Publications by authors named "Jinyang Zhu"

Article Synopsis
  • Long-wavelength afterglow emitters are important for fields like optoelectronics and information security, but achieving high efficiency is challenging due to poor electronic coupling and nonradiative transitions.
  • Researchers demonstrate a hybrid system using organic carbon dots that achieves bright afterglow emission at 600 nm with nearly perfect luminescence efficiency through a method involving space-confined energy transfer.
  • The study highlights how energy transfer from carbon dot triplet excitons to singlets and minimizing energy loss through structural modifications lead to successful yellow and near-infrared emissions, making these materials promising for lighting and secure data transmission.
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Lead-halide perovskite nanocrystals (NCs) are promising for fabricating deep-blue (<460 nm) light-emitting diodes (LEDs), but their development is plagued by low electroluminescent performance and lead toxicity. Herein, the synthesis of 12 kinds of highly luminescent and eco-friendly deep-blue europium (Eu)-doped alkali-metal halides (AX:Eu; A = Na, K, Rb, Cs; X = Cl, Br, I) NCs is reported. Through adjustment of the coordination environment, efficient deep-blue emission from Eu-5 → Eu-4 transitions is realized.

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Article Synopsis
  • A study aimed to assess the effectiveness of high-intensity laser therapy (HILT) combined with targeted hand function training on pain relief and grip strength in women with early-stage thumb osteoarthritis.
  • The research involved 42 female patients, aged 58 to 80, divided into two groups: one receiving HILT and hand training, and the other receiving traditional treatment with ultrashort wave therapy and an orthosis, over a 4-week period.
  • Results showed that the HILT group experienced significantly greater reductions in pain and improvements in lateral pinch force compared to the control group, indicating that HILT combined with training is more beneficial for treating this condition.
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Thermally activated delayed fluorescence (TADF) materials, which can harvest both singlet and triplet excitons for high-efficiency emission, have attracted widespread concern for their enormous applications. Nevertheless, luminescence thermal quenching severely limits the efficiency and operating stability in TADF materials and devices at high temperature. Herein, a surface engineering strategy is adopted to obtain unique carbon dots (CDs)-based thermally enhanced TADF materials with ≈250% enhancement from 273 to 343 K via incorporating seed CDs into ionic crystal network.

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Wide-coverage near infrared (NIR) phosphor-converted LEDs possess promising potential for practical applications, but little is developed towards the efficient and wide-coverage NIR phosphors. Here, we report the single-component lanthanide (Ln ) ions doped Cs M(In Sb )Cl (M=alkali metal) nanocrystals (NCs), exhibiting emission from 850 to 1650 nm with high photoluminescence quantum yield of 20.3 %, which is accomplished by shaping the multiple metal halide octahedra of double perovskite via the simple alkali metal substitution.

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The structure of CsPbI nanocrystals (NCs) with excellent photoelectric properties easily collapses, which hinders their application in light-emitting diodes (LEDs). Herein, we accomplished the synthesis of efficient and stable CsPbI NCs by regulating structural rigidity under the synergistic effect of Mg and AcO ions. The introduced AcO and Mg ions increase surface steric hindrance and defect formation energy, which enhances the structural rigidity of the perovskite.

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Highly efficient emission has been a long-lasting pursuit for carbon dots (CDs) owing to their enormous potential in optoelectronic applications. Nevertheless, their room-temperature phosphorescence (RTP) performance still largely lags behind their outstanding fluorescence emission, especially in the blue spectral region. Herein, high-efficiency blue RTP CDs have been designed and constructed via a simple molecular engineering strategy, enabling CDs with an unprecedented phosphorescence quantum efficiency of to 50.

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The System #2 flow loop used in this study is a 4-inch-diameter, high-temperature, high-pressure system. In situ corrosion and electrochemical measurements were performed using a homemade flat corrosion specimen and a three-electrode probe. The experiment results show that temperature has an accelerated influence on the corrosion of antibacterial alloy steel.

