels on the gaseous and solid exhaust emissions of a 220 kW Euro II engine equipped with a sintered metal active–passive filter, focusing on the regeneration phenomenon. The results show that the efficiency for filtering the maximum number of particles was 99.9% and that the average was above 99% for steady-state operating conditions for both high-sulphur diesel (7700 ppm) and medium-sulphur diesel (229 ppm). The removal efficiency of the particle mass was low in the case of high-sulphur diesel owing to the sulphate condensate collection effect as the result of using a non-heated sample line. During regeneration, the number of particles increased in comparison with that in the filtration phase but the total number of emitted particles was less than the engine baseline value. The results for both fuels were the same, and the only measurable difference was the high sulphur dioxide production in the high-sulphur diesel during regeneration. This study demonstrates the potential of this type of filter technology for the effective removal of solid particles independent of the sulphur content of the fuel. With the exception of the decrease in the removal efficiency of the particle mass and the high sulphur dioxide production, no other notable difference was observed to be caused by the change in the sulphur content of the diesel fuel.

Highly blue emission of ZnO nanoparticles embedded in a SiO2 matrix

The main drawbacks of fluorescent ZnO nanoparticles in practical optoelectronic applications are fast particle growth and agglomeration in water, causing a periodic decrease of light emission intensity. In this work, ZnO nanoparticles were successfully embedded within a silica matrix to prevent their agglomeration. The ZnO NPs were synthesized by the polyol method, using ethylene glycol and glycerol in sizes ranging from 5–6 nm. The as-obtained ZnO particles were dispersed in an amorphous silica matrix under three different ZnO:SiO2 molar ratios: 20:80, 15:85 and 10:90. With the aim of enhancing the luminescent properties of the ZnO@SiO2 composites, various annealing treatments in the range of 150–210 °C were carried out. The chemical analyses of the bare ZnO and the composites were carried out by Fourier transform infrared spectroscopy, which confirmed the presence of functional groups attached to the ZnO surface. By means of thermogravimetric analysis, it was determined that the evaporation of solvents shifted to lower temperatures (180 °C) when silica was added to the ZnO colloidal solution. By means of photoluminescence, a bright blue emission, centered at 440 nm, was observed in all of the samples, even at high temperatures (i.e., 210 °C); only a red shift of 20 nm was observed. Interestingly, the emission intensity of the sample 20:80, when annealed at 170 °C for 4 h, was enhanced 2.6 times, compared to the bare ZnO.

Spectroscopic characterization and docking studies of ZnO nanoparticle modified with BSA

Nanoparticles (NP) into a biological environment are an interesting topic for diagnosis and therapy in applications for medicine or environment and the knowledge about this interaction is important from the perspective of safe use of nanomaterials. In the current study, we characterized the type of interaction and the orientation of bovine serum albumin (BSA) adsorbed on ZnO nanoparticle surfaces as a function of size, using molecular docking. To probe experimentally different theoretical hypothesis about the interaction, ZnO-NPs were prepared in aqueous solution, and then were bioconjugated with BSA. Transmission electron microscopy (TEM) and Raman spectroscopy confirm the spherical shape of NP and the irreversible adsorption of BSA on NP surface. Raman and Infrared spectroscopy (FTIR) reveal that BSA interaction with ZnO nanoparticle produced a conformational rearrangement into protein, observing changes in Tyr and Trp environment, a minor percentage of α-helix structure and a more extended chain. The fluorescence analysis demonstrated that when BSA concentration higher than 30μM is used the signal due to the self-oligomerization of protein overlaps with the ZnO nanoparticle emission. The results predicted that the most probable interaction site is near to domain IB and IIA and ionic interactions are the major responsible for the binding. Thermal stability studies reveals that the denaturalization temperature of BSA increase from 57°C to 65°C in presence of ZnO NP and their esterase-like activity was improved.

