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JOURNAL OF MATERIALS SCIENCE · 2023 ·Vol. 58 ·期 15 ·6743-6756 · IF 4.5

Preparation of near-infrared light responsive upconversion nanoparticles TiO2/(Ca,Y)F2:Tm,Yb for photodynamic antitumor therapy

Zhou Huan,Wang Jie,Yang Bing,Sun Manna,Liang Chunyong,Yang Lei,Zhao Xiaoyan,Wang Hongshui

In this work, near-infrared light responsive upconversion nanoparticles TiO 2 /(Ca,Y)F 2 :Tm,Yb were hydrothermally prepared for tumor control. Moreover, femtosecond laser was adopted to reduce particle size and aggregation of TiO 2 /(Ca,Y)F 2 :Tm,Yb, as a strategy to enhance its dispersity. In vitro studies of the biocompatibility and tumor control efficacy of TiO 2 /(Ca,Y)F 2 :Tm,Yb were carried out via co-culturing human pancreatic carcinoma cells (CFPAC-1). It was found in the absence of near-infrared light, TiO 2 /(Ca,Y)F 2 :Tm,Yb showed no toxicity to CFPAC-1 cells. On contrast, when exposed to near-infrared light, particles exhibited irradiation time, irradiation interval and particle concentration dependent suppression of CFPAC-1 cells proliferation along with portion of S phase cells increase. A nude mouse model with CFPAC-1 cells injection was established and TiO 2 /(Ca,Y)F 2 :Tm,Yb was subsequently applied for in vivo tumor control. A 15 days tracking confirmed the antitumor capability of near-infrared light excited TiO 2 /(Ca,Y)F 2 :Tm,Yb. Overall, we anticipate that the here-introduced TiO 2 /(Ca,Y)F 2 :Tm,Yb can serve as an effective agent for photodynamic antitumor therapy. Graphical Abstract

研究领域: 纳米技术 · 生物医学工程 · 癌症研究 · 光动力治疗 · 材料科学
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ACS Applied Nano Materials · 2025 · IF 5.5

A High Anti-interference Trimode Hydrogen Peroxide Sensing Strategy via Inner Filter Effect between the Anthracene-Based Probes and NaYF4:Yb/Tm/Er Nano Hexagonal Prisms

Zhongfei Shang,Meimei Wang,Honghong Li,Jiahao Dong,Luyan Yang,Xincun Dou,Baiyi Zu

The exploration of efficient hazardous chemical sensing technology is of great importance to protect the environment and maintain public security. Here, a design strategy of a trimode upconversion nanoprobe was developed for H2O2 detection through establishing the inner filter effect (IFE) between the anthracene-based probes and the NaYF4:Yb/Tm/Er upconversion nanoparticles (UCNPs). The trimode nanoprobe exhibits superior H2O2 detection performance, including a low limit of detection (LOD) of 152 nM, fast response (<3 s), outstanding selectivity, and robust anti-interference ability even in the presence of 15 common interferents. Furthermore, the practical utility of this design is conclusively demonstrated through a sensing chip capable of accurately and selectively identifying H2O2 even in the presence of more than 7 types of coexisting multicolor interferents. This sensing strategy, characterized by its strong anti-interference capability even when facing extremely complex real-world samples, is expected to establish a promising framework for ultra-accurate detection of hazardous substances.

研究领域: 分析化学 · 纳米技术 · 传感器 · 环境监测 · 生物工程
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LANGMUIR · 2022 · IF 4.331

3D TM-N-C Electrocatalysts with Dense Active Sites for the Membraneless Direct Methanol Fuel Cell and Zn-Air Batteries

Xiaoting Cao,Ruili Song,Xiaoshuang Zhou,Xi Wang,Xu Dong,Ningyi Yuan,Jianning Ding

