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CHEMICAL ENGINEERING SCIENCE · 2025 · IF 4.3

High-performance F, Mn co-doped VO2(B) cathode material in the form of multilayered nanosheets curled rods and its aqueous zinc ion battery applications

Changqing Yuan,Xiaorong Meng,Han Shen,HaoHao Wei

To address the shortcomings of VO 2 (B) when utilized as cathode materials for aqueous zinc ion batteries (AZIB), this study prepared a fluorine and manganese co-doped VO 2 (B) with a nanorod-like structure, formed from convoluted multilayered nanosheets, was synthesized via a solvothermal method. It was established that F and Mn doping effectively broadens the lattice structure and tunneling space of VO 2 (B) and induces lattice distortion of VO 2 (B) through the high electronegativity of F element, leading to the ductile growth of FMVO into a nanorod-like structure made of multilayered ultrathin nanosheets curled. The increased tunneling space and active sites of FMVO, compared to pure VO 2 (B), significantly enhanced the de-embedding rate of Zn 2+ and reduced diffusion resistance. The specific capacity of F 0.06 M 0.02 VO is 523.92 mAh/g (0.2 A/g) with 88.64 % capacity retention after 2,000 cycles (5 A/g). This research provides a novel approach to the development of cathode materials for AZIB.

CAS / MDL: 1314-62-1 54010-75-2
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SOLID STATE IONICS · 2025 · IF 3.3

Synergistic effect of ball milling time and Mn-Fe ratio on the electrochemical performance of paper-based LiMn1-XFeXPO4/C cathodes for Lithium-ion batteries

Peng Xu,Haiwei Wu,Haiwen Li,Hanbin Liu,Zhijian Li

In recent years, with the continuous development of high-voltage cathode materials for lithium-ion (Li + ) batteries, the LiMn 1-X Fe X PO 4 solid solution obtained by using Mn element to replace part of Fe on the basis of LiFePO 4 (LFP) has received extensive attention. It shows significantly improved voltage and capacity than LFP, which is currently regarded as a leading update for the traditional LFP cathode. At present, preparation of high-performance LiMn 1-X Fe X PO 4 using common high-temperature solid-state method is still challenging and the basic intricate coupling of the Mn-Fe ratio and ball milling time parameters on its electrochemical performance is still need to be fully studied due to the parametric complexity. Herein, the carbon wrapped LiMn 1-X Fe X PO 4 /C material was prepared by high-temperature solid-phase method, and paper-based LiMn 1-X Fe X PO 4 /C electrodes were also fabricated to fully study the synergistic effects of ball milling times (0.5 h, 1 h, 2 h) and Mn-Fe ratios (5:5, 6:4, 7:3, 8:2) on their electrochemical performance. It was found that there happened to be optimized ball milling time for each Mn-Fe ratio based LiMn 1-X Fe X PO 4 /C materials. The higher Mn-Fe ratio, the longer ball milling time that is needed to achieve high electrochemical performance of paper-based LiMn 1-X Fe X PO 4 /C cathodes. Through detailed analysis of cyclic voltammetry (CV) curves, cycling and rate performance, it was found that LiMn 1-X Fe X PO 4 /C cathode prepared by ball milling for 1 h and Mn-Fe ratio of 7:3 has the best optimized voltage, cycling and rate performance.

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SENSORS AND ACTUATORS B-CHEMICAL · 2018 · IF 5.667

Facile, rapid synthesis of N,P-dual-doped carbon dots as a label-free multifunctional nanosensor for Mn(VII) detection, temperature sensing and cellular imaging

Fangfang Du,Gan Li,Xiaojuan Gong,Guo Zhonghui,Shaomin Shuang,Ming Xian,Chuan Dong

