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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2024 · IF 9.4

Engineering atomically dispersed Mn and Fe sites on hollow nitrogen-doped carbon for high-performance Zn-air batteries

Qiyu Li,Lei Zhao,Zhaozhao Zhu,Pei Xiong,Jiayu Zuo,Jun Song Chen,Rong Li,Rui Wu

Zinc-air batteries (ZABs) have garnered significant interest due to their environmental friendliness, low cost, and high energy density. However, their practical application is significantly hindered by high overpotential and sluggish reaction kinetics. Here, we propose a hollow nitrogen-doped carbon supported atomically dispersed Fe and Mn sites (FeMn-HNC) through a facile NaCl-assisted pyrolysis strategy. The synthesized FeMn-HNC catalyst possesses a hollow porous structure, resulting in exceptional oxygen reduction reaction (ORR) catalytic activity, remarkable durable stability, and good tolerance to methanol. Furthermore, integrating this catalyst into ZABs demonstrates significant performance advantages, achieving a maximum power density of 223.1 mW cm −2 and a high specific capacity of 804.3 mAh g −1 . This study offers a promising approach for boosting the power density and specific capacity of nitrogen-doped carbon catalysts in ZABs.

研究领域: 材料科学 · 电化学 · 能源存储
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NMR IN BIOMEDICINE · 2025 ·Vol. 38 ·期 9 ·e70116 · IF 2.7

Preparation of Fe–Mn Codoped 2D MXene Nanoprobes and Feasibility Study of Combining With CEST for Multimodal Imaging

Fei-Xiang Hu,Deng-Deng Liu,Xiao-Wen Ma,Pu-Yeh Wu,Wei-Jun Peng,Dan Wang,Tong Tong

This study aims to design and evaluate a two-dimensional Ti 3 C 2 -MXene contrast agent, codoped with iron and manganese, with the aim of achieving T 1 /T 2 dual-mode magnetic resonance imaging contrast, and to investigate its effect on Chemical Exchange Saturation Transfer (CEST) contrast agents. Single-layer Ti 3 C 2 was synthesized via the HCL/LiF etching technique, with the flake size subsequently tailored and the hydroxylated surface modified through a hydrothermal process. Fe 3 O 4 nanoparticles and MnO 2 nanosheets were integrated onto the two-dimensional Ti 3 C 2 -MXene surface using an in situ doping approach, and the final modification was achieved with carboxymethyl chitosan. Various characterization techniques were employed to assess the physical and chemical properties of the probe, which were then combined with a CEST contrast agent to investigate the mechanisms of multimodal magnetic resonance imaging and in vitro photothermal effects. Upon integrating the multi-modal molecular probe with Ioversol for imaging purposes, at a magnetic field strength of B 1 = 1.25 μT and with a molecular probe concentration of 0.5 mg/mL, the CEST signal from Ioversol is almost entirely suppressed. This allows for the successful identification of a distinct concentration range where both contrast agents can coexist. In vitro photothermal studies on MXene codoped with iron and manganese have shown that the composite molecular probe exhibits excellent photothermal efficiency. The method combining complex nanoprobes with CEST contrast agents successfully achieved simultaneous imaging of both contrast agents. In vitro MRI experiments successfully obtained distinguishable concentration ranges for both, with changes in CEST signals reflecting the concentration variations of the complex molecular probes, which also exhibit good photothermal therapy (PTT) capabilities.

CAS / MDL: 1122-58-3
研究领域: 纳米材料 · 磁共振成像 · 对比剂 · 多模态成像 · 光热治疗 · 生物医学工程 · 材料科学
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JOURNAL OF POWER SOURCES · 2022 · IF 9.794

Study on the influence of Cu/F dual-doping on the Fe–Mn based compound as cathode material for sodium ion batteries

Yixuan Zhang,Guoqiang Liu,Chang Su,Guangyin Liu,Hongda Sun,Danlei Qiao,Lei Wen

This work focuses on the improvement on the electrochemical performances of Fe–Mn based oxides as cathode for sodium ion batteries by doping Cu and F elements. The synthesized doped-compounds exhibit extremely excellent electrochemical performance. For instance, it's initial discharge capacity can reach 195.6 mAh g −1 at a current density of 10 mA g −1 . Meanwhile, after 200 cycles at 200 mA g −1 , it still remains a capacity of 124.1 mAh g −1 , 87.8% of the initial capacity of 141.3 mAh g −1 . More significantly, it can deliver a high capacity of 106.4 mAh g −1 at a high current density of 1000 mA g −1 . It is found that F/Cu co-substitution obviously improve the discharge capacity and cycle stability of Fe–Mn based oxide especially at higher current densities. Doping Cu and F elements has influence on the structure and morphology of the material, which results in the improvement of charge-discharge characteristics.