Studies on Opuntia dilenii haw mediated multifunctional ZnFe2O4 nanoparticles: Optical, magnetic and catalytic applications

The sustainable and eco friendly green synthesis report on the use of plant extract alternate to chemicals has been discussed. In this work, opuntia plant extract is used as a natural reagent to synthesize nanoparticles. Herein, we demonstrate two methods namely, conventional and microwave method for the synthesis of nanoparticles using plant extract, due to its easy handling and bio-compatibility. Both the methods were carried out under the same conditions to explore the comparison of the data. Various characterization techniques were used to determine the crystallinity, crystallite size, lattice parameter, morphology, elemental composition, band gap energy, emission, saturation magnetization, and coercivity of the as-synthesized nanoparticles. A brief discussion about the importance of using the plant extract as well as the importance of microwave heating were discussed and summarized. The phase identification was examined using XRD analysis, which showed the formation of single and pure phase without any post annealing in microwave heating method. The formation of pure phase ferrites is also confirmed by Fourier Transform Infrared Spectroscopy (FTIR). The surface morphology of ZnFe2O4 nanoparticles showed spherical shape and the size difference depends upon the method of synthesis. EDX analysis confirms the phase-purity of the as-synthesized nanoparticles. UV–Vis DRS of the as-obtained nanospheres exhibited the absorbance in the visible region. VSM analysis showed that the sample prepared by microwave technique exhibited better magnetic behaviour at room temperature than that of the ones prepared by the conventional heating method. The microwave heating technique produces nano-ferrites with high yield, low crystallite size, uniform morphology, and good absorption properties than the conventional heating method. Zinc ferrites were used in the catalytic reaction for the oxidation of glycerol into formic acid. The catalyst exhibit good catalytic performance and better selectivity of formic acid throughout the reaction. The plausible mechanism has been proposed.

Characterization of Emissions from a Desktop 3D Printer

Summary3D printers are currently widely available and very popular among the general public. However, the use of these devices may pose health risks to users, attributable to air‐quality issues arising from gaseous and particulate emissions in particular. We characterized emissions from a low‐end 3D printer based on material extrusion, using the most common polymers: acrylonitrile‐butadiene‐styrene (ABS) and polylactic acid (PLA). Measurements were carried out in an emission chamber and a conventional room. Particle emission rates were obtained by direct measurement and modeling, whereas the influence of extrusion temperature was also evaluated. ABS was the material with the highest aerosol emission rate. The nanoparticle emission ranged from 3.7·108 to 1.4·109 particles per second (# s−1) in chamber measurements and from 2.0·109 to 4.0·109 # s−1in room measurements, when the recommended extruder temperature was used. Printing with PLA emitted nanoparticles at the rate of 1.0·107 # s−1 inside the chamber and negligible emissions in room experiments. Emission rates were observed to depend strongly on extruder temperature. The particles’ mean size ranged from 7.8 to 10.5 nanometers (nm). We also detected a significant emission rate of particles of 1 to 3 nm in size during all printing events. The amounts of volatile organic and other gaseous compounds were only traceable and are not expected to pose health risks. Our study suggests that measures preventing human exposure to high nanoparticle concentrations should be adopted when using low‐end 3D printers.

Role of epithelial-mesenchymal transition (EMT) and fibroblast function in cerium oxide nanoparticles-induced lung fibrosis

The emission of cerium oxide nanoparticles (CeO2) from diesel engines, using cerium compounds as a catalyst to lower the diesel exhaust particles, is a health concern. We have previously shown that CeO2 induced pulmonary inflammation and lung fibrosis. The objective of the present study was to investigate the modification of fibroblast function and the role of epithelial-mesenchymal transition (EMT) in CeO2-induced fibrosis. Male Sprague-Dawley rats were exposed to CeO2 (0.15 to 7mg/kg) by a single intratracheal instillation and sacrificed at various times post-exposure. The results show that at 28days after CeO2 (3.5mg/kg) exposure, lung fibrosis was evidenced by increased soluble collagen in bronchoalveolar lavage fluid, elevated hydroxyproline content in lung tissues, and enhanced sirius red staining for collagen in the lung tissue. Lung fibroblasts and alveolar type II (ATII) cells isolated from CeO2-exposed rats at 28days post-exposure demonstrated decreasing proliferation rate when compare to the controls. CeO2 exposure was cytotoxic and altered cell function as demonstrated by fibroblast apoptosis and aggregation, and ATII cell hypertrophy and hyperplasia with increased surfactant. The presence of stress fibers, expressed as α-smooth muscle actin (SMA), in CeO2-exposed fibroblasts and ATII cells was significantly increased compared to the control. Immunohistofluorescence analysis demonstrated co-localization of TGF-β or α-SMA with prosurfactant protein C (SPC)-stained ATII cells. These results demonstrate that CeO2 exposure affects fibroblast function and induces EMT in ATII cells that play a role in lung fibrosis. These findings suggest potential adverse health effects in response to CeO2 nanoparticle exposure.