We rapidly synthesized N,P-dual-doped carbon dots (N,P-CDs) via the acid-base neutralization spontaneous heat using a simple blend of phthalic acid, 1,2-ethylenediamine, and concentrated phosphoric acid. The approach is automatic without external heat treatment to speedily produce dozens of N,P-CDs, which refrain high temperature, sophisticated manipulations, and long reaction times. As-fabricated N,P-CDs with excellent luminescent properties, superior biocompatibility and respectable fluorescence quantum yield (QY) of 15% have been employed for the development of a label-free multifunctional fluorescence sensing platform for the detection of Mn(VII), temperature sensing and cellular imaging. Mn(VII) is able to effectively quench the fluorescence of N,P-CDs based on inner filter effect (IFE) because the absorption bands of Mn(VII) can perfectly overlap the emission and excitation wavelengths of N,P-CDs. The system had high selectivity toward Mn(VII) and the detection limit was 48.3 nM in the broad linear span from 10 μM to 200μM. Moreover, the N,P-CDs were extended for sensing Mn(VII) in living cell due to favorable biocompatibility and negligible cytotoxicity. Furthermore, the sensors showed a linear and reversible variation of emission intensity for a temperature range from 25℃ to 80℃, with a sensitivity of −1.79% per ℃. The practical implications of N,P-CDs for Mn(VII) detection have been demonstrated in Teas leaves and Medicinal herbs samples with satisfactory results.

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JOURNAL OF COORDINATION CHEMISTRY · 2024 · IF 2.2

Zn(II), Cd(II), Mn(II), and Cu(II) complexes based on an imidazole derivative and carboxylic acids: synthesis, crystal structures, and DNA-binding properties

Ying Zhou,Xiao-Tong Song,Hui-Chao Guan,Shu-Mei Yue

In this investigation, six new metal complexes with 2-(pyridin-2-yl)benzo[d]imidazole (bpm) were synthesized and analyzed by single-crystal X-ray diffraction (XRD), including catena-bis[(µ-2,2-bis(4-carobxyphenyl)hexafluoropropane)-(2-(pyidin-2-yl)-1H-benzimidazole)-aqua-zinc] (1), catena-[(µ-2,2-bis(4-carobxyphenyl)hexafluoropropane)-(2-(pyidin-2-yl)-1H-benzimidazole)-aqua-cadmium] (2), aqua-[2,2-bis(4-carobxyphenyl)hexafluoropropane]-bis[2-(pyridin-2-yl)-1H-benzimidazole]-manganese (3), μ-[2-nitrobenzene-1,4-dicarboxylato]-μ-[2-nitrobenzene-1,4-dicarboxylato]-bis[2-(pyridin-2-yl)-1H-benzimidazole]-di-zinc (4), catena-[bis(µ-2-nitrobenzene-1,4-dicarboxylato)-diaqua-bis(2-(pyridin-2-yl)-1H-benzimidazole)-di-cadmium] (5), aqua-[pyridine-2,6-dicarboxylato]-[2-(pyridin-2-yl)-1H-benzimidazole]-copper hydrate (6) (H2hfipbb = 2,2-bis(4-carboxyphenyl)hexafluoropropane, H2nbdc acid = Nitroterephthalic acid, and H2pda = 2,6-pyridinedicarboxylic acid). Complex 1 crystallized in a monoclinic system with space group P21/n; 2 crystallized in a monoclinic system with space group C2/c; 3 crystallized in an orthorhombic system with space group Pna21; 5 crystallized in a monoclinic system with space group P21/c; 4 and 6 crystallized in triclinic systems with space group P-1. The DNA-binding modes of the complexes were investigated by several analysis methods (e.g. viscosity analysis, circular dichroism spectroscopy, fluorescent spectroscopic analysis, as well as UV spectroscopic analysis). Complexes 1-6 bind to calf thymus DNA via an intercalative mode. The results of this study provide insights into the mechanism of DNA binding and provide a basis for rationally designing new powerful reagents for DNA detection and targeting.

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ACTA MATERIALIA · 2026 · IF 10.7

Conventional solid-state synthesis achieves advanced P'2-type Mn-rich cathodes for sodium-ion batteries with 35 mA·h·g−1 capacity increase and 28.7% stability improvement

Qi-Lin Zheng,Wei-Wei Yuan,Min Wen,Shengqi Chu,Min Lin,Zhensheng Hong,Jiaxin Li,Lituo Zheng,Zhigao Huang,Hu-Rong Yao

