JOURNAL OF POWER SOURCES
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2024
·
IF 8.1
Lu Sai,Zhongsheng Dai,Zhenbo Wang,Huiling Zhao,Ying Bai
Li-rich layered oxides with high energy densities have become one kind of promising cathode for advanced lithium-ion batteries, however some issues are severely hindering their practical applications. To address these challenges, fast ion conductive LiTi 2 (PO 4 ) 3 (LTPO) is employed to modify the typical Li-rich cathode Li 1 · 2 Mn 0 · 56 Ni 0 · 17 Co 0 · 07 O 2 (LMNCO) via a sol-gel process combined with a two-step annealing treatment in this work. Serving as a physical separator, LTPO coating effectively depresses the side reactions at cathode-electrolyte interface and the transition-metal dissolution from LMNCO active material under harsh electrochemical environment. Meanwhile, LTPO layer with high ion conductivity could facilitate the interfacial Li + diffusion during charge/discharge process. In addition, partial Ti 4+ ions doped into LMNCO effectively elevate the oxygen electronegativity and restrain the excessive oxidization of lattice oxygen, thus stabilizing the crystal structure and alleviating the stress-strain propagation upon cycling. Electrochemical characterization results demonstrate that the LTPO-modified LMNCO cathode exhibits a superior capacity retention of 86.5 % after 400 cycles at room temperature and that of 73.7 % even under an elevated temperature of 45 °C after 250 cycles under 1C. This study provides a facile strategy for the surface modification of Li-rich layered-structure oxides, which also sheds light in enhancing electrochemical performances for various cathode materials .
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CERAMICS INTERNATIONAL
·
2025
·
IF 5.6
Fanlin Kong,Yi liu,Shiyu Cao,Huimin Chen,Yanwei Fan,Junhua Wang,Jincheng Yao,Aimin Chang
In this study, single-phase high-entropy ceramics (HECs) with the composition (Co,Mn,Fe,Zn,Ni,Mg,Al,Cr) 3 O 4 were successfully synthesized using five different types of spinel raw materials. The resulting material demonstrates excellent performance in the negative temperature coefficient (NTC) thermistor field. X-ray diffraction (XRD) analysis confirmed the structure as a cubic spinel with a single Fd-3m space group. The electron microscope image reveals the growth of ceramic grains with increasing sintering temperature, with a uniform distribution of all elements. After 1800 h of accelerated aging at 150 °C, the Δ R / R 0 value was only 0.41 %, indicating the ceramic's exceptional structural stability. X-ray photoelectron spectroscopy(XPS) analysis reveals that electrical conductivity are mainly governed by electron hopping between Mn 3+ and Mn 4+ ions in the octahedral sublattice sites. Impedance spectroscopy further shows that grain boundary resistance is the dominant contributor to the total resistance. This study provides new insights into the synthesis of single-phase HECs materials and proposes strategies to enhance material stability for future applications.
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GREEN CHEMISTRY
·
2024
·Vol. 26
·期 10
·6131-6138
·
IF 9.3
Yan Wang,Xuan Wang,Yonghao Dong,Mingli Peng,Lina Guo,Mengyao Cui,Yuan He,Jiabao Yi,Huijun Ma,Huan Zhang,Haiming Fan
The selective oxidation of alcohols has drawn significant attention in heterogeneous catalysis with the increasing use of Pickering interfacial catalysis (PIC) for green transformations of alcohols. However, it is still highly desirable to design and develop a solid catalyst with easy separation and recycling, made from abundant resources through a simple synthesis route, for the selective oxidation of alcohols. In this study, ferrite nanoparticles, synthesized via a hydrothermal process, were employed to act as a stabilizer and catalyst in PIC for the oxidation of benzyl alcohol using H2O2. The ferrite nanoparticles exhibited higher catalytic performance in PIC than in acetonitrile. The turnover number (TON) of the nanocatalyst in PIC was found to be 1.5–4 times higher than that in acetonitrile, and the reaction constant in PIC (kPIC = 0.712 h−1) was almost twice that in acetonitrile (kCH3CN = 0.310 h−1) for MnFe2O4 nanoparticles. Moreover, other alcohols could also be oxidized with moderately high conversion and selectivity in PIC. Significantly, the ferrite nanocatalyst could be easily separated from PIC using a magnet for reuse, achieving 88% BzOH conversion after five cycles. The use of hazardous organic solvents was avoided in PIC, making it a more advanced, green and sustainable reaction system.