研究领域: 材料科学 · 电化学 · 能源存储
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Coatings · 2025 ·Vol. 15 ·期 7 ·825 · IF 2.8

Preparation of S-Doped Ni-Mn-Fe Layered Hydroxide for High-Performance of Oxygen Evolution Reaction

Jiefeng Wang,Shilin Li,Yifan Guo,Jiaqi Ding,Zhi Lu

A novel catalyst with a metal sulfide/hydroxide heterostructure was prepared by introducing sulfur ions into NiMnFe layered hydroxide by a simple hydrothermal method, using a series of characterization methods and electrochemical tests to explore the optimal sulfur ion doping amount. The XPS results show that the introduction of sulfur ions leads to a change in metal electron delocalization, which is conducive to the OER procedure. The newly formed metal sulfide can not only improve the conductivity of NiMnFe LDH/NF electrode materials but also enhance the intrinsic catalytic activity of the materials. The electrochemical performance indicated that the S2-NiMnFe LDH/NF catalyst required only 205 mV overpotential to provide a current density of 10 mA−2, and the Tafel slope was only 45.79 mV dec−1. In addition, the large turnover frequency value (1.2614 S−1) reflects the excellent intrinsic activity of the novel catalytic material.

研究领域: 材料科学 · 电化学 · 催化 · 纳米技术 · 能量转换
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ANALYTICAL AND BIOANALYTICAL CHEMISTRY · 2017 ·Vol. 409 ·期 10 ·2675-2683 · IF 3.431

Near-infrared-emitting NaYF4:Yb,Tm/Mn upconverting nanoparticle/gold nanorod electrochemiluminescence resonance energy transfer system for sensitive prostate-specific antigen detection

Gao Ni,Ling Bo,Gao Zhongling,Wang Lun,Chen Hongqi

An electrochemiluminescence resonance energy transfer (ECL-RET) system that detects prostate-specific antigen (PSA) was created. Near-infrared (NIR)-emitting NaYF 4 :Yb,Tm/Mn upconverting nanoparticles (UCNPs) are used as donors, and gold nanorods (GNRs) are used as acceptors. The ECL was enhanced nearly threefold by Mn 2+ doping, with an emission peak appearing at an NIR wavelength of 808 nm. Anti-PSA 1 (Ab 1 ) was bound to the surfaces of UCNPs after being modified with poly(acrylic acid) (PAA). As for acceptors, cetyltrimethylammonium bromide (CTAB)-capped GNRs were treated with 11-mercaptoundecanoic acid (MUDA) and then conjugated with Anti-PSA 2 (Ab 2 ). When PSA was added, donors and acceptors were brought in close proximity through specific interactions of antibodies and antigens, resulting in high quenching efficiency levels. Under optimal conditions, the linear range of detection was 3.75–938 pg/mL for PSA ( R  = 0.999), with a detection limit as low as 3.16 pg/mL. This method can be applied to detect PSA in human serums with satisfactory results. An electrochemiluminescence resonance energy transfer system was developed for determination of prostate-specific antigen using near-infrared-emitting NaYF 4 :Yb,Tm/Mn upconverting nanoparticles as donors and gold nanorods as acceptors.

研究领域: 分析化学 · 纳米技术 · 生物传感器 · 癌症诊断
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2025 · IF 21.1

Selective catalytic oxidation of sulfonamides for targeted hydroxybenzene sulfonate production via modulating surface complexes on Mn-doped Co3O4

Jia-Ying Zhang,Lin-Feng Zhai,Sheng-Nan Tang,Hao-Li,Zhuo-Feng Hu,Min Sun

This study presents a novel nonradical catalytic oxidation system for targeted p-hydroxybenzene sulfonate (PHS) production from sulfonamides (SAs). A positive external electric field was applied to induce the in-situ activation of O 2 on Mn-doped Co 3 O 4 surface, with Mn-doping used to manipulate the reactivity of surface complexes. Theoretical simulations predicted CoMn-peroxides as thermodynamically favorable candidates for the targeted PHS production. Experimental validation achieved PHS yields of 18.4–32.6 % from five typical SA compounds. While 1 O 2 also actively participated in the oxidation of SAs, disruption of the 1 O 2 oxidation pathway significantly enhanced the PHS yields to 47.6–50.3 %. The intensity of electric field regulated the O 2 activation pathways by influencing the stability of CoMn-peroxides. This nonradical catalytic oxidation system demonstrated excellent catalyst reusability and environmental robustness for energy-efficient SAs removal and PHS recovery. These findings provide new insights into leveraging nonradical = pathways to advance catalytic oxidation technology for sustainable water management.

