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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2023 ·Vol. 34 ·期 12 ·1-16 · IF 2.8

Modification of BaTiO3 for diversified applications by single Nd element substitution with wide doping range

Wang Fenglin,Mao Haijun,Chen Xingyu,Li Wei,Liu Zhuofeng,Zhang Weijun,Bai Shuxin

In this work, A -site Nd doped BaTiO 3 ceramics in the form of Ba 1− x Nd 2 x /3 TiO 3 with a wide substitution level range of x  = 0–0.2 have been prepared via solid-state reaction method. Powder X-ray diffraction results reveal that Nd is completely incorporated into the BaTiO 3 lattice in all specimens. Further analyses based on Rietveld refinement suggest that tetragonal and pseudo-cubic phases coexist in Ba 1− x Nd 2 x /3 TiO 3 ceramics with x  ≤ 0.06, and the amount of tetragonal phase is raised with the increase of x value. When x value is larger than 0.08, only pseudo-cubic is observed. The generated \(V^{\prime\prime}_{{{\text{Ba}}}}\) , \({\text{Nd}}_{{{\text{Ba}}}}^{\cdot }\) and \(V_{{\text{O}}}^{{\cdot \cdot }}\) defects, which are identified by X-ray photoelectron spectra, make the grain size displays a tendency of decrease first mainly due to the pining effect, and then increase ascribed to the accelerate of mass diffuse. By introducing such wide range of substitution level, Ba 1− x Nd 2 x /3 TiO 3 ceramics with colossal dielectric constant ( x  = 0.08), temperature-stable dielectric properties ( x  = 0.15), especially relaxor behavior ( x  = 0.20) noticed for the first time, are, respectively, received, which is closely related to the variation of phases and defects induced by the addition of Nd. This study may provide a special idea to modify BaTiO 3 to satisfy diversified applications by single element with a wide doping range, and could lay the foundation of future works focusing on the various potential applications of Ba 1− x Nd 2 x /3 TiO 3 ceramics.

研究领域: 材料科学 · 物理学
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JOURNAL OF POWER SOURCES · 2026 · IF 8.4

A dual-regulation strategy for constructing Na2Ti6O13-CeO2(Nd) heterostructures enabling superior-power fuel cells

Ruoming Wang,Yanbei Liu,Yuzheng Lu,Sining Yun

Limited catalytic activity and inefficient ionic transport are major obstacles that compromise the overall performance of low-temperature fuel cells. To address this, we present a novel dual-regulation strategy that synergistically enhances electrolyte ion transport and electrode charge transfer. This approach achieves pre-reconstructed interfacial engineering through in situ phase reconstruction of the electrolyte during heat pretreatment, rather than through real-time interfacial evolution under operating conditions. By tuning the Ti:Ce ratio in the precursor composites, the Na 2 CO 3 -triggered reconstruction converted TiO 2 into oxygen vacancies Na 2 Ti 6 O 13 and formed Na 2 Ti 6 O 13 -CeO 2 (Nd) heterostructure electrolytes. Assembled with LiNi 0.8 Co 0.15 Al 0.05 O 2 electrodes, the optimized Ti:Ce-6%(PS) fuel cell achieves a superior power density of 1011 mW cm −2 at 550 °C. Its excellent structural stability enables stable cell operation for over 45 h at 100 mA cm −2 . This study provides a synergistic and scalable material design strategy for high-efficiency fuel cells.

CAS / MDL: 8000-41-7
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MATERIALS & DESIGN · 2026 · IF 8.2

Preparation of composite ceramics with microwave–sintered uranium tailings for fixing Sr/Nd binary radionuclides

