Water Cycle
·
2024
·
IF 0
Guoting Li,Haozhe Li,Shude Zhang,Xiao Mi,Yujie Guo,Zhixin Song,Yuhao Liu,Hongwei Pan,Baogui Wang,Yingxu Liu,Weigao Zhao,Tannaz Pak
Mn oxides are confined within the porous structure of activated coke (ACO) via impregnation followed by calcination treatment. The Mn-ACO sample calcined at 600°C (Mn-ACO600) demonstrated superior performance despite containing only a minute atomic ratio of 0.11% Mn on its surface. This treatment led to a slight increase in the specific surface area and pore volume of ACO, with a significant enhancement in the proportion of micropores, rising from 54.2% in ACO to 71.8% in Mn-ACO600. Raman spectroscopy indicated additional defects in Mn-ACO, while XPS analysis confirmed the coexistence of Mn(II), Mn(III), and Mn(IV) oxides. Although ACO adsorption alone was ineffective in removing acesulfame (ACE), Mn-ACO600 achieved a removal rate of 19.0%. The introduction of peroxydisulfate (PDS) further boosted the degradation of Mn-ACO600, with a K app value that was 2.28 times of that of the combined Mn-ACO600 adsorption and PDS oxidation process, indicating a remarkable synergistic effect. To optimize the experimental conditions, a response surface methodology design analysis was conducted, revealing that solution pH and the dosage of Mn-ACO600 were crucial factors. Furthermore, the study confirmed non-radical oxidizing species, such as 1 O 2 and h + , played a predominant role in the process, with relatively minor contributions from radical oxidizing species.
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JOURNAL OF SOLID STATE ELECTROCHEMISTRY
·
2024
·Vol. 28
·期 8
·2547-2560
·
IF 2.6
Wan Huan,Wang Wei,Bu Lu-xia
In this study, Al-Fe and Al-Fe-Mn alloy anodes are prepared and examined. The influence of impurity Fe on the microstructure and properties of Al alloy anodes is investigated using scanning electron microscopy (SEM), X-ray diffraction (XRD), and electrochemical testing techniques. The results reveal that the presence of impurity Fe in Al alloys significantly shifts the open-circuit potential of the Al anode towards the positive side and reduces its discharge efficiency. However, the adverse impact of impurity Fe is mitigated by alloying with Mn. Specifically, the open-circuit potential of Al-0.20%Fe-0.20%Mn anodes is observed to shift negatively by 70 mV when compared to that of Al-0.20%Fe in a 3 M KOH solution. Furthermore, the anode utilization of Al-0.20%Fe-0.20%Mn anodes, following continuous discharge at 30 mA·cm −2 and 100 mA·cm −2 for 30 min, is found to be 70% and 52% higher, respectively, than that of Al-0.20%Fe anodes. This highlights the effectiveness of Mn modification as a preferable approach to ameliorate the detrimental effects of impurity Fe.
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高影响因子
Frontiers in Energy Research
·
2022
·
IF 3.858
Zhang Shuai,Ren Huixue,Fu Kaifang,Cheng Wenqing,Wu Daoji,Luo Congwei,Jiang Shengyun,Li Jie,Zhang Mingyue
The printing and dyeing wastewater produced by different dyes, as well as different printing and dyeing processes, have different components. These wastewater have high toxicity, high organic concentration, and deep chromaticity. Ozone catalytic oxidation is a very promising technical method for wastewater treatment. In this paper, Mn/Mg/Ce ternary catalyst was prepared, and the ozone catalytic oxidation treatment of actual and simulated printing and dyeing wastewater was performed to study the performance of four different carrier catalysts, namely, molecular sieve (MS), silica gel (SG), attapulgite (ATP), and nano alumina (Al2O3), by simulated dynamic test. The effects of reaction time, pH, and catalyst dosage on methyl orange degradation were studied. The results showed that under the optimum treatment conditions (120 min, pH 11, and 12.5 g/L catalyst dosage), the degradation rate of methyl orange reached 96% and the removal rate of the chemical oxygen demand of printing and dyeing wastewater reached 48.7%. This study shows that the treatment effect of ozone catalytic oxidation on printing and dyeing wastewater is remarkably improved after catalyst addition. This study provides a new choice of ozone catalyst for the degradation of printing and dyeing wastewaters in the future.