研究领域: 环境化学 · 催化 · 水处理技术 · 材料科学 · 化学工程 · 可持续水资源管理
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2024 · IF 3.8

A Novel Mn-Based Film with Oxygen Vacancy for Efficient and Selective K+ Separation

Zhenkun Li,Peifen Wang,Xinglong Zhang,Xiaowei An,Xuli Ma,Yongguo Li,Xiao Du,Xiaogang Hao,Guoqing Guan

In this study, a novel electrical Mn-based film was developed for selective potassium (K+) separation, in which delaminated MnOx was obtained with the assistance of Ho3+ using a facile coprecipitation method and coated on carbon paper with poly(vinylidene fluoride) (PVDF) and graphitized carbon black. With the scanning electron microscope (SEM) and transmission electron microscope (TEM) observations, it was found that abundant multiphase interfaces and lattice dislocations appeared on the bulk of Ho-MnOx. Brunauer–Emmett–Teller (BET) analysis verified that the delamination assisted by Ho3+ increased the specific surface area from 110.3 m2/g (MnOx) to 166.8 m2/g (1% Ho-MnOx), which should be beneficial for the exposing of more electrochemical active areas and active sites for K+ adsorption and separation. Particularly, 1% Ho-MnOx had a high concentration of oxygen vacancies and showed a better K+ adsorption ability than MnOx. It was considered that the adsorption of K+ was mainly affected by the ion memory toward K+ for the 1% Ho-MnOx. In addition, the 1% Ho-MnOx film had good stable retention and regeneration capability for the separation of K+; after 10 cycles of adsorption and desorption, the film still retained 87.24% of the maximum adsorption capacity for K+. It is expected to provide an effective preparation method to obtain a high-performance K+ removal film electrode for the separation of K+ under a low concentration.

CAS / MDL: 14483-18-2
研究领域: 材料科学 · 电化学 · 环境工程
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Surfaces and Interfaces · 2024 · IF 5.7

Outside-to-inside: Efficacy comparation of Mn bulk and surface-doped TiO2{201} in E-fueled solar flow battery system

Ping Lu,Zixing Gu,Zihan Zhang,Huaneng Su,Qiang Ma,Chunsheng Li,Lei Wei,Qian Xu

The all-in-one E-fueled solar flow battery system that can be recharged with liquid fuel is a new type of power system. It can continuously convert solar energy into liquid fuel without relying on external power supply equipments. However, the interface between the photoanode and the electrolyte often exhibits unsteady behavior, resulting in poor performance of the system. In this work, the {201} facets are selected and the impact of two doping treatment strategies for TiO 2 {201} photoanode on the performance of the E-fueled solar flow battery system is systematically studied through the I-t curve, linear sweep voltammetry, Mott-Schottky plot. The results show that the un-biased photocharging current of bulk-doped TiO 2 can reach 2.7 mA·cm −2 in the battery system test, only relying on the self-built electric field at the interface, and the energy conversion efficiency approaches 2.67 %. In addition, the performance is analyzed by the combination of transmission electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy and other characterizations, with the aim of distinguishing the effects of bulk- and surface-doped Mn and accurately revealing the mechanism of their influences from the outside to the inside. Finally, the optimization rules of the un-biased light charging mode of the system are explored.

研究领域: 材料科学 · 电化学 · 太阳能转化 · 电池技术
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FUEL · 2025 · IF 7.5

Smooth charge transfer at the Ag2MoO4/Mn-Fe PBAs S-scheme interface for photo-driven CO2 reduction

Lina Dai,Qiang Li,Xianglan Dong,Enqi Zhang,Yufeng Hu,Xin Guo,Yanduo Liu

Photocatalysis exhibits great potential for applications in solving energy and environmental problems, and has received widespread attention. This article constructs a new type of Mn-Fe Prussian blue analogues S-scheme mechanism photocatalytic material. The material is composed of oxidized photocatalysts (Ag 2 MoO 4 ) and reduced photocatalysts (Mn-Fe PBAs). The composite photocatalyst constructed in this way shows advantages such as a wide spectral response range, high charge carrier separation efficiency, and strong oxidation–reduction ability, which can significantly enhance photocatalytic efficiency. By studying the construction method and CO 2 reduction performance of the photocatalyst, the structure-performance relationship can be clarified. The CO production rate is 43.3 μmol/g/h, and the selectivity can reach 94.9 %, which is far superior to the current mainstream photocatalytic system. The electron transfer kinetics and S-scheme charge separation mechanism between the Mn-Fe PBAs and Ag 2 MoO 4 interfaces are explained by steady-state surface photovoltage spectroscopy (SS-SPS) and near ambient pressure XPS (NAP-XPS). In-situ DRIFTS techniques are used to monitor the changes of transition intermediates, and combined with theoretical calculations, the activation mechanism of CO 2 by the Mn-Fe catalytic site is deeply revealed at the atomic level. This study provides new theoretical guidance and profound insights for the construction of Prussian blue analogues photocatalysts.

