Journal of Materials Chemistry C
·
2024
·Vol. 12
·期 45
·18300-18307
·
IF 5.7
Xu Yang,Zihao Ren,Tao Yin,Jialong Yu,Xinying Song,Yuansheng Ma,Xu Li,Li Guan,Yingnan Guo,Fenghe Wang
Near-infrared (NIR) phosphors have been extensively used in the fields of biological imaging, night vision monitoring, and food safety inspection. Although Cr3+ doping phosphors have been widely reported, achieving broadband and tunable NIR emissions remains challenging. In this work, Cr3+-doped LiSc2SbO6 broadband NIR phosphors were synthesized by a high-temperature solid-phase method. LiSc2SbO6:Cr3+ exhibits a wide emission band of 780–1400 nm. By [Mg2+–Mg2+] co-substituting the [Li+–Sc3+] chemical units, controllable emission is achieved with the emission peak tuning in the range of 890–950 nm, FWHM in the range of 215–239 nm, and the maximum intensity increased by 1.51 times. On co-doping with Yb3+ ions, the luminous intensity of the Li0.7Mg0.6Sc1.7SbO6:0.02Cr3+,0.05Yb3+ (LMSS:Cr3+,Yb3+) phosphor has been further enhanced by 5.62 times. Thus, the LMSS:Cr3+,Yb3+ phosphor has great potential in the field of anti-counterfeiting and information encryption. By combining LMSS:Cr3+,Yb3+ with a commercial blue LED chip, the obtained NIR pc-LED performs well in night vision and non-destructive testing applications.
研究领域:
材料科学
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光学材料
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固态照明
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光子学
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防伪技术
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高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2026
·
IF 9.6
Xuejie Zhang,Huijie Zhang,Yanyang Jia,Guihua Liu,Aijia Wei,Yongguang Zhang,Jingde Li
Innovatively proposed Mg 2+ & Ti 4+ co-doped to efficiently suppress Mn 3+ -induced Jahn-Teller distortion and stabilize LMFP's olivine framework. • In-situ characterizations combined with DFT calculations clarify the intrinsic mechanism of co-doped regulating LMFP's crystal/electronic structures. • Co-doped significantly boosts LMFP's electronic conductivity and capacitive contribution, realizing superior high-rate performance and structural reversibility. • Co-doped LMFP@C-MT reduces Mn dissolution by alleviating Jahn-Teller distortion, further enhancing the cathode's structural and electrochemical stability. LiMn x Fe 1-x PO 4 (LMFP) cathodes are considered promising candidates for next-generation lithium-ion (Li + ) batteries due to their high safety, low cost, environmental benignity, and relatively high energy density. However, they suffer from severe Jahn-Teller distortion and sluggish Li + kinetics, leading to poor structural stability and rate performance. Herein, a synergistic Mg 2+ and Ti 4+ co-doping strategy is proposed to concurrently regulate the crystal structure and electronic properties of LMFP. Structural and electrochemical analyses show that Mg 2+ and Ti 4+ effectively suppress Mn 3+ -induced Jahn-Teller distortion. This helps stabilize the olivine framework while causing a small shrinkage in the crystal lattice, thereby improving Li + diffusion capability. In situ XRD reveals that un-doped lithium manganese iron phosphate (LMFP@C) undergoes a distinct phase transition during the high-voltage plateau, as evidenced by peak splitting, whereas Mg 2+ and Ti 4+ co-doped lithium manganese iron phosphate (LMFP@C-MT) exhibits a continuous peak shift, indicative of a solid-solution reaction with improved structural reversibility. Density functional theory (DFT) calculations further demonstrate that Mg 2+ lowers the Li + migration energy barrier, while Ti 4+ stabilizes the Mn electronic structure near the Fermi level. This synergistic effect suppresses Jahn-Teller distortion, thereby enhancing both structural stability and electrochemical kinetics. This enables the LMFP@C-MT cathode to deliver a high initial capacity of 158.35 mAh g −1 at 0.2C, along with outstanding cycling stability, retaining 91.39% capacity after 500 cycles at 1C. This work both presents an effective structural modification strategy and supplies theoretical guidance for the development of high-performance LMFP-based cathode materials. The LMFP@C-MT synthesized by the high-temperature solid-state method suppresses the Jahn–Teller distortion induced by Mn 3+ and stabilizes the lattice. Combined with the ordered carbon coating, it enhances the charge transfer kinetics, thereby achieving excellent structural reversibility and electrochemical performance. Download: Download high-res image (196KB) Download: Download full-size image
