Journal of Materials Chemistry A
·
2016
·Vol. 4
·期 25
·9789-9796
·
IF 8.262
Xihui Nan,Chaofeng Liu,Changkun Zhang,Wenda Ma,Kan Wang,Zhuoyu Li,Guozhong Cao
V2(PO4)O/C is a promising new anode material for lithium ion batteries with excellent electrochemical properties, synthesized by a facile one pot hydrothermal method, followed by a two-step calcination process. The composite can deliver a reversible capacity of 445 mA h g−1, 409 mA h g−1 and 382 mA h g−1 at 1.0, 1.5 and 2.0 A g−1. The capacity retentions of V2(PO4)O/C cycled at 1 and 5 A g−1 for 200 cycles are 90% and 80%, respectively. The excellent electrochemical properties are mainly attributed to the following three factors: (1) face-sharing [VO6] octahedral arrays endow the crystal with a high intrinsic electronic conductivity; (2) the good lithium ion diffusion coefficient of the material contributes for reducing electrochemical and concentration polarization in the charge–discharge process; and (3) porous microstructure and nanoscale particles not only permit effective contact between the electrolyte and active material, but also provide more space to accommodate volume change during the discharge/charge processes. The results in this study provide convincing evidence that V2(PO4)O/C has significant research value for future practical applications.
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DOI
高影响因子
FUEL
·
2021
·
IF 6.609
Ze Fang,Zhiguo Zhao,Nan Li,Zhexin Zhu,Wangyang Lu,Fengtao Chen,Wenxing Chen
An environmentally friendly desulfurization technology was constructed innovatively through coupling extraction and oxidation technique under mild conditions. A biomimetic catalytic system was built by O-bridged diiron perfluorophthalocyanine (FePcF 16 -O-FePcF 16 ) and hydrogen peroxide, and its displayed excellent catalytic activity and satisfactory regenerative performance for the oxidative desulfurization reaction. A mixed solvent of ethanol and water (volume ratio 9:1) was used as a “green” extractant with the property of low cost and low toxicity. It was found that 99% of the conversion rate of dibenzothiophene was achieved successfully after 2 h operation at 30 °C. The catalyst system was cycled 6 times without significantly reducing the removal of DBT. The catalytic activity was in the order of dibenzothiophene > 4,6-dimethyldibenzothiophene > benzothiophene. In addition, a possible reaction mechanism of the extraction and oxidative desulfurization was proposed and confirmed by electron paramagnetic resonance tests, gas chromatograph-mass spectrometer and electrospray ionization–mass spectrometry. The results demonstrated that the high-valent iron-oxo (Fe(IV) = O) was the main active species and this technology provides a novel idea for the design of high-efficiency, energy-saving and environmentally friendly desulfurization system.
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高影响因子
Advanced Science
·
2025
·
IF 14.1
Lili Liu,Chen Wang,Luxin Zhao,Yayun Xiao,Weiwei Fang,Lanling Zhao,Faxing Wang,Yuping Wu
The practical development of Li-O 2 batteries (LOBs) urgently needs to explore robust cathode catalysts to boost the sluggish Li 2 O 2 reaction kinetics and parasitic reactions despite their theoretically high specific energy. Profound understanding of the cathode properties and the battery performance is rather critical in developing rational-designed electrocatalysts. In this study, a Co-N x /Co (111) decorated N-doped hierarchical carbon framework (Co-N x /Co@NHCF) is proposed as an efficient cathode in LOBs. Spectroscopic analysis coupled with experimental results suggests that the Co-N x /Co (111) catalytic center can significantly reduce the battery overpotential, and meanwhile, the hierarchical carbon framework ensures rapid mass transportation and provides sufficient space to accommodate Li 2 O 2 deposition. Density functional theory calculations reveal that the incorporated Co (111) facet can effectively regulate the electronic distribution of N-carbon, optimize the adsorption of desirable intermediates, and eventually facilitate oxygen reduction reaction/oxygen evolution reaction kinetics. As expected, the Co-N x /Co@NHCF catalyzed LOBs deliver a high discharge/charge capacity of 6.15/ 6.22 mAh cm −2 with a columbic efficiency of 98.9%, along with a high rate cycling of 700 h at 0.3 mA cm −2 . This work provides valuable instruction for the rational design of efficient catalysts for high-performance LOBs via optimization of the crystal structure and the adsorption of intermediates.