Amplified stimulated emission in upconversion nanoparticles for super-resolution nanoscopy.

Lanthanide-doped glasses and crystals are attractive for laser applications because the metastable energy levels of the trivalent lanthanide ions facilitate the establishment of population inversion and amplified stimulated emission at relatively low pump power. At the nanometre scale, lanthanide-doped upconversion nanoparticles (UCNPs) can now be made with precisely controlled phase, dimension and doping level. When excited in the near-infrared, these UCNPs emit stable, bright visible luminescence at a variety of selectable wavelengths, with single-nanoparticle sensitivity, which makes them suitable for advanced luminescence microscopy applications. Here we show that UCNPs doped with high concentrations of thulium ions (Tm3+), excited at a wavelength of 980 nanometres, can readily establish a population inversion on their intermediate metastable 3H4 level: the reduced inter-emitter distance at high Tm3+ doping concentration leads to intense cross-relaxation, inducing a photon-avalanche-like effect that rapidly populates the metastable 3H4 level, resulting in population inversion relative to the 3H6 ground level within a single nanoparticle. As a result, illumination by a laser at 808 nanometres, matching the upconversion band of the 3H4 → 3H6 transition, can trigger amplified stimulated emission to discharge the 3H4 intermediate level, so that the upconversion pathway to generate blue luminescence can be optically inhibited. We harness these properties to realize low-power super-resolution stimulated emission depletion (STED) microscopy and achieve nanometre-scale optical resolution (nanoscopy), imaging single UCNPs; the resolution is 28 nanometres, that is, 1/36th of the wavelength. These engineered nanocrystals offer saturation intensity two orders of magnitude lower than those of fluorescent probes currently employed in stimulated emission depletion microscopy, suggesting a new way of alleviating the square-root law that typically limits the resolution that can be practically achieved by such techniques.

Laser-induced atomic emission of silicon nanoparticles during laser-induced heating.

The temporal luminescence behavior of silicon atoms during and after laser-heating of gas-borne silicon nanoparticles was investigated. Silicon nanoparticles were formed in the exhaust stream of a microwave plasma reactor at 100 mbar. The observed prompt atomic line intensities correspond with thermal excitation of the evaporated species. A prompt signal at 251.61 and 288.15 nm originating from the 3s23p2→3s23p4s transitions showed a lifetime of 16 ns that matches the documented excited-state lifetime for the respective transitions. A secondary delayed signal contribution with similar peak intensities was observed commencing approximately 100-300 ns after the laser pulse and persisting for hundreds of nanoseconds. This signal contribution is attributed to electron impact excitation or recombination after electron impact ionization of the silicon evaporated as a consequence of the laser heating of the plasma leading to non-thermal population of electronically excited silicon. The observations support a nanoparticle evaporation model that can be used to recover nanoparticle sizes from time-resolved LII data.

Assessment of airborne nanoparticles present in industry of aluminum surface treatments

ABSTRACTConventional industrial processes are emission sources of unintended nanoparticles which are potentially harmful for the environment and human health. The aim of this study is to assess airborne nanoparticle release from aluminum surface treatment processes in various workplaces. Two direct reading instruments, a scanning mobility particle sizer to measure size distribution and a nanoparticle surface area monitoring to measure the surface area of particles deposited in the human lung, were employed to perform area monitoring.The lacquering paint was the process which released the highest concentration of particles from 10–487 nm (7.06 × 106 particles/cm3). The lacquering baths process emitted particles of the largest average size (76.9 nm) and the largest surface area deposited in the human lung (167.4 µm2/cm3). Conversely, the anodizing bath process generated particles of the smallest average size (44.3 nm) and the lowest human lung-deposited surface area (1.2 µm2/cm3). The total number of particles and the surface area can only be fairly correlated for environments in which the surface area presented higher values. The transmission electron microscopy analysis confirmed the presence of aluminum oxide particles of different dimensions near the LB and AB areas and polymeric-based particles near the LP areas.The findings of this study indicated that lacquering and anodizing surface treatments are indeed responsible for the emission of airborne nanoparticles. It also highlights the importance of control strategies as a means of protecting workers' health and environment.