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高影响因子
JOURNAL OF MEMBRANE SCIENCE
·
2026
·
IF 8.8
Xin Shi,Qiuyan Bi,Zizhen Peng,Zhicheng Wang,Xiaodan Zhang,Yakai Lin,Wenzhong Ma,Shiai Xu
Thin-film composite (TFC) nanofiltration (NF) membranes generally face a challenging balance between permeability and selectivity when separating saline water with a high Mg 2+ /Li + ratio, and are also vulnerable to fouling and operational instability during prolonged operation. This study presents a dual ionic liquid (IL) mediated reverse interface polymerization (RIP) strategy. A hydrophilic polar intermediate layer is generated on the PES substrate via the co-deposition of tannic acid (TA) and [HEMIm][BF 4 ]. Subsequently, the organic phase containing TMC is first introduced on the surface of this intermediate layer, and then the PEI aqueous phase doped with hydrophobic IL ([C 6 mim] [Tf 2 N]) is introduced to trigger the RIP reaction. TIL-PIL membranes with rapid hydration behavior, a high positive surface charge (IEP pH = 9.5), excellent antifouling properties, and a uniform pore-size distribution were constructed for Mg 2+ /Li + separation. The separation factor (SF) of the membrane attained 88 at a feed Mg 2+ /Li + mass ratio of 300, while maintaining a high salt water permeation flux of 13.58 LMH. Throughout the permeation process, the Mg 2+ /Li + ratio diminished from 300 in the feed to 1.2 during permeation. Moreover, the membrane demonstrated exceptional long-term stability throughout a continuous 100 h filtration experiment, with the Mg 2+ rejection rate consistently surpassing 98.5%. Compared with the RNFm membranes prepared on PES substrates without IL incorporation, the TIL-PIL membranes exhibit significantly improved antifouling performance.
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高影响因子
CERAMICS INTERNATIONAL
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2026
·
IF 6
Dan Yang,Jiajin Lin,Xingzhong Liu,Hanxing Liu,Zhonghua Yao,Hua Hao
The development of base metal electrode multilayer ceramic capacitor (BME-MLCC) dielectric materials that combine high reduction resistance with superior energy storage performance is crucial to meet the demands of next-generation high-power electronic devices and power modules. In this study, a series of BaTiO 3 –MnO 2 –Yb 2 O 3 – x MgO (BMYT- x Mg, x = 0–3) ceramics were successfully produced in a reducing atmosphere. The influence of Mg 2+ acceptor doping on the anti-reduction resistance mechanism and energy storage behavior was systematically investigated. The results indicate that Mg 2+ doping promotes the formation of [Mgʹʹ Ti-V•• O] defect dipoles, which effectively suppresses the generation and migration of charge carriers. This mechanism enables the BMYT-2Mg ceramic to maintain an insulation resistivity as high as 3.6 × 10 11 Ω m even after sintering in a reducing atmosphere. Additionally, Mg 2+ doping optimizes the phase structure, refines the grain size, increases the grain boundary density, and synergistically enhances the relaxor characteristics of the system. As a result, the BMYT-2Mg ceramic achieves a recoverable energy storage density ( W rec ) of 1.75 J/cm 3 and an energy storage efficiency ( η ) of 72.65% under an electric field of 270 kV/cm. It also demonstrates excellent energy storage stability and electrical reliability across a temperature range of 40–120 °C and over 10 5 charge–discharge cycles at 130 kV/cm. This work provides an effective design strategy for fabricating BaTiO 3 -based dielectric ceramics with both high reduction resistance and superior energy storage performance in a reducing atmosphere.