研究领域: 材料科学 · 环境科学 · 物理化学 · 纳米技术 · 催化 · 能量转换
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Catalysts · 2025 ·Vol. 15 ·期 6 ·545 · IF 4

Tailoring Pore Size in Bimetallic Nb-Mn/MCM-41 Catalysts for Enhanced Plasma-Driven Catalytic Oxidation of Toluene

Xiaohong Yao,Jian Zhang,Chao Long

This study explored how pore size engineering in Nb-Mn/MCM-41 catalysts affects plasma-catalytic toluene oxidation. Adjusting the pore diameter (2.49–3.98 nm) modulated metal-support interactions and oxygen dynamics, with pore expansion to 3.73 nm (M3) optimizing the Mn4+/(Mn2++ Mn3+) ratio (XPS: 36.8%), the amount of lattice oxygen species (O2-TPD: 0.222 mmol/g), and crystallite size control (1.5 ± 0.2 nm, TEM). Smaller pores (M1: 2.49 nm) enhanced toluene adsorption but limited active site accessibility, while oversized pores (M4: 3.98 nm) reduced oxygen storage capacity (0.600→0.412 mmol/g). The Nb-Mn/M3 catalyst achieved superior performance with 96.8% toluene conversion, 55.0% CO2selectivity, and 85.4% carbon balance, while minimizing organic byproducts (GC-MS). Mechanistic studies revealed pore-mediated oxygen storage-transport cycles as critical for decoupling adsorption and oxidation steps. This study reveals fundamental mechanisms linking pore architecture to plasma-catalytic synergy in toluene oxidation, offering critical insights for the systematic design of energy-efficient, plasma-catalytic systems targeting industrial VOCs remediation.

CAS / MDL: 6156-78-1
研究领域: 催化化学 · 环境化学 · 材料科学 · 等离子体化学 · 纳米技术 · 表面科学
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Surfaces and Interfaces · 2025 · IF 6.3

Bimetallic Fe/Mn Doped Zeolite Imidazolate Organic Framework with Peroxidase-like Activity for Dopamine Detection and Antibacterial Application

Qingtao Zeng,Bingjie Zhang,Shengzhi Jiao,Mingyue Gao,Ruyu Li,Haiyan Xiao,Longgang Wang

The emergence of nanozymes based on metal-organic frameworks has successfully addressed some limitations of natural enzymes. ZIF-8 is a framework with high pore rate consisting of Zn 2+ and 2-methylimidazole, but its catalytic activity is limited. In this study, a new metal organic framework named ZIF-8 (FM) was prepared by doping iron and manganese in ZIF-8, which exhibited enhanced catalytic performance. ZIF-8(FM) showed the peroxidase-like (POD-like) activity by oxidizing chromogenic substrates and was capable of colorimetric detection of dopamine in actual samples. In addition, in order to improve the photothermal conversion efficiency, ZIF-8(FM) was wrapped with polydopamine (PDA) to prepare ZIF-8(FM)@PDA. The antibacterial experiments of Escherichia coli and Staphylococcus aureus showed that ZIF-8(FM)@PDA had strong antibacterial effect. Nanomaterials based on ZIF-8(FM) have great potential in dopamine detection and effective photothermal antibacterial treatment.

研究领域: 纳米技术 · 生物分析化学 · 材料科学 · 酶模拟 · 抗菌治疗
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Surfaces and Interfaces · 2025 · IF 6.3

Insight into the role of Si/Al of MCM-41 zeolite in non-thermal plasma-assisted catalytic oxidation of toluene over bimetal Nb-Mn supported on MCM-41

Xiaohong Yao,Jian Zhang,Chao Long

This study explored how the Si/Al ratio in Nb-Mn/MCM-41 catalysts affect toluene degradation via plasma catalysis. Adjusting the Si/Al ratio altered catalyst acidity and redox properties, decreasing the Si/Al ratio led to increased acidity, higher Mn 3+ /Mn 4+ ratio and greater O ads /O lat ratio as indicated by NH 3 -TPD, XPS, and O 2 -TPD analysis. Lower Si/Al (Nb-Mn/M(25)) boosted toluene removal efficiency to 98.2% under dry conditions due to increased oxygen vacancies and acidity. Moderate humidity enhanced conversion, but higher humidity levels proved detrimental, especially for low Si/Al catalysts. At a humidity level of 3.11 vol%, the toluene removal efficiency of Nb-Mn/M(25) exhibited a reduction of 15.3%, while Nb-Mn/M(200) with higher Si/Al ratio decreased only by 3%. Hydrophobic, higher Si/Al catalysts showed better resistance to humidity's negative impact. These findings offered insights into designing efficient catalysts for VOC removal by optimized Si/Al ratio and managing humidity.

CAS / MDL: 6156-78-1
研究领域: 环境催化 · 材料科学 · 化学工程 · 等离子体化学
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