JOURNAL OF POWER SOURCES
·
2012
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IF 4.951
Jing Lin,Daobin Mu,Ying Jin,Borong Wu,Yunfeng Ma,Feng Wu
Li-rich layered composite Li[Li 0.2 Ni 0.2 Mn 0.6 ]O 2 is prepared by a novel approach in which carbon felt acts as a carrier for synthesis reaction . The as-prepared material is characterized by SEM, ICP and XRD , its electrochemical performance is also examined with galvanostatic charge/discharge and CV measurements. It is showed that the facile process controls effectively the particle growth (in size around 100–200 nm) of the composite and its chemical composition . The as-prepared material shows a high initial discharge capacity about 288 mAh g −1 when charged to 4.8 V, and a retained value of 246.8 mAh g −1 in the 40th cycle. The crystalline structure of the composite is simulated further by Material Studio. It is revealed that the composite has a compatible layer structure merged by Li 2 MnO 3 and LiNi 0.5 Mn 0.5 O 2 , which makes substantial contribution to the cycleability of the electrode. In addition, the lithiation/delithiaion properties including charge transfer resistance and lithium ion diffusion coefficient are studied with electrochemical impedance spectra.
研究领域:
材料科学
·
电化学
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DOI
高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2025
·
IF 8.3
Daming Yang,Yingyue Zhang,Jiaqi Sun,Xinyu Zhang,Ze Gao,Qilong Sun,Tong Wu,Wei Lu,Guiru Sun,Ming Feng
The photo-assisted strategy is viewed as a promising method to improve the ORR and OER performance of Li–O 2 batteries. Nevertheless, designing a photocatalyst that ensures wide light absorption and minimizes the recombination of photoinduced electrons and holes is still a notable challenge. In this study, 2D porous Co 3 O 4 nanosheets are synthesized as photocatalysts for photo-assisted Li–O 2 batteries. Their unique structure improves surface area, facilitates O 2 transport, and stores discharge products. Equally, the Co 3 O 4 nanosheets exhibit strong light responsiveness and photocatalytic activity. Upon optical field, photoinduced electrons and holes are successfully separated on Co 3 O 4 nanosheets, which promotes the formation and decomposition of Li 2 O 2 , respectively. Li–O 2 cells using Co 3 O 4 nanosheets display a low overpotential of 0.15 V and good cycling stability under optical field. These findings highlight the potential of Co 3 O 4 nanosheets as photocatalysts for photo-assisted Li–O 2 batteries, providing a foundation for future energy storage advancements.
研究领域:
材料科学
·
能源化学
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DOI
高影响因子
IET Nanobiotechnology
·
2020
·Vol. 14
·期 5
·347-356
·
IF 1.859
Mei Yang,Qingyuan Gui,Jinlei Ma,Lei Qi,Bijun Bao,Yida Huang
In this study, Gd 2 O 2 S:Ln 3+ (Ln 3+ = Yb 3+ , Er 3+ ) upconversion nanotubes (UCNTs) were synthesised by using Gd(OH) 3 :Ln 3+ (Ln 3+ = Yb 3+ , Er 3+ ) nanotubes as the template. The luminescent and biological properties of Gd 2 O 2 S:Ln 3+ (Ln 3+ = Yb 3+ , Er 3+ ) UCNTs, along with photodynamic therapy (PDT) applications of the Gd 2 O 2 S:8%Yb 3+ , 2%Er 3+ UCNT–Ce6 (chlorin e6) nanocomposites, were systematically studied. The resultant UCNTs showed excellent biocompatibility with human retinal pigment cells (ARPE-19) even after a prolonged incubation time of 72 h, and could be used as luminescent probes. Microscopic imaging revealed that the UCNTs existed mainly in cytoplasm. PDT studies on the Gd 2 O 2 S:8%Yb 3+ , 2%Er 3+ UCNT–Ce6 nanocomposites indicate that the growth of the tumour (cell) could be inhibited dramatically when it was injected (incubated) with Gd 2 O 2 S:8%Yb 3+ , 2%Er 3+ UCNT–Ce6 nanocomposites under the irradiation of 980 nm laser.
