Journal of Energy Chemistry
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2026
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IF 15.6
Yifei Ye,Zhuoshen Huang,Hao Pan,Zhaokun Wang,Wei Xia,Guangtong Hai,Ge Wang,Xiubing Huang
Transition metal oxyhydroxides are crucial for the electrochemical oxidation of 5-hydroxymethylfurfural (HMF), though the co-adsorption and activation mechanisms of HMF and hydroxyl species require further clarification. This study designs cerium-doped Co-based layered double hydroxide (LDH) arrays, including 3%Ce-Co 3 Fe 1− x Al x -LDH/NF, to investigate Fe as a secondary active center and the role of Ce–O–TM (Transition metal) bridges in regulating HMF/OH − adsorption. Theoretical calculations indicate that Ce–O–TM bridges induce f – p – d gradient orbital coupling, optimizing HMF/OH − adsorption configurations and facilitating the HMF oxidation reaction (HMFOR). Synchrotron radiation characterization and in situ Raman spectroscopy reveal that Fe enhances electronic interaction between Ce and Co/Fe sites, strengthening the stability of M–O bonds, suppressing metal dissolution, and further optimizing reactant adsorption. Fe doping also modulates charge distribution and accelerates charge transfer. The optimized 3%Ce-Co 3 Fe 1 -LDH/NF delivers industrial current density (0.1 A cm −2 ) at 1.44 V RHE , with 98.1% HMF conversion, 99.6% FDCA yield, and 99.8% Faradaic efficiency. In an anion exchange membrane (AEM) electrolyzer, it achieves 0.5 A cm −2 at 2.1 V while maintaining high stability across 0.1–0.5 A cm −2 . These results provide an effective strategy for designing high-performance HMFOR catalysts through electronic structure modulation.
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Journal of Materials Chemistry C
·
2025
·
IF 5.1
Shan shan Zhao,He-He Dong,Weichang Li,Lei Zhang,Shikai Wang,Chun Yu,Hu Li
Upconversion emission materials have many advantages, such as narrowband sharp line emission, excellent photochemical stability, and long lifespan. In particular, under 980 nm invisible laser-beam irradiation, materials with visible light upconversion luminescence have vital application value in optical anti-counterfeiting and laser displays. In this study, a library of upconversion phosphors of CaLaAl3O7:RE3+/Yb3+ (RE=Tm, Ho) was produced through a high-temperature solid-state reaction method. The powders exhibited different color emissions under different excited wavelengths. Under 980 nm laser excitation, Tm3+/Yb3+ co-doped phosphors exhibited upconversion emission of 474 nm blue light, which was attributed to the 1G4→3H6 transition of Tm3+, and the fitting slope of the upconversion luminescence intensity vs. laser-pump power density was n450-500=2.83, which indicated the three-photon absorption upconversion process. Additionally, Ho3+/Yb3+ co-doped phosphors had the strongest red emission at 660 nm, originating from the 5F4/5S2→5I8 transition of Ho3+, which belongs to the two-photon absorption process. Subsequently, the changes in chromaticity coordinates of the prepared samples were analyzed under different light excitations, and different light color emissions were observed. The color purities of Ho3+/Yb3+ and Tm3+/Yb3+ co-doped samples were 99.9% and 65.4%, respectively. Finally, we verified the practical application value of the prepared powder in the fields of multi-color luminescence optical anti-counterfeiting and laser displays. The results show that the produced phosphors have vital application potential in information security protection, optical data storage, and 3D laser displays.
研究领域:
材料科学
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光学工程
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高影响因子
ACS Applied Materials & Interfaces
·
2025
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IF 8.2
Gulizhabaier Abulipizi,Juanjuan Zhou,Chaomin Qu,Leping Ding,Ziang Zong,Yanlun Fang,Zimin Yu,Xingyuan Shi,Fanwen Yang,Zhanjun Li
Lanthanide-doped materials were developed with interesting near-infrared (NIR) persistent luminescence (PersL) properties after X-ray irradiation but are limited by poor charging ability based upon biocompatible red light. In this study, CaTiO3:Tm (CTT) was found to emit an unusual single band PersL at ∼800 nm, which was rechargeable by red-NIR light excitation (∼650 to 720 nm). Moreover, blue or deep red light could charge more intense PersL than UV light in CTT, which was quite different from all the other known lanthanide-activated NIR PersL materials. An upconverting-energy transfer PersL mechanism was proposed based on the upconverting property of Tm3+ and its energy transfer to Ti3+ in the CaTiO3 matrix. The interaction of Tm3+ and Ti3+ in CaTiO3 quite possibly played an important role in the unusual PersL process of CTT, which avoided the band-pass transition of the CaTiO3 matrix. By comparison with a series of Tm-doped phosphors, CaTiO3 was found to be an optimal PersL matrix to generate the unique PersL properties of Tm3+. The in situ charged NIR PersL imaging of a medical stent implant in the neck of a chicken model was demonstrated. This study reveals the unusual PersL properties of CTT and will promote advanced biomedical applications of rare-earth-doped PersL biomaterials.