Electrocatalysts with high cost-effectiveness for the oxygen reduction reaction (ORR) are essential for fuel cells (FC) and Zn-Air batteries (ZAB), which need highly active sites and suitable carbon substrates to accelerate the charge transfer kinetics. Herein, a simple and extensible method using ball milling and space-confinement pyrolysis is reported to prepare a series of transition metals and N-C catalysts (M-NLPC), which possess three-dimensional porous carbon substrates and dense active sites for efficient ORR. M-NLPC catalysts (especially Fe-NLPC) exhibit outstanding ORR activity with a half-wave potential (E1/2, 0.88 V) in an alkaline medium, high stability, and strong methanol resistance. The M-N4 sites are proven to be the active centers in M-NLPC by theoretical calculation, and methanol molecules are more likely to desorb than react on the Fe-N4 sites, which is the origin of the inactivity for the methanol oxidation reaction (MOR). Furthermore, Fe-NLPC was applied to membraneless alkaline direct methanol FC (DMFC) in practice, exhibiting outstanding performance. Meanwhile, the Fe-NLPC-based ZAB also shows excellent electrochemical performance.

研究领域: 材料科学 · 电化学 · 能源存储与转换
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JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY · 2019 · IF 5.04

Preparation and hydrogen storage properties of MgH2-trimesic acid-TM MOF (TM=Co, Fe) composites

Zhewen Ma,Jianxin Zou,Darvaish Khan,Wen Zhu,Chuanzhu Hu,Xiaoqin Zeng,Wenjiang Ding

Two kinds of metal-organic frameworks (MOFs) based on Co (II) and Fe (II) as metal ions and trimasic acid (TMA) as organic linker were synthesized. They were used to prepare corresponding MgH 2 -TM MOF (TM = Co, Fe) composites via ball-milling. X-ray diffraction analyses show the formation of Mg 2 Co and α-Fe phases in MgH 2 -TM MOF composites after decomposition. Both of the well dispersed Mg 2 Co and α-Fe nanoparticles exhibit considerable catalytic efficiency in accelerating the sorption kinetics of MgH 2 . The dehydrogenated MgH 2 -Fe MOF composite shows faster hydriding kinetics than the pure MgH 2 and MgH 2 -Co MOF. Meanwhile, the apparent dehydrogenation activation energy ( E d ) of the MgH 2 -Co MOF and MgH 2 -Fe MOF composites are 151.3 ± 9.4 and 142.3 ± 6.5 kJ/mol H 2 , both of which are lower than that of pure MgH 2 (181.4 ± 9.2 kJ/mol H 2 ). The improvement on the sorption kinetics of the MgH 2 -TM MOF powders is mainly attributed to the catalytic effects of nano-sized Mg 2 Co and α-Fe formed on the surface of Mg/MgH 2 particles.

研究领域: 材料科学 · 能源储存
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Sustainable Energy & Fuels · 2020 ·Vol. 4 ·期 5 ·2192-2200 · IF 5.503

Nano Fe and Mg2Ni derived from TMA-TM (TM = Fe, Ni) MOFs as synergetic catalysts for hydrogen storage in MgH2

Zhewen Ma,Qiuyu Zhang,Wen Zhu,Darvaish Khan,Chuanzhu Hu,Tianping Huang,Wenjiang Ding,Jianxin Zou

TMA-TM (TM = Fe, Ni) MOFs were synthesized successfully by a facile method. A MgH2-TM MOF (TM = Fe, Ni) composite was obtained via ball milling and the corresponding hydrogen storage performance was investigated. Particularly, high-resolution transmission electron microscopy was performed to in situ characterize the dehydrogenation behavior of the MgH2-TM MOF composite. The results reveal that nano α-Fe and Mg2NiH4/Mg2Ni derived from the TMA-TM MOFs display a synergetic improving effect on the de/hydrogenation of MgH2. During the hydrogen desorption process, Mg2NiH4/Mg2Ni works as a “hydrogen pump” to quickly deliver hydrogen and facilitates hydrogen diffusion. Meanwhile, α-Fe accelerates the nucleation and growth of Mg by reducing the nucleation energy of Mg from MgH2. The hydriding activation energy of the MgH2-TM MOF declines to 45.3 kJ mol−1 H2. Meanwhile, the peak dehydriding temperature of the MgH2-TM MOF is 530.9 K, which is much lower compared with the MgH2–Fe MOF composite (541.7 K) and as-milled MgH2 (685.2 K). Therefore, nano Mg2Ni and α-Fe derived from the TMA-TM MOFs can remarkably improve the hydrogen storage properties of the MgH2/Mg system due to their synergetic catalytic effects.