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DOI
PubMed
高影响因子
Journal of Materials Chemistry A
·
2021
·Vol. 9
·期 42
·24056-24063
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IF 12.732
Yanfang Chen,Xuemei Yan,Jixiang Xu,Lei Wang
H2O2 has a wide range of uses as an oxidant and is also utilized as a high density and environmentally friendly fuel. In this study, crystalline g-C3N4 was modified with K+, Ni and N-doped carbon by thermal-polymerization of Ni2+-anchored and polyvinyl pyrrolidone-encapsulated melamine-cyanuric acid supramolecules, followed by re-calcination in a KCl–LiCl mixture. The obtained strip-like g-C3N4 nanocrystals exhibited high charge separation efficiency and good light absorption capability. Density-functional theory calculations confirmed that the orbital hybridization of Ni–N atoms enabled the formation of charge-transfer channels, which can capture electrons, achieve enhanced oxygen adsorption and reduction via a two-electron pathway. Under the synergistic effects of K+, Ni and N-doped carbon dopants and crystallinity, the obtained sample exhibited high photocatalytic H2O2 yields of 79.6 μM in O2-saturated pure water, which was 10-fold higher than the yield using pristine g-C3N4. This work provides a novel design for production of highly efficient photocatalysts for H2O2 production.
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DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2018
·
IF 6.735
Bin He,Huanhuan Liu,Zheng Lin,Lei Yan,Jiqiang Ning,Yijun Zhong,Changcheng Zheng,Ziyang Zhang,Yong Hu
The practical application of photocatalytic water splitting is essentially limited by the slow kinetic nature of the water oxidation process. Therefore, it is highly desirable but challenging to explore a low-cost and high-efficiency water oxidation catalyst for the aim of commercialization and industrialization. We herein report the first-time synthesis of a novel and high-efficiency visible-light-driven photocatalyst composed of flower-like Co(CO 3 ) 0.5 (OH)·0.11H 2 O (CCO) nanowires and Bi 2 WO 6 (BWO) nanosheets, i.e. CCO/BWO nanocomposite, via a facile hydrothermal method. Without utilizing any additional cocatalyst, the composite of CCO/BWO in 30% weight ratio exhibits extraordinarily high photoactivity and photostability towards O 2 evolution, achieving an average O 2 generation rate of 953 µmol h −1 g −1 under visible-light irradiation (λ > 420 nm).
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高影响因子
Science Bulletin
·
2018
·
IF 4.136
Zhen-Dong Yang,Zhi-Wen Chang,Qi Zhang,Keke Huang,Xin-Bo Zhang
A facile synthesis of the hierarchically porous cathode with Mo 2 C nanoparticles through the electrospinning technique and heat treatment is proposed. The carbonization temperature of the precursors is the key factor for the formation of Mo 2 C nanoparticles on the carbon nanofibers (MCNFs). Compared with the Mo 2 N nanoparticles embedded into N-doped carbon nanofibers film (MNNFs) and N-doped carbon nanofibers film (NFs), the battery with MCNFs cathode is capable of operation with a high-capacity (10,509 mAh g −1 at 100 mA g −1 ), a much reduced discharge-charge voltage gap , and a long-term life (124 cycles at 200 mA g −1 with a specific capacity limit of 500 mAh g −1 ). These excellent performances are derived from the synergy of the following advantageous factors: (1) the hierarchically self-standing and binder-free structure of MCNFs could ensure the high diffusion flux of Li + and O 2 as well as avoid clogging of the discharge product, bulk Li 2 O 2 ; (2) the well dispersed Mo 2 C nanoparticles not only afford rich active sites, but also facilitate the electronic transfer for catalysis.