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ENVIRONMENTAL RESEARCH
·
2025
·
IF 7.7
Hao Meng,Yue Wang,Haiyan Yang,Jinglong Han,Dillirani Nagarajan,Shih-Hsin Ho,Jo-Shu Chang
Advanced oxidation processes, especially those engaging in persulfate activation, are one of the emerging technologies for the degradation of recalcitrant organic pollutants. This study used Fe and Mn-loaded Prussian blue analogs (FeMn-PBA) as precursors to synthesize a nitrogen-doped graphene shell (FeMn@NG) through calcination in a nitrogen atmosphere. This was then employed as a catalyst to initiate the degradation of sulfadiazine (SD) using persulfate. The encapsulated FeMn bimetallic nanoparticles with various oxidation states undergo redox cycling, which promotes the rapid generation of free radicals and maintains the stability of FeMn@NC by sustaining continuous persulfate (PDS) activation. The results showed that nearly 96 % of SD was degraded within 45 min. Experiments involving free radical quenching and electron paramagnetic resonance spectroscopy demonstrated that sulfate radicals (SO 4 ·− ) and superoxide radicals (O 2 ·− ) were primarily responsible for the degradation of SD. The impact of different process parameters on the degradation efficiency of SD was simultaneously investigated. The degradation products of SD were examined, and a degradation pathway was proposed according to the LC-MS findings. XPS analysis indicated the presence of Fe/Mn redox cycling, which played a role in the equilibrium electron transfer during PDS activation. This study provides insights into the rational design of efficient catalysts by combining Prussian blue analogs with FeMn, while also promoting the remediation of polluted water bodies.
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高影响因子
MICROCHEMICAL JOURNAL
·
2025
·
IF 5.1
Siyu Wu,Xiaojuan Niu,Jiali Chen,Wangni Meng,Han Tao,Jianli Zhou,Yuangen Wu
Kanamycin (KAN) can generate a serious threat to human health due to its tendency to accumulate in food. Current colorimetric strategy for KAN detection still faces some challenges, and nanozyme-based colorimetry is an ideal alternative approach. Herein, a non‑copper-based multivalent laccase mimic named Mn-Car is first synthesized through a self-assembly of manganese ions and the endogenous biomolecule carnosine, which is further used to develop a novel colorimetric method for ultrasensitive and selective detection of KAN. The laccase-like catalytic center is formed through the multidentate chelation bonds between manganese ions and imidazolium groups of histidine as well as carboxyl groups of β-alanine in carnosine. The multivalent oxidation states of manganese dynamically regulate electron transfer pathways through synergistic coordination. The unique Mn-Car architecture drives the efficient generation of superoxide radicals (O 2 · − ) and semiquinone radicals (SQ· − ). Leveraging the excellent laccase-like activity of Mn-Car , a highly sensitive colorimetric method for KAN detection is developed. Mn-Car forms polydentate chelation with the amino and hydroxyl groups in KAN, which can trigger multi-step cascade oxidation reactions that disrupt the structural core of Mn-Car and lead to reduced colorimetric signals. The colorimetric method achieves a limit of detection (LOD) of 0.102 μM and is successfully applied for on-site detection of KAN in water samples and honey, providing a novel platform for antibiotic residue analysis.
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MATERIALS SCIENCE IN SEMICONDUCTOR PROCESSING
·
2025
·
IF 4.6
Yaqi Wu,Jianhua Qian,Jinjuan Xing,Junhua Li,He Huang,Yanan Wang,Xueming Kang,Lijuan Wang,Jiasheng Xu
Volatile organic compounds (VOCs), as hazardous environmental pollutants emitted from chemical industries, cause significant threats to human health and ecological environment owing to their inherent toxicity and carcinogenicity. Catalytic oxidation has emerged as a promising technology for VOC elimination, enabling complete degradation of pollutants into CO 2 and H 2 O. This study investigates transition metal oxide (TMO x , TM = Mn, Co, Fe, Ni, Cu, Zn)/TiO 2 catalysts for toluene degradation. Since the catalytic efficacy of TiO 2 -based catalysts critically depends on the quantity of surface oxygen vacancy (O v ) in heterogeneous processes, we engineered O v -rich interfaces by breaking atomic periodicity arrangements and generating unsaturated coordination sites. These structural modifications enhanced oxygen migration rates and increased reactive oxygen species availability. Among the synthesized catalysts, CuO/TiO 2 exhibited the highest performance, achieving 90 % toluene conversion (T 90 ) at 286 °C under a weight hourly space velocity (WHSV) of 20,000 mL/(g·h) with an initial toluene concentration of 1000 ppm. The measurement of in-situ DRIFTS suggested that toluene oxidation process abided by the path of toluene → benzaldehyde → benzoic acid → anhydride →CO 2 and H 2 O. Furthermore, the by CuO/TiO 2 catalyst demonstrated great reusability, and long-term stability, highlighting its potential for industrial-scale VOC abatement applications.