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DOI
PubMed
高影响因子
ACS Nano
·
2025
·
IF 16
Jimin Qiu,Yuchen Ji,Wenfang Li,Yuhang Li,Wenguang Zhao,Yunxing Zuo,Weiyuan Huang,Chen Zhu,Mingjian Zhang,Guorui Zheng,Luyi Yang,Feng Pan,Zu-Wei Yin
Lithium cobalt oxide (LiCoO2) cathodes suffer serious structure instability when charged to high voltage (>4.5 V), including H1-3 phase transition, cobalt dissolution, and interfacial side reactions, which are closely related to the instability of surface lattice oxygen. Herein, an interfacial B–O complexing strategy was proposed to stabilize the surface lattice oxygen of LiCoO2 at 4.6 V, through the preferential coordination between derived products of the tris(pentafluorophenyl)borane electrolyte additive and LiCoO2. Combining a series of in situ and ex situ characterization methods with temporal and spatial resolution, it was revealed that the emergence of peroxy-like species (O22–) at high potentials is one of the origins of the instability of LiCoO2, which can be well inhibited thanks to interfacial B–O complexing. Thus, oxygen loss and interfacial side reactions can be drastically retarded, which consequently provides a more stable chemical environment for Co element, avoiding the dissolution and valence reduction of Co. Owing to the well-anchored Co and O elements, undesirable phase transition and local coordination structure change are suppressed, hence improving the capacity retention and rate performance of LiCoO2 at 4.6 V. This study provides an interfacial complexing strategy to stabilize the high-voltage LiCoO2 cathode.
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DOI
PubMed
高影响因子
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
·
2019
·
IF 3.571
Linhui Qin,Jianping Wang,RongRong Zhao,Xiao Zhang,Yingwu Mei
Ginsenoside-Rb1 (Rb1), a major active component of ginseng, has many benefits for cardiovascular disease and diabetes mellitus (DM), but the effect and mechanism on diabetic cardiomyopathy are not clear. In the present study, we found that Rb1-feeding significantly improved cardiac dysfunction and abnormal cardiomyocytes calcium signaling caused by diabetes. This improved calcium signaling was because Rb1 reduced Ca2+ leakage caused by overactivated ryanodine receptor 2 (RyR2) and increased Ca2+ uptake by sarcoplasmic reticulum Ca2+-ATPase 2a (SERCA 2a). Furthermore, we found that Rb1 not only enhanced energy metabolism like metformin and eliminated O-GlcNAcylation of calcium handling proteins to regulate calcium signaling but also directly inhibited RyR2 activity to regulate calcium signaling. The present study indicated that as a health supplement or drug, Rb1 was a relatively effective auxiliary therapeutic substance for diabetic cardiomyopathy.
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DOI
PubMed
高影响因子
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE
·
2025
·Vol. 29
·期 23
·e70940
·
IF 4.2
Hao Tan,Cao Fang,Yiyun Tan,Zhi Wang,Yun Zhou,Xing Li
Astragalus polysaccharides (APS) are a crucial bioactive component known for their various pharmacological properties. Abnormal O‐linked β‐N‐acetylglucosamine modification (O‐GlcNAcylation) is noted in cases of intervertebral disc degeneration (IVDD). Nonetheless, it remains uncertain whether APS regulates the process of O‐GlcNAcylation associated with IVDD. We employed molecular docking, cycloheximide chase assay, immunohistochemistry, and immunoprecipitation to investigate APS‐mediated OGT/O‐GlcNAcylation regulation of Nrf2. The effects of APS and its role in promoting the O‐GlcNAcylation of Nrf2 in IVDD through both in vivo and in vitro studies are discussed. In vitro investigations demonstrated an increase in the levels of OGT and O‐GlcNAcylation in nucleus pulposus cells (NPCs) following exposure to tert‐butyl hydroperoxide (TBHP). APS further facilitated improvements in OGT expression and O‐GlcNAcylation processes, restoring the viability of NPCs inhibited by TBHP and promoting the synthesis of collagen II and aggrecan, while reducing apoptosis. Mechanistically, APS promotes the expression of OGT by targeting it. Furthermore, O‐GlcNAcylation mediated by OGT stabilizes the expression of Nrf2 via the ubiquitin‐proteasome pathway. Rescue experiments indicated that the disruption of either OGT or Nrf2 expression negated the protective role of APS on NPCs. Ultimately, both in vitro and in vivo studies indicated that APS significantly enhanced OGT expression and O‐GlcNAcylation, which subsequently improved Nrf2 expression and contributed to the alleviation of IVDD in rats. APS promotes O‐GlcNAcylation through OGT, thereby stabilizing the expression of Nrf2, which in turn contributes to the improvement of IVDD.
