ACS Sustainable Chemistry & Engineering
·
2025
·
IF 7.3
Meiqing Yan,Jiapeng Yang,Enrou Mei,Ye He,Zhaoping Chen,Weiwei Huan,Xiaojuan Liang,Weidong Xiang
To address the issues of Pb toxicity and stability in traditional lead halide perovskite materials, this study presented an environmentally benign aqueous-phase synthesis method for the fabrication of a series of high-performance, green-emitting, lead-free organic–inorganic hybrid manganese(II) halide (OIMnHs) materials, (C12H28N)2Mn(1–x)ZnxBr4. Through Zn2+ doping, the optical properties and stability of the materials were significantly enhanced. Notably, (C12H28N)2Mn0.95Zn0.05Br4 exhibited a remarkable photoluminescence quantum yield (PLQY) of 97.2% and narrow-band green emission at 520 nm with a full width at half-maximum (fwhm) of 43 nm. Furthermore, (C12H28N)2Mn0.95Zn0.05Br4@PET composite films, fabricated via a double-layered PET film encapsulation technique, demonstrated exceptional environmental stability, including resistance to air, heat, water, and blue light. Finally, by integrating (C12H28N)2Mn0.95Zn0.05Br4 with commercial K2SiF6:Mn4+ red phosphor, a composite light conversion film was developed, achieving an impressive wide color gamut coverage of 116.73% NTSC 1953 and 86.82% Rec. 2020. Importantly, the aqueous-phase method exhibited excellent scalability, as demonstrated by a successful 20-fold scale-up production without compromising the optical properties or crystal structure of the materials, highlighting its potential for large-scale manufacturing. This study paved the way for the development of high-performance, environmentally friendly, low-cost, and readily scalable lead-free halide materials for wide-color-gamut backlight displays.
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JOURNAL OF NANOBIOTECHNOLOGY
·
2025
·Vol. 23
·期 1
·1-18
·
IF 12.6
Wen E.,Tian Yu,Chen Yu,Wang Zhigang,Feng Yi,Liao Zhen
Despite the encouraging developments in tumor immunotherapy, the complex tumor microenvironment (TME) and abnormal energy metabolism persist as key factors facilitating immune escape. Recent research has emphasized the significant potential of the Manganese ions (Mn 2+ ) as a “immune ion reactors” have the potential to stimulate cGAS-STING signaling pathway in modulating tumor immunotherapy. However, their efficacy is limited by insufficient targeting and lack of tumor specificity. To address these challenges, we have developed a nano-drug named as LT@MnO@MON-HA (LMMH), which incorporates manganese oxide (MnO) nanoparticles as the core and organic mesoporous silica as the outer layer. The mitochondrial glycolysis inhibitor lonidamine (LT) is encapsulated within the mesopores of LMMH and subsequently coated with hyaluronic acid to achieve precise tumor-targeted drug delivery. After reaching the tumor site, LMMH can decompose in the reducing and acidic TME, releasing LT and Mn 2+ . Once internalized by cells, LT rapidly localizes to mitochondria via functional groups, disrupting mitochondrial metabolism and increasing intracellular reactive oxygen species levels. Mn 2+ catalyze the conversion of hydrogen peroxide (H₂O₂) into more cytotoxic hydroxyl radicals (·OH), thereby enhancing chemodynamic therapy (CDT). The mesoporous silica shell of LMMH is capable of depleting glutathione in the TME, enhancing CDT. Moreover, LMMH functions as an agonist of the cGAS-STING pathway, stimulating cytokine release and activating effector T cells, which in turn triggering systemic immune responses against primary and metastatic cancers. Collectively, these finding highlights the dual mechanisms by which LMMH enhances combination immunotherapy by regulating the TME and tumor metabolism. Graphical
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PubMed
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JOURNAL OF FOOD COMPOSITION AND ANALYSIS
·
2025
·
IF 4.6
Huakuo Zhou,Peng Li,Yifei Li,Yi Ke,Xia Zhang,Jun Meng
In recent years, most of the studies on nanozymes have focused on improving their catalytic activity and direct synthesis, but this task is still very complex. Bimetallic oxides are particularly popular due to their mixed valence and synergistic effects between different metal ions. In this study, Fe-Mn bimetallic oxide nano-cubes were prepared by fast and effective solvothermal synthesis, and nano-flower-like structures were grown on the surface of Fe-Mn oxide nanocubes via controlled etching. The synthesized Fe-Mn bimetallic oxide nano-flowers (FMBO NFs) have great oxidase-like activity. On this basis, a simple, economical and accurate colorimetric sensor was established by combining 3,3',5,5'-tetramethylbenzidine (TMB). Exposure to L-cysteine (L-Cys) inhibited the catalytic activity of FMBO NFs. As the concentration of L-Cys increased, the absorbance at 652 nm decreased, with a good linear relationship in the range of 0.01-1000 μM, with a limit of detection (LOD) of 3.99 × 10 -11 M, and the detection of L-Cys in the actual sample egg yolk was successfully achieved. This study provides theoretical support for the effective design of bimetallic oxide nanozyme activity, and can guide the development of an accurate detection system for the analysis of L-Cys in food.