P'2-type manganese-rich layered oxides are promising cathodes for sodium-ion batteries. However, their synthesis requires unconventional rapid quenching to prevent O₂ absorption and P'2-P2 phase transformation during cooling, which compromises scalability and safety. Moreover, Jahn-Teller active ion enrichment and irreversible phase transitions during cycling impair structural stability. These synthesis challenges and inadequate electrochemical performance hinder practical applications. Herein, we report for the first time a simple solid-state synthesis of P'2-Na 0.55 Mg 0.05 Mn 0.90 O 2 (Na□MM□) cathode with a 3.78% lattice distortion through a dual-vacancy strategy. The Na□MM□ cathode delivers an ultrahigh energy density of 786 Wh·kg −1 . Na vacancies stabilize P'2 structure and enable a reversible P'2-OP4 transition, delivering 35 mA·h·g⁻¹ extra capacity. TM vacancies further synergize with Na vacancies to stabilize the TM-O framework, suppressing lattice oxygen loss and Mn³⁺ enrichment, which improves 100 cycles capacity retention by 28.7%. This work advances the synthesis and electrochemistry of P'2-type materials, offering a practical path toward application. Download: Download high-res image (286KB) Download: Download full-size image

CAS / MDL: 1309-48-4
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JOURNAL OF HAZARDOUS MATERIALS · 2023 · IF 13.6

Electrons of d-orbital (Mn) and p-orbital (N) enhance the photocatalytic degradation of antibiotics by biochar while maintaining biocompatibility: A combined chemical and biological analysis

Jinrui Dong,Pin Li,Xiaoyuan Ji,Yong Kang,Xue Yuan,Jingchun Tang,Boxiong Shen,Huajiang Dong,Honghong Lyu

Photocatalytic oxidation technology holds promise for ideal advanced treatment of antibiotic wastewater. Single-atom catalysts (SACs) are a new hotspot in catalytic science, but the photochemical studies on the removal of antibiotics from water and biocompatibility after entering the environment are scarce. In this work, we prepared a single Mn atom immobilized on N-doped biochar (Mn@N-Biochar) by impregnation calcination method for enhancing photocatalytic degradation of sulfanilamide (SNM) in different types of various water systems. Compared with the original biochar, Mn@N-Biochar showed enhanced SNM degradation and TOC removal capacity. DFT calculation concluded that the electrons of d‐orbital (Mn) and p-orbital (N) altered the electronic structure of biochar and enhanced the photoelectric performance. It was shown that Mn@N-Biochar caused negligible systemic inflammation and tissue damage when given orally in mice, and also did not alter cell death and ROS production in human lung, kidney, and liver cells, as compared with biochar. We are convinced that Mn@N-Biochar could enhance the photocatalytic degradation of antibiotics while maintaining biocompatibility, which could be a promising strategy for wastewater treatment .

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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH · 2023 · IF 5.8

Performance and mechanism analysis of sludge-based biochar loaded with Co and Mn as photothermal catalysts for simultaneous removal of acetone and NO at low temperature

Wang Hongqiang,Huang Sheng,Liao Lei,Mo Shengpeng,Zhou Xiaobin,Fan Yinming

Replacing NH 3 in NH 3 -SCR with VOCs provides a new idea for the simultaneous removal of VOCs and NO x , but the technology still has urgent problems such as high cost of catalyst preparation and unsatisfactory catalytic effect in the low-temperature region. In this study, biochar obtained from sewage sludge calcined at different temperatures was used as a carrier, and different Co and Mn injection ratios were selected. Then, a series of sludge-based biochar (SBC) catalysts were prepared by a one-step hydrothermal synthesis method for the simultaneous removal of acetone and NO in a low-temperature photothermal co-catalytic system with acetone replacing NH 3 . The characterization results show that heat is the main driving force of the reaction system, and the abundance of Co and Mn atoms in high valence states, surface-adsorbed oxygen, and oxygen lattice defects in the catalyst are the most important factors affecting the performance of the catalyst. The performance test results showed that the optimal pyrolysis temperature of sludge was 400 °C, the optimal dosing ratio of Co and Mn was 4:1, and the catalyst achieved 42.98% and 52.41% conversion of acetone and NO, respectively, at 240 °C with UV irradiation. Compared with the pure SBC without catalytic effect, the SBC loaded with Co and Mn gained the ability of simultaneous removal of acetone and NO through the combined effect of multiple factors. The key reaction steps for the catalytic conversion of acetone and NO on the catalyst surface were investigated according to the Mars-van Krevelen (MvK) mechanism, and a possible mechanism was proposed. This study provides a new strategy for the resource utilization of sewage sludge and the preparation of photothermal catalysts for the simultaneous removal of acetone and NO at low cost.

