SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
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2025
·
IF 4.6
Wei Gao,Hao Hu,Jinkun Xue,Yongrun Dong,Wen Li,Xia Zhao,Xiang Mao,Zequan Li
Carbon dots (CDs) have attracted considerable interest as fluorescent nanomaterials; however, their long-afterglow emission properties remain underexplored. In this study, we synthesized dual-mode afterglow CDs exhibiting room-temperature phosphorescence (RTP) and thermally activated delayed fluorescence (TADF) via fluorine-sodium (F, Na) co-doping, achieving an extended afterglow lifetime of 574 ms. Under 365 nm UV excitation, the afterglow emission persists for 14 s (naked-eye observation) and 40 s (instrumentally quantified), demonstrating exceptional temporal resolution. Na doping enhances afterglow intensity by 11.3 %, while fluorine doping reduces the singlet–triplet energy gap (ΔE ST ) to 0.036 eV, facilitating efficient Reverse Intersystem Crossing and enabling TADF behavior. These synergistic effects position the developed CDs as promising candidates for anti-counterfeiting systems, multilevel data encryption, and high-security optical tagging.
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DOI
PubMed
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2025
·
IF 9.7
YuKai Hua,MingPei Tan,Ming Liu,Xiao Yu,Donghai Wang,Yong Liu
P2-type layered metal oxides are promising cathode materials for Na-ion batteries (NIBs), but they suffer from Na + /vacancy ordering and P2-O2 phase transitions during charge–discharge processes, resulting in rapid capacity decay and poor rate performance. In this study, a non-equimolar five-component medium-entropy strategy was employed to design a Na 0.67 Ni 0.19 Cu 0.07 Zn 0.07 Mn 0.60 Ti 0.07 O 2 (NNCZMT) material. Unlike equimolar high-entropy designs, Ni and Mn remain as the main components, with Ni providing high capacity through the Ni 2+ /Ni 4+ redox couple and Mn stabilizing the P2 structure. The introduction of Cu 2+ , Zn 2+ , and Ti 4+ , which have slightly larger ionic radii and the same valence states as Ni 2+ and Mn 4+ , respectively, allows for mutual substitution, synergistically promoting a solid-solution reaction and excellent Na + diffusion kinetics. The NNCZMT electrode delivers a high reversible capacity of 110 mAh g −1 at 10 mA g −1 , an initial Coulombic efficiency of 96.8 %, remarkable cycling stability (94.7 % capacity retention after 100 cycles at 200 mA g −1 ), and excellent rate performance (57.2mAh g −1 at 2000 mA g −1 ).
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PubMed
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JOURNAL OF CHEMICAL AND ENGINEERING DATA
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2025
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IF 2.1
Jing Li,Linglin Fu,Zongde Ma,Jinniu Chen,Changhao Wu,Nan Zhang,Xudong Yu
To understand the interrelationships within the multi-ion coexisting sulfate system during the solid–liquid transformation of polyhalite in the Bieletan area, phase equilibria of ternary systems M, Ca2+//SO42–-H2O (M = Na+, K+, Mg2+) at 288.2 K were studied by the isothermal dissolution equilibrium method. The solubility and density of the equilibrium liquid phases of the system were measured experimentally, and the composition of the equilibrium solid phase at the ternary invariant point was determined by X-ray powder diffractometry. It is found that the ternary system K+, Ca2+//SO42–-H2O at 288.2 K forms the double salt syngenite (K2SO4·CaSO4·H2O), while the systems Na+, Ca2+//SO42–-H2O and Mg2+, Ca2+//SO42–-H2O at 288.2 K only form with the formation of CaSO4·2H2O and Na2SO4·10H2O (MgSO4·7H2O). Multitemperature comparison of the M, Ca2+//SO42–-H2O (M = Na+, K+, Mg2+) systems shows that the phase diagrams of Mg2+, Ca2+//SO42–-H2O are consistent at the selected temperature, only containing CaSO4·2H2O and MgSO4·nH2O (n = 1, 6, 7). While K+, Ca2+//SO42–-H2O and Na+, Ca2+//SO42–-H2O change from 288.2 and 298.2 to 348.2 K, the phase diagram forms double salt(s) K2SO4·5CaSO4·H2O (Na2SO4·5CaSO4·3H2O and Na2SO4·CaSO4).