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产品关联
DOI
PubMed
高影响因子
CORROSION SCIENCE
·
2019
·
IF 6.355
Mingjun Cui,Siming Ren,Jibin Pu,Yonggang Wang,Haichao Zhao,Liping Wang
In this research, soluble poly(o-phenylenediamine) nanoparticles were synthesized to noncovalently functionalize the graphene nanosheets via π-π interactions, and the corresponding protective performance of epoxy composite coatings was also investigated. Results showed that the impedance modulus of the composite coatings incorporated with 0.5–1.0% G-Popd was about 10 10 Ω cm 2 after 60 days of immersion. Furthermore, the corrosion of substrate was still retarded even if there is an artificial scratch to the composite coatings. The superior protective performance of the composite coating derived from the synergistic action in the barrier property of graphene nanosheets and metal surface passivation by Popd nanoparticles.
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高影响因子
Nature Communications
·
2020
·Vol. 11
·期 1
·1-7
·
IF 12.121
Yu Fei-Yang,Lang Zhong-Ling,Yin Li-Ying,Feng Kun,Xia Yu-Jian,Tan Hua-Qiao,Zhu Hao-Tian,Zhong Jun,Kang Zhen-Hui,Li Yang-Guang
The oxidized platinum (Pt) can exhibit better electrocatalytic activity than metallic Pt 0 in the hydrogen evolution reaction (HER), which has aroused great interest in exploring the role of oxygen in Pt-based catalysts. Herein, we select two structurally well-defined polyoxometalates Na 5 [H 3 Pt (IV) W 6 O 24 ] (PtW 6 O 24 ) and Na 3 K 5 [Pt (II) 2 (W 5 O 18 ) 2 ] (Pt 2 (W 5 O 18 ) 2 ) as the platinum oxide model to investigate the HER performance. Electrocatalytic experiments show the mass activities of PtW 6 O 24 /C and Pt 2 (W 5 O 18 ) 2 /C are 20.175 A mg −1 and 10.976 A mg −1 at 77 mV, respectively, which are better than that of commercial 20% Pt/C (0.398 A mg −1 ). The in situ synchrotron radiation experiments and DFT calculations suggest that the elongated Pt-O bond acts as the active site during the HER process, which can accelerate the coupling of proton and electron and the rapid release of H 2 . This work complements the knowledge boundary of Pt-based electrocatalytic HER, and suggests another way to update the state-of-the-art electrocatalyst.
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高影响因子
JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS
·
2024
·
IF 5.8
Xian Huang,Shangshu Peng,Shengshang Lu,Xinhai Wang,Yang Wu,Linxi Dai,Bo Chen,Quan Xie,Yunjun Ruan
Considerable attention has been devoted to creating porous carbons with exceptional surface area and porosity from biomass waste for energy storage devices. Herein, we employed a straightforward high-temperature carbonization and KOH activation method to synthesize nitrogen (N) and oxygen (O) co-doped porous activated carbons derived from luffa vines (LVACs). The impact of varying KOH concentrations on the morphology, structure, and electrochemical properties of LVACs was thoroughly investigated. The optimal mass ratio of KOH to LVACs at 1:6 achieved the maximum specific surface area of 3369 m 2 g −1 . At a current density of 1 A g −1 , the LASC-6 electrode exhibits an impressive specific capacitance of 348.5 F g −1 . It also demonstrates exceptional rate performance, retaining 70.6 % of its capacitance at a current density of 20 A g −1 . The electrode possesses robust cycling stability, retaining 90 % of the initial capacitance after 5000 cycles. We assessed the practicality of LVAC-6 by constructing symmetric supercapacitors (SSCs) using KOH and [BMIM]BF 4 electrolytes. The KOH and [BMIM]BF 4 SSCs achieved specific capacitances of 86.75 and 50.31 F g −1 , respectively, at a current density of 0.25 A g −1 . Moreover, the [BMIM]BF 4 SSC exhibited an impressive energy density of 51.05 Wh kg −1 at a power density of 346.15 W kg −1 . Therefore, we propose a simple and cost-effective strategy to produce porous carbon materials with excellent electrochemical performance from discarded biomass waste, facilitating the preparation of environmentally friendly electrode materials for high-performance supercapacitors.
