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JOURNAL OF RARE EARTHS · 2026 · IF 9.6

Highly efficient adjustable photoluminescence with negative thermal expansion/quenching of SrGa2B2O7: Bi/Na/Tb/Eu for LEDs via synergistic alkali metal ions and Sr/O vacancies regulations

Biao Xu,Zihao Xu,Chunyu Li,Jian Peng,Xingyu Li,Wubin Dai

Phosphor with thermally stable and highly efficient photoluminescence (PL) is a premise/challenge for use in high-quality phosphor-converted light-emitting diodes (pc-LEDs). Herein, via a facile solid-phase sintering method in air, a negative thermal quenching (TQ) blue emitting SrGa 2 B 2 O 7 (SGB): Bi is reported, mainly associating with the underlying collaborative effect of negative volumetric thermal expansion of rigid host, heterovalent substitution (Bi 3+ → Sr 2+ )-induced V Sr /V O vacancies, and generating self-reduction ions (Bi 2+ ). For charge balance under the condition of temperature rising, both opposite process of self-oxidation (Bi 2+ to Bi 3+ ) and charge release from trap levels can compensate blue-PL loss. This phosphor is comparable to Eu 2+ /Ce 3+ -activated blue-emitting phosphors, and even boasts superior quantum efficiency (QE) and thermal stability. Via artificially codoping Na + for charge compensation, the QE of the SGB:Bi/Na can be further significantly enhanced. Color-tunable PL is achieved via cascade-connected energy transfer (ET) from Bi 3+ to Tb 3+ (green)/Eu 3+ (red) in SGB: Bi/Na/Tb/Eu that possesses high QE/stability than the case of blue/green/red tricolor phosphor blends adopted in warm white LEDs (wLEDs). Finally, the SGB: Bi/Na and SGB: Bi/Tb/Eu/Na are respectively, encapsulated with distinct encapsulants via either traditional or remote “capping” packaging strategy to form blue LEDs and wLEDs, showcasing splendid electroluminescence behaviors and luciferous application prospects.

✓ 已验证 产品关联 DOI 高影响因子
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Food Packaging and Shelf Life · 2026 · IF 10.8

Bilayer pH-responsive intelligent active packaging film based on gelatin/Na-doped rice bran carbon dots and chitosan/shikonin for real-time salmon freshness monitoring and preservation

Hongkai Xie,Yinlei Mao,Xinhao Wan,Hailu Liao,Chunhao An,Fengjiao Fan,Tao Zhang,Yinji Chen

Aggregated carbon dots exhibit weak antibacterial and antioxidant activities, limiting their application in packaging systems. Metal doping is an effective strategy to enhance their performance. Herein, Na-doped rice bran carbon dots (Na-RBCDs) were synthesized hydrothermally from rice bran and NaOH. A pH-sensitive bilayer film was fabricated via layer-by-layer casting, comprising an outer gelatin layer containing Na-RBCDs and an inner chitosan layer loaded with shikonin for indication/sustained release. Optimal antioxidant and antibacterial activities of Na-RBCDs were achieved at a 10:1 rice bran/NaOH mass ratio, and they exhibited no cytotoxicity toward HaCaT cells below 2 mg/mL. Scanning electron microscopy confirmed their uniform dispersion within the film matrix, ensuring a smooth surface and strong interlayer adhesion. Fourier transform infrared spectroscopy and thermogravimetric analysis indicated that Na-RBCDs formed hydrogen bonds with the polymer matrix, thereby improving the film’s thermal stability. Incorporating 5% Na-RBCDs enhanced UV-blocking ability, hydrophilicity (water contact angle >75°), and tensile strength (1.7-fold increase). The film demonstrated effective sustained release of both active components, alongside improved antioxidant, antibacterial, and pH-responsive colorimetric properties. When applied to refrigerated salmon, the film containing 5% Na-RBCDs extended the shelf life from 3 to 9 days by enhancing chemical and microbial stability. A pronounced color change was observed between days 9 and 12 (ΔE from 15.7 to 30.6), demonstrating its ability to monitor salmon freshness. This gelatin/chitosan-based intelligent active packaging system shows promising applicability for muscle food preservation and freshness monitoring. Further research is needed to establish a precise correlation between colorimetric response and specific spoilage indicators.