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CERAMICS INTERNATIONAL
·
2025
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IF 5.6
Weichen Xu,Xiaomeng Li,Hong Wang,Fuliang Wang,Shouqiang Han,Jing Guo
Microwave dielectric ceramics are critical components in wireless communications. However, it is still a challenge to develop microwave dielectric ceramics with reduced sintering temperatures, high thermal stabilities and good dielectric properties at the same time. Herein, the entropy value, which is able to modulate the grain boundary energy and adjust the inherent sintering temperature, is engineered to develop high-performance microwave dielectric ceramics with low sintering temperatures. The structure-property relationships of AWO 4 ceramics, including (NaCaBi) 1/3 WO 4 , (NaCaSrBi) 1/4 WO 4 , (NaLiCaBiSm) 1/5 WO 4 and (NaLiCaSrBiSm) 1/6 WO 4 with increased entropy values are investigated systematically. X-ray diffraction and high-resolution TEM analyses confirm the formation of single-phase solid solutions with the tetragonal scheelite structure in AWO 4 ceramics. As the number of elements in the A-site varies, the relative permittivities, Q × f values and TCF values shift in the range of 12.2–16.5, 8,000–25,000 GHz and −32.3–31.6 ppm/°C, respectively. Simultaneously, the high-entropy samples demonstrate the lowest sintering temperature of 750 °C among the four formulations. Phillips-Van Vechten-Levine (PVL) complex chemical bond theory reveals that the covalency, lattice energy and bond energy affect the relative permittivity, Q × f value and TCF value, respectively. Raman spectra suggest that high entropy value leads to increased disorder, and infrared reflectivity spectra illustrate that the dielectric response is dominated by polarized optical phonons of [WO 4 ] tetrahedron. It is anticipated that entropy design will facilitate the development of microwave dielectric ceramics in low temperature co-fired ceramic applications.
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Journal of Water Process Engineering
·
2025
·
IF 6.7
Junguo He,Yuanyi Zhao,Heliang Pang,Yili Wang,Lin Li,Yunlong Liu,Xinxin Cui,Tong Wei,Shengye Duan,Suiyin Yu
Sulfaquinoxaline sodium (SQ-Na), a veterinary sulfonamide antibiotic, poses potential risks to anaerobic digestion (AD) systems due to its antimicrobial properties, yet its impacts on methanogenic efficiency and microbial dynamics remain poorly understood. This study systematically evaluated the effects of SQ-Na (0–50 mg/L) on AD of simulated wastewater through batch experiments, integrating methane yield analysis, enzyme activity assays, 16S rRNA sequencing and metagenomic insights. Results demonstrated a dose-dependent inhibition of cumulative methane production, with 1 and 5 mg/L SQ-Na reducing yields to 41.21 % and 8.12 % of the control, respectively, while 20–50 mg/L caused near-complete stagnation. The modified Gompertz equation revealed prolonged lag phases (up to 53.52 % extension) and suppressed maximum methane production rates (Rmax). Function enzyme analyses indicated SQ-Na-induced adenosine triphosphatase (ATPase) inhibition (0.26–0.63–fold reduction) alongside accumulated Acetyl-CoA (A-CoA, 0.23–2.32 folds) and Coenzyme F 420 (F 420 , 0.48–2.52 folds), suggesting metabolic imbalance. Microbial shifts highlighted SQ-Na-driven suppression of acetoclastic methanogens (e.g., Methanosaeta ). Metagenomic evidence further pinpointed decreases in the abundance of methanogenesis-associated genes (e.g., EC 7.2.1.4, EC 2.8.4.1) and folate biosynthesis pathways, revealing an inhibition mechanism where SQ-Na competitively inhibits dihydropteroate synthase (EC 2.5.1.15), impairing the metabolic chain of energy, enzymes and function substances. This study offering critical data for optimizing SQ-Na-wastewater treatment and sustainable bioenergy recovery.
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Biomaterials Advances
·
2025
·
IF 6
Chen Wang,Yin Li,Xiaoxue Shen,Shiwei Xiao,Huiying Du,Qianye Zhao,Ying Wang,Qiangtao Zhang,Shuxin Wen
Background Patients with locally advanced head and neck squamous cell carcinoma (HNSCC) exhibit poor survival due to tumor microenvironment (TME) barriers and systemic toxicity of chemo-immunotherapy associated with chemo-immunotherapy. Methods An injectable thermoresponsive hydrogel was engineered by crosslinking D-α-tocopheryl polyethylene glycol succinate (TPGS) with Na₂CO₃ (15 % w/v TPGS: 9 % w/v Na₂CO₃). This platform co-encapsulated doxorubicin-loaded nanoparticles (DOX NP) synthesized via PEI-cis-aconitic acid conjugation and CpG-loaded adjuvant nanoparticles (CpG NP) prepared through genipin-mediated PEI crosslinking. The hydrogel exhibited rapid temperature-triggered gelation, shear-thinning injectability, and a macroporous architecture that enabled dual drug retention and immune cell infiltration. Results In vitro , the hydrogel provided the sustained release of DOX NP with pH-responsive acceleration in acidic TME. In vivo , localized delivery of Gel-DOX NP-CpG NP significantly suppressed tumor growth ( p < 0.05) and enhanced cytotoxic CD8 + T-cell infiltration in TME (3.1-fold) and spleens (2.4-fold). RNA sequencing revealed 88 immune-related differentially expressed genes, including downregulated immunosuppressors and enriched cytokine pathways. Conclusion This TPGS/Na₂CO₃ hydrogel platform coordinates chemotherapy-induced immunogenic cell death (DOX NP) with CpG-driven innate immunity, overcoming TME barriers to enhance localized and systemic anti-tumor responses in HNSCC.