Jiawei Li,Gaiyuan Chen,Min Chen,Zhengxin Wu,Yong Liu

Uranium tailings are directly upcycled into composite ceramics waste forms via microwave sintering. • A dual-phase SrZP/monazite structure enables simultaneous immobilization of Sr 2+ and Nd 3+ . • Rapid microwave sintering achieves high densification (4.24 g·cm −3 ) within 50 min at 1200 °C. • The composite ceramics exhibit enhanced mechanical strength up to 714.1 HV 1 . • Ultra-low leaching rates of Sr (10 –4 ) and Nd (10 –7 g·m −2 ·d –1 ) ensure long-term stability. As a primary byproduct of uranium mining and processing, Uranium tailings result in significant hazards for environment and human health owing to the presence of multivalent radioactive nuclides, especially for 226 Ra(II), 144 Nd(III), and 237 Np (III). Herein, we proposed a microwave one–step sintering of the uranium tailings to fabricate novel composite ceramics as (1– x )SrZP– x NdPO 4 ( x  = 0, 0.2, 0.4, 0.6, 0.8, 1), suggesting the dual purposes of treating uranium tailings and immobilizing divalent fission products (FPs) and trivalent simulated nuclide. The phase evolution, microstructure, density, and chemical stability were systematically investigated for the sintered samples with different Sr/Nd ratios. As presented, the ceramics exhibit high densification without elemental enrichment via sintering at 1200 °C with a 50–min soak . As  x  increases in the crystalline phase, the content of monazite synchronously increases, leading to a maximum density of 4.24 g·cm −3 and a maximum Vickers hardness of 714.1 HV1 in final SrZP–NdPO 4 composite ceramics. More importantly, the SrZP–NdPO 4 composite ceramics demonstrate an excellent leaching resistance, correponding to the leaching rates of Sr and Nd as low as 10 –4 g·m −2 ·d –1 and 10 –7 g·m −2 ·d –1 over a 42–day period, respectively. This study offers a promising strategy for the long-term stabilization and safe disposal of the divalent FPs and trivalent radionuclides in uranium tailings via a ceramic solid-solution approach. A novel (1– x )SrZP– x NdPO 4 composite ceramic was designed to simultaneously enable uranium tailings utilization and the immobilization of divalent fission products (Sr) and trivalent surrogate nuclides (Nd). Download: Download high-res image (264KB) Download: Download full-size image

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APPLIED CATALYSIS B-ENVIRONMENTAL · 2026 · IF 19.7

Coordination and K-induced electronic effects promote efficient COS hydrolysis over K-Nd/Al2O3 catalysts

Yuran Li,Yu Zhang,Yuting Lin,Guangyan Xu,Ruixiang Xu,Wei Su,Tingyu Zhu

A K-Nd/Al 2 O 3 catalyst achieves a COS capacity of 1.46 g/g under H 2 S/O 2 co-feeding. • K modulates Nd Lewis acidity and facilitates the dissociative activation of H 2 O. • Synergistic K and Nd sites enable the formation of key *HOCOS and *HSCOO intermediates. • Adaptive Nd-O x sites, enhanced by K-induced effects, promote H 2 S desorption. The development of efficient alumina-based catalysts for carbonyl sulfide (COS) hydrolysis remains a significant challenge, as their application in real blast furnace gas is largely hindered by insufficient activity and poor long-term durability. Here, K-Nd/Al 2 O 3 maintains nearly complete COS conversion for 20 h at 120 °C and achieves a cumulative COS conversion capacity of 1.46 g/g under a simplified H 2 S/O 2 -containing atmosphere. Comprehensive characterization reveals that K-Nd co-modulation tailors acid-base site distribution, preserving active sites. Aberration-corrected HAADF-STEM and XAFS analyses confirm that Nd is predominantly atomically dispersed, existing as isolated, low-coordinated Nd-O x single-sites. During reaction, the Nd-O coordination number increases from 4.2 to 8.0 without aggregation, demonstrating reaction-induced reconstruction of the first coordination shell. Surface characterization, in-situ DRIFTS, and DFT calculations further show that K enhances surface electron density and fine-tunes Nd Lewis acidity, promoting H 2 O dissociation and nucleophilic *OH attack on COS, stabilizing *HOCOS and *HSCOO intermediates while facilitating H 2 S desorption. The synergy between Nd-O x centers and K-induced electronic regulation reconcile durable COS hydrolysis under harsh conditions. Download: Download high-res image (225KB) Download: Download full-size image

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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2025 ·Vol. 36 ·期 25 ·1-13 · IF 2.8

High-temperature thermistors using novel double perovskite Ba2ReNbO6 (Re = La, Nd, and Sm) NTC ceramics