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高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2026
·
IF 12.5
Xin Shi,Qiuyan Bi,Zizhen Peng,Zhicheng Wang,Fangbo Zhu,Yakai Lin,Wenzhong Ma,Chuanjie Fang,Shiai Xu
RIP microenvironment regulation and amino acid functionalization synergize NF design. • BDM scavenges H + to suppress PEI protonation and preserve reactivity. • L-Arginine functionalization enhances membrane hydration and positive charge. • P-B-0.8/A-0.1 membrane achieves 99.5% Mg 2+ rejection and an SF of 131.7. • After 80 h, MgCl 2 rejection >98%, showing stable and antifouling performance. Thin-film composite (TFC) nanofiltration (NF) membranes show great potential for Mg 2+ /Li + separation. However, during conventional interfacial polymerization, excessively rapid amine diffusion and local acidification at the reaction interface can lead to nonuniform interfacial reactions. This study proposes a synergistic construction strategy of membrane forming microenvironment regulation and amino acid interface empowerment. Bis (2-dimethylaminoethyl) ether moderated the apparent migration and protonation behavior of polyethylenimine and alleviated local acidification at the reaction front. Subsequent L-arginine post modification enhanced surface hydration and modified the acid–base/charge characteristics of the polyamide layer interface. P-B-0.8/A-0.1 membrane with high positive surface charge (IEP pH = 8.5), excellent antifouling properties, and a uniform pore-size distribution were constructed for Mg 2+ /Li + separation. In the MgCl 2 /LiCl mixed salt system, the membrane achieved an Mg 2+ rejection rate of 99.5% and a separation factor of 131.7. During 80 h of continuous operation, the Mg 2+ rejection rate remained above 98%. Moreover, the P-B-0.8/A-0.1 membrane exhibited excellent flux recovery and anti-scaling stability during BSA and lysozyme fouling cycles, as well as in CaSO 4 and CaCO 3 inorganic scaling systems.
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高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2026
·
IF 9.1
Chenxu Wang,Wanting Yang,Yuchen Shi,Hongchang Liu,Hongfei Ba,Baojun Yang,Jun Wang
In high-Mg 2+ wastewater systems, the sulfidization flotation of malachite is severely inhibited. This study systematically investigated the effect of mechanical sulfidization on the flotation behavior of malachite in comparison with conventional stirring sulfidization. Pure mineral flotation tests showed that in a 100 mmol/L Mg 2+ solution, mechanical sulfidization achieved a maximum malachite recovery of 83.77%, significantly superior to stirring sulfidization. Actual ore flotation further confirmed that the copper recovery increased from 74.16% to 84.33% using mechanical sulfidization. Characterization results indicated that mechanical sulfidization effectively reduced magnesium ion adsorption on the malachite surface, promoted the rapid formation of Cu S hydrophobic species with a higher Cu(I) proportion, suppressed hydrophilic Cu–SO species, and generated a denser sulfidization layer. Electrochemical measurements revealed that mechanical sulfidization facilitated xanthate oxidation and constructed a stable hydrophobic barrier. DFT calculations further demonstrated that the mechanically sulfidized surface exhibited a higher Cu S bond population and a significantly lower activation energy barrier for xanthate oxidation than stirring sulfidization. In summary, mechanical sulfidization constructs a highly covalent Cu S network enriched with Cu(I) that lowers the kinetic barrier for xanthate oxidation, effectively alleviating the interference of high Mg 2+ ions. This study fills the gap in understanding the surface chemical states and electronic structure mechanisms underlying mechanical activation in malachite sulfidization flotation, providing a theoretical basis for high-Mg 2+ wastewater recycling in copper oxide ore flotation.
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高影响因子
Materials Futures
·
2024
·
IF 12
Xiang Xu,Yi Wang,Siyu Zhu,Rui Jia,Zulan Liu,Guotao Cheng,Dingpei Long,Lan Cheng,Fangyin Dai
Severe bone defects remain a significant clinical challenge, necessitating the development of advanced bone repair scaffolds with excellent biocompatibility, precise immune modulation, and robust support for vascularization and osteogenesis. Silk fibroin (SF), a polymer renowned for its outstanding biocompatibility, has been widely used in bone repair scaffold materials. However, its complex fabrication process limits its broader clinical application. In this study, flat silkworm cocoon (FSC), characterized by continuous silk fibers, a porous hierarchical structure, and superior mechanical properties, was utilized for the first time to fabricate bio-scaffolds (TH-PDA@Mg) designed for sustained magnesium ion release in bone repair applications. FSC scaffolds featuring surface pores and extracellular matrix-like structures were successfully prepared using hot-press and surface modification techniques. Magnesium ions were effectively assembled onto FSC scaffolds via polydopamine (PDA)-mediated adhesive interactions. The resulting TH-PDA@Mg scaffolds demonstrated enhanced osteogenic properties, exceptional mechanical strength, superior surface characteristics, and excellent biocompatibility. In vitro analyses revealed that these scaffolds supported cell adhesion, promoted stem cell proliferation, and facilitated osteogenic differentiation due to the synergistic effects of SF and magnesium ions. Furthermore, they exhibited immunomodulatory properties by promoting M2 macrophage polarization while suppressing M1 macrophage activity. In vivo studies using a rat model of critical-sized cranial bone defects showed that the TH-PDA@Mg scaffolds accelerated bone regeneration, enhanced angiogenesis, and mitigated inflammation. These findings highlight the remarkable osteogenic and immunomodulatory potential of functional bio-spinning silk fiber scaffolds, underscoring their promise as a therapeutic strategy for the clinical treatment of bone defects.