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高影响因子
CRYSTENGCOMM
·
2021
·Vol. 23
·期 21
·3892-3900
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IF 3.545
Dandan Ju,Xiaoli Gao,Shouchao Zhang,Yang Li,Wenjing Cui,Yinhui Yang,Mingyan Luo,Shujing Liu
Temperature is one of the physical parameters that affects the emission luminescence properties of upconversion (UC) materials. Temperature-dependent emission color tuning and good temperature sensitivity in multifunctional β-NaYF4:Yb/Er@β-NaYF4:Yb/Tm microcrystals were achieved under 980 nm excitation. Based on the different emission bands (blue, green and red bands) and spectral sensitivities of the core–shell structured microcrystals to temperature, intense white-light emission was obtained at room temperature and a real-time naked-eye recognizable emission color change from white to the purplish-pink region was realized with the temperature increasing from 300 to 500 K. Furthermore, optical temperature sensing properties of the sample with good sensitivity (from 0.0034 to 0.0044 K−1) were investigated by using a fluorescence intensity ratio between 521 nm (2H11/2 → 4I15/2 transition) and 540 nm (4S3/2 → 4I15/2 transition) in the temperature range from 300 to 500 K. The results indicate that the sample has high sensitivity in a relatively wide range of temperature intervals, especially in the low temperature region. We believe that the multifunctional core–shell structured microcrystals exhibit promising applications in white-light emitting diodes, the anti-counterfeiting field, and temperature sensing.
研究领域:
材料科学
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光学
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高影响因子
ANALYTICAL CHEMISTRY
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2013
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IF 5.695
Ji-Wei Shen,Cheng-Xiong Yang,Lu-Xi Dong,Hao-Ran Sun,Kai Gao,Xiu-Ping Yan
Rational design and fabrication of multimodal imaging nanoprobes are of great significance for in vivo imaging. Here we report the fabrication of a multishell structured NaYF4:Yb/Tm@NaLuF4@NaYF4@NaGdF4 nanoprobe via a seed-mediated epitaxial growth strategy for upconversion luminescence (UCL), X-ray computed tomography (CT), and magnetic resonance (MR) trimodal imaging. Hexagonal phase NaYF4:Yb/Tm is used as the core to provide UCL, while the shell of NaLuF4 is epitaxially grown on the core not only to provide an optically inert layer for enhancing the UCL but also to serve as a contrast agent for CT. The outermost NaGdF4 shell is fabricated as a thin layer to give the high longitudinal relaxivity (r1) desired for MR imaging. The transition shell layer of NaYF4 not only provides an interface to facilitate the formation of NaGdF4 shell but also inhibits the energy transfer from inner upconversion activator to surface paramagnetic Gd3+ ions. The fabricated multishell structured nanoprobe shows intense near-infrared UCL, high r1 value of 3.76 mM–1 s–1, and in vitro CT contrast effect. The multishell structured nanoprobe offers great potential for in vivo UCL/CT/MR trimodal imaging. Further covalent bonding of folic acid makes the multishell structured nanoprobe promising for in vivo targeted UCL imaging of tumor-bearing mice.
研究领域:
生物医学工程
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材料科学
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影像医学
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高影响因子
JOURNAL OF LUMINESCENCE
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2015
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IF 2.719
ShaoZhen Wang,Jianguo Zhang,Hongqi Chen,Lun Wang
A new serum ferritin (SF) biosensor based on fluorescence resonance energy transfer (FRET) from Mn 2+ -doped NaYF 4 :Yb,Tm up-converting rare-earth nanophosphors (UCNPs, donor) to gold nanorods (GNRs, acceptor) was developed in the near-infrared (NIR) region. The as-prepared Mn 2+ -doped NaYF 4 :Yb,Tm UCNPs exhibited a strong emission at 807 nm in the NIR region and were modified with poly-(acrylic acid) (PAA) before conjugating with anti-SF (Ab 1 ). The negatively charged donor (Ab 1 -UCNPs) and the positively charged acceptor (GNRs) were mixed in close proximity due to electrostatic interactions, which quenched the fluorescence emission of the Mn 2+ -doped NaYF 4 :Yb,Tm UCNPs. However, added SF combines with the anti-SF because the binding affinity between SF and Ab 1 is stronger than the electrostatic interactions. Thus, the acceptor separated from the donor, and the fluorescence was restored. Under optimal conditions, the restored fluorescence exhibited a linear relationship with SF concentrations ranging from 0.23 to 16.88 ng/mL and a limit of detection as low as 0.12 ng/mL. The proposed method was also used to monitor SF in human serum samples.