Lu Jiajun,Kong Wenwen,Xie Juntao,Zhao Yan,Zhao Qing,Chang Aimin

High-temperature thermistors face significant challenges in maintaining stability under extreme temperature conditions, meaning that stringent requirements for material selection and structural design are needed. To address this issue, negative temperature coefficient (NTC) thermistor ceramics of Ba 2 ReNbO 6 (Re = La, Nd, and Sm) were successfully prepared using the solid-state reaction method. X-ray diffraction (XRD) analysis revealed that Ba 2 ReNbO 6 (Re = La, Nd, and Sm) had an ordered double perovskite structure. Scanning electron microscopy (SEM) revealed that as the difference in cationic radii between B′/B″ decreased, the porosity of the materials gradually increased. After Ba 2 ReNbO 6 (Re = La, Nd, and Sm) underwent aging tests at 1173 K for 720 h, the resistance drift rates were 1.33, 3.80, and 5.88%, respectively, and the aging mechanism was explained using cation diffusion theory. These ceramics exhibited typical NTC characteristics over a wide temperature range from 773 to 1473 K, with the degree of linearity exceeding 0.999 for all the samples.

CAS / MDL: 12047-27-7
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2015 ·Vol. 26 ·期 9 ·6807-6813 · IF 1.569

Investigation on structural and functional properties of Nd doped BiFeO3 particles prepared by hydrothermal method

Guan Xiao Ying,Qiao Zhong Wang,Yan Deng Zhou,Sun Yan Fei,Li Jin

This study reports the effect of Nd-doping on structural, morphological and optical properties of BiFeO 3 synthesized by hydrothermal method. The X-ray diffraction’s results indicate that the samples possess single phase up to 12.5 % Nd doping at the Bi site, and all the samples were pure phase microcrystal having a perovskite structure with a space group of R3c. Through the scanning electron microscope, we find that the particles are nearly spherical morphology and the size decreases with Nd doping. The study of Fourier transform infrared spectroscopy confirms the formation of perovskite structure of prepared BiFeO 3 . Photoluminescence spectroscopy shows Nd doping enhanced the Photoluminescence intensity. Ultraviolet–visible absorption spectrum shows BiFeO 3 have a wide absorption band in 550–650 nm wavelength range. The corresponding energy band gap of the samples decreases with the increase of Nd-doping concentration. BiFeO 3 valence band electrons will be excited to the conduction band when the wavelength of visible light is 600–800 nm. It can be used in visible light catalysis. The value of remnant magnetization has improved due to the continuing collapse of the space-modulated spin structure of Bi 0.925 Nd 0.075 FeO 3 microcrystals.

研究领域: 材料科学 · 凝聚态物理 · 纳米材料 · 功能材料
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Cell Communication and Signaling · 2023 ·Vol. 21 ·期 1 ·1-17 · IF 8.4

Endothelial cell-derived MMP19 promotes pulmonary fibrosis by inducing E(nd)MT and monocyte infiltration

Zhao Weiming,Wang Lan,Yang Juntang,Chen Xinyu,Guo Xiaoshu,Xu Kai,Wang Ningdan,Zhao Wenyu,Xia Cong,Lian Hui,Rosas Ivan,Yu Guoying

Background Matrix metalloproteinases (MMPs) play important roles in remodeling the extracellular matrix and in the pathogenesis of idiopathic pulmonary fibrosis (IPF). MMP19, which is an MMP, was significantly upregulated in hyperplastic alveolar epithelial cells in IPF lung tissues and promoted epithelial-mesenchymal transition (EMT). Recent studies have demonstrated that endothelial-to-mesenchymal transition (E(nd)MT) contributes to pulmonary fibrosis. However, the role of MMP19 in pulmonary vascular injury and repair and E(nd)MT remains unclear. Methods To determine the role of MMP19 in E(nd)MT and pulmonary fibrosis. MMP19 expressions were determined in the lung endothelial cells of IPF patients and bleomycin (BLM)-induced mice. The roles of MMP19 in E(nd)MT and endothelial barrier permeability were studied in the MMP19 cDNA-transfected primary human pulmonary microvascular endothelial cells (HPMECs) and MMP19 adenoassociated virus (MMP19-AAV)-infected mice. The regulatory mechanism of MMP19 in pulmonary fibrosis was elucidated by blocking its interacting proteins SDF1 and ET1 with AMD3100 and Bosentan, respectively. Results In this study, we found that MMP19 expression was significantly increased in the lung endothelial cells of IPF patients and BLM-induced mice compared to the control groups. MMP19 promoted E(nd)MT and the migration and permeability of HPMECs in vitro, stimulated monocyte infiltration into the alveolus, and aggravated BLM-induced pulmonary fibrosis in vivo. SDF1 and Endothelin-1 (ET1) were physically associated with MMP19 in HPMECs and colocalized with MMP19 in endothelial cells in IPF patient lung tissues. AMD3100 and bosentan alleviated the fibrosis induced by MMP19 in the BLM mouse model. Conclusion MMP19 promoted E(nd)MT by interacting with ET1 and stimulated monocyte infiltration into lung tissues via the SDF1/CXCR4 axis, thus aggravating BLM-induced pulmonary fibrosis. Vascular integrity regulated by MMP19 could be a promising therapeutic target for suppressing pulmonary fibrosis. Video abstract