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RSC Advances
·
2025
·Vol. 15
·期 28
·22605-22615
·
IF 4.6
Jujiao Zhao,Xianjuan Xu,Qiao Zhang,Feilan Qi,Haoxuan Wei,Quanfeng Wang,Youzhou He,Xiaoxia Bai,Shun Guan,Ming Zhu,Xingmin Wang
Transforming Mn residues into catalysts for activating peroxymonosulfate (PMS) for the degradation of organic pollutants is a promising method that could not only mitigate environmental pollution caused by Mn residues, but could also provide inexpensive catalysts for PMS-based wastewater treatment. Herein, a two-step method involving alkali-reduction treatment is proposed for improving the catalytic activity of Mn residues. The proposed alkali treatment successfully reduced the content of Si from 261.0 mg g−1 to 80.5 mg g−1, leading to relatively increased contents of Fe and Mn. Moreover, alkaline NaBH4 reduction treatment introduced more oxygen vacancies, further enhancing the performance. The sample treated with the two-step method exhibited rhodamine B (RhB) degradation kinetics of 0.034 min−1, which was 2.43 times higher than that of the control sample. Quenching experiments and electron paramagnetic resonance demonstrated the vital role of 1O2 in the degradation of RhB, and the mechanism was investigated. Furthermore, 18 types of degradation intermediates were detected, and the possible degradation pathway for RhB was proposed. Through employing a toxicity estimate software tool, it is indicated that RhB toxicity continuously decreases during RhB degradation. The findings of this work could shed light on the reutilization of Mn residues and the development of inexpensive catalysts for PMS-based wastewater treatment.
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CHEMICAL ENGINEERING SCIENCE
·
2025
·
IF 4.3
Xiaoqiang Li,Xin Zhang,Xiaorui Zhang,Hao Lu,Jian Wang,Siyuan He,Xiaoxiao Duan,Yongsheng Ren
2-Mercaptobenzothiazole (MBT), a widely utilized metal corrosion inhibitor in industrial production processes, has become a typical persistent organic pollutant (POP) in the circulating water of coal chemical pipelines. In this study, Fe/Mn bimetallic MOF materials supported on carbon fiber paper (PC) were employed for the first time as an electro-Fenton cathode (Fe/Mn@MPC) in a heterogeneous electro-Fenton system, achieving efficient degradation of MBT. Specifically, this novel cathode enabled 96.35 % removal of MBT within 2 h. The uniformly rough fiber morphology presented by the Fe/Mn@MPC cathode results in an increased electrochemically active surface area and reduced resistance. Remarkably, it maintains a very stable catalytic activity over a wide pH range (3–11) and after 10 h of continuous operation, which confirms that the bimetallic synergistic effect enhances the stability of the system. EPR and quenching experiments identified hydroxyl radicals as the primary active species. Based on HPLC-MS results, MBT degradation pathways involving sulfur oxidation intermediate cleavage and benzothiazole ring detachment were proposed. This work presents a promising cathode design for the treatment of thiol-containing wastewater and offers new insights into the efficient remediation of coal chemical wastewater.
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ADVANCED FUNCTIONAL MATERIALS
·
2024
·
IF 18.5
Qianqian Qiao,Zerui Liu,Fei Hu,Ziqiang Xu,Ying Kuang,Cao Li
Catalytic medicine, using enzymes or nanozymes, is an emerging method for cancer treatment. However, its applicability is limited by the low catalytic activity in the tumor microenvironment (TME). In this work, a versatile and synthesis-friendly nanozyme, CeO 2 Mn 1.08 O x nanoclusters, is prepared. This novel Ce─Mn heterojunction is formed by oxidation of CeO 2 nanoparticles through H 2 SO 4 /KMnO 4 . CeO 2 Mn 1.08 O x exhibits high multi-enzymatic catalytic activities and acts as a catalase (CAT), peroxidase (POD), and oxidase (OXD) mimics under acidic conditions. It can regulate the TME by relieving hypoxia and consuming endogenous glutathione (GSH). Glucose oxidase (GOx) is then incorporated into CeO 2 Mn 1.08 O x and linked with poly(ethylene glycol) (PEG) to obtain the cascade enzyme system (Ce─Mn)-PEI/GOx-PEG. CeO 2 Mn 1.08 O x exhibits CAT-like properties, which sensitize GOx-based starvation therapy, and POD- and OXD-like properties, which generate highly cytotoxic reactive oxygen species (ROS) in cancer cells. The glucose catabolic product, H 2 O 2 , is also used to generate O 2 and ROS. In addition, the heterojunction structure provides CeO 2 Mn 1.08 O x with near-infrared (NIR) photothermal capability, making it suitable for photothermal therapy (PTT). Density functional theory (DFT) calculations provide possible reasons for the high catalytic activity and photothermal capability of CeO 2 Mn 1.08 O x . When combining mild PTT with catalytic therapy, the cascade enzyme system (Ce─Mn)-PEI/GOx-PEG can efficiently ablate tumors.