研究领域:
生物化学
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纳米医学
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分析化学
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高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
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2020
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IF 4.65
Tianping Huang,Jianxin Zou,Huabing Liu,Wenjiang Ding
Three kinds of transition metal fluorides TMF x (TM = Nb, Co, Ti) were introduced into the 3NaBH 4 -GdF 3 hydrogen storage system via mechanical milling. Their effects on the hydrogen storage behaviors of 3NaBH 4 -GdF 3 were systematically investigated by means of DSC and volumetric methods. All TMF x exhibited promoting effect on hydrogen desorption properties of 3NaBH 4 -GdF 3 to different degrees, especially when NbF 5 or TiF 3 was added. For example, the hydrogen desorption peak temperature was decreased by 17 °C with doping 3 mol% of NbF 5 . Besides, TiF 3 improved also the hydrogen absorption capacity and reversibility of 3NaBH 4 -GdF 3 . Based on XRD analyses, the role of TMF x on the dehydrogenation and the promoting effect of TiF 3 on the reversibility of 3NaBH 4 -GdF 3 were clarified. This work helped to understand the combination effect of rare earth metal fluoride (GdF 3 ) and transition metal fluorides on the reversible hydrogen storage properties of NaBH 4 .
研究领域:
材料科学
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化学工程
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Chemistry-An Asian Journal
·
2022
·Vol. 17
·期 14
·e202200161
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IF 4.839
Bo Ling,Yaguang Wang,Ruo Mi,Di Wang,Hongqi Chen,Xiaohu Li,Ye Zhang,Lun Wang
Graphical NaGdF 4 ,Yb,Er@NaGdF 4 ,Yb,Tm@NaYF 4 core@shell@shell three-layer structure of upconversion nanoparticles coated with Fe−TCPP metal-organic frameworks nanocomposite was designed and constructed for multimodal imaging and synergetic chemodynamic therapy/photodynamic therapy of tumors. Here, NaGdF 4 ,Yb,Er@NaGdF 4 ,Yb,Tm@NaYF 4 core@shell@shell three-layer structure of upconversion nanoparticles (UCNPs) coated with Fe−Tetrakis (4-carboxyphenyl) porphine (TCPP) metal-organic frameworks (Fe-MOFs) nanocomposite (UCNPs@MOFs) was designed and constructed for multimodal imaging and synergetic chemodynamic therapy (CDT)/photodynamic therapy (PDT) of tumors. The UCNPs@MOFs were successfully applied for tumor cells imaging in vitro and in vivo in near-infrared (NIR) region. The doped Gd was used as contrast agent for the magnetic resonance imaging (MRI) of mouse tumors. The luminescence in the UV-vis region was absorbed by the Fe-MOFs to produce singlet oxygen ( 1 O 2 ) for PDT. The Fe 3+ doped in the MOFs can catalyze H 2 O 2 to produce oxygen and hydroxyl radical (⋅OH). Hydroxyl radical is used in CDT and cooperates with the 1 O 2 of PDT. Based on the CDT/PDT synergistic effects, the UCNPs@MOFs nanocomposite had obviously enhanced tumor inhibitory efficiency in vivo. These results described that the asprared UCNPs@MOFs nanocomposite have great potential in the effective multimodal imaging and treatment of tumors.
研究领域:
生物医学工程
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纳米医学
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肿瘤学
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高影响因子
CRYSTENGCOMM
·
2023
·Vol. 25
·期 38
·5452-5460
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IF 3.1
Huimin Du,Yunhao Liang,Xingzuo Liu,Yue Deng,Jie Yang,Jun Yang,Shanshan Hu
Yb2(MoO4)3:Ln3+ (Ln = Ho, Tm, Er) phosphors were synthesized by a hydrothermal method with further calcination. The crystal structure and morphology of the samples were characterized by X-ray diffraction and scanning electron microscopy. The effects of rare earth ion interaction in the Yb2(MoO4)3:Ln3+ phosphors on the upconversion (UC) luminescence properties and energy transfer process at different doping concentrations were discussed. It is concluded that by doping Ho3+, Tm3+, and Er3+ in the Yb2(MoO4)3 host, the phosphors emit orange-yellow, blue and green light, respectively, and the energy transfer from Yb3+ → Ho3+/Er3+ and Yb3+ → Tm3+ is a two and three photon process, respectively. Under the excitation of a 980 nm laser, by changing the Ho3+/Tm3+ ratio in doped Yb2(MoO4)3, we have realized the transition of phosphors from cold white light to warm white light. The temperature sensitivity of the 2H11/2 and 4S3/2 energy levels of Yb2(MoO4)3:Er3+ in the range of 323–573 K was studied by the FIR technology. The experimental results show that the maximum absolute sensitivity was 0.0081 K−1 at 573 K and the maximum relative sensitivity was 0.01 K−1 at 323 K. Compared with other materials, the Er3+ doped Yb2(MoO4)3 phosphor is an excellent optical temperature sensing material.
