- 标题
- 摘要
- 关键词
- 实验方案
- 产品
-
Vertically-grown few-layer MoS2 nanosheets on hierarchical carbon nanocages for pseudocapacitive lithium storage with ultrahigh-rate capability and long-term recyclability
摘要： Molybdenum disulfide (MoS2) are intensively studied anode materials for lithium-ion batteries (LIBs) owing to the high theoretical capacity, but still confront the severe challenges of unsatisfied rate capability and cycle life to date. Herein, few-layer MoS2 nanosheets are vertically grown on the hierarchical carbon nanocages (hCNC) via a facile hydrothermal method, which introduce pseudocapacitive lithium storage owing to the highly-exposed MoS2 basal planes, enhanced conductivity and facilitated electrolyte access arising from the well hybridization with hCNC. As a result, the optimized MoS2/hCNC exhibits the reversible capacity of 1670 mAh g-1 at 0.1 A g-1 after 50 cycles, 621 mAh g-1 at 5.0 A g-1 after 500 cycles, and 196 mAh g-1 at 50 A g-1 after 2,500 cycles, staying at the top level of the MoS2-based anode materials. The specific power and specific energy can reach to 16.1 kW kg-1 electrode and 252.8 Wh kg-1 electrode after 3,000 cycles, respectively, showing the great potential in high-power and long-life LIBs. This finding suggests a promising strategy for exploring advanced anode materials with high reversible capacity, high-rate capability and long-term recyclability.
关键词： pseudocapacitive lithium storage,vertical few-layer MoS2,hierarchical carbon nanocages,long-term recyclability,ultrahigh-rate capability
更新于2025-09-23 15:23:52
-
Self-hybridized coralloid graphitic carbon nitride deriving from deep eutectic solvent as effective visible light photocatalysts
摘要： The room temperature deep eutectic solvent (DES) is demonstrated as an ideal precursor to prepare self-hybridized graphitic carbon nitride (g-C3N4) for the first time, for its special components, randomly reorganized molecules and extensive hydrogen bonds. In this work, by adjusting the proportion of urea and ammonium thiocyanate in the precursor DES, the self-hybridized coralloid g-C3N4, stacked by a mass of double-layer g-C3N4/g-C3N4 nanocages, were prepared without any templates. Compared to conventional g-C3N4 prepared using melamine, urea and AT as precursors, the improved charge transfer between the interfaces of the self-hybridized g-C3N4 has been demonstrated, which is attributed to the well-matched electronic band structures of the two g-C3N4 species, the abundant 2D/2D interfacial contact and increased photocatalytic active sites. As expected, it exhibits highly enhanced photocatalytic activity, which is among the best g-C3N4 photocatalysts without doping any other elements.
关键词： G-C3N4/g-C3N4 heterojunction,Graphitic carbon nitride,Photocatalysis,Nanocages,Deep eutectic solvents
更新于2025-09-23 15:23:52
-
Multifunctional Nanotheranostic Gold Nanocages for Photoacoustic Imaging Guided Radio/Photodynamic/Photothermal Synergistic Therapy
摘要： In this work, we developed a novel multifunctional nanoplatform based on hyaluronic acid modified Au nanocages (AuNCs-HA). The rational design of AuNCs-HA renders the nanoplatform three functionalities: (1) AuNCs-HA with excellent LSPR peak in the NIR region act as contrast agent for enhanced photoacoustic (PA) imaging and photothermal therapy (PTT); (2) the nanoplatform with high-energy rays (X-ray) absorption and auger electrons generation acts as a radiosensitizer for radiotherapy; (3) good photocatalytic property and large surface area make AuNCs-HA a photosensitive agent for photodynamic therapy (PDT). In vivo results demonstrated that AuNCs-HA presented excellent PA imaging performance after intravenous injection, which provided contour, size, and location information of the tumor. Moreover, because AuNCs-HA could combine radiotherapy and phototherapy together, the tumors treated with AuNCs-HA showed complete growth inhibition, comparing to that with each therapy alone. Taken together, our present study demonstrates that AuNCs-HA is of great potential as a multifunctional nanoplatform for PA imaging-guided radio- and photo-therapy of tumor.