研究领域:
生物材料
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组织工程
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再生医学
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免疫学
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高影响因子
JOURNAL OF MEMBRANE SCIENCE
·
2024
·
IF 8.4
Xin Mao,Nuanyuan Xu,Xinyu Shi,Hui Wen,Changkun Liu
Nanofiltration (NF) is commonly recognized as one of the effective technologies for the separation of magnesium (Mg 2+ ) and lithium (Li + ) from salt-lake brines. Charge repulsion and size exclusion effects often play an important role, whose functions primarily occur at the top surface and the matrix, respectively, of the skin layer. In this study, a novel nanofiltration (NF) membrane is prepared that integrates both size exclusion and charge repulsion effects into the matrix of the skin layer for enhanced Mg 2+ /Li + separation. With the surface-modified hydrophilic polyethylene (PE) membrane as the supporting layer, the prepared NF membrane successfully incorporated Fe 3+ ions into the matrix of the skin layer during the interfacial polymerization (IP). Fe 3+ ions which chelate with amine groups of PEI (aqueous-phase monomers during IP) ensure abundant positive charges within the matrix of the skin layer, providing good hydrophilicity and sustained electrostatic repulsive force against the transmembrane transport of Mg 2+ , and thus the enhanced rejection. Results exhibited a remarkable 92.6 % rejection rate for MgCl 2 and a higher water permeance of 22 LMH/bar, which is 1.57 times greater than that of the traditional PEI-TMC membranes. The nanofiltration process effectively reduced the Mg 2+ /Li + ratio from 50 in the feed to 5.4 in the permeate solution. It is also interesting to find that although the pore size of the skin layer (0.53 nm in radius) exceeds both the hydrated radii of Mg 2+ and Li + , the positive charges within the matrix of the skin layer still provide good selective separation performance, thus effectively breaking the trade-off of permeability and selectivity. This study offers a fresh perspective on the preparation of nanofiltration membranes by systematically exploring the potential of integration of charge repulsion and size exclusion effects into one location, i.e., the matrix of the skin layer for enhanced Mg 2+ /Li + separation performance.
研究领域:
材料科学
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环境工程
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高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2019
·
IF 5.107
Changsheng Guo,Nan Li,Xiaoming Qian,Jie Shi,Miaolei Jing,Kunyue Teng,Zhiwei Xu
To explore nanofiltration (NF) membrane with high permeability and good separation for Li + from salt-lake, a triple-layered ultra-thin double Janus NF membrane was prepared with polyethersulfone (PES) substrate membrane, a carboxylated cellulose nanocrystal (CNC-COOH) interlayer and an ultra-thin polyamide (PA) layer via interfacial polymerization of polyethylenimine and trimesoyl chloride. The interlayer contain a large number of carboxyl groups, which could improve not only the negative potential of interlayer, but also the positive potential of the PA layer because of the increase of unreacted NH 2 . In addition, the hydrophilic of interlayer was stronger than the PA layer. Therefore, the interlayer and the ultra-thin PA layer could construct a double Janus NF membrane with hydrophobic/hydrophilic, positive/negative charge. It was found that the content of carboxyl groups and unreacted amino groups on the surface of Janus PES/CNC-COOH/PA NF membrane was increased obviously. The thickness of Janus NF membrane PA layer was 60.29 nm, 55.56% thinner than that in traditional PES/PA NF membrane and 25.89% thinner than that in weak Janus PES/cellulose nanocrystal/PA NF membrane. The Janus NF membrane had a minimum average surface roughness of 6.21 nm, an effective pore diameter of 1.38 nm, and exhibited a positive surface charge with a highly hydrophilic nature. Under the Mg 2+ /Li + ratio of 30 and 60, the Janus NF membrane exhibited the rejection difference between Mg 2+ and Li + reached to 74.35% and 83.96%, the water flux was 4.17 and 3.4 L/(m 2 ·h·bar), respectively, and the separation factor S Li,Mg was 12.15 and 5.84, respectively.