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CHEMICAL ENGINEERING JOURNAL
·
2025
·
IF 13.2
Mufan Wang,Shiying Fan,Shaomin Liu,Xinyong Li
5-Hydroxymethylfurfural (HMF) serves as a key platform molecule for producing high-value chemicals via green and efficient photocatalytic oxidation. Transition metal oxides, particularly spinel substances, are promising heterogeneous catalysts due to their ability to promote interfacial electron transfer. However, the impact of interfacial electron transfer in HMF photocatalytic oxidation on spinel catalysts remains largely unexplored. In this study, we engineered Mn 4+ -O V -Co 2+ active sites in cobalt-based spinel by in-situ (MCO 4-δ -1) and post-doping (MCO 4-δ -2) strategies to investigate their impact on photocatalytic HMF oxidation. The microstructure morphology, chemical valence states, and band structure of prepared catalysts were systematically characterized by transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and UV–vis diffuse reflectance spectra (DRS) techniques. The results revealed that the post-doping catalyst (MCO 4-δ -2) exhibited a higher density of surface oxygen vacancy (Ov), significantly enhancing charge transfer and HMF photocatalytic conversion activity. Specifically, MCO 4-δ -2 achieved an outstanding HMF oxidation product yield of 356.55 μmol g −1 under visible light over 4 h. Furthermore, density functional theory (DFT) calculations provided mechanistic insights, revealing that the oxygen in the aldehyde group of HMF preferentially occupies surface Ov sites at Mn 4+ -Ov-Co 2+ interfaces, thereby facilitating selective HMF oxidation pathways. This study not only expand the application scope of cobalt-based spinel photocatalysts in biomass valorization but also provides an insight on the effects of doping-induced interfacial electronic effects in photocatalytic oxidation reactions.
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Journal of Environmental Chemical Engineering
·
2025
·
IF 7.2
Yuqiu Fan,Dawei Liu,Haipeng Wan,Xingyu Liu,Jun Wang,Kun Xiong
For rapid and efficient removal of tetracycline (TC), a new cobalt (Co) and manganese (Mn) co-doped zinc ferrite (CoMnZFO) photoanode was synthesized in this study. Compared to the pure zinc ferrite (ZFO), CoMnZFO exhibited stronger enhanced light harvesting ability and a narrower band gap. Although there were oxygen vacancies in both CoMnZFO and ZFO lattices, CoMnZFO possessed more double-exchange interaction pathways in comparison with ZFO. Besides the Fe 2 + /Fe 3+ pathway, CoMnZFO also had the Mn 3+ /Mn 4+ pathway, which facilitates the transfer of photogenerated electrons ( e - ) and holes (h + ), thereafter enabling CoMnZFO better photoelectrocatalytic (PEC) activity. Since CoMnZFO had a significantly smaller Helmholtz layer resistance than ZFO, it enhanced TC adsorption onto its surface. Exposed to simulated solar light for 12 min, CoMnZFO was able to make the complete degradation of TC (20 mg/L, 70 mL) when a voltage of 0.2 V was applied, while ZFO only achieved a TC degradation rate of 50.85 ± 5.77 % under the same condition. In addition, CoMnZFO achieved a TC mineralization rate of 41.89 ± 1.72 %, while that of ZFO was 13.87 ± 1.94 %. Furthermore, a quantitative structure-activity relationship (QSAR) method was applied to evaluate the ecotoxicological impact of the degradation products. The results demonstrate that the toxicity and mutagenicity of TC were weakened after experiencing the PEC treatment of CoMnZFO. Overall, this work offers a rapid and efficient way for PEC removal of TC-contaminated wastewater.