CAS / MDL: 57-55-6
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MATERIALS & DESIGN · 2023 · IF 8.4

Designing Nd-doped bismuth selenide nanosheets with boosted photothermal conversion for imaging guided cancer therapy

Yanbang Lian,Congcong Wang,Yu Meng,Junqiang Dong,Jianbin Zhang,Gongxun Bai,Jianbo Gao

Rational design and preparation of multifunctional low dimensional nanomaterials are of great importance for in vivo imaging and safety therapy. Meanwhile, nanomaterials with good bio-compatible and effectively photothermal conversion are still demanded to be fabricated in biomedicine. In this work, we have developed two-dimensional bismuth selenide nanosheets as the imaging and photothermal nanoagents. Through doping engineering, the near infrared photothermal conversion of Nd doped nanosheets was boosted by 52 %, which is higher than many previous works. Besides, the prepared nanomaterials can realize infrared and in vivo computed X-ray tomography bioimaging, due to the rich optical-magnetic properties of Nd atoms. The in vitro and vivo experiments with mice display that the Nd doped nanosheets have low toxicity and high biocompatibility. More importantly, the nanomaterials can efficiently achieve photothermal tumor ablation. It is suggested that designed and developed nanosheets have promising applications for biomedicine.

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JOURNAL OF ALLOYS AND COMPOUNDS · 2022 · IF 6.371

Rare earth Nd-doping lead-free double perovskite Cs2AgBiBr6 films with improved resistive memory performance

Chongguang Lyu,Chang Liu,Huihua Min,Xinyu Shi,Ran Jiang,Zhikang Ao,Xu Zhang,Chunli Wang,Huifang Ma,Lin Wang

Lead-free double perovskites have been an excellent candidate for resistive memories due to their mixed electronic-ionic properties, remarkable ambient stability and nontoxicity. However, the studies on resistive memories of rare-earth ion doping lead-free double perovskite are scarce to date. Here, we report the lead-free double perovskite Cs 2 AgBiBr 6 films with tuning rare earth Nd 3+ content by the vacuum sublimation and solution processing. The X-ray diffraction (XRD) pattern and scanning electron microscopy (SEM) confirm that Nd-doped Cs 2 AgBiBr 6 films show high crystallinity and phase purity. We also systematically investigate the resistive memory properties of the resulted Cs 2 AgBiBr 6 films doped by different content Nd 3+ . The resistive memory devices demonstrate a typical write-once-read-many-times (WORM) behavior with low on-set voltage and long retention time. Particularly, the ON/OFF ratio of Nd-doped Cs 2 AgBiBr 6 film is 1000 times higher than that of the undoped Cs 2 AgBiBr 6 film. This study exhibits that Nd-doped Cs 2 AgBiBr 6 film provide a new material platform for lead-free perovskite-based application in future electronics and optoelectronics .

