MATERIALS RESEARCH BULLETIN
·
2024
·
IF 5.3
Jiaping Guan,Guomin Sun,Gaoyuan Yu,Yu Chen,Jiawen Wei,Xiaohui Zhu,Xiaogu Huang
Sodium-ion batteries (SIBs) have garnered significant interest due to their cost-effectiveness and operational similarities to lithium-ion batteries. Amongst the various components, the cathode plays a pivotal role in determining the energy density of these batteries. Mn-based layered oxides stand out as promising cathode materials, owing to their abundance and non-toxicity. However, these oxides tend to suffer from structural instability during high-voltage cycling, leading to a decline in capacity. In this work, we have designed Ce-doped Na 0.6 Li 0.2 Mn 0.79 Ce 0.01 O 2 cathodes through a solid-state reaction process. This innovation aims to inhibit undesirable phase transitions and enhance the electrochemical performance of the electrodes. By integrating electrochemical testing with a suite of characterization techniques, we have shown that 1 mol% Ce doping effectively suppresses the formation of birnessite and the irreversible oxygen redox reactions in the high-voltage region. Moreover, our findings indicate that the detrimental phase transitions can be significantly mitigated throughout the electrochemical cycling process, thereby bolstering structural stability. Notably, the capacity of the Ce-doping cathode after 20 cycles substantially exceeds its initial discharge specific capacity, reaching 169.3 mAh g –1 . This research introduces a strategy for stabilizing the cathode structure of P2-type Mn-based layered oxides through Ce-doping, offering valuable insights for the advancement of next-generation SIBs.
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JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY
·
2022
·
IF 10.319
Qi Xue,Tao Hang,Jianghu Liang,Chun-Chao Chen,Yunwen Wu,Huiqin Ling,Ming Li
Memristors have been seen as promising candidates for next-generation nonvolatile memory and neuromorphic computing . Solution-processed memristors can offer many advantages, such as low-cost fabrication, large-area uniformity, and high versatility. However, the high annealing temperature of the solution process and unsatisfactory performance are impeding the advancement of flexible memristors. In this work, the combustion method was proposed to fabricate the Mn-ZnO-based memristor without a high-temperature process on the flexible substrate. The device demonstrates stable bipolar resistive switching behavior with ultralow switching voltage (−0.6 V/0.71 V), high on/off ratio (˃ 2 × 10 3 ), multilevel storage capability, and uniform resistance distribution ( σ / µ = 18%/16%). The flexible device with a bend radius of 10 mm shows no obvious performance degeneration compared with the device in the flat state. Furthermore, tunable repetitively synaptic weight was achieved by the memristor. Synaptic plasticity functions, such as excitatory postsynaptic current, paired-pulse facilitation, and learning/forgetting behaviors, have been emulated. This work provides a simple and feasible strategy for fabricating the flexible high-performance memristor, with the expectation to facilitate the development of flexible electronics.
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Journal of Cleaner Production
·
2023
·
IF 11.1
Xiaoyang Wang,Xiaoqing Si,Jianwei Gao,Qihan Zhou,Chun Li,Mingshen Li,Junlei Qi,Jian Cao
The high preparation cost and poor density of spinel coatings for stainless steel interconnect have always been puzzling conundrums for the solid oxide fuel cell stack developers. Herein, the microwave heating technology for fabricating Mn–Co spinel coating is developed to address these issues. We designed a device spontaneously providing reducing atmospheres and realized the low-cost, high-efficiency reduction of Mn–Co spinel via microwave heating. Dense coatings (MnO + Co) are formed on the steel surface at ∼1100 °C. The excellent density is related to the melting of Co particles induced by microwave selective heating. At initial, microwave heating is dominated by dipolar polarization, interfacial polarization, and natural resonance. After forming metallic Co, conductive loss and the lens effect further accelerate the reduction process. High-quality spinel coatings are formed during the subsequent oxidation at 800 °C, exhibiting an extremely low area-specific resistance increase rate.