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Zero-dimensional (0D) crystal structure perovskite NCs have reemerged as promising materials owing to their superior long-term stability; however, their poor conductivity leads to the inferior electrical performances and critically restricts the optoelectronic application of 0D perovskite materials. Herien, the alloyed 0D crystal structure CsZnPbCl nanorods (NRs) have been synthesized by the modified hot-injection method, which emits bright blue-violet light at 408 nm, and the optimized photoluminescence quantum yield (PLQY) reaches 26%. The CsZnPbCl NRs display more excellent air stability and an order of magnitude higher conductivity than CsPbCl nanocube films.

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Oleylamine and oleic acid are common organic capping ligands used in the hot injection preparation of perovskite quantum dots (QDs). Their labile nature is responsible for the poor colloidal stability and conductivity that affect the performance of perovskite QD light-emitting diodes (LEDs). We introduced 4-trifluoro phenethylammonium iodide (CFPEAI) directly in the synthesis and found that CFPEAI efficiently modified the I vacancy defects on the QD surface and partially substituted the surface capping ligand oleylamine.

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Carbon dot (CD) based long-lived afterglow emission materials have attracted attention in recent years, but demonstration of white-light room-temperature afterglow remains challenging, due to the difficulty of simultaneous generation of multiple long-lived excited states with distinct chromatic emission. In this work, a white-light room-temperature long-lived afterglow emission from a CD powder with a high efficiency of 5.8% and Commission International de l'Eclairage (CIE) coordinates of (0.

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Light-emitting devices (LEDs) with inorganic perovskite nanocrystals (PNCs) fabricated through the all-solution process have tremendous potential for new-generation illumination and displays on account of their large area and cost-effective manufacturing. However, the development of efficient solution-processed PNC LEDs remains challenge, which mainly results from the fact that only a few types of charge transport layers can be employed for the subsequent deposition steps, thus leading to injection barriers and charge injection imbalance inside these LEDs. Herein 4,4'-bis(carbazole-9-yl) biphenyl (CBP) is introduced as a dopant into the poly(9,9-dioctylfluorene---(4-(3-methylpropyl)) diphenylamine) (TFB) hole transport layer (HTL), which efficiently modulates the mobility of charge carrier as well as the energy level of the HTL, resulting in the barrier-free injection of the charge carrier in the as-fabricated solution-processed PNC LEDs.

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In recent years, significant advances have been achieved in the red and green perovskite quantum dot (PQD)-based light-emitting diodes (LEDs). However, the performances of the blue perovskite LEDs are still seriously lagging behind that of the green and red counterparts. Herein, we successfully developed Ni ion-doped CsPbClBr PQDs through the room-temperature supersaturated recrystallization synthetic approach.

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Article Synopsis
  • - The corrosion of 13Cr martensitic steel increases significantly at higher CO partial pressures, specifically reaching up to 20-180 times the rate seen at lower pressures.
  • - At lower CO pressures (4-12 MPa), a protective Cr(OH) passive film completely covers the steel, whereas at 28 MPa, the corrosion film is more complex, featuring both a damaged inner Cr(OH) layer and an outer FeCO layer.
  • - The observed corrosion behavior correlates with the acidic conditions (lower pH of about 2.75) and increased HCO concentration in the environment at higher CO pressures.
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All-inorganic cesium lead halide perovskite nanocrystals (NCs) have demonstrated excellent optical properties and an encouraging potential for optoelectronic applications; however, mixed-halide perovskites, especially CsPb(Cl/Br) NCs, still show lower photoluminescence quantum yields (PL QY) than the corresponding single-halide materials. Herein, anhydrous oxalic acid is used to post-treat CsPb(Cl/Br) NCs in order to initially remove surface defects and halide vacancies, and thus, to improve their PL QY from 11% to 89% for the emission of 451 nm. Furthermore, due to the continuous chelating reaction with the oxalate ion, chloride anions from the mixed-halide CsPb(Cl/Br) perovskite NCs could be extracted, and green emitting CsPbBr NCs with PL QY of 85% at 511 nm emission are obtained.