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高影响因子
Desalination and Water Treatment
·
2024
·
IF 1
Temitope F. Ajibade,Jiaoxing Xu,Huali Tian,Lunhui Guan,Kaisong Zhang
Removal of emulsified oil droplets less than 20 μm and maintaining operational stability remains a key concern in the field of oily wastewater treatment. In this work, a major breakthrough was achieved via modification of polyacrylonitrile/polyvinylidene fluoride (PAN/PVDF) blended ultra-filtration (UF) membrane with oxidized multiwall carbon nanotubes (O-MWCNT) to tailor the membrane chemical properties for boosted oil and water separation. Overall, a high separation performance of oily emulsion (99%) and simultaneous increase in flux up to 65% was achieved using the novel O-MWCNT/PAN/PVDF membrane. Moreover, the performance of the O-MWCNT/PAN/PVDF membrane was consistent after 28-cycles of oil separation and the antifouling properties were exceptionally enhanced by 96%. In addition, there was a significant decrease in fouling in terms of the cake, pore, and intrinsic resistance. Furthermore, evidence of even dispersal of nanofillers was confirmed by an increase of casting solution viscosity with increasing O-MWCNT. Consequently, this provides a remarkable mechanical/tensile strength of 5.94 MPa, and 16.05% elongation of the O-MWCNT/PAN/PVDF fingerlike structured UF membrane. The novel O-MWCNT/PAN/PVDF membrane demonstrated promising properties that balanced the membrane tradeoff between permeability and selectivity, as well as, improved mechanical strength and operational stability that can elongate the life span of the membrane in oily wastewater treatment.
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高影响因子
ACS Applied Nano Materials
·
2024
·
IF 5.3
Hao Gu,Yi Jiang,Xijia Yang,Yue Yang,Xuesong Li,Liying Wang,Wei Lü
Flexible and wearable pressure sensors have attracted significant attention due to their wide range of potential applications. However, they often suffer from low sensitivity, narrow pressure detection range, and poor mechanical flexibility. In this work, a multifunctional 3D pressure sensor based on a ternary metal oxide@carbon-based sponge (C–NiCoZn–O/CMF) was developed by the hydrothermal method. The pressure feedback layer of the sensor was uniformly coated with C–NiCoZn–O on the surface of the framework, which improved the device’s conductivity, sensitivity, and stability significantly. The sensitivities of 41.99, 23.39, and 11.19 kPa–1 are in the ranges 0–4.01, 4.01–8.39, and 8.39–20.1 kPa, respectively, and the cyclic retention rate exceeded 90% after 2000 cycles. The C–NiCoZn–O/CMF composite demonstrated excellent electrochemical performance as an electrode for supercapacitors, with a high specific capacity of 2030 mF/cm2 at a current density of 1 mA/cm2 and a high capacity retention rate of 81.55% after 4000 cycles. As a multifunctional device, when integrated with a microprocessor, it can easily detect and process a large amount of human physiological signal data in daily work scenarios. Present composites maintain adjustable conductivity and extremely high elasticity even under extreme conditions such as liquid nitrogen and high temperatures up to 85.6 °C. This work is expected to play a great role in polar exploration, volcano survey, deep space exploration, etc.
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高影响因子
APPLIED CATALYSIS A-GENERAL
·
2023
·
IF 5.5
Jiacheng Xu,Tiantian Zhang,Yan Sun,Shiyu Fang,Zuliang Wu,Jiali Zhu,Lianxin Dai,Weihua Liu,Buhe Zhang,Junwei Zhang,Shuiliang Yao,Erhao Gao,Jing Li
MnO 2 is a promising catalyst due to its abundant metal valence and good redox ability. Different crystal phases of MnO 2 have different oxygen species, but the relationship between their catalytic activity and crystal structures is unclear. In this study, four MnO 2 catalysts with crystal structures ( α -, β -, γ -, and δ -MnO 2 ) were selected to unveil the roles of terminal-type (Mn O), superoxide-type Mn(-O-) 2 Mn, and bridge-type (Mn-O-Mn) oxygen species in CO oxidation . γ -MnO 2 has the best CO oxidation performance. Density functional theory calculation results show that Mn O on γ- MnO 2 can adsorb CO easier than other two types of oxygen species. Operando TPR-DRIFTS-MS results show that Mn O on the surface of γ- MnO 2 can react with CO to form terminal-type oxygen vacancies (M 2+ =□ 2– ) at low temperatures. Meanwhiles, Mn(-□-)(-O-)Mn and Mn-□-Mn can dissociate O 2 to form Mn O under certain conditions to promote CO oxidation. MnO 2 catalysts with more Mn O oxygen species are of great significance for CO oxidation at a low temperature.
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高影响因子
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