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WATER RESEARCH
·
2020
·
IF 9.13
Dandan Rao,Jie Chen,Hongyu Dong,Junlian Qiao,Baoxue Zhou,Yuankui Sun,Xiaohong Guan
Although permanganate activation by sodium sulfite (Mn(VII)/Na 2 SO 3 ) has shown great potential for rapid abatement of organic contaminants , the limited reactivity under alkaline conditions and undesirable Mn residual may prevent its widespread application. To solve these challenges, calcium sulfite (CaSO 3 ) was employed as a slow-release source of SO 3 2− /HSO 3 − (S(IV)) to activate Mn(VII) in this study. It was found that the application of CaSO 3 solid could extend the effective working pH range of Mn(VII)/S(IV) from ≤7.0 to ≤9.0. Moreover, due to the enhanced precipitation of MnO 2 with the presence of Ca 2+ , very low Mn residual (<0.05 mg/L) was achieved in Mn(VII)/CaSO 3 system. Mn(VII)/CaSO 3 system is a unique two-stage oxidation process in terms of reaction kinetics and reactive oxidants. Specifically, Mn(VII) was rapidly consumed and reactive Mn intermediates (e.g., Mn(VI), Mn(V)), SO 4 •− , and HO • were produced in the first stage. However, the second stage was governed by the interaction between MnO 2 and S(IV), with SO 4 •− and HO • serving as the dominant reactive oxidants. Taking advantage of an automatic titrator, excess S(IV) was found to greatly quench the generated radicals, whereas it did not cause a significant consumption of reactive Mn species. All these results improved our understanding of the Mn(VII)/S(IV) process and could thus facilitate its application.
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高影响因子
MOLECULES
·
2023
·Vol. 28
·期 14
·5544
·
IF 4.6
Min Wang,Shilin Zhang,Juejin Teng,Shunsheng Zhao,Zhongtao Li,Mingbo Wu
An efficient and low-cost oxygen catalyst for the oxygen reduction reaction (ORR) was developed by in situ growth of Mn-Mo oxide nanoparticles on nitrogen-doped carbon nanotubes (NCNTs). Doped nitrogen effectively increases the electron conductivity of the MnMoO4@NCNT complex and the binding energy between the Mn-Mo oxide nanoparticles and carbon nanotubes (CNTs), leading to fast charge transfer and more catalytically active sites. Combining Mn and Mo with NCNTs improves the catalytic activity and promotes both electron and mass transfers, greatly enhancing the catalytic ability for ORR. As a result, MnMoO4@NCNT exhibited a comparable half-wave potential to commercial Pt/C and superior durability, demonstrating great potential for application in renewable energy conversion systems.Keywords:MnMoO4/NCNT composites;nitrogen doping;oxygen reduction reaction;platinum group metal (PGM)-free catalyst;electrocatalysis
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CERAMICS INTERNATIONAL
·
2023
·
IF 5.2
Zhihao Liang,Rongxia Huang,Tianbao Xie,Yi Zhang,Hua-Tay Lin,Yejing Dai
Bi 4 Ti 3- x (Mn 1/3 Ta 2/3 ) x O 12 piezoelectric ceramics were prepared by conventional sintering and direct-reaction sintering in this study. The effect of B-site Mn/Ta co-substitution and sintering method on the microstructure and electrical properties of Bi 4 Ti 3- x (Mn 1/3 Ta 2/3 ) x O 12 piezoelectric ceramics was systematically investigated. The experimental results show that the combination of high-valent Ta and low-valent Mn ions replacing Ti 4+ ions reduce the concentration of oxide vacancy defects in BITMT ceramics. The direct-reaction sintering is a simpler preparation method and the prepared samples have more uniform grain distribution and higher density. The resistivity of the direct reaction sintered sample with x = 0.05 at 500 °C is 7.19 × 10 5 Ωcm, the residual polarization is 8.1 μC/cm 2 , and the temperature stability of the piezoelectric constant is good. Therefore, the present study suggests that the piezoelectric properties of Mn and Ta co-doping of BIT ceramics could be greatly enhanced via the direct-reaction sintering, which provides a promising alternative to the conventionally sintered for a more cost-effective preparation for BIT ceramics.