✓ 已验证 DOI 高影响因子
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FOOD RESEARCH INTERNATIONAL · 2025 · IF 8

Modulating the aggregation pattern of interface myofibrillar protein in emulsion gel to enhance Na+ inhomogeneous distribution during microwave heating: The effects of hydrophobic interactions and disulfide bonding

Min Zhang,Yaqi Hou,Shuqin Xia,Khizar Hayat,Di Hua,Heping Cui,Jingyang Yu,Shahzad Hussain

Nowadays, modulating microstructure of matrix to achieve salt reduction on diverse food have attract widespread attention. Our previous study found that the spatial site resistance effect of oil droplets attenuated the inhomogeneous distribution of Na + in microwave processing, which was detrimental to the enhancement of saltiness perception. This study promoted the extent of inhomogeneous Na + distribution by 39.79 % through regulating interfacial protein aggregation pattern. The protein aggregation pattern is mainly accomplished through the regulation of hydrophobic interaction and disulfide bonding of interfacial proteins by octenyl succinic anhydride and reduced glutathione, respectively. The results showed that droplet and interfacial tension of myofibrillar protein (MP) increased significantly, while the fluorescence intensity of hydrophobic groups decreased with the increase of hydrophobic interactions regulation. However, regulation of disulfide bonds conducive to the exposure of more hydrophobic amino acids and rapid adsorption of MPs at the oil-water interface to form more stable droplets. The unstable droplets regulated by hydrophobic interactions inhibited the inhomogeneous distribution of Na + in gel matrix, whereas the regulation of disulfide bonds promoted the inhomogeneous distribution of Na + . This work is expected to give some insights into the development of emulsified salt-reduced meat products by microwave processing.

CAS / MDL: 3625-57-8 7385-67-3
✓ 已验证 产品关联 DOI PubMed 高影响因子
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Advanced Science · 2020 ·Vol. 7 ·期 18 ·1903045 · IF 15.84

Graphene-Like Carbon Film Wrapped Tin (II) Sulfide Nanosheet Arrays on Porous Carbon Fibers with Enhanced Electrochemical Kinetics as High-Performance Li and Na Ion Battery Anodes

Zhe Cui,Shu-Ang He,Qian Liu,Guoqiang Guan,Wenlong Zhang,Chaoting Xu,Jinqi Zhu,Ping Feng,Junqing Hu,Rujia Zou,Meifang Zhu

SnS, is a promising anode material for lithium ion batteries (LIBs) and sodium ion batteries (SIBs), however, undergoes poor cyclic lifespan due to its huge volume changes and bad electroconductivity. Here, a modified CVD method is used to directly grow graphene-like carbon film on the surface of SnS nanosheet arrays which are supported by Co-, N-modified porous carbon fibers (CCF@SnS@G). In the strategy, the SnS nanosheet arrays confined into the integrated carbon matrix containing porous carbon fibers and graphene-like carbon film, perform a greatly improved electrochemical performance. In situ TEM experiments reveal that the vertical graphene-like carbon film can not only protect the SnS nanosheet from destruction well and enhance the conductivity, but also transforms SnS nanosheet into ultrafine nanoparticles to promote the electrochemical kinetics. Systematic electrochemical investigations exhibit that the CCF@SnS@G electrode delivers a stable reversible capacity of 529 mAh g −1 at a high current density of 5 A g −1 for LIBs and 541.4 mAh g −1 at 2 A g −1 for SIBs, suggesting its good potential for anode electrodes.

研究领域: 材料科学 · 电化学
✓ 已验证 DOI 高影响因子
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INORGANIC CHEMISTRY · 2018 · IF 4.7

Effect of Element Substitution on Structural Transformation and Optical Performances in I2BaMIVQ4 (I = Li, Na, Cu, and Ag; MIV = Si, Ge, and Sn; Q = S and Se)

Leyan Nian,Kui Wu,Guijie He,Zhihua Yang,Shilie Pan

In the exploration of new infrared nonlinear optical (IR NLO) materials, element substitution has been developed as an effective way to adjust the structural features and material performances. A series of new IR NLO materials have been discovered in the I–Ba–MIV–Q system (I = Li, Na, Cu, and Ag; MIV = Si, Ge, and Sn; Q = S and Se), and they undergo interesting structural transformation with different element substitution except Li analogues. Herein, we have successfully synthesized three selenides with different space groups (Ag2BaSiSe4: I4̅2m; Ag2BaGeSe4 and Ag2BaSnSe4: I222) in the above system and studied their properties through experimental and theoretical methods. Remarkably, the detailed analysis on the structural changes and properties comparison was also systematically investigated in the I–Ba–MIV–Q system and the results indicate that the distortion degrees of different IQ4 tetrahedra play the critical role to cause the structural transformation with the M or Q elements substitution. More importantly, we have also found that the structural changes have the close relationship with the distance d(I–I) between adjacent I cations in the I2BaSnSe4 system, which makes the four-membered rings formed by edge-sharing BaSe8 units change from the square to rhombus with the increase of d(I–I). The properties comparisons (band gap and NLO effect) in this system have been also systematically studied.