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Catalysts
·
2023
·Vol. 13
·期 11
·1398
·
IF 3.9
Wei Qian,Yi Fang,Hui Liu,Yili Deng,Yingying Li,Yongzheng Zhang,Zenghui Diao,Mingyu Li
The environmental pollution caused by antibiotics is becoming more serious. In this study, the Mn/BiPO4/g-C3N4composite (Mn-BPC) and the Ti/g-C3N4/BiPO4composite (Ti-BPC) were prepared by hydrothermal reaction method and solvent method, respectively, and applied to the degradation of tetracycline (TC) in an aqueous environment. The XRD and HRTEM results showed that these materials had the crystalline rod-like structure of BiPO4and abundant carbon, nitrogen and carbon–oxygen surface functional groups. The degradation of TC by Ti-BPC and Mn-BPC were nearly 92% and 79%, respectively. The degradation processes of TC were well consistent with the pseudo-second-order kinetics model and R2values were closer to 1. The trapping experiment showed that electron holes (h+) were the main reactive species for the degradation of tetracycline, OH· and O2−also have certain effects. Also, the possible photocatalytic degradation mechanism of Ti-BPC and Mn-BPC composites was thereby proposed. TC was firstly adsorbed on the surface of catalysts, and subsequently degraded by reactive species such as h+, OH· and O2−generated under visible light excitation. This study shows that the Ti-BPC and Mn-BPC photocatalysts have great potential in antibiotic degradation and can provide new ideas for antibiotic removal in aqueous environments.Keywords:bismuth phosphate;graphite phase carbon nitride;tetracycline (TC)
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Transactions of the Indian Ceramic Society
·
2020
·
IF 0.952
Shifa Wang,Huajing Gao,Hong Yu,Peiying Li,Yanwu Li,Chaoli Chen,Yong Wang,Liang Yang,Zijuan Yin
MgAl2O4:M (M = Ti, Mn, Co, Ni) phosphors were successfully prepared by a modified polyacrylamide gel method. Calcination temperature and metal particle has significant effects on the phase transition, optical and color properties of Mg Al2O4: M phosphors. Ti, M n, Co and Ni metal particles introduced into the MgAl2O4 system can produce a variety of colours from white, grayish black, blue to turquoise blue. Mn, Co and Ni metal particles added into MgAl2O4 system can extend their light absorption to visible light range, while the Ti metal particles clad into the system did not improve significantly. Co metal particles appended into the MgAl2O4 system can cause fluorescence quenching of emission peak at 395 nm and enhancement of emission peak at 405 nm, while the Ti and Mn metal particles infused into the system can bring the enhancement of visible emission peak at 425 nm. The fluorescence quenching of the peak at 395 nm can be ascribed to the wavelength of Co metal particles matching the surface plasmon absorbance band of MgAl2O4:M phosphor. A reduction in emission intensity at 425 nm can be assigned to electron transfer from the conduction band (CB) of MgAl2O4 to the CB of metal particles causing non-radiative decay.
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Protection of Metals and Physical Chemistry of Surfaces
·
2017
·Vol. 53
·期 1
·118-126
·
IF 0.707
Fashu S.,Khan R.