研究领域: 材料科学 · 能源科学
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CHEMICAL ENGINEERING JOURNAL · 2023 · IF 15.1

Defect engineering enabling p-type Mo(S,Se)2:TM (TM = V, Nb, Ta) towards high-efficiency kesterite solar cells

Junjie Fu,Afei Zhang,Dongxing Kou,Zewen Xiao,Wenhui Zhou,Zhengji Zhou,Shengjie Yuan,Yafang Qi,Zhi Zheng,Sixin Wu

One important issue limiting the development of Cu 2 ZnSn(S,Se) 4 (CZTSSe) solar cells is the severe recombination loss at CZTSSe/Mo(S,Se) 2 /Mo back contact, primarily arising from the non-matched potential barrier and inferior electric contact between absorber and weak n -type Mo(S,Se) 2 interfacial layer. It is expected that a p-type Mo(S,Se) 2 can effectively improve the hole extraction and enhance the device performance. In this work, we propose a plausible direction to build up an electrically benign back surface field by in-situ doping Mo(S,Se) 2 with group VB elements (TM = V, Nb and Ta). It is turned out that the generated V Mo , Nb Mo , or Ta Mo shallow acceptors could convert Mo(S,Se) 2 from weak n -type to p-type conductivity and increase its work function ( W F ) and hole concentration. With the contact of p-type absorber ( W F,absorber  <  W F,Mo(S,Se)₂ ), a benign ohmic contact with favorable downward band bending is formed, thereby accelerating the holes extraction and minimizing interface recombination loss. With significant gains in open-circuit voltage ( V oc ) and fill factor (FF), the Mo(S,Se) 2 :Ta device finally increases the efficiency from 10.82 % to 12.72 %. This convenient in-situ Mo(S,Se) 2 doping strategy is different from previous complicated or unstable cases and should serve as a basis for high-quality back contact engineering in kesterite photovoltaics.

研究领域: 材料科学 · 光伏技术 · 半导体物理
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Food Analytical Methods · 2022 ·Vol. 15 ·期 6 ·1535-1544 · IF 3.498

Screening and Identification of Specific Aptamers for Shellfish Allergen Tropomyosin with Capillary Electrophoresis-SELEX

Li Linfang,Zhou Jinru,Wang Kuiwu,Chen Xiaojing,Fu Linglin,Wang Yanbo

Tropomyosin (TM), known as the major allergen in shellfish, has gained increasing concerns in industrialized countries, resulting in an urgent need for an accurate, simple, and sensitive method for TM detection in food products. Nucleic acid aptamers, short single-stranded oligonucleotides chains, can bind to various targets with a high affinity and specificity and hence have the potential to be used for the accurate detection of targets. Here, we proposed capillary electrophoresis-systematic evolution of ligands by exponential enrichment (CE-SELEX) for rapid selection and identification of specific aptamers against shellfish TM. A selected aptamer IX exhibited high specificity and high binding affinity against TM with K d determined (0.95 nM). In addition, the aptamer IX has great potential to be employed in the establishment of various aptasensors for TM detection in shellfish products. Furthermore, the CE-SELEX method may provide a universal and convenient method for the aptamer selection against more targets.

研究领域: 食品科学 · 分子生物学
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BRAZILIAN JOURNAL OF CHEMICAL ENGINEERING · 2024 · IF 1.5

Preparation of layered high nickel cobalt-free LiNi0.8Mn0.17Fe0.03O2 cathode material for lithium-ion batteries