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高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
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2023
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IF 6.2
Yanyan Ma,Hongwei Zhang,Haofei Cong,Yuxiao Wang,Shuwen Xin,Peilong Xu,Yuanbin Qin,Guangxu Xu,Xiaochan Kang,Fengyun Wang
Transition metal phosphides (TMPs) are considered satisfactory anode candidates for sodium-ion batteries (SIBs) due to their high energy density and modest plateau. However, the TMPs anode suffers from poor cycling and rate properties owing to the negative effects of severe volumetric expansion and sluggish reaction kinetics. Herein, a novel structure of porous core/shell CoP@N-C nano polyhedral embedding on 2D MXene nanosheets (CoP@N-C/MXene) was synthesized by self-assembly and in-situ phosphorization methods. The porous CoP@N-C with the unique core/shell structure benefits the infiltration of electrolytes and alleviates the volumetric change. Besides, high-conductive 2D MXene nanosheets could enhance electrical conductivity and charge transfer kinetics, and effectively inhibit CoP@N-C pulverization and agglomeration. Based on the above advantages, the as-prepared CoP@N-C/MXene anode delivers an excellent cycling capacity, outstanding rate capability and low-temperature high-rate capability. This synthetic strategy of CoP@N-C/MXene architecture can be extended to other materials which are promising for SIBs electrodes.
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Journal of Materials Chemistry A
·
2019
·Vol. 7
·期 44
·25268-25273
·
IF 10.733
Jun Han,Kunjie Zhu,Pei Liu,Yuchang Si,Yujun Chai,Lifang Jiao
Herein, the preparation of CoSb nanoparticles embedded in carbon nanofibers with a raised surface (N-doped CoSb@C nanofibers) via the electrospinning method is reported for the first time. The distinct structure facilitates the pseudocapacitive behaviors, which is the key to obtain fast kinetics and long cyclability. N and Co elements can not only optimize the electronic configuration but also buffer the volume changes of the material during cycling. For potassium-ion batteries, the capacity maintains 250 mA h g−1 after 500 cycles at 1 A g−1, and for sodium-ion batteries, the capacity keeps 413 mA h g−1 after 1000 cycles at 1 A g−1. Thus, this work makes a great contribution towards exploring high-capacity anodes for practical potassium-ion batteries and sodium-ion batteries.
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JOURNAL OF MEMBRANE SCIENCE
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2022
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IF 10.53
Jiang Fan,Wufeng Wu,Zong Lu,Yanying Wei
The Metal-Organic Framework (MOF) materials are ideal molecular sieving membrane materials due to the regular pores with high-density and good designability, which have been widely studied in gas separation, desalination, and nanofiltration , etc. However, most preparation methods of MOF polycrystalline membranes are always time-consuming and the as-synthesized MOF membranes are thick. Here in this work, the ultrathin 210 nm-UiO-66 polycrystalline membranes are rapidly synthesized in 1 h, where sonication is utilized to generate massive tiny nucleation followed with rapid microwave-assisted membrane growth. The Na + rejection of the UiO-66 membrane maintains at 99.6% for 700 h long-term experiment with 0.16 L/(m 2 h bar) of water flux in forward osmosis, indicating the good quality and excellent stability of the as-synthesized membrane. This strategy is also expected to synthesize many other continuous defect-free MOF membranes with ultrathin thickness rapidly.