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DOI
PubMed
高影响因子
SOLID STATE IONICS
·
2016
·
IF 2.38
Cheng-Dong Li,Jin Xu,Ji-Sheng Xia,Wei Liu,Xin Xiong,Zhu-An Zheng
The FeF 3 -coated Li[Li 0.2 Mn 0.54 Ni 0.13 Co 0.13 ]O 2 cathode materials were synthesized via a wet chemical process followed by a solid state reaction . The physical properties of the as-prepared samples were conducted using X-ray diffraction, scanning electron microscopy, and transmission electron microscopy . The results indicated that the surface of cathode particles was covered by FeF 3 film (about 5–15 nm thick). Compared with the bare cathode, the FeF 3 -coated Li[Li 0.2 Mn 0.54 Ni 0.13 Co 0.13 ]O 2 one delivered the higher coulombic efficiency, better rate capability, longer cycle life, and better structure stability. A high capacity retention of 95% (190 mAh g − 1 ) after 100 cycles at 0.5 C rate was obtained for the FeF 3 -coated Li[Li 0.2 Mn 0.54 Ni 0.13 Co 0.13 ]O 2 cathode. Besides, the results from cyclic voltammetry and electrochemical impedance spectra revealed that the noteworthy enhanced electrochemical properties of the surface-modified sample were due to the presence of FeF 3 coating layer , which suppressed the side reaction between the Li[Li 0.2 Mn 0.54 Ni 0.13 Co 0.13 ]O 2 particles with electrolyte and further stabilized the Li[Li 0.2 Mn 0.54 Ni 0.13 Co 0.13 ]O 2 structure with cycling.
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高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2022
·
IF 5.518
Wenjing Shen,Dandan Xiang,Junnan Yang,Yanting Tang,Changhui Xin,Quanhui Guo,Xin Yu
In this work, beta zeolite supported Ti 3+ -TiO 2 /CdS heterojunction was prepared for photodegradation of tetracycline under visible-light irradiation, and zeolite served as a support for the high dispersions of the Ti 3+ -TiO 2 nanoparticles . The obtained zeolite/Ti 3+ -TiO 2 /CdS heterojunction showed a relatively high surface areas of approximately 63.2 m 2 g −1 , much higher than those of the prepared Ti 3+ -TiO 2 /CdS (27.1 m 2 g −1 ), Ti 3+ -TiO 2 (36.5 m 2 g −1 ), and CdS (31.1 m 2 g −1 ), strongly demonstrating the significant of zeolite for high dispersion of the Ti 3+ -TiO 2 /CdS composite. Besides, the experimental results also showed that the photocatalytic degradation efficiency could reach 78 % in 3 min for the zeolite/Ti 3+ -TiO 2 /CdS heterojunction, and the corresponding rate constant was as high as 0.788 min −1 , which was 26.90 times that of pristine Ti 3+ -TiO 2 , 2.24 times of pristine CdS , and 2.04 times of the Ti 3+ -TiO 2 /CdS composite, mainly because of the supporting effects of zeolite and the formation of Ti 3+ -TiO 2 /CdS heterostructure for highly enhanced charge separation. In addition, the trapping experiment revealed that the main reactive species involved in tetracycline degradation were attributed to the photo-generated holes and ⸱O 2 - species.
研究领域:
环境科学
·
材料科学
·
化学
✓ 已验证
DOI
高影响因子
Science Bulletin
·
2024
·
IF 18.8
Zhihong Bi,Anping Zhang,Gongrui Wang,Cong Dong,Pratteek Das,Xiaoyu Shi,Zhong-Shuai Wu
High-voltage and fast-charging LiCoO 2 (LCO) is key to high-energy/power-density Li-ion batteries. However, unstable surface structure and unfavorable electronic/ionic conductivity severely hinder its high-voltage fast-charging cyclability. Here, we construct a Li/Na-B-Mg-Si-O-F-rich mixed ion/electron interface network on the 4.65 V LCO electrode to enhance its rate capability and long-term cycling stability. Specifically, the resulting artificial hybrid conductive network enhances the reversible conversion of Co 3+/4+ /O 2−/ n − redox by the interfacial ion–electron cooperation and suppresses interface side reactions, inducing an ultrathin yet compact cathode electrolyte interphase. Simultaneously, the derived near-surface Na + /Mg 2+ /Si 4+ -pillared local intercalation structure greatly promotes the Li + diffusion around the 4.55 V phase transition and stabilizes the cathode interface. Finally, excellent 3 C (1 C = 274 mA g −1 ) fast charging performance is demonstrated with 73.8% capacity retention over 1000 cycles. Our findings shed new insights to the fundamental mechanism of interfacial ion/electron synergy in stabilizing and enhancing fast-charging cathode materials.