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JOURNAL OF SOLID STATE CHEMISTRY · 2021 · IF 3.498

A nanoscale Nd-based metal-organic framework electrochemical sensor for rapid detection of Rhodamine B

Shaoxiong Feng,Weigang Ding,Yan Zhang,Jingwei Wu,Zhiming Zou,Tongfa Wu,Qun Tang

A novel neodymium-based metal-organic framework (Nd-MOF) {[Nd 2 (Hpdc) 3 (H 2 O) 6 ]·3H 2 O} n (H 3 pdc ​= ​1H-pyrazole-3,5-dicarboxylic acid) was synthesized by a simple hydrothermal method and structurally characterized. By dropped onto glassy carbon electrodes (GCE), the prepared Nd-MOF was applied to construct an efficient electrochemical sensor for the rapid and reliable electrochemical detection of Rhodamine B (RhB). This proposed Nd-MOF/GCE sensor exhibited strong accumulation ability and high electrocatalytic activity for RhB. Electrochemical oxidation signal of RhB at the Nd-MOF/GCE was greatly enhanced as compared to that at the bare GCE. The effective factors such as pH of buffer solution , amount of Nd-MOF suspension and accumulation time were optimized for the quantitative detection of RhB. Under optimum conditions, the fabricated sensor showed two wide linear ranges of 0.08–2.0 and 2.0–40 ​μM with a low detection limit of 3.6 ​nM, which was ascribed to the advantages of Nd-MOF such as large specific surface area, multiple active sites, strong accumulation ability. Moreover, the developed Nd-MOF/GCE sensor displayed good selectivity and accuracy towards RhB detection in the actual samples. Thus, this simple and efficient approach for RhB detection has good prospective for application in environmental monitoring.

CAS / MDL: 81-88-9
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JOURNAL OF NANOPARTICLE RESEARCH · 2020 ·Vol. 22 ·期 11 ·1-10 · IF 2.132

Preparation of SiO2/YPO4:Nd/SiO2 composite microspheres with near-infrared luminescence and surface functionalization

Yang Yunjiang,Zhu Xiaowei,Bao Jinrong,Bai He,Wu Anping,Qiao Yan,Bian Yulong,Zhao Xin,Li Wenxian,Liu Ying

In this study, the core/shell/shell-structured SiO 2 /YPO 4 :Nd/SiO 2 composite microspheres with near-infrared luminescence property were prepared by sol-gel method. The morphology and structure of the as-prepared microspheres were observed by transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), and infrared spectroscopy (IR). These tests show that the composite microspheres have a sandwich structure. The diameter of the core SiO 2 microspheres is ~ 220 nm, the intermediate layer thickness of rare-earth phosphate is ~ 5 nm, and the outer SiO 2 layer is ~ 20 nm thick. The core/shell/shell microspheres are emitted at 1063 nm in the near-infrared region, which attributes to optical transparent windows of biological tissues. Meanwhile, the interaction between the composite microspheres and bovine serum albumin (BSA) was investigated. The results showed that the composite microspheres could quench the emission intensity of BSA by binding the tryptophan residues in BSA. The synthesized core/shell/shell composite microspheres may be used as near-infrared luminescence probes in the field of biological tissue imaging.

CAS / MDL: 99-05-8 24801-88-5
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Science Advances · 2020 ·Vol. 6 ·期 32 · IF 13.117

Multifunctional bioactive Nd-Ca-Si glasses for fluorescence thermometry, photothermal therapy, and burn tissue repair

Lingling Ma,Yanling Zhou,Zhaowenbin Zhang,Yaqin Liu,Dong Zhai,Hui Zhuang,Qin Li,Jianding Yuye,Chengtie Wu,Jiang Chang

Photothermal therapy (PTT), an emerging tumor treatment technology, has attracted tremendous interest, but excessive heat will cause damage to surrounding healthy tissues. Therefore, in situ temperature monitoring during PTT is of great importance to determine optimal treatment temperature and repair heat-damaged normal tissues. Here, we report the preparation of multifunctional Nd-Ca-Si silicate glasses and glass/alginate composite hydrogels that not only have photothermal property but also emit fluorescence under 808-nm laser irradiation, and its fluorescence intensity is linearly correlated with in situ temperature. With this feature, optimal PTT temperature for effective tumor treatment with minimal normal tissue damage can be obtained. In addition, because of the bioactive silicate components, the composite hydrogel has bioactivity to repair heat damage caused by PTT. This implantable multifunctional material with unique temperature monitoring, photothermal function, and wound healing bioactivity can be used for localized thermal therapy.

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