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ADVANCED FUNCTIONAL MATERIALS
·
2025
·
IF 19
Yong-Qi Ye,Si-Heng Liu,Wen-Qi Lv,Ding-Rong Deng,Gui-Fang Li,Ye Zeng,Jia-Xi Song,Hai Huang,Shuang-Lin Cai,Yu-Han Yuan,Xiao-Hong Fan,Jian-Chun Weng,Qi-Hui Wu
Iron-based sulfides are promising anode materials for sodium-ion batteries (SIBs) due to high theoretical capacities, but their short cycle life—caused by volume expansion and polysulfide shuttle effect—limits wide-temperature applications. To solve this, a novel three-dimensional MFS@rGO composite anode was prepared via one-step solvothermal method followed by annealing sulfurization, composed of Mn-doped Fe 7 S 8 (MFS) embedded in nitrogen-doped reduced graphene oxide (N-doped rGO). Mn doping enlarges Fe 7 S 8 lattice spacing, reducing Na⁺ diffusion resistance to boost ionic conductivity and Na storage. DFT calculations confirm Mn increases Fermi-level electronic density, lowers Na⁺ migration energy barrier, and accelerates ion transport. N-doped rGO builds a stable conductive network and synergizes with Mn to suppress shuttle effect and alleviate volume expansion, enhancing structural stability. Benefiting from this synergy, MFS@rGO performs well at −40–60 °C: 282.71 mAh g −1 after cycling at −40 °C, 310 mAh g −1 over 500 cycles at −20 °C, 450 mAh g −1 over 1000 cycles (60 °C, 2 A g −1 ). At room temperature, it retains 407.09 mAh g −1 ; over 100 cycles (1 A g −1 ); even at 50 A g −1 , it maintains 206.14 mAh g −1 over 100,000 cycles with negligible degradation. It also works well in full cells, offering a strategy for high-performance SIBs under extreme conditions.
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ACS Applied Materials & Interfaces
·
2021
·
IF 9.229
Xueqian Ji,Yuxing Xu,Hailan Feng,Pengfei Wang,Yuncheng Zhou,Jiechen Song,Qing Xia,Qiangqiang Tan
To improve the initial Coulombic efficiency, cycling stability, and rate performance of the Li-rich Mn-based Li1.2Mn0.54Ni0.13Co0.13O2 cathode, the combination of LiMn1.4Ni0.5Mo0.1O4 coating with Mo doping has been successfully carried out by the sol–gel method and subsequent dip-dry process. This strategy buffers the electrodes from the corrosion of electrolyte and enhances the lattice parameter, which could inhibit the oxygen release and maintain the structural stability, thus improving the cycle stability and rate capability. After LiMn1.4Ni0.5Mo0.1O4 modification, the initial discharge capacity reaches 272.4 mAh g–1 with a corresponding initial Coulombic efficiency (ICE) of 84.2% at 0.1C (1C = 250 mAh g–1), far higher than those (221.5 mAh g–1 and 68.9%) of the pristine sample. Besides, the capacity retention of the coated sample is enhanced by up to 66.8% after 200 cycles at 0.1C. Especially, the rate capability of the coated sample is 95.2 mAh g–1 at 5C. XRD, SEM, TEM, XPS, and Raman spectroscopy are adopted to characterize the morphologies and structures of the samples. This coating strategy has been demonstrated to be an effective approach to construct high-performance energy storage devices.
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高影响因子
ACTA PHYSICO-CHIMICA SINICA
·
2017
·Vol. 33
·期 8
·1672-1680
·
IF 0.767
LIAO Pei-Yi,ZHANG Chen,ZHANG Li-Jun,YANG Yan-Zhang,ZHONG Liang-Shu,GUO Xiao-Ya,WANG Hui,SUN Yu-Han
A series of Cu/Co/Mn/Al catalysts derived from hydrotalcite precursors with different Cu/Co molar ratios (0, 0.1, 0.5, 1.0, and 2.0) were prepared and used for the synthesis of higher alcohols from syngas. N2 physical adsorption desorption, inductively coupled plasma atomic
emission spectrometry (ICP-AES), X-ray diffraction (XRD), scanning electron microscopy (SEM), hydrogen temperature-programmed reduction (H2-TPR), thermogravimetry (TG), and high-resolution transmission electron microscopy (HRTEM) techniques were employed to investigate the physical
and chemical properties of the Cu/Co/Mn/Al catalysts. The results show that the optimum Cu content can increase specific surface area, improve reducibility, and form regular layered structure to provide more uniform distribution of active sites, thereby enhancing catalytic activity and alcohol
selectivity. When the Cu/Co molar ratio was 0.5, the yield of alcohol and the alcohol selectivity reached the maximum values of 0.071 g·g-1·h-1 and 35.9%, respectively.
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