Tailoring of size, emission and surface chemistry of germanium nanoparticles via liquid-phase picosecond laser ablation

We report on the tailoring of the size and emission of germanium nanoparticles via liquid-phase picosecond laser ablation.

A soluble conjugated porous organic polymer: efficient white light emission in solution, nanoparticles, gel and transparent thin film.

A tetraphenylcyclopentadiene based multifunctional, solution processable, fluorescent, ultramicroporous polymer exhibiting high hydrogen uptake was employed for encapsulation of dyes to obtain enhanced white light emission in solution, nanoparticles, gel and transparent thin film. Hybrid nanoparticles showed a quantum yield of 35% with a high color rendering index.

Energy and charge transfer cascade in methylammonium lead bromide perovskite nanoparticle aggregates.

Highly photoluminescent hybrid lead halide perovskite nanoparticles have recently attracted wide interest in the context of high-stake applications, such as light emitting diodes (LEDs), light emitting transistors and lasers. In addition, they constitute ideal model systems to explore energy and charge transport phenomena occurring at the boundaries of nanocrystalline grains forming thin films in high-efficiency perovskite solar cells (PSCs). Here we report a complete photophysical study of CH3NH3PbBr3 perovskite nanoparticles suspended in chlorobenzene and highlight some important interaction properties. Colloidal suspensions under study were constituted of dispersed aggregates of quasi-2D platelets of a range of thicknesses, decorated with 3D-like spherical nanoparticles. These types of nanostructures possess different optical properties that afford a handle for probing them individually. The photophysics of the colloidal particles was studied by femtosecond pump-probe spectroscopy and time-correlated single-photon counting. We show here that a cascade of energy and exciton-mediated charge transfer occurs between nanostructures: upon photoexcitation, localized excitons within one nanostructure can either recombine on a ps timescale, yielding a short-lived emission, or form charge-transfer states (CTSs) across adjacent domains, resulting in longer-lived photoluminescence in the millisecond timescale. Furthermore, CTSs exhibit a clear signature in the form of a strong photoinduced electroabsorption evidenced in femtosecond transient absorption measurements. Charge transfer dynamics at the surface of the nanoparticles have been studied with various quenchers in solution. Efficient hole transfer to N,N,N',N'-tetrakis(4-methoxyphenyl)benzidine (MeO-TPD) and 1,4-bis(diphenyl-amino)benzene (BDB) donors was attested by the quenching of the nanoparticles emission. The charge transfer rate was limited by the organic layer used to stabilize the nanoparticles, which acted as a wide spacer between reactants. The forward charge transfer was found to take place in the sub-microsecond time-scale in competition with slow carrier recombination, while back transfer was shown to occur with a time-constant τ = 25 ms.

Investigations on emission of nanoparticulates under free acceleration test condition

Considering the dangerous effects of ultrafine particles and air quality concerns worldwide, this work investigates the possibility of identifying operating criterion over which there is a greater tendency of formation of nanoparticle emissions in Diesel engines. The objective of this analysis is to study the emission of particles in the size range of 10 nm to 700 nm by subjecting a diesel engine to free acceleration tests. Details on the emission characteristics such as Particulate number, Particle mass, Particle diameter and the Lung deposition surface area in the size range 10–700 nm during specific conditions of acceleration and deceleration has been studied in this work. Maximum effect of the particles occurs during rapid acceleration. At idle speed, the Particle number, particle mass and Lung deposition surface area are very low indicating that the nanoparticle formation is low at idle condition. With increase in Particulate number, there is an increase in the Particulate mass and the LDSA. The particulate diameter is distributed across the PN range.

Investigations on emission of nanoparticulates under free acceleration test condition

Considering the dangerous effects of ultrafine particles and air quality concerns worldwide, this work investigates the possibility of identifying operating criterion over which there is a greater tendency of formation of nanoparticle emissions in Diesel engines. The objective of this analysis is to study the emission of particles in the size range of 10 nm to 700 nm by subjecting a diesel engine to free acceleration tests. Details on the emission characteristics such as Particulate number, Particle mass, Particle diameter and the Lung deposition surface area in the size range 10–700 nm during specific conditions of acceleration and deceleration has been studied in this work. Maximum effect of the particles occurs during rapid acceleration. At idle speed, the Particle number, particle mass and Lung deposition surface area are very low indicating that the nanoparticle formation is low at idle condition. With increase in Particulate number, there is an increase in the Particulate mass and the LDSA. The particulate diameter is distributed across the PN range.