研究领域:
材料科学
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光学
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高影响因子
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES
·
2024
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IF 2.8
Yiwen Zhang,Yang Guo,Liang Song,Wenshuai Liu,Rui Nian,Xiying Fan
This study introduces an efficient on-column refolding and purification method for preparing nanobodies (Nbs) expressed as inclusion bodies and fusion proteins. The HisTrap TM FF system was successfully employed for the purification of the fusion protein FN1-ΔI-CM-2D5. The intein ΔI-CM cleavage activity was activated at 42 °C, followed by incubation for 4 h. Leveraging the remarkable thermal stability of Nbs, 2D5 was further purified through heat treatment at 80 °C for 1h. This method yielded up to 107.2 mg of pure 2D5 with a purity of 99.2 % from just 1L of bacterial culture grown in a shaker flask. Furthermore, this approach successfully restored native secondary structure and affinity of 2D5. Additionally, the platform was effectively applied to the refolding and purification of a polystyrene-binding nanobody (B2), which exhibited limited expression in the periplasmic and cytoplasmic spaces of E. coli . This endeavor resulted in the isolation of 53.2 mg of pure B2 Nb with a purity exceeding 99.5 % from the same volume of bacterial culture. Significantly, this approach restored the native secondary structure of the Nbs, highlighting its potential for addressing challenges associated with expressing complex Nbs in E. coli . Overall, this innovative platform provides a scientifically rigorous and reproducible method for the efficient preparation of Nbs, offering a valuable tool for antibody research and development.
研究领域:
生物技术
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蛋白质工程
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分子生物学
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抗体研究
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PubMed
高影响因子
ACS Photonics
·
2024
·
IF 6.5
Wenxia Wu,Yazhao Wang,Limin Wu,Huiting Zhang,Zhonghua Zhu,Shengdi Ta,Peng Zhang,Shoulei Xu,Bernard A. Goodman,Wen Deng
Under excitation at 980 nm, Tm3+ may emit ultraviolet, blue, and red light, and Ho3+ may emit green light through multiphoton upconversion processes in Yb/Tm/Ho codoped materials. However, because the probability of the electron population of the higher excited state energy levels is much lower than that of the lower ones in multiphoton upconversion processes, it is difficult to observe the ultraviolet emission of Tm3+-doped single crystals under excitation at 980 nm. Here, we report that high-quality single crystals of cubic ZrO2 codoped with Tm2O3, Ho2O3, and Yb2O3 are successfully grown by the optical floating zone method, and ultraviolet emission at 308 nm was observed for the first time from multiphoton upconversion transitions in these highly transparent, low phonon energy single crystals under excitation at 980 nm. This result demonstrates the prospect of making ultraviolet solid-state lasers pumped by near-infrared light. Moreover, bright white light was emitted from the single crystal prepared with 5.00 mol % Yb2O3, 0.75 mol % Tm2O3, 0.0075 mol % Ho2O3, 2.2425 mol % Y2O3, and 92.00 mol % ZrO2 under excitation at 980 nm, and a bright solid white light source excited by a near-infrared light-emitting diode for practical use is presented.
研究领域:
材料科学
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光学
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高影响因子
Materials Today Communications
·
2024
·
IF 3.7
Bingxin Yuan,Meiting Li,Chi Zhang
The RE 3+ doped YbNbO 4 and Yb 3 NbO 7 nanophosphors (RE=Ho, Er and Tm) were synthesized via a calcination-assisted hydrothermal procedure. YbNbO 4 intensified almost the whole up-conversion (UC)/down-conversion (DC) emissions of RE 3+ by ∼2 times when compared with Yb 3 NbO 7 components, indicating that a lower symmetry environment in the former case is more favorable for photoluminescence. UC luminescence in each case was dominated by a green band at ∼539 nm for Ho 3+ and a NIR band at ∼803 nm for Tm 3+ , while doping YbNbO 4 and Yb 3 NbO 7 with Er 3+ separately yielded the slightly stronger green 556 nm and red 658 nm emissions. The UC/DC luminescence mechanisms were elaborated via Yb 3+ → RE 3+ forward/backward energy transfer and cross relaxation.
研究领域:
材料科学
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光学
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高影响因子