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Article Synopsis
  • All-inorganic CsPbX3 perovskite quantum dots (QDs) have great photoluminescence properties but struggle with low blue-violet fluorescence and stability issues that limit their use.
  • A new method involving co-doping with La3+ and F- ions was developed to enhance these optical properties, resulting in bright blue-violet emissions and a significantly improved photoluminescence quantum yield of 36.5%.
  • The improvements are due to better defect management and increased radiative recombination rates, making these co-doped CsPbCl3 QDs suitable for applications such as anti-counterfeiting.
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White light-emitting diodes (WLEDs) based on all-inorganic perovskite CsPbX (X = Cl, Br, I) nanocrystals (NCs) have attracted extensive interests. However, the native ion exchange among halides makes them extremely difficult to realize the white emission. Herein, we demonstrate a novel strategy to obtain WLED phosphors based on the codoping of different metal ion pairs, such as Ce/Mn, Ce/Eu, Ce/Sm, Bi/Eu, and Bi/Sm into stable CsPbCl and CsPbCl Br NCs.

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Drug release systems with fluorescence detection have emerged as a potential application for the biological area of diagnosis and therapy. Carbon dots (CDs) are a promising fluorescence probe for application in a drug release system due to their excellent biocompatibility, low toxicity, chemical inertness, and non-blinking fluorescence emission. Herein, we developed a composite nanocarrier based on fluorescent CDs and polyvinylpyrrolidone (PVP) through an electrospinning technology.

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CsPbX3 (X = Cl, Br or I) perovskite quantum dots (PQDs) have attracted tremendous attention due to their extraordinarily excellent optical properties. However, there is still an obstacle for their bio-application, which is limited by their water-instability. In this work, we have designed a novel visible light triggered photoelectrochemical (PEC) sensor for dopamine (DA) based on CsPbBr1.

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Inorganic perovskite quantum dots (QDs) have attracted wide attention in display and solid-state lighting because of their easily tunable band-gaps and high photoluminescence quantum yields (PLQY) of green light emission. However, some drawbacks limit their practical applications, including the low PLQY of blue light emission and the instability in the moisture environment. In this work, efficient blue-light emitting CsPbBr perovskite QDs with PLQY of 72% were developed through a bandgap engineering approach.

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Article Synopsis
  • Carbon dots (CDs) are new fluorescent materials with advantages like high luminescence and low toxicity, but their photoluminescence mechanism is not fully understood.
  • The study synthesized CDs from citric acid and urea and identified three different emitting states contributing to their light emissions.
  • The research led to the development of a pH sensor and white light-emitting films, resulting in promising applications for solid-state lighting and LEDs.
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Carbon dots (CDs) have attracted extensive attention over the past decade due to their excellent advantages. However, few attempts have been reported for realizing the long-wavelength emission, especially for obtaining efficient solid-state red emission with high photoluminescence quantum yield (QY). Herein, we developed highly red light emitting CDs by the step-by-step surface modifications of the nitrogen-doped CDs.

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Intracellular pH sensing is of importance and can be used as an indicator for monitoring the evolution of various diseases and the health of cells. Here, we developed a new class of surface-functionalized MXene quantum dots (QDs), TiC, by the sonication cutting and hydrothermal approach and further explored their intracellular pH sensing. The functionalized TiC QDs exhibit bright excitation-dependent blue photoluminescence (PL) originating from the size effect and surface defects.

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Colloidal perovskite nanocrystals (NCs), especially the fully inorganic cesium lead halide (CsPbX, X = Cl, Br, I) NCs, have been considered as promising candidates for lighting and display applications due to their narrow band emission, tunable band gap and high photoluminescence quantum yields (QYs). However, owing to the anion exchange in the CsPbX NCs, stable multi-color and white light emissions are difficult to achieve, thus limiting their practical optoelectronic applications. In this work, dual ion Bi/Mn codoped CsPbCl perovskite NCs were prepared through the hot injection method for the first time to the best of our knowledge.

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Carbon dots (CDs), one of the most significant classes of carbon-based nanophosphors, have attracted extensive attention in recent years. However, few attempts have been reported for realizing CDs with tunable emissions, especially for obtaining the red-light emissions with high photoluminescence quantum yields. Herein, we synthesized CDs with different chromatic blue, green and red emissions by facilely changing the reaction solvent during hydrothermal conditions.

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