A one-pot synthesis of water soluble highly fluorescent silica nanoparticles.

We report a one-pot synthesis of water dispersible fluorescent silica nanoparticles (NPs) functionalized with terminal amine groups, starting from silicon tetrabromide (SiBr4) and aminopropyltriethoxy silane (APTES). The NPs range from 1 to 2 nm in diameter, and exhibit an intense blue emission with a quantum yield (QY) of around 34% in water. They were characterized using XRD, XPS, TEM and FTIR spectroscopy for structural analysis. A tentative mechanism explaining the origin of the NPs emission in the blue region is presented based on the distinctive features of their low temperature photoluminescence (PL), photoluminescence excitation (PLE) spectrum and time correlated single photon counting lifetime decay profiles. The outstanding PL QY and photostability of the NPs, together with their water dispersibility and biocompatibility, constitute a unique set of properties among existing silica NPs and enable the application of the NPs in various fields.

Amplified Fluorescence from Polyfluorene Nanoparticles with Dual State Emission and Aggregation Caused Red Shifted Emission for Live Cell Imaging and Cancer Theranostics.

A newly synthesized polyfluorene derivative with pendant di(2-picolyl)amine (PF-DPA) shows dual state emission and aggregation caused red shifted emission that was utilized for cell imaging and cancer theranostics. PF-DPA was nontoxic to normal cells but showed cytotoxicity against cancer cells, suggesting its utility for cancer therapy. PF-DPA exhibits a large and unique red shifted emission at 556 nm at higher water ratio of THF:H2O (10:90) due to the formation of polymer nanoparticles or PDots spontaneously by intra- and intermolecular self-assembly induced aggregation. Dual state emission and aggregation caused red shifted emission (>100 nm) in PF-DPA homopolymer nanoparticles is very unique and attributed to the combined effect of intramolecular planarization and J-type aggregate formation in the PDots (25 ± 5 nm). The PF-DPA PDots exhibit bright green and orange fluorescence with exceptional live cell imaging properties and potential applications in cancer theranostics due to their selective cytotoxic nature toward cancer cells.

Bioethanol Blending Reduces Nanoparticle, PAH, and Alkyl- and Nitro-PAH Emissions and the Genotoxic Potential of Exhaust from a Gasoline Direct Injection Flex-Fuel Vehicle.

Bioethanol as an alternative fuel is widely used as a substitute for gasoline and also in gasoline direct injection (GDI) vehicles, which are quickly replacing traditional port-fuel injection (PFI) vehicles. Better fuel efficiency and increased engine power are reported advantages of GDI vehicles. However, increased emissions of soot-like nanoparticles are also associated with GDI technology with yet unknown health impacts. In this study, we compare emissions of a flex-fuel Euro-5 GDI vehicle operated with gasoline (E0) and two ethanol/gasoline blends (E10 and E85) under transient and steady driving conditions and report effects on particle, polycyclic aromatic hydrocarbon (PAH), and alkyl- and nitro-PAH emissions and assess their genotoxic potential. Particle number emissions when operating the vehicle in the hWLTC (hot started worldwide harmonized light-duty vehicle test cycle) with E10 and E85 were lowered by 97 and 96% compared with that of E0. CO emissions dropped by 81 and 87%, while CO2 emissions were reduced by 13 and 17%. Emissions of selected PAHs were lowered by 67-96% with E10 and by 82-96% with E85, and the genotoxic potentials dropped by 72 and 83%, respectively. Ethanol blending appears to reduce genotoxic emissions on this specific flex-fuel GDI vehicle; however, other GDI vehicle types should be analyzed.