CAS / MDL: 6147-53-1 6156-78-1
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Materials · 2022 ·Vol. 15 ·期 12 ·4149 · IF 3.748

Study of Ce, Ca, Fe, and Mn-Doped LaCoO3 Perovskite Oxide for the Four-Way Purification of PM, NOx, CO, and HC from Diesel Engine Exhaust

Yinghui Wang,Xiurong Guo,Danfeng Du,Shaochi Yang

Perovskite-type catalysts were widely used in the field of automobile exhaust purification due to their inherent physicochemical properties and excellent doping characteristics. A series of La1−xMxCo1−yNyO3(M = Ce, Ca; N = Fe, Mn) perovskite-type catalyst samples were prepared by sol-gel method for the four-way purification of PM, NOx, CO, and HC emitted by diesel exhaust. The activity of catalyst samples was tested by simulation experiments and hydrogen temperature-programmed reduction (H2-TPR). Catalyst samples were characterized by means of XRD, FT-IR, SEM, BET, and XPS analysis. The results demonstrated that the perovskite-type catalyst samples with a particle pore size of 3–5 μm can be prepared by sol-gel method. When A-site of LaCoO3perovskite-type oxide was doped by cerium ions, the catalyst samples produced small distortion. The doping of cerium ions to A-site was more conducive to the four-way purification of diesel exhaust than calcium ions. La0.8Ce0.2CoO3perovskite-type samples showed the best purification efficiency, and the purification efficiencies of PM, NOx, CO, and HC were 90%, 85%, 94%, and 100%, respectively. When the B-site of La0.8Ce0.2CoO3perovskite was doped with iron ions, the purification efficiency of catalyst samples for PM and NOxcan be further enhanced. When the B-site of La0.8Ce0.2CoO3perovskite was doped with manganese ions, the purification efficiency of the catalyst samples for PM can be further enhanced. It can be seen from the simulation experiments that La0.8Ce0.2Co0.7Fe0.3O3perovskite was the best doping amount, and the purification efficiencies of PM, NOx, CO, and HC were 95%, 92%, 94%, and 100%, respectively.Keywords:perovskite-type catalyst;diesel exhaust;sol-gel method;four-way purification;doping amount

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APPLIED SURFACE SCIENCE · 2023 · IF 6.7

Deep eutectic solvent mediated synthesis of Mn-based hybrid electrocatalyst for oxygen evolution reaction: Insights into the effect of anion on the evolution of structure-activity

Mengwei Guo,Bo Zhang,Qibo Zhang

In this work, sulfur-doped manganese (S-Mn/CP) pre-catalysts supported by carbon paper (CP) were prepared from choline chloride/ethylene glycol-based deep eutectic solvent containing different manganese salts via electrodeposition method. The effect of anions, including NO 3 – , Cl - , SO 4 2- , CH 3 COO – , and crystal water (H 2 O), on the evolution of the structure and OER activity of as-prepared Mn-based pre-catalysts was analyzed. It turns out that the NO 3 – and H 2 O can be reduced during the electroreduction of Mn(II) species and induce the formation of manganese oxide/hydroxide. Thiourea (TU), used as a sulfur source, decomposes at the cathode and releases S 2- . The TU and H 2 O replace the Cl - in the [Mn(Cl) 6 ] 4- to form [Mn(Cl) 6- x (H 2 O) x ] x -4 and [Mn(Cl) 6- x - y (TU) y (H 2 O) x ] x + y -4 complexes, promoting the electroreduction of Mn(II) species. The OER intrinsic catalytic activity of the amorphous Mn 3 O 4 pre-catalyst is 16.3 times lower than that of the metallic Mn 0 pre-catalyst in a 1.0 M KOH solution. After annealing in an argon atmosphere, the surface of metallic Mn 0 is in-situ converted into Mn 3 O 4 and exhibits superior activity (0.0395 A g −1 cm -2 ECSA ) than the ordinary Mn 3 O 4 electrode (0.0088 A g −1 cm -2 ECSA ). This study brings insights into the effect of anion on the evolution of structure-activity of Mn-based pre-catalysts during the electrodeposition and OER catalytic process.