研究领域: 材料科学 · 无机化学 · 光学材料 · 固态化学
✓ 已验证 DOI 高影响因子
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CERAMICS INTERNATIONAL · 2025 · IF 5.6

On the photoluminescence differences of Eu3+-activated layered perovskite La2Ti2O7 and A2La2Ti3O10 (A = Li, Na, K) phosphors for potential applications in white LEDs and plant growth lighting

Dong Yi,Jiawei Fu,Fenzhong Long,Jin Han,Fangui Meng,Xinmin Zhang

To improve the quality of white LED and develop plant growth lighting, considerable efforts have been devoted to investigating red phosphor. Eu 3+ -activated phosphors are well-known red-emitting components due to their 5 D 0 - 7 F 1,2 transitions in various applications. It is also found that its 5 D 0 - 7 F 4 transition in the range of far-red wavelengths has potential applications in the fields of daily and agricultural lighting. In this study, two kinds of Eu 3+ -doped layered perovskite La 2 Ti 2 O 7 and A 2 La 2 Ti 3 O 10 (A = Li, Na, K) phosphors were synthesized by the solid-state method. The crystal structure, absorption, excitation, and emission spectra of all the samples were investigated in detail. Dissimilar luminescent behaviors of the studied samples were observed. Due to the different crystal structure and chemical composition of the host matrix, each compound exhibits a different emission spectrum. Specifically, Eu 3+ occupies a lower symmetric La 3+ site in A 2 La 2 Ti 3 O 10 (A = Li, Na, K) phosphors, resulting in an intense 5 D 0 - 7 F 4 far-red emission, while in La 2 Ti 2 O 7 :Eu 3+ , Eu 3+ gives a weak 5 D 0 - 7 F 4 emission. To the best of our knowledge, this is the first report that Eu 3+ exhibits a strong 5 D 0 - 7 F 4 far-red emission in the titanate host lattices with perovskite structure. Besides, A 2 La 2 Ti 3 O 10 :Eu 3+ (A = Li, Na, K) phosphors achieve higher photoluminescence efficiency than La 2 Ti 2 O 7 :Eu 3+ . Among them, the internal quantum efficiency of the optimized Li 2 La 2 Ti 3 O 10 :1.2Eu 3+ is about 84.7 %, and it has a better thermal stability (80 % at 125 °C). Furthermore, good photoelectric performances of red/white-LEDs fabricated by utilizing the representative Li 2 La 2 Ti 3 O 10 :1.2Eu 3+ as red/far-red components indicate that it has potential applications in indoor/outdoor lighting and plant growth lighting. This study provides a feasible way for developing efficient Eu 3+ -activated far-red optical materials.

✓ 已验证 产品关联 DOI 高影响因子
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JOM · 2024 ·Vol. 76 ·期 8 ·4169-4178 · IF 2.1

Synthesis and Electrochemical Performance of Na and F Elements Co-Doped LiFePO4/C as a Cathode Material for High-Rate Lithium-Ion Batteries and the Mechanism of Modification

He Jie,Liu Jiaming,Yu Xiuyuan,Yang Chao,Liu Qingsheng

LiFePO 4 has become a mainstream cathode material, owing to its good safety and low price. However, its intrinsic limitations in terms of electronic and ionic conductivities hinder its further advancements. To overcome this challenge, element doping has been explored to enhance its conductivity. Here, Na and F co-doped LiFePO 4 /C was successfully synthesized via a carbothermic method. Structural characterization techniques were employed to confirm the formation of Li 0.97 Na 0.03 FePO 3.97 F 0.03 with controllable particle sizes. The incorporation of Na and F ions into the LiFePO 4 lattice results in a reduction of the Li-O bond energy. This decrease in bond energy facilitates the extraction and insertion of lithium ions during the charge and discharge processes, subsequently improving the overall kinetics of lithium-ion diffusion. Simultaneously, lattice distortion induced by doping led to charge compensation and accelerated Li + migration. Benefiting from the enhancement of intrinsic conductivity and Li + diffusivity, the specific capacitance of the co-doped LiFePO 4 /C cathode material was found to be 160 and 110 mAh g −1 at 0.1 and 5 C, respectively. Further, density functional theory calculations showed that Na/F co-doping enhanced the structural evolution in the material and increased free carrier concentration in LiFePO 4 . This work demonstrates that synergistic Na and F co-doping can optimize the rate performance of LiFePO 4 by enhancing intrinsic conductivity and Li + diffusivity, suggesting promising applications of the co-doped LiFePO 4 /C in high-power lithium-ion batteries for electric vehicles and grid-level energy storage systems.