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2021
·
IF 5.316
Zilei Liu,Feng Li,Gaoxiang Huang,Feng Zhao,Weiwei Zhang,Guangyu Jiang,Sunhuizi Cheng,Zixin Fang,Quanshui Zhu,Yan Huang
Perovskite quantum dots (PQDs) suffer from the long-time stability owing to their strong ionic structure. Wrapping them with silica or doping them with ions have been used to improve their structural stabilities. Here, transitional metal doping and surface engineering are employed to synthesize silica-coated Mn:CsPbCl 3 QDs for the fabrication of photoluminescent QD-based light-emitting diodes (QLEDs). The as synthesized QDs have dual emission, one is the intrinsic emission of the perovskite host, and the other is the Mn-related emission. The as synthesized Mn-doped CsPbCl 3 exhibit improved stability of luminous spectra compared to those of the pure ones. We also integrate the silica-coated Mn:CsPbCl 3 QDs as color converters with a purple chip. The luminous spectra of the photoluminescent QD-based light-emitting diodes (QLEDs) can be adjusted by controlling the QD concentration. Twenty-day observation and measurement show that devices based on the silica-coated Mn:CsPbCl 3 exhibit enhanced performance stabilities, including a maximum CRI fluctuation of 2.3, a maximum CCT fluctuation of 7 K and a maximum LER fluctuation of 5.2 lm/W opt . These results indicate that manganese doping and silica shell are helpful for the stability improvement of perovskite QDs, and the potential applications of silica-coated Mn:CsPbCl 3 QDs in lighting fields.
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高影响因子
ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
·
2021
·Vol. 29
·期 1
·1289-1300
·
IF 4.223
Huang Tao,Du Jing,Yu Danni,Deng Shihan,Zhang Shuwen,Liu Longfei
Aqueous Fe(II)-catalyzed activation commonly deteriorates the oxidation performance of persulfate (PS) to the treatment of organic contaminants. In this study, a PS-doped layered bimetallic hydroxide (Fe–Mn hydroxide) was synthesized to construct a heterogeneously catalytic system to solve the issue brought by homogeneity. The molar ratio of Fe(II) to Mn(II) and the mass ratio of PS to Fe–Mn hydroxide both had a significant impact on the catalytic degradation of p-CP. Reaction temperatures engaged in the most essential role in influencing the degradation and removal of p-chlorophenol (p-CP). The optimal combination of factors for the preparation of PS-hydroxide and the treatment of p-CP was finally determined by significance analysis. The degradation process was appropriately fitted by the pseudo-first-order kinetic model. The benzene ring in p-CP was broken by PS-hydroxide during the adsorption. The surface modification of PS-hydroxide caused by the valence transition of Mn was beneficial to the adsorption and catalytic degradation of p-CP.
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高影响因子
Journal of Energy Storage
·
2023
·
IF 9.4
Yao Lu,Miaoyan Song,Jieyou Huang,Le Zhang,Binyu Zhao,Wenwei Wu,Xuehang Wu
Charging P2-type Na 0.66 Ni 0.33 Mn 0.67 O 2 (NNM) to a high upper cut-off voltage of 4.3 V (vs. Na + /Na) can yield a competitive discharge voltage (3.6 V-class) and capacity. However, achieving stable cycling for NNM under this condition remains challenging owing to an unfavorable phase transition and a large lattice-volume change. Herein, a dual-site doping strategy is used to simultaneously realize a pinning effect at the Na and transition metal sites. Incorporating pinned K + and Zn 2+ ions considerably enhances the structural stability of NNM, affording a complete single-phase reaction with ultralow strain (only 0.54 % variation in volume) during Na + insertion/extraction. The synergistic contributions of dual-site doping to the enhanced electronic conductivity , lowered Na + migration barrier, and increased Na + diffusion coefficients are confirmed via theoretical calculations. Consequently, the K + /Zn 2+ dual-site-doped Na 0.63 K 0.03 Ni 0.26 Zn 0.07 Mn 0.67 O 2 delivers satisfactory discharge capacities of 118.6 and 63.2 mAh g −1 at 10 and 2000 mA g −1 , respectively, and achieves an excellent capacity retention of 81.2 % after 200 cycles at 500 mA g −1 . This study provides a promising method to strengthen the stability of the Ni − Mn-based layered framework and optimize other high-voltage and high-capacity layered oxide cathode materials .