Su Yongyou,Zhu Bowen,Zhang Yingjie,Meng Qi,Dong Peng

With the rapid development of the global economy, energy crisis and environmental protection problems are in urgent need of solution. And the development of energy-saving and new energy vehicles is an inevitable trend to improve the energy structure, alleviate the conflict between oil supply and demand, and improve the living environment of human beings. Layered high nickel material is considered as one of the most promising cathode materials for power batteries because of its high energy density, high platform potential and good rate capability. However, it has problems such as high dependence on cobalt resources and poor cycling stability. In this paper, the preparation of layered high nickel cobalt-free cathode materials is investigated. Because Fe element has the advantages of large reserves and low price. At the same time, Fe makes the layered structure of the positive electrode more stable. In this paper, LiNi 0.8 Mn 0.17 Fe 0.03 O 2 (Li/TM = 1.01, 1.03, 1.05) materials with different Li/TM ratios were prepared by solid-phase method to investigate the effects of different Li/TM ratios on the structural and electrochemical properties of LiNi 0.8 Mn 0.17 Fe 0.03 O 2 materials. The results show that the materials synthesized with different Li/TM ratios have a layered structure. When the Li/TM ratio is 1.03, the crystal structure is the best and the degree of Li/Ni mixing is the least. The electrochemical performance study shows that the synthesized materials have the optimal electrochemical performance at the Li/TM ratio of 1.03. The electrochemical behavior during lithium embedding/delithiation was also investigated by quasi-in situ XRD, dQ/dV and CV tests. This study will provide some reference and guidance for the development and application of next-generation low-cost cobalt-free lithium-ion batteries.

CAS / MDL: 1310-66-3
研究领域: 材料科学 · 能源科学
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CHEMICAL ENGINEERING JOURNAL · 2018 · IF 6.735

Efficient near-infrared photocatalysts based on NaYF4:Yb3+,Tm3+@NaYF4:Yb3+,Nd3+@TiO2 core@shell nanoparticles

Huining Huang,Huiliang Li,Zeyan Wang,Peng Wang,Zhaoke Zheng,Yuanyuan Liu,Ying Dai,Yingjie Li,Baibiao Huang

In this work, we fabricated NaYF 4 :Yb 3+ ,Tm 3+ @NaYF 4 :Yb 3+ ,Nd 3+ @TiO 2 (Tm@Nd@TiO 2 ) core@shell nanoparticles and investigated their near-infrared (NIR) photocatalytic activities. Comparing to traditional TiO 2 based upconversion (UC) photocatalysts (i.e., NaYF 4 :Yb 3+ ,Tm 3+ @TiO 2 , named Tm@TiO 2 ), Tm@Nd@TiO 2 exhibits enhanced photocatalytic activity under NIR light irradiation. The photocatalytic activity of Tm@Nd@TiO 2 under 980, 808, and 980 + 808 nm laser irradiation is 4.40, 5.84, and 9.83 times as high as that of Tm@TiO 2 under only 980 nm irradiation, respectively. The ethylene degradation rate of Tm@Nd@TiO 2 under 980 + 808 nm laser irradiation is 6.4 times as that of Tm@TiO 2 . The photocatalytic activity of Tm@Nd@TiO 2 under visible + NIR irradiation is even comparable with (∼2/3) that under UV light irradiation during Rhodamine B (RhB) degradation. The enhanced photocatalytic activity of Tm@Nd@TiO 2 can be attributed to the stronger light absorption in NIR region ascribed to Nd 3+ , lower water absorption and the enhanced UC emission of Tm@Nd with unique core@shell nanostructures. This work can provide a possible route to improve the NIR photocatalytic activity and stimulate the applications in many other fields.

研究领域: 材料科学 · 光催化技术
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MICROPOROUS AND MESOPOROUS MATERIALS · 2025 · IF 4.7

Highly controllable CO2 capture performance under varied humidity conditions by finely tuned metal and organic ligand compositions of DMOF adsorbents

Xinyu Chen,Jinhai Leng,Fengying Ma,Jianqing Wu,Yi Jin,Miao Yu,Haomin Huang,Shanshan Shang,Daiqi Ye