研究领域: 材料科学 · 电化学
✓ 已验证 DOI 高影响因子
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JOURNAL OF ALLOYS AND COMPOUNDS · 2024 · IF 5.8

The interference mechanism of Na+ and Cl- on photocatalytic properties of phosphate-oxygen co-doped graphite carbon nitride for hydrogen production from water splitting: Experimental and theoretical calculations

Longde Jiang,Jingde Luan,Yu Zhang,Qingyu Chi,Wengang Liu,Zheng Yan,Shaobai Li,Chen Zhao

Phosphorus-oxygen co-doped graphite carbon nitride (POx-CN) are successfully fabricated by in situ impregnation and two-stage thermal polycondensation to investigate the effect of Na + and Cl - on the photocatalytic hydrogen evolution from artificial seawater splitting. The as-prepared POx-CN exhibits a hydrogen evolution rate of 1054.29 μmolg −1 h −1 in artificial seawater , lower than fresh water , indicating that Na + and Cl - play an inhibitory effect on hydrogen evolution reaction . The theoretical calculation indicates that the phosphorus-oxygen binary doping changed the electrostatic potential of the modified layer in carbon nitride molecule, accelerating the electron transfer rate from the structural O in triazine ring to P-N bond. In artificial seawater, the competition between Na + and Pt 2+ at active sites in the modified layer and electron capture by Cl - in the mutual conversion of Cl - and chlorine radicals result in the reduction of hydrogen evolution efficiency.

CAS / MDL: 108-78-1
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2022 · IF 8.025

Synthesis of cellulose-based superabsorbent hydrogel with high salt tolerance for soil conditioning

Yu Guo,Rongbo Guo,Xiaoshuang Shi,Shujuan Lian,Qiannan Zhou,Ying Chen,Weifeng Liu,Wei Li

In this study, cellulose-based superabsorbent hydrogel was synthesized from sodium carboxymethyl cellulose (CMC-Na), acrylic acid (AA), and 2-acrylamido-2-methylpropanesulfonic acid (AMPS) to enhance its water absorbency and salt tolerance for soil-conditioning applications in areas suffering from drought and soil salinization. Superabsorbent hydrogels (SHs) were prepared by CMC-Na and AMPS successfully, using chemical graft technology. Structure, morphology, thermal stability , and water absorbency of SHs were deduced. The cellulose-based hydrogel showed a high salt tolerance that the maximum water absorbency reached 604 and 119% in distilled water and saline water, respectively. The swelling behavior in aqueous solvents indicated that the water absorption of hydrogels was improved with the increasing ratio of CMC-Na. All SHs exhibited adsorption of nitrogen with the maximum adsorption of ammonia nitrogen 30 mg·g −1 and the presence of hydrogels could slow down the loss of nutrients in the soil. This study provided a feasible strategy that AMPS was substituted by CMC-Na to synthesize SHs with strong water absorbency and high salt tolerance which could be efficiently applied in agriculture as a soil conditioner.

研究领域: 材料科学 · 环境科学 · 农业科学
✓ 已验证 DOI 高影响因子
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CERAMICS INTERNATIONAL · 2022 · IF 5.532

Influence of alkali metal and alkaline earth metal oxides on physical and optical properties of TeO2–WO3–GdF3-R2O-ZO: Eu3+ glasses (R = Li, Na, K, Z = Mg, Ca, Ba)

Ce Li,Xu Zhang,V.C. Onah,Weiling Yang,Zhuang Leng,Xiliang Jiang,Fangming Zhang,Shasha Li,Yong Zhang,Yu Han,Huisheng Liu,Chun Li,Dingfu Zhou,Fanming Zeng