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高影响因子
ACS Applied Materials & Interfaces
·
2023
·
IF 9.5
Kunli Song,Kaiyu Guo,Yixuan Lv,Dandan Ma,Yonghong Cheng,Jian-Wen Shi
Selective catalytic reduction with ammonia is the mainstream technology of flue gas denitration (de-NOx). The reducibility and acid site are two important factors affecting the de-NOx performance, and effective regulation between them is the key to obtain a highly efficient de-NOx catalyst. Herein, a series of Mn–Fe–BTC with different ratios of Mn and Fe are synthesized, among which 2Mn-1Fe-BTC with 2:1 molar ratio of Mn and Fe has excellent low-temperature (LT) de-NOx performance (above 90% NO conversion between 60 and 270 °C) and good tolerance to H2O and SO2 poisoning (88% NO conversion at 150 °C with 100 ppm of SO2 and/or 6% H2O). It is revealed that the reducibility properties and acid sites of Mn–Fe–BTC can be flexibly tuned by the ratio of Mn and Fe. The difference in electronegativity between Fe and Mn leads to the redistribution of valence electrons, which enables the controllable reducibility of Mn–Fe–BTC. Furthermore, different amounts of Mn and Fe lead to different electron transport, which determines the type and number of acid sites. The synergistic effect of Mn and Fe endows Mn–Fe–BTC with enhanced surface molecular adsorption capacity and enables the catalyst to selectively chemisorb NH3 and NO at different active sites. This research provides guidance for the flexible regulation of reducibility and acid site of LT de-NOx catalyst.
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高影响因子
FOOD CHEMISTRY
·
2025
·
IF 9.8
Jianfang Jiang,Kuaqian Deng,Rui Duan,Cong An,Fanglin Dao,Jiali Huang
Organophosphorus pesticides (OPs) are extensively utilized in agricultural production, but they pose significant threats to environment and organisms. This study aims to develop a novel method for the rapid and efficient detection of OPs. Initially, an iron/manganese zeolitic imidazolate framework (Fe/Mn-ZIF) with excellent oxidase-like activity was synthesised. The catalytic performance was evaluated, and the main factors influencing catalytic activity were investigated. Subsequently, a combined acetylcholinesterase assay was employed to detect three OPs. The specificity and recyclability of Fe/Mn-ZIF were also studied. The proposed colorimetric strategy demonstrated strong linear relationships: 0.1–2 mg/L for trichlorfon, 0.2–14 mg/L for glyphosate, and 0.4–10 mg/L for glufosinate, with the low detection limits of 0.024, 0.080, and 0.121 mg/L (3 S/N) respectively. Good recoveries were observed in real sample detection. This work lays a foundation for enhancing the catalytic performance of Fe/Mn-ZIF, which holds promise for biosensing applications.
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PubMed
高影响因子
CHEMICAL PHYSICS LETTERS
·
2025
·
IF 3.1
Simin Li,Ziran Chang,Fengbing Tang,Tianshuo Sui,Lemin Li,Jingbo Mu,Zhennan Shi
The QS@PDA/Co-Mn-ZIF catalyst, synthesized using quartz sand as a base material, effectively degrades TCH through the activation of PMS. The Co-Mn-ZIF component activates PMS, while PDA ensures the adhesion of ZIF to quartz, facilitating catalyst recovery. This design enhances electron transport and metal ion redox reactions, generating reactive species that degrade TCH. It achieves a 94 % TCH removal rate from a 100 mg/L solution within 40 min, demonstrating stability under various pH and water conditions. The catalytic mechanism was elucidated·through radical trapping experiments and electron paramagnetic resonance analysis. QS@PDA/Co-Mn-ZIF shows great potential for treating recalcitrant and high-concentration organic wastewater.
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高影响因子
RSC Advances
·
2025
·Vol. 15
·期 16
·12364-12371
·
IF 4.6
Chang Man,Chunpeng Xu,Jinfeng Wang,Xiangli Li,Tong Li,Yanhua Ma,Shalu Zhang,Yongfeng Qiao,Qiong Wu
Organic–inorganic hybrid materials have significant potential in the photocatalytic degradation of Rhodamine B (RhB). In this study, five hybrid materials were successfully synthesized by modifying silicotungstic acid (H4SiW12O40, abbreviated SiW12O40) with diverse MnL [L = Salen(L1), 5-Br-Salen(L2), 5-Cl-Salen(L3), 3-Me-Salen(L4), di-tBu-Salen(L5)] complexes, specifically derivatives featuring various substituents. All the compounds are characterized by IR spectra, elemental analyses and thermogravimetric analyses (TGA). The band gaps of 1.33–1.52 eV and energy bands are obtained through the measurement of UV-Vis DRS and Mott–Schottky. Photocatalytic experiments of (MnL1)4SiW12O40 (compound 1), (MnL2)4SiW12O40 (compound 2), (MnL3)4SiW12O40 (compound 3), (MnL4)4SiW12O40 (compound 4) and (MnL5)4SiW12O40 (compound 5) indicate that compound 2 catalyst exhibits the best photocatalytic properties (RhB degrades to 6% during 70 min) while all of them possess catalytic activity for photodegradation of RhB under UV irradiation. Free radical trapping experiments show that the addition of PBQ (·O2− trapping agents) makes the RhB residual ratio increase from 6% to 60% and indicates that ·O2− is playing a pivotal role. A possible mechanism of RhB photodegradation in the presence of compound 2 is proposed based on free radical trapping experiments and the energy bands. Future work could focus on fine-tuning the molecular architecture through strategic modification of the organic ligands and precise control of the metal-to-POM ratio, potentially leading to optimized electronic structures and enhanced charge transfer kinetics for superior photocatalytic performance in environmental applications.