研究领域:
材料科学
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化学工程
·
膜技术
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Journal of Materials Chemistry A
·
2018
·Vol. 6
·期 21
·9922-9929
·
IF 9.931
Yang Chen,Bohan Shan,Chengyin Yang,Jiangfeng Yang,Jinping Li,Bin Mu
Two environmentally friendly and efficient synthesis methods, NH3-assisted synthesis and solvent-evaporated conversion, have been developed for the synthesis of a series of M(NA)2 (M = Zn, Co, Cu, Cd; NA = nicotinate) flexible MOFs. The two-dimensional M(NA)2 (M = Zn, Co) and three-dimensional M(NA)2 (M = Cu, Cd) materials exhibit peculiar structural transformation. These frameworks can be obtained from dehydration of M(NA)2(H2O)4 (M = Zn, Co, Cu, Cd) which are zero-dimensional supramolecular structures. Interestingly, the structural transformation of M(NA)2 (M = Zn, Co, Cd) is reversible after liquid water adsorption. Due to the flexible structure of these MOFs, they exhibit abnormal NH3 adsorption properties. The two-dimensional Zn(NA)2 shows a gate-opening behavior for NH3 adsorption. Its layers opened at a pressure of 0.22 bar in the first cycle, resulting in a two-step NH3 uptake with a capacity of 10.2 mmol g−1 at 1 bar. The gate-opening pressure shifted to a lower value with cycles. Co(NA)2 has a huge NH3 uptake of 17.5 mmol g−1, which is top-ranking among the reported values. For the NH3 adsorption over Cu(NA)2 and Cd(NA)2, the adsorption rates increase and adsorption equilibrium is achieved faster after three cycles. Their maximum capacity at 1 bar is 13.4 and 6 mmol g−1, respectively. More importantly, all MOFs can be regenerated under vacuum and heating conditions of 150 °C for 70 min, and they all retained the capacity. The advantages of environmentally friendly synthesis, large adsorption capacity, and regenerable properties indicate that M(NA)2 (M = Zn, Co, Cu) are promising candidates for NH3 adsorption.
研究领域:
材料科学
·
化学工程
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MATERIALS RESEARCH BULLETIN
·
2023
·
IF 5.4
Zhiwei Li,Zhengxiang Bian,Yurong Ren,Zhihui Chen,Jiujun Xu
(1-x)(0.9Ba 1.003 Ti 0.97 Ca 0.03 O 3 –0.1(Bi 0.51 Na 0.47 ) 0.94 Ba 0.06 TiO 3 )-xNa(Nb 0.85 Ta 0.15 )O 3 ( x = 0.03–0.15) ceramics were designed and fabricated through a bidirectional optimization strategy using traditional solid reaction method. The results revealed that the introduction of Na(Nb 0.85 Ta 0.15 )O 3 increased the vacancy concentration at the A site , conducing to improved polarization and reduced grain size. The substitution at the B site disrupted the long-range ordered ferroelectric domains and generated polar nanodomains, leading to enhanced relaxation behavior. The optimum energy storage density of 3.57 J/cm 3 and efficiency of 87.5% were simultaneously achieved under the electric field of 220 kV/cm in the sample with x = 0.09. Moreover, it also exhibits extremely high-power density (∼57 MW/cm 3 ), ultrafast discharge time (∼103 ns), high discharge density (1.35 J/cm 3 ), along with excellent temperature (30‒120 °C) and frequency stability (1‒100 Hz) under the equivalent electric field of 120 kV/cm. This novel design strategy provides theoretical guidance for the development of advanced electrical energy storage devices.
研究领域:
材料科学
·
能源存储
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DOI
高影响因子
FUEL
·
2022
·
IF 8.035
Quanwang Zhong,Junwei Liao,Qian Zhang,Songbai Qiu,Qingwei Meng,Xiaoping Wu,Tiejun Wang
Developing biomass-derived fuels is a highly competent approach towards the current serious carbon emission issue caused by fossil fuel. The direct upgrading of the aqueous bio-ethanol to higher alcohols as diesel blending and bio-jet fuel precursors showed great potential in techno-economic. In this work, a water-tolerant Na-doped porous carbon encapsulated Ni nanocomposite was fabricated by direct pyrolyzing of Na-containing organic precursors for direct upgrading of aqueous ethanol. The higher alcohols yield of 35.0 C-mol% with C4-C7 selectivity of 51.9% and C8-C16 selectivity of 33.8% were achieved. The C4-C7 alcohols showed the excellent inter-miscibility with diesel at the 0–90% blending proportion. The C8-C16 higher alcohols with iso/n-OH (isomerized/normal alcohol) ratio of 1.86 can be directly used to produce desired jet fuel by hydrodeoxygenation treatment. Experiment and characterization results indicated that the Ni@C catalyst could spontaneously transfer from aqueous phase to the produced oil (higher alcohols) phase. The coupling of phase-transfer and basic sites of Ni@C-NaGlu effectively promoted the secondary C C coupling of higher alcohols to form C8-C16 alcohols. In general, this work provides a novel feasible approach to produce higher alcohol diesel blending and bio-jet fuel precursors from widely available bio-ethanol.
研究领域:
能源化学
·
催化化学
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危险品化学品经营许可证（带存储）