关键词： PTT,Au nanocages,radiotherapy,PDT,theranostic nanoplatform,PA imaging
更新于2025-09-23 15:21:21
-
Biocompatible Chitosan-Carbon Nanocage Hybrids for Sustained Drug Release and Highly Efficient Laser and Microwave Co-irradiation Induced Cancer Therapy
摘要： Graphitic carbon nanocages (GCNCs) are unique graphene-based nanomaterials that can be used for cancer photothermal therapy (PTT). However, low toxicity GCNC-based organic/inorganic hybrid biomaterials for microwave irradiation assisted PTT have not yet been reported. In the present study, chitosan (CS)-coated GCNCs (CS-GCNCs) loaded with 5-fluorouracil (5Fu) were used for cancer therapy when activated by 808-nm laser and microwave co-irradiation. The cytotoxicity of GCNCs was significantly reduced after coating with CS. For example, fewer cell-cycle defects were caused by CS-GCNCs in comparison with non-coated GCNCs. The release rate of 5Fu from CS-GCNCs was significantly slower than that of 5Fu from GCNCs, providing sustained release. The release rate could be accelerated by 808-nm laser and microwave co-irradiation. The 5Fu in CS-GCNCs retained high cancer cell killing bioactivity by enhancing the caspase-3 expression level. The cancer cell killing and tumor inhibition efficiencies of the 5Fu-loaded nanomaterials increased significantly under 808-nm laser and microwave co-irradiation. The strong cell killing and tumor ablation activities were due to the synergy of the enhanced GCNC thermal effect caused by laser and microwave co-irradiation and the chemotherapy of 5Fu. Our research opens a door for the development of drug-loaded GCNC-based nano-biomaterials for chemo-photothermal synergistic therapy with the assistance of microwave irradiation.
关键词： sustained drug release,cancer therapy,low cytotoxicity,Graphitic carbon nanocages,laser microwave co-irradiation
更新于2025-09-12 10:27:22
-
Triple-Shelled Co-VSex Hollow Nanocages as Superior Bifunctional Electrode Materials for Efficient Pt-Free Dye-Sensitized Solar Cells and Hydrogen Evolution Reactions
摘要： Complex nanostructures with distinct spatial architectures and more active sites hold broad prospects in new energy conversion fields. Herein, a facile strategy was carried out to construct triple-shelled Co-VSex nanocages, starting via an ion-exchange process about Co-based zeolitic imidazolate framework-67 (ZIF-67) nanopolyhedrons and VO3?, followed by the formation of triple-shelled Co-VSex hollow nanocages during the process of rising the solvothermal temperature under the assistance of SeO32?. Meanwhile, triple-shelled Co-VSx and yolk-double shell Co-VOx nanocages were fabricated as references by a similar process. Benefiting from the larger surface areas and more electrolyte adsorption sites, the triple-shelled Co-VSex nanocages exhibited excellent electrocatalytic performances when applied as the electrochemical catalysts for dye-sensitized solar cell (DSSC) and hydrogen evolution reaction (HER). More concretely, the DSSC based on Co-VSex counter electrode (CE) showed outstanding power conversion efficiency of 9.68% when Pt counterpart was 8.46%. Moreover, Co-VSex electrocatalyst exhibited prominent HER performance with a low onset overpotential of 40 mV and a small Tafel slope of 39.1 mV dec?1 in acid solution.
关键词： Dye-sensitized solar cells,Hydrogen evolution reactions,Pt-free catalysts,Triple-shelled nanocages,Co-VSex,Bifunctional electrocatalysts
更新于2025-09-11 14:15:04
-
A Flexible Photothermal Cotton-CuS Nanocage-Agarose Aerogel towards Portable Solar Steam Generation
摘要： Solar-steam generation provides an economically efficient pathway to produce clean water by using solar light as an energy source. While this strategy is highly suitable for portable and small scale water purification for individuals, families and those living in remote areas, the development of highly efficient and flexible photothermal materials which can be easily transported for storage and deliver is required. In this study, a commercial degreasing cotton, photothermal CuS yolk-shell nanocages and agarose were combined to produce a highly flexible photothermal aerogel which delivered a high energy efficiency (94.9%) for solar-steam generation under 1.0 sun irradiation, corresponding to a water evaporation rate of 1.63 kg m-2 h-1. The preparation of the photothermal aerogel can be easily scaled up due to the simplicity of the applied casting method. The obtained aerogel showed excellent stability for solar steam generation with no degradation in performance after at least 15 cycles. The salinity of the clean water produced during solar-thermal desalination of seawater was only 0.54 ppm. The raw materials of cotton, agarose and CuS are all cost effective, thus this flexible photothermal aerogel has showed great potential for practical application in portable solar-thermal evaporators.
关键词： solar-thermal energy,nanocages,aerogel,water evaporation,Photothermal
更新于2025-09-09 09:28:46