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Journal of Materials Chemistry B
·
2021
·Vol. 9
·期 15
·3401-3411
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IF 6.331
Ming Wang,Miao Li,Yunli Wang,Yiran Shao,Yingchun Zhu,Shiping Yang
Hydroxyapatite (HA) has attracted wide attention for medical application due to its biocompatibility and bioactivity. However, the infection problems of HA remain among the leading reasons for implantation failure. Thus, it is urgent to endow HA biomaterials with antibacterial activity. Herein, the high antibacterial activity was achieved by introducing trace Mn3+ and H vacancy couples in HA through a facile heat-treatment strategy in air. The theoretical results indicated that Mn3+ was preferentially substituted for the Ca(2) site in the HA structure with a charge-compensating H vacancy appearing at the adjacent OH− site. The antibacterial tests showed that Mn-HA possessed antibacterial activity towards both E. coli and S. aureus with trace Mn content at the ppm level, and implied that Mn3+ and centers may play an important role in the antibacterial process. The Mn3+ and couples in Mn-HA, serving as oxidative and reductive centers respectively, could then collectively participate in the CoQ/CoQH2 redox cycling and synergistically facilitate the accumulation of CoQ˙− and ROS radicals. This enhanced ROS production was the main factor to endow Mn-HA with efficient antibacterial activity. Moreover, the in vitro bioactivity assay showed that Mn-HA materials exhibited enhanced osteogenic activity and good biocompatibility. Therefore, this work not only provides a feasible method to control the oxidation state of Mn elements in HA, but also proposes a novel trace Mn3+-doped HA for potential applications in tissue engineering.
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BIOMASS & BIOENERGY
·
2025
·
IF 5.8
Hongrui Guo,Chengjie Sun,Mo Qiu,Hejuan Wu,Zhihui Ma,Jirui Yang,Feng Shen
The catalytic oxidation of glucose to formic acid (FA) represents a crucial route for biomass valorization. Metal–organic framework (MOF)-derived carbon composites offer exceptional tunability for catalyst design. Herein, a series of carbon-regulated Mn x O y /C catalysts from Mn-MOF-74 precursors via controlled calcination atmospheres and temperatures, achieving satisfactory performance in glucose-to-FA conversion. Comprehensive characterization reveals that the carbon matrix plays a synergistic effect: dispersing Mn x O y nanoparticles to enhance substrate accessibility, and preventing Mn leaching to improve stability. The FA yield is determined by fine-tuning key parameters: the (Mn 2+ +Mn 3+ )/Mn valence ratio and Mn x O y particle size. Combined DFT and experimental analyses demonstrate that Mn valence states determine reaction kinetics: Mn 3 O 4 exhibits elevated glucose adsorption energy and reduced formic acid (FA) desorption energy, while MnO displays an opposing trend, rationalizing the activity differences. This work establishes a carbon-mediated synergy strategy for designing efficient Mn-based catalysts in biomass oxidation upgrading.
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Materials
·
2024
·Vol. 17
·期 5
·1200
·
IF 3.1
Wei Tong,Weiqiang Wang,Xiayu Leng,Jianli Song
To enhance the comprehensive performance of solid oxide fuel cells (SOFCs) ferritic stainless steel (FSS) interconnectors, a novel approach involving composite electrodeposition and thermal conversion is proposed to prepare Ni-doped Co-Mn composite spinel protective coatings on FSS surfaces. The process involves the composite electrodeposition of a Ni-doped Co-Mn precursor coating, followed by thermal conversion to obtain the Co-Mn-Ni composite spinel coating. Crofer 22H was used as the substrate and orthogonal experiments were designed to investigate the influences of deposition solution pH, stirring rate, cathode current density, and the element content of Mn and Ni on the surface morphology and properties of the composite coatings, respectively. The characterization of the prepared coatings was conducted through macroscopic and microscopic morphology observations of the component surface, energy dispersive spectroscopy (EDS) analysis, and area specific resistance (ASR) testing, etc. Finally, the optimized composite electrodeposition parameters and the Mn-Ni content ratio in the solution were obtained. Experimental results indicated that the composite spinel coating prepared with the optimized process parameters exhibited excellent adhesion to the substrate, and the diffusion and migration of Cr element has been effectively inhibited. Compared with the substrate, the ASR of the coated components has also been decreased simultaneously, which provided an effective method for the surface modification of SOFC FSS interconnectors.