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PubMed
高影响因子
ChemSusChem
·
2024
·
IF 7.5
Tao Xu,Meihui Jiang,Siyu Mo,Xianhui Wang,Tianlin Ren,Zhichen Liu,Zhicheng Wang,Yicheng Qiu,Lingying Gu,Xu Wang,Xuhui Mao
Graphical We designed a carbon-coated aluminum oxide carrier and reinforced it with Mn−Fe bimetal assemblages to prepare a high-performance catalyst Mn−Fe/C-Al 2 O 3 . Mn−Fe/C-Al 2 O 3 catalyst exhibited satisfactory catalytic ozonation activity and stability in the degradation of p -nitrophenol. Experiments and theoretical calculations revealed the internal degradation mechanism of the Mn−Fe/C-Al 2 O 3 catalyst, underscoring the role of the carbon-coated and bimetallic active unit in O 3 activation. Catalysts with high catalytic activity and low production cost are important for industrial application of heterogeneous catalytic ozonation (HCO). In this study, we designed a carbon-coated aluminum oxide carrier (C-Al 2 O 3 ) and reinforced it with Mn−Fe bimetal assemblages to prepare a high-performance catalyst Mn−Fe/C-Al 2 O 3 . The results showed that the carbon embedding significantly improved the abundance of surface oxygen functional groups, conductivity, and adsorption capacity of γ-Al 2 O 3 , while preserving its exceptional mechanical strength as a carrier. The prepared Mn−Fe/C-Al 2 O 3 catalyst exhibited satisfactory catalytic ozonation activity and stability in the degradation of p -nitrophenol (PNP). Electron paramagnetic resonance (EPR) and quenching experiments reveal that radical ( ⋅ OH and ⋅ O 2 ⋅ ) and nonradical oxidation ( 1 O 2 ) dominated the PNP degradation process. Theoretical calculations corroborated that the anchored atomic Fe and Mn sites regulated the local electronic structure of the catalyst. This modulation effectively promoted the activation of O 3 molecules, resulting in the generation of atomic oxygen species (AOS) and reactive oxygen species (ROS). The economic analysis on Mn−Fe/C-Al 2 O 3 revealed that it was a cost-competitive catalyst for HCO. This study not only deepens the understanding on the reaction mechanism of HCO with transition metal/carbon composite catalysts, also provides a high-performance and cost-competitive ozone catalyst for prospective application.
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PubMed
高影响因子
Energy Materials
·
2025
·Vol. 5
·期 4
·N
·
IF 11.2
Dongwei Zhou,Guiyang Gao,Zhanlin Yang,Weibin Guo,Liang Lin,Yinggan Zhang,Chengkun Zhang,Saichao Li,Yuanyuan Liu,Baisheng Sa,Guoying Wei,Dong-Liang Peng,Jie Lin,Qingshui Xie
Li-rich Mn-based cathode materials (LRM) have received great attention owing to their high capacity and low cost. However, the mismatch between the widely used carbonate electrolyte and the LRM cathode and lithium metal anode causes a series of problems, such as electrolyte continuous oxidation, cathode structure degradation, and Li dendritic growth. Herein, inorganic oxide B2O3 is introduced as a dual-functional high-voltage electrolyte additive to construct stable cathode electrolyte interphase and solid electrolyte interphase for Li||LRM batteries. The modified interface derived from the additive can induce dendrite-free Li deposition, stabilize cathode structure, and inhibit transition metal dissolution. Moreover, the adverse side reactions are mitigated, thus enhancing Li+ transport rate and reducing interface impedance. With the addition of B2O3 into the carbonate electrolyte, the Li||LRM battery exhibits an enhanced discharge capacity of 221 mAh g-1 after 200 cycles, equaling a capacity retention of 92.1%. When the upper cut-off voltage is increased to 5 V, a superior capacity retention of > 85% can still be achieved after 150 cycles at 1 C. In addition, the low cost of B2O3 benefits for commercial application. This work offers new guidance for the research of low-cost, high-voltage dual-functional additives for advanced lithium metal batteries.
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