Excessive CO 2 emissions significantly contribute to global warming, promoting the advancement of carbon capture and storage (CCS) technologies. Metal-organic frameworks (MOFs) are promising candidates for selective CO 2 adsorption; however, their effectiveness is often compromised in humid environments, such as flue gas streams. To overcome this limitation, this study synthesizes six isostructural DABCO-pillared MOFs (DMOFs) by finely tuning metal nodes (from Zn to Ni) and integrating methyl (-CH 3 ) functional groups on the organic ligand to enhance CO 2 adsorption performance, especially under humid conditions. Single gas adsorption isotherms reveal that the Ni-TM DMOF achieves the highest CO 2 adsorption capacity of 5.0 mmol g −1 and maintains 100 % regenerability after five cycles. Binary CO 2 /N 2 dynamic breakthrough experiments further demonstrate that the Ni-TM DMOF excels in both CO 2 uptake and CO 2 /N 2 separation performance under both dry and humid conditions (80 % relative humidity). Mechanistic insights from in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) and density functional theory (DFT) calculations elucidate the molecular interactions between CO 2 and the DMOF structure, revealing that CO 2 adsorption predominantly occurs via physisorption, enhanced by C-H·O interaction from the -CH 3 groups. This work provides a strategic approach for enhancing the stability and efficiency of MOFs in industrial CO 2 sequestration applications.

研究领域: 材料科学 · 环境科学 · 化学工程
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JOURNAL OF LUMINESCENCE · 2021 · IF 3.599

Simultaneous luminescence enhancement and lifetime tuning of deep UV-NIR upconversion through controlling dopant concentration

Dangli Gao,Yuqian Liang,Jie Gao,Hong Xin,Long Wang,Sining Yun,Xiangyu Zhang

Applications of rare-earth (Re)-doped upconversion (UC) micro/nanocrystals in varying areas have sparked a growing, constant demand for deliberate control over the luminescent profile and lifetime. A general strategy for adjusting UC luminescence is to control the dopant Re 3+ concentration. However, the progress of elevating dopant concentration is significantly limited owing to frequently encountering severe concentration quenching. Herein, by designing UC system using Tm 3+ with super long intermediate energy level lifetime and Yb 3+ with a simple two-level structure as a activator/sensitizer combination, we have achieved the unusually intense deep ultraviolet (UV) UC emissions at 290 nm and 345 nm, near UV emission at 361 nm, visible blue emissions at 452 nm and 478 nm, and near infrared (NIR) emission at 803 nm in NaYF 4 :Yb/Tm microtubes under 980 nm excitation. The luminescence intensity reaches about 56 times and 8 times enhancement for the UV and blue emission, respectively, with the increase of dopant Yb 3+ contents from 20 to 80 mol%. While luminescence lifetimes for all emissions decrease, particularly, for NIR emission at 803 nm, from 1507 μs down to 384 μs. Importantly, upon 980 nm irradiation, these UC NaYF 4 :Yb/Tm microtubes exhibit superior optical performance as a promising candidate of advanced anti-counterfeiting applications and other applications including UV light triggered reactions and multiplexing information storage.

研究领域: 材料科学 · 光学
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International Journal of Applied Ceramic Technology · 2024 · IF 1.8

Composition optimization of (Hf, Ta, Zr, Cr)C high-entropy carbides for good oxidation resistance

Shuaijun Yang,Mei Wang,Yetong Lv,Huilin Sheng,Yexia Qin

Oxidation resistance is crucial to the potential applications of high-entropy carbides (HECs) at elevated temperatures. Here, we realize the exploration of (Hf, Ta, Zr, Cr)C high-entropy carbides (HEC-TM, TM = Hf, Zr, Ta, and Cr) with good oxidation resistance by optimizing their compositions. To be specific, 21 kinds of HEC- x TM ( x = 0–25 mol%) samples are fabricated by a high-throughput ultrafast high-temperature sintering technique, followed by oxidation testing at 1673 K for 30 min. Among all the HEC samples, the as-fabricated HEC-0Zr samples are proved to possess the best oxidation resistance with an oxidation depth of only 53 µm. Further study on isothermal oxidation kinetics demonstrates that the as-fabricated HEC-0Zr samples follow a linear oxidation law. The good oxidation resistance of the as-fabricated HEC-0Zr samples is believed to result from the (Ta, Me) 2 O 5 phase with a low melting point, which can promote the densification of the oxide layer. This research opens up a new way for efficiently discovering new HECs for extreme applications.

CAS / MDL: 7440-44-0
研究领域: 材料科学 · 高温材料
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