研究领域:
材料科学
·
电化学
·
能源存储
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DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2024
·
IF 13.3
Yu Luo,Chenchen Liu,Jiahui Liu,Xueming Liu,Yang Zhou,Xinwen Ou,Bo Weng,Jin Jiang,Bin Han
Photocatalytic O 2 reduction presents a sustainable strategy for H 2 O 2 synthesis, while the in-situ decomposition of H 2 O 2 significantly deteriorates the activity and stability. Here, by introducing anthraquinone centers into covalent organic frameworks (DQTb-COFs), for the first time, we realized the suppression of in-site decomposition of generated H 2 O 2 via site-engineering of COFs. Under visible light irradiation, DQTb-COFs achieves an H 2 O 2 generation rate of 1844.1 μmol h −1 g −1 without sacrificial agents, which is about 3.4 times that of its counterpart without anthraquinone centers (DATb-COFs). The generated H 2 O 2 on DATb-COFs is readily reduced into hydroxyl radicals (•OH), which is not observable on DQTb-COFs. Experiments and calculations demonstrated that the anthraquinone centers of DQTb-COFs can enhance the generation of H 2 O 2 by facilitating the utilization of O 2 and promoting the desorption of H 2 O 2 . This work highlights how to inhibit the in-situ decomposition of H 2 O 2 via site-engineering of COFs, and blazes a new trail for highly efficient H 2 O 2 photosynthesis.
研究领域:
材料科学
·
环境科学
·
化学工程
✓ 已验证
产品关联
DOI
高影响因子
CATALYSIS TODAY
·
2024
·
IF 5.2
Jipeng Wang,Xinli Tong,Chen Guo,Yahui Wei
The high entropy oxides are widely studied as the potential catalytic materials owing to their unique structure and excellent properties. In this work, a new high entropy oxide catalyst MnFeCoNiCuO x was successfully prepared and used for the oxidative condensation reaction of furfural (FUR) and aliphatic alcohol , where the carbon-chain length can be selectively increased under the mild conditions. For the selective oxidative transformation of FUR with n-butanol, a more than 99.0 % conversion of FUR and 91.5 % selectivity of 2-(furanyl-2-methylene) butanal was obtained at 80 ºC for 2 h. In addition, the oxidative condensation of FUR with ethanol, n-propanol, n-pentanol, n-hexanol and n-heptanol was also carried out with the MnFeCoNiCuO x - LiOH as catalyst system in the presence of molecular oxygen , where a moderate to high product yields were acquired. Furthermore, the characterizations of catalyst showed that the existence of abundant oxygen vacancy and high specific area was greatly important to the catalytic reactions .
研究领域:
化学工程
·
催化科学
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DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2025
·
IF 6.3
Yajuan Jiang,Shining Zhang,Chunyu Xu,Bin Jia,Shijie Ren,Wenyu Zheng,Yicong Huang,Kunpeng Jiang,Xiuyun Zhang,Yunyun Zhao,Guisheng Zhu,Huarui Xu
In this paper, biomass carbon@Li(Ni 0.6 Co 0.4 )O 2 (BC@LNCO) micron-tube is successfully synthesized via a bio-templating method as cathodic material for lithium-ion hybrid supercapacitors. Cobalt nickel subcarbonates nanowires arrays are homogeneously grown on bagasse substrate via a unique synthesis strategy using a toluene-water interface reaction process, which subsequently transform as BC@LNCO micron-tube after lithiation process. The distinctive biomass fibre structure of bagasse biomass carbon leads to a significant enhancement in active sites in the BC@LNCO composite, which facilitates lithium-ion diffusion and enhances the contact area between the electrode and electrolyte. So, the prepared BC@LNCO electrode demonstrates improved electrical performances with a high specific capacitance of 921 F g −1 at 1 A g −1 and a good rate performance with 72 % retention at 10 A g −1 . In addition, the lithium-ion hybrid supercapacitor is fabricated with BC@LNCO and activated carbon (AC) as positive and negative electrodes, respectively. The BC@LNCO//AC device demonstrates a good energy density of 56.25 Wh kg −1 at 818.4 W kg −1 , and maintains 25.06 Wh kg −1 when the power density is up to 8143.42 W kg −1 , indicating that the prepared BC@LNCO composite can be a promising candidate as electrode material for Li-ion hybrid supercapacitor.
研究领域:
材料科学
·
能源存储
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产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）