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Materials · 2023 ·Vol. 16 ·期 20 ·6667 · IF 3.4

Ce/Mn/Cr: (Re,Y)3Al5O12 Phosphor Ceramics (Re = Gd, Tb and Lu) for White LED Lighting with Significant Spectral Redshift and Improved Color-Rendering Index

Yukun Li,Svenja Hanson,Cheng Heng Pang,Peng Lyu,Jun Jiang

In order to attain phosphor ceramics with a high Color-Rendering Index (CRI), samples with the composition of Y0.997−xRexCe0.003)3(Al0.9748Mn2+0.024Cr3+0.0012)5O12(Rex= 0, Gd0.333, Gd0.666, Gd0.997, Tb0.333, Tb0.666, Tb0.997and Lu0.997were prepared by solid-state reaction and vacuum sintering, and exhibited potential for high-quality, solid-state lighting. Doping with Cr3+and Mn2+effectively enhanced the red component of Ce3+spectra through the intense energy transfer from Ce3+ions to Mn2+/Cr3+ions. The crystal field splitting of [GdO8] and [TbO8] was more extensive than that of [YO8], causing a massive redshift in the Ce3+emission peaks from 542 to 561 and 595 nm, while [LuO8] had an opposite effect and caused a blueshift with a peak position at 512 nm. White LED devices incorporating Ce/Mn/Cr: (Gd0.333Y0.664)3Al5O12phosphor ceramic exhibited a high CRI of 83.97, highlighting the potential for enhancing the red-light component of white LED lighting.Keywords:garnet phosphor;laser lighting;full spectrum;spectral modulation;Ce/Mn/Cr: (Re,Y)3Al5O12

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CERAMICS INTERNATIONAL · 2023 · IF 5.2

The effect of B-site ions on crystal structure evolution and microwave dielectric properties of gillespite-type SrCu0.95B0.05(B2+: Cu, Co, Mn, Ni, Mg, Zn)Si4O10

Zelai Cheng,Liming Xu,Xi Wang,Xiaohui Wu,Fangyi Huang,Yulan Jing,Hua Su

Gillespite-type SrCu 0.95 B 0.05 (B 2+ :Cu,Co,Mn,Ni,Mg,Zn)Si 4 O 10 (SCBS) ceramics were prepared by high-temperature solid-state method. Their microwave dielectric properties and crystal structure evolution were studied by P–V-L theory, bond valence model, and X-ray photoelectron spectroscopy. Varying B 2+ ion changed ionic polarizability and bond ionicity, causing dielectric constant ε r of SCBS to change. The change in quality factor Q  ×  f was explained by lattice energy, oxidation state of Cu, and internal strain/fluctuation. The temperature coefficient of resonator frequency τ f was regulated by B–O bond length and valence. The optimal microwave dielectric properties were exhibited by SrCu 0.95 Mn 0.05 Si 4 O 10 after sintering at 1050 °C: ε r ∼5.8 ± 0.03, Q  ×  f ∼65,589 ± 2611 GHz (@15.8 GHz), and τ f  ∼ -50 ± 4 ppm/°C. These materials show great potential application prospects for 5G/6G wireless communication.

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ENVIRONMENTAL RESEARCH · 2023 · IF 8.3

Synthesis of X@DRHC (X=Co, Ni, Mn) catalyst from comprehensive utilization of waste rice husk and spent lithium-ion batteries for efficient peroxymonosulfate (PMS) activation

Zhenyi Hu,Geng Su,Shujun Long,Xiaoting Zhang,Linkun Zhang,Yilin Chen,Chang Zhang,Gonggang Liu

Highly efficient resource recycling and comprehensive utilization play a crucial role in achieving the goal of reducing resource wasting, environmental protection, and achieving goal of sustainable development . In this work, the two kinds waste resources of agricultural rice husk and metal ions (Co, Ni, and Mn) from spent lithium-ion batteries have been skillfully utilized to synthesize novel Fenton-like catalysts. Desiliconized rice husk carbon (DRHC) with rich pore structure and large specific surface area from rice husk has been prepared and used as scalable carrier, and dandelion-like nanoparticles cluster could be grown in situ on the surface of the carrier by using metal ions contained waste water. The designed catalysts (X@DRHC) as well as their preparation process were characterized in detail by SEM, TEM, BET, XRD and XPS, respectively. Meanwhile, their catalytic abilities were also studied by activating potassium peroxomonosulfate (PMS) to remove methylene blue (MB). The results indicate X@DRHC displays excellent degradation efficiency on MB with wide pH range and stable reusability, which is suitable for the degradation of various dyes. This work has realized the recycling and high-value utilization of waste resources from biomass and spent lithium-ion batteries, which not only creates an efficient way to dispose waste resources, but also shows high economic benefits in large-scale water treatment .

CAS / MDL: 106-51-4 67-56-1 57-13-6
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