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CHEMICAL ENGINEERING JOURNAL
·
2022
·
IF 16.744
Fawen Liang,Zhang Liu,Xueding Jiang,Jiesen Li,Kaibang Xiao,Weicheng Xu,Xin Chen,Jinzhi Liang,Zhifeng Lin,Meng Li,Xiaolian Wu,Hailong Wang
In this study, NaOH-modified biochar supported Fe/Mn bimetallic composite (Fe-Mn/AW-BC) was prepared to remove tetracycline (TC) through activating peroxymonosulfate (PMS). Results showed that about 97.9 % of TC was degraded and the rate constant of Fe-Mn/AW-BC + PMS system was 37 folds higher than BC + PMS system. Experimental results confirmed that both radical and non-radical pathway were contribute to the catalytic system. Density functional theory (DFT) results also suggested that Fe-Mn/AW-BC sample was favorable for adsorbing PMS based on the length O O bond from PMS and the E ads of catalysts. The superior activation ability was ascribed to the accelerating formation of reaction active species and other oxidation species by bimetallic structures of Fe-Mn and oxygenated functional groups of BC. Additionally, the redox cycles of Fe 3+ /Fe 2+ and Mn 3+ /Mn 2+ under Fe-Mn-BC synergism promoted the generation of the radicals, whereas the carbon shell effectively inhibited metals leaching of Fe-Mn/AW-BC, and 77.8 % of TC can be still removed within 60 min after five consecutive cycles. Notably, Fe-Mn/AW-BC system has special characteristic of wide pH usable range and broad-spectrum adaptability towards various organic pollutants and various water environments. Based on intermediate identification and Fukui function calculation, the degradation pathways of TC were also proposed. This study highlights the applications of biochar for the environmental catalysis.
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Materials
·
2021
·Vol. 14
·期 20
·5958
·
IF 3.623
Xusheng Ren,Zhiliang Ou,Bang Wu
The activated coke is a promising support for catalysts, and it is important to study the performance of the activated coke catalyst on the removal of NOx. In the current research, a series of the activated coke-supported Mn–Cu catalysts are prepared by the incipient wetness impregnation method. The effects of the molar ration of Mn/Cu, the content of Mn–Cu, the calcination temperature, and reaction space velocity on NO conversion are investigated, and it was found that the 8 wt.% Mn0.7Cu0.3/AC had the best catalytic activity when the calcination temperature was 200 °C. The existence of SO2caused the catalyst to deactivate, but the activity of the poisoning catalyst could be recovered by different regeneration methods. To uncover the underlying mechanism, BET, XPS, XRD, SEM and FTIR characterizations were performed. These results suggested that the specific surface area and total pore volume of the poisoning catalyst are recovered and the sulfite and sulfate on the surface of the poisoning catalysts are removed after water washing regeneration. More importantly, the water washing regeneration returns the value of Mn3+/Mn4+, Cu2+/Cu+, and Oα/Oβ, related to the activity, basically back to the level of the fresh catalyst. Thus, the effect of water washing regeneration is better than thermal regeneration. These results could provide some helpful information for the design and development of the SCR catalysts.Keywords:activated coke;low-temperature NH3-SCR;sulfur poisoning;regeneration
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Journal of Materials Chemistry C
·
2023
·Vol. 11
·期 14
·4837-4845
·
IF 6.4
Yao Zhang,Chengpeng Hu,Yu Wang,Xiaolin Huang,Xuejie Sun,Mingxuan Liu,Bohan Xing,Xing Wen,Hao Tian
The improvement of piezoelectric properties is always a key issue in the study of piezoelectric materials. The construction of composition gradient (CG) is a novel method to improve piezoelectric properties. However, the physical mechanism of CG influence on the piezoelectric properties has to be analyzed further. We investigate the origin of the CG-affected piezoelectric property using a manganese-doped potassium sodium niobate single crystal (that is Mn: KNN) as a model system. The relationship between CG, microstructure and spontaneous polarization was explored by designing and growing Mn:KNN single crystals with different CGs. It is found that the built-in electric field (Ein) in single crystals is constructed by introducing the CG in the crystals. The large Ein induces a more ordered, large-sized striated domain structure. The Mn: KNN single crystal with a large CG has a uniform orientation of spontaneous polarization and large macro-piezoelectric properties (83 pC N−1). Therefore, it is important to explore the relationship between CG and the piezoelectric properties of single crystals in lead-free piezoelectric materials. The results can be used to further develop high-performance lead-free piezoelectric materials.
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