In analyzing the effect of alkali metal and alkaline earth metal oxide on the properties of tellurite glass , a series of tellurite glass samples doped with alkali metals and alkaline earth metals were prepared based on the TeO 2 -WO 3 -GdF 3 glass system by melt quenching method. Through tests and comprehensive analysis, the results show that after the F − ions successfully enter the glass network, the substitution of TeO 2 by alkali and alkaline earth metals could reduce the molar volume , which means the glass becomes more compacted. The influence on the glass network is mainly shown in [TeO 3 ] and [TeO 4 ] units. Alkali metals and alkaline earth metals could increase the asymmetry of the TWG: Eu 3+ glass network, shorten the critical distance, and increase luminescence intensity by 8.6 times and improve color purity to 94%. In addition, alkali metals could prolong the fluorescence lifetime , while alkaline earth metals could shorten it. Te 4+

研究领域: 材料科学 · 光学材料 · 玻璃物理 · 发光光谱学 · 无机化学
✓ 已验证 DOI 高影响因子
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Advanced Materials Interfaces · 2020 ·Vol. 7 ·期 19 ·2000684 · IF 4.948

In Situ Electrospinning Synthesis of N-Doped C Nanofibers with Uniform Embedding of Mn Doped MFe1−xMnxPO4 (M = Li, Na) as a High Performance Cathode for Lithium/Sodium-Ion Batteries

Wenyan Chen,Donghui Xu,Yuancheng Chen,Tang Tang,Shaojie Kuang,Haikuo Fu,Wuyi Zhou,Xiaoyuan Yu

Using polyvinyl alcohol and N-rich polyacrylonitrile as carbon sources, uniform MFe 1– x Mn x PO 4 (M = Li, Na)/N-doped C nanofibers are synthesized by sol–gel pretreatment and an electrospinning method followed by calcination. The as-prepared nanofibers exhibit a 3D homogenous network with uniform distribution of MFe 1− x Mn x PO 4 nanoparticles. The lattice distorts after Mn-doping without altering the original crystalline structure, increasing conductivity and enhancing the efficiency of Li + /Na + diffusion. When applied for lithium ion batteries, the optimized LiFe 0.8 Mn 0.2 PO 4 /C nanofibers deliver a considerable initial capacity of 169.9 mAh g −1 with coulombic efficiency of 92.4%. It also displays the excellent cycling stability with reversible capacity of 160 mAh g −1 after 200 cycles at 0.1 C and high rate performances with the specific capacity of 93 mAh g −1 at 5 C. Furthermore, NaFe x Mn 1− x PO 4 /N-doped C nanofibers are also synthesized by the same method for sodium-ion batteries, which exhibit an initial capacity of 134 mAh g −1 and specific capacity of 106 mAh g −1 at 0.1 C and 90 mAh g −1 at 1 C after 200 cycles. Owing to the facile fabrication process, these nanofibers are promising cathodes for lithium/sodium ion batteries with excellent electrochemical performances.

研究领域: 材料科学 · 电化学 · 纳米科技 · 能源存储 · 固态化学
✓ 已验证 DOI 高影响因子
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Small · 2021 ·Vol. 17 ·期 46 ·2101887 · IF 13.281

Rational Design of Yolk–Shell Zn?Co?Se@N-Doped Dual Carbon Architectures as Long-Life and High-Rate Anodes for Half/Full Na-Ion Batteries

Jian Feng,Shao-hua Luo,Sheng-xue Yan,Yang Zhan,Qing Wang,Ya-hui Zhang,Xin Liu,Long-jiao Chang

Transition-metal selenides (TMSs) have emerged as prospective anode materials for sodium ion batteries (SIBs), owing to their considerable theoretical capacity and intrinsic high electronic conductivity. Whereas, TMSs still suffer from poor rate capability and inferior cycling stability induced by sluggish kinetics and severe volume changes during de/sodiation processes. Herein, a hierarchical composite consisting of a zinc-cobalt bimetallic selenide yolk and nitrogen-doped double carbon shell (denoted as Zn  Co  Se@NDC) is engineered and fabricated successfully. The architecture of the as-fabricated material improves the Na-ion storage performance via increasing the electron transfer kinetics, accommodating volume expansion, and mitigating the generation of by-products. As expected, the Zn  Co  Se@NDC electrode delivers superior sodium storage performance with long cycling stability (344.5 mAh g −1 at 5.0 A g −1 over 2000 long-term cycles) and high-rate performance (319.2 mAh g −1 at 10.0 A g −1 ). Meanwhile, the NVP@C//Zn  Co  Se@NDC full SIB cells are constructed successfully, retaining 96.3% of its initial capacity at 0.5A g −1 after 200 loops. The outstanding electrochemical performance and the construction of hybrid SIBs will have far-reaching influences on the development of the various rechargeable batteries.

研究领域: 材料科学 · 能源存储
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