Nanoparticle emission characteristics and reduction strategies by boost pressure control and injection strategies in a passenger diesel engine

This research attempted to analyze nanoparticles and other harmful exhaust emissions in accordance with injection strategies and air-fuel ratio (AFR) changes for small diesel engines. The emission characteristics were analyzed in the medium-speed condition, which is the main driving range of a diesel engine. In the case of particulate matter (PM), the number of particles was measured, analyzed, and compared to identify the correlation and emission characteristics of nanoparticles by using a dilution device and condensation particle counter (CPC), which are international standards for particle measurement recommended by the Particulate Measurement Programme (PMP). The engine torque tended to be reduced as pilot injections were added, and the torque was increased by the increased boost pressure, but reduced by the exhaust pressure increase in a part of the low-load range. The number of nanoparticles was not influenced greatly by the change in AFR, but the reduction effect on the PM weight was great depending on the boost pressure increase. In addition, the number of nanoparticles tended to increase as the fuel injection timing became closer to TDC in all conditions, and its difference became larger with an increase in AFR. In addition, in the case of the pilot injection, nanoparticle emission showed similar characteristics depending on the main injection timing, but it was increased by advanced injection timing when performing the main injection only, and the number of the nanoparticles increased as pilot injections were added. Last, the optimal conditions for EMS calibration were analyzed by selecting the conditions of torque reduction and NOx increase within 5 % from all of the engine operating conditions; optimized conditions are presented.

Morphology and oxidation kinetics of CI engine’s biodiesel particulate matters on cordierite Diesel Particulate Filters using TGA

The impact of small compression ignition (CI) engine operation conditions and fuel properties on diesel and biodiesel particulate matters (PMs) quantity using opacity smoke meter is investigated. The biodiesel engine’s PMs are around a half of diesel engine PMs under the same engine operation conditions. Morphology of both engine’s PMs are also studied using a Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM) and image processing method. The average primary nanoparticle sizes of diesel and biodiesel engine’s PMs are approximately 34 nm and 32 nm, respectively. The result shows that engine operation condition and fuel property are strongly impact on the quantity and size distribution of primary nanoparticles emission. PM oxidation kinetics on conventional cordierite Diesel Particulate Filters (DPFs) powders by Thermo-gravimetric analysis (TGA) is also successfully studied. The calculated apparent activation energies of biodiesel engine’s PM oxidation on conventional cordierite DPFs powders are lower than that of diesel engine’s PM and carbon black because of unburned oxygenated molecule. The calculated apparent activation energy of biodiesel engine’s PM and diesel engine’s PM oxidize on conventional cordierite DPFs powders with pure air are in the range of 109 ~ 131 kJ/mole and 117 ~ 130 kJ/mole, respectively. It might be expected that smaller primary nanoparticle size of biodiesel engine’s PMs and bio-oxygenate unburned hydrocarbon can promote more PM oxidation rate during vehicle’s DPF regeneration process.

Optimization of Bi3+ in Upconversion Nanoparticles Induced Simultaneous Enhancement of Near-Infrared Optical and X-ray Computed Tomography Imaging Capability.

Bioimaging probes have been extensive studied for many years, while it is still a challenge to further improve the image quality for precise diagnosis in clinical medicine. Here, monodisperse NaGdF4:Yb3+,Tm3+,x% Bi3+ (abbreviated as GYT-x% Bi3+, x = 0, 5, 10, 15, 20, 25, 30) upconversion nanoparticles (UCNPs) have been prepared through the solvothermal method. The near-infrared upconversion emission intensity of GYT-25% Bi3+ has been enhanced remarkably than that of NaGdF4:Yb3+,Tm3+ (GYT) with a factor of ∼60. Especially, the near-infrared upconversion emission band centered at 802 nm is 150 times stronger than the blue emission band of GYT-25% Bi3+ UCNPs. Such high ratio of NIR/blue UCL intensity could reduce the damage to tissues in the bioimaging process. The possibility of using GYT-25% Bi3+ UCNPs with strong near-infrared upconversion emission for optical imaging in vitro and in vivo was performed. Encouragingly, the UCL imaging penetration depth can be achieved as deep as 20 mm. Importantly, GYT-25% Bi3+ UCNPs exhibit a much higher X-ray computed tomography (CT) contrast efficiency than GYT and iodine-based contrast agent under the same clinical conditions, due to the high X-ray attenuation coefficient of bismuth. Hence, simultaneous remarkable enhancement of NIR emission and X-ray CT signal in upconversion nanoparticles could be achieved by optimizing the doping concentration of Bi3+ ions. Additionally, Gd3+ ions in the UCNPs endow GYT-25% Bi3+ UCNPs with T1-weighted magnetic resonance (MR) imaging capability.