研究领域:
纳米技术
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膜科学
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材料科学
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化学工程
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环境科学
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高影响因子
COMPOSITES PART B-ENGINEERING
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2021
·
IF 9.078
Shuangli Zhu,Qiyuan Dai,Longtao Yao,Zetao Wang,Zhichao He,Maocai Li,Hao Wang,Qingtao Li,Huichang Gao,Xiaodong Cao
Diabetic ulcers are common and severe chronic wound. For the treatment of diabetic ulcers, due to the existence of sinus and fistula in the wound sites, the prefabricated hydrogel could not cover the deep wounds well and result in further presence and proliferation of bacteria at the deep wound site, which increases the risk of secondary infection. In addition, most current hydrogel dressings do not rapidly repair wounds due to the lack of bioactivity . Therefore, it's essential to develop a bioactive hydrogel dressing with self-adaption to solve the above clinical problems. In this work, HQ hydrogel was fabricated by the self-crosslinking of hyaluronic acid modified with phenyl boronate acid (HA-PBA) by boronate ester dynamic bonds and electronic interaction between quaternized chitosan (QCS) and HA-PBA, which possessed good injectability , self-healing, adhesion and antibacterial properties . Especially, HQ hydrogel with good self-adaption can be shaped as needed and automatically adapt to the wounds with all kinds of shapes. In addition, Magnesium-containing bioactive glasses (BGs) with a uniform spherical morphology and amorphous structure were incorporated into HQ hydrogel to achieve nanocomposite hydrogel (HQB), which possessed good bioactivity and could slowly release magnesium to recruit cells, promote vascularization and anti-inflammation. More importantly, animal experiments showed that HQB hydrogel can strikingly accelerate wound healing of diabetic SD rats by improving granulation tissues formation, collagen deposition, the formation of blood vessels and decreasing inflammation in the wound sites, indicating a good clinical application prospect as wound dressing for diabetic wound healing.
研究领域:
材料科学
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生物医学工程
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伤口愈合
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DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
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2023
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IF 15.1
Tong Wen,Yunliang Zhao,Xingwen Wang,Licai Chen,Renbo Gao,Shutong Wang,Tingting Zhang
Recent innovations have created various two-dimensional membranes to break the Li + /Mg 2+ selectivity limit of traditional separation membranes. However, the simultaneous achievement of ultrafast transport and high selectivity is still below the theoretical prediction. Herein, for overcoming these shortcomings, the two-dimensional montmorillonite membrane (2D MMT membrane) consisting of sulfonated polyvinyl alcohol (SPVA), ethylene glycol (EG), and polyacrylamide (PAM) is proposed based on the design of porous 2D nanochannels. It is found that the SPVA can effectively improve the membrane stability, but will densify the channel, and prevent ion transport. When the appropriate EG is included in the membrane component, the transport rate of Li + can be increased from 0.29 mol h −1 m −2 to 0.56 mol h −1 m −2 . However, because the transport of Mg 2+ needs to overcome the high dehydration energy barrier, the J Mg2+ changes little, hence increases in S Mg 2+ Li + from 4.1 to 7.3. In addition, the selectivity regulation of PAM can be further integrated, and the permselectivity of the membrane is improved to 9.2 due to the strong selective coordination of amide groups to Mg 2+ . This novel strategy provides a valuable reference for developing high-performance 2D MMT membranes, which can also promote the application of 2D membranes in the Li + /Mg 2+ separation.
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高影响因子
Journal of Materials Chemistry C
·
2017
·Vol. 5
·期 34
·8828-8835
·
IF 5.256
Yibo Chen,Kuanglun Wu,Jin He,Zhengbin Tang,Jianxin Shi,Yiqin Xu,Zhao-Qing Liu
The rational and delicate synthesis of Mn4+ activated red-emitting oxide phosphors with high photoluminescence quantum yield (PLQY) and photo-stability for developing high-quality w-LEDs still remains a great challenge. Herein, we demonstrate a simultaneous ion co-substitution design strategy to synthesize a red-emitting Lu3Al5O12:Mn4+,Mg2+ garnet phosphor delicately with the assistance of MgF2. The Mn4+ activated garnet phosphor exhibits superior moisture resistance properties and high PLQY (ca. 72.41%), which emits a bright and narrow-band red light peaking at ∼670 nm due to the 2E–4A2 spin-forbidden transition of Mn4+ upon UV excitation. Remarkably, MgF2 as a charge compensator & flux can not only accelerate the solid state reaction, but also greatly improve the emission intensity. Furthermore, by employing the as-prepared Lu3Al5O12:Mn4+,Mg2+ as a red component, we fabricate a warm w-LED with a high color rendering index (Ra = 81.4) and low color temperature (CCT = 4766 K) based on a UV chip and commercial blue and yellow phosphors.
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
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