Ternary Zn–Mn–Ni alloy coatings were electrodeposited for the first time from a choline chloride based ionic liquid with the aim of collecting properties of binary Zn–Mn and Zn–Ni alloys into one alloy system. The effect of electrodeposition potential on the composition and corrosion performance of the obtained ternary Zn–Mn–Ni deposits was investigated and contrasted with the characteristics of Zn–Mn and Zn–Ni deposits. Cyclic voltammetry revealed that the deposition of ternary Zn–Mn–Ni alloys behaved differently from the deposition of binary Zn–Mn and Zn–Sn alloys and that Mn deposition takes place at positive potentials in the Zn–Mn–Ni electrolyte than in the Zn–Mn electrolyte due to the presence of Ni 2+ ions in the electrolyte. X-ray diffraction studies showed that the Zn–Mn–Ni ternary alloys consist of a lattice of Zn (with Mn and Ni imbedded inside) at low electrodeposition potentials and MnZn(with Ni imbedded inside) phase at high electrodeposition potentials. Chemical composition analysis show that the Mn content in the ternary Zn–Mn–Ni alloy increased with increase in electrodeposition potential, whereas Zn and Ni contents are suppressed. The corrosion tests results indicate that through addition of Ni into the Zn–Mn binary alloy, the Zn–Mn–Ni alloy tailored are more corrosion resistant than the Zn–Mn binary alloy whilst the passivation behavior is still preserved.
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APPLIED CATALYSIS B-ENVIRONMENTAL
·
2019
·
IF 14.229
Yuxian Wang,Lulu Chen,Hongbin Cao,Zhaoxu Chi,Chunmao Chen,Xiaoguang Duan,Yongbing Xie,Fei Qi,Weiyu Song,Jian Liu,Shaobin Wang
La-based perovskites are catalytically active owing to the oxygen vacancies, redox metal centers of B sites and surface hydroxyl groups. Nevertheless, the insights into these active centers on environmental catalysis are still insufficient. In this study, hierarchical mixed oxides perovskite microspheres were synthesized for catalytic ozonation over oxalic acid and benzotriazole. LaMn 4 O x , with LaMnO 3-δ as the dominant crystal phase, demonstrated superior catalytic activity to Mn 2 O 3 and LaMnO 3 synthesized from citric acid sol-gel method. Temperature-programmed desorption of NH 3 (NH 3 -TPD) and pyridine-Fourier transform infrared spectroscopy (pyridine-FTIR) tests proved Lewis acid as the main acid type. Temperature-programmed reduction of H 2 (H 2 -TPR), O 2 -TPD and X-ray photoelectron spectroscopy (XPS) analysis indicated the presence of oxygen vacancies and mixed valences of Mn in the crystal structure facilitated the catalytic process. Moreover, the content of oxygen vacancy was calculated by iodometric titration method. With the aid of theoretical calculations, oxygen vacancies were found to exhibit a strong affinity toward ozone adsorption, where ozone molecules spontaneously dissociated into reactive oxygen species (ROS) such as O 2 − and 1 O 2 . The B site of Mn facilitated ozone decomposition by extending the O O bond of ozone due to the electron transfer from Mn 3+ /Mn 4+ redox cycle. In-situ EPR and quenching tests confirmed the contribution of O 2 − and 1 O 2 in benzotriazole degradation along with OH. This study stepped further to unveil the ozone adsorption/decomposition and ROS generation on nanoscale perovskite-based composites.
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DESALINATION
·
2025
·
IF 9.8
Zhiqiang Wu,He Ren,Hao Zhou,Jianeng Ji,Haiyun Ding,Chunyan Li,Minjie Shi,Ying Hong,Jun Yang
Prussian Blue analogs (PBAs) have emerged as one of the promising materials for capacitive deionization (CDI) due to their excellent specific capacity and outstanding ion adsorption capability. However, Mn-based hexacyanoferrate Prussian Blue (MnHCF) suffers from insufficient utilization of active sites and poor ion kinetics during the electrochemical process, resulting in weak ion adsorption capacity and easy destruction of its stable structure. In this work, CuMnHCF was synthesized by incorporating Cu into the MnHCF framework via an in situ solvothermal approach. The appropriate introduction of Cu effectively occupied the interstitial sites of the MnHCF structure, optimized its electronic configuration, and successfully activated both the metal–N bonds and the Fe–CN dual redox-active sites within the framework (evidenced by in situ Raman measurements). These merits collectively led to a significant enhancement in the electrosorption capacity of CuMnHCF toward Na ions. The CuMnHCF electrode exhibits excellent cycling stability in aqueous NaCl electrolyte. After 5000 cycles, the specific capacitance decay is minimal, with a capacity retention rate of approximately 61.5% (5 A g −1 ). As applied in electrochemical desalination experiment at a voltage of 1.2 V for 50 cycles, the retention rate of CuMnHCF electrode reached as high as 82.2%. Additionally, it not only exhibits a high salt removal capacity of 58.4 mg g −1 (salt removal rate: 1.95 mg g −1 min −1 ), but also a peak salt removal rate of 15.7 mg g −1 min −1 . As an application extension, the CuMnHCF electrode also shows excellent desalination performance for K + , Ca 2＋ , and Mg 2 + .
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2025
·
IF 9
Zhengming He,Cong Li,Jingzhen Su,Kai Zhang,Jiaxue zhu,Ren Cai,Yunshu Zhang,Jieming Yuan,Xiaohong Guan
Iron-based catalysts are generally used to activate oxidizing species, such as hydrogen peroxide by increasing homogeneous active substances like free radicals, to promote the degradation of organic matter. However, less attention has been paid to the reactions on the surface or the generation of heterogeneous metal-oxo species. Herein, oxygen vacancies (Vo) were introduced into Fe oxides by a calcination-induced hetero-atom doping modification. The characteristic peak of the heterogeneous hypervalent iron-oxo [≡Fe IV =O] species in the UV–Vis spectrum at 371 nm was observed. In the context of electrochemical experiment, Vo-rich Mn-Fe 2 O 3 significantly enhanced the electron conduction of sulfamethoxazole and H 2 O 2 , while simultaneously inhibiting the self-decomposition of potassium ferrate (Fe(VI)). Regarding the H 2 O 2 generated during the self-decomposition process of Fe(VI), Vo-rich Mn-Fe 2 O 3 can accelerate the degradation of sulfamethoxazole, increasing the reaction rate to 0.1081 min −1 (with a 30.05 % improvement in removal efficiency). Density functional theory calculations indicate that Vo leads to an enhanced capture of O atoms by the low-coordinated Fe atoms, promoting the anchoring of H 2 O 2 and the formation of the active ≡Fe IV =O with a higher spin state. This work proposes heterogeneous reactive species on the surface of metal oxidase, constructing Vo as the O atom capture sites in iron-based oxides to facilitate the formation of ≡Fe IV =O and the degradation of organic compounds.
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RSC Advances
·
2018
·Vol. 8
·期 5
·2338-2349
·
IF 2.936
Jing Deng,Chen Ya,Yongjian Ge,Yongqing Cheng,Yijing Chen,Mengyuan Xu,Hongyu Wang
Various transition metals (Fe, Mn, Cu and Ni) were doped into ordered mesoporous Co3O4 to synthesize Co3O4-composite spinels. Their formation was evidenced by transmission electronic microscopy (TEM), X-ray diffraction (XRD) and Brunauer–Emmett–Teller (BET) analysis. It was found that Co3O4-composite spinels could efficiently activate peroxymonosulfate (PMS) to remove enrofloxacin (ENR) and the catalytic activity followed the order Co3O4–CuCo2O4 > Co3O4–CoMn2O4 > Co3O4–CoFe2O4 > Co3O4–NiCo2O4. Moreover, through the calculation of the specific apparent rate constant (ksapp), it can be proved that the Co and Cu ions had the best synergistic effect for PMS activation. The Co3O4-composite spinels presented a wide pH range for the activation of PMS, but strong acidic and alkaline conditions were detrimental to ENR removal. Higher reaction temperature could promote the PMS activation process. Sulfate radical was identified as the dominating reactive species in Co3O4-composite spinel/PMS systems through radical quenching experiments. Meanwhile, the probable mechanisms concerning Co3O4-composite spinel activated PMS were proposed.
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