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1.
    
Carbon dots (CDs), a class of carbon-based nanomaterials with dimensions less than 10 nm, have attracted significant interest since their discovery. They possess numerous excellent properties, such as tunability of photoluminescence, environmental friendliness, low cost, and multifunctional applications. Recently, a large number of reviews have emerged that provide overviews of their synthesis, properties, applications, and their composite functionalization. The application of CDs in the field of optoelectronics has also seen unprecedented development due to their excellent optical properties, but reviews of them in this field are relatively rare. With the idea of deepening and broadening the understanding of the applications of CDs in the field of optoelectronics, this review for the first time provides a detailed summary of their applications in the field of luminescent solar concentrators (LSCs), light-emitting diodes (LEDs), solar cells, and photodetectors. In addition, the definition, categories, and synthesis methods of CDs are briefly introduced. It is hoped that this review can bring scholars more and deeper understanding in the field of optoelectronic applications of CDs to further promote the practical applications of CDs.  相似文献   

2.
High purity semiconducting single‐walled carbon nanotubes (s‐SWCNTs) with a narrow diameter distribution are required for high‐performance transistors. Achieving this goal is extremely challenging because the as‐grown material contains mixtures of s‐SWCNTs and metallic‐ (m‐) SWCNTs with wide diameter distributions, typically inadequate for integrated circuits. Since 2000, numerous ex situ methods have been proposed to improve the purity of the s‐SWCNTs. The majority of these techniques fail to maintain the quality and integrity of the s‐SWCNTs with a few notable exceptions. Here, the progress in realizing high purity s‐SWCNTs in as‐grown and post‐processed materials is highlighted. A comparison of transistor parameters (such as on/off ratio and field‐effect mobility) obtained from test structures establishes the effectiveness of various methods and suggests opportunities for future improvements.  相似文献   

3.
以韭菜为前驱体,采用微波法一步绿色合成N,S共掺杂的粒径均匀、分散性好的碳点。所合成的碳点近似球状,粒径2.0-5.0 nm。在365 nm的紫外灯照射下发明亮的蓝色荧光,发射峰具有激发波长依赖性。Fe3+对所制备的碳点有明显选择性荧光猝灭现象。在5-300μmol/L的范围内,荧光猝灭程度(F/F0)与Fe3+浓度呈现良好的线性关系(R=0.9930),检测限为4.0μmol/L。同时探测温度对制备碳点的影响,在20-55℃范围内,碳点荧光强度与温度具有较好的线性响应。由于生理温度范围在此温度范围内,所制备的碳点可用于细胞温度传感。  相似文献   

4.
    
Carbonaceous materials are promising anodes for potassium‐ion batteries (PIBs). However, it is hard for large K ions (1.38 Å) to achieve long‐distance diffusion in pristine carbonaceous materials. In this work, the following are synthesized: S/N codoped carbon nanofiber aerogels (S/N‐CNFAs) with optimized electronic structure by S/N codoping, enhanced interlayer spacing by S doping, and a 3D interconnected porous structure of aerogel, through a pyrolysis sustainable seaweed (Fe‐alginate) aerogel strategy. Specifically, the S/N‐CNFAs electrode delivers high reversible capacities of 356 and 112 mA h g?1 at 100 and 5000 mA g?1, respectively. The capacity reaches 168 mA h g?1 at 2000 mA g?1 after 1000 cycles. A full cell with a S/N‐CNFAs anode and potassium prussian blue cathode displays a specific capacity of 198 mA h g?1 at 200 mA g?1. Density functional theory calculations indicate that S/N codoping is beneficial to synergistically improve K ions storage of S/N‐CNFAs by enhancing the adsorption of K ions and reducing the diffusion barrier of K ions. This work offers a facile heteroatom doping paradigm for designing new carbonaceous anodes for high‐performance PIBs.  相似文献   

5.
    
Aqueous zinc-ion batteries (ZIBs) using the Zn metal anode have been considered as one of the next-generation commercial batteries with high security, robust capacity, and low price. However, parasitic reactions, notorious dendrites and limited lifespan still hamper their practical applications. Herein, an eco-friendly nitrogen-doped and sulfonated carbon dots (NSCDs) is designed as a multifunctional additive for the cheap aqueous ZnSO4 electrolyte, which can overcome the above difficulties effectively. The abundant polar groups (-COOH, -OH, -NH2, and -SO3H) on the CDs surfaces can regulate the solvation structure of Zn2+ through decreasing the coordinated active H2O molecules, and thus redistribute Zn2+ deposition to avoid side reactions. Some of the negatively charged NSCDs are adsorbed on Zn anode surface to isolate the H2O/SO42- corrosion through the electrostatic shielding effect. The synergistic effect of the doped nitrogen species and the surface sulfonic groups can induce a uniform electrolyte flux and a homogeneous Zn plating with a (002) texture. As a result, the excellent cycle life (4000 h) and Coulombic efficiency (99.5%) of the optimized ZIBs are realized in typical ZnSO4 electrolytes with only 0.1 mg mL-1 of NSCDs additive.  相似文献   

6.
    
In recent years, carbon dots (CDs) have garnered increasing attention due to their simple preparation methods, versatile performances, and wide-ranging applications. CDs can manifest various optical, physical, and chemical properties including quantum yield (QY), emission wavelength (Em), solid-state fluorescence (SSF), room-temperature phosphorescence (RTP), material-specific responsivity, pH sensitivity, anti-oxidation and oxidation, and biocompatibility. These properties can be effectively regulated through precise control of the CD preparation process, rendering them suitable for diverse applications. However, the lack of consideration given to the precise control of each feature of CDs during the preparation process poses a challenge in obtaining the requisite features for various applications. This paper is to analyze existing research and present novel concepts and ideas for creating CDs with different distinct features and applications. The synthesis methods of CDs are discussed in the first section, followed by a comprehensive overview of the important properties of CDs and the modification strategy. Subsequently, the application of CDs and their requisite properties are reviewed. Finally, the paper outlines the current challenges in controlling CDs properties and their applications, discusses potential solutions, and offers suggestions for future research.  相似文献   

7.
    
As a new class of luminescent nanomaterials, carbon dots (CDs) have aroused significant interest because of their fascinating photoluminescence properties and potential applications in biological, optoelectronic, and energy‐related fields. Strikingly, embedding CDs in host matrices endow them with intriguing luminescent properties, in particular, room temperature phosphorescence and thermally activated delayed fluorescence, due to the confinement effect of the host matrix and the H‐bonding interactions between CDs and the matrix. Here, the state‐of‐the‐art strategies for introducing CDs in various host matrices are summarized, such as nanoporous materials, polyvinyl alcohol, polyurethane, potash alum, layered double hydroxides, amorphous silica, etc. The resultant luminescent properties of the composites and their emission mechanisms are discussed. Their applications in bioimaging, drug delivery/release, sensing, and anticounterfeiting are also presented. Finally, current problems and challenges of CDs‐based composites are noted for future development of such luminescent materials.  相似文献   

8.
荧光碳点的制备和性质及其应用研究进展   总被引:1,自引:0,他引:1       下载免费PDF全文
荧光碳点是继碳纳米管、纳米金刚石和石墨烯之后,最受关注的碳纳米材料之一。与传统半导体量子点相比,碳点具有优异的荧光性能、小尺寸特性、良好的生物相容性、低毒性以及表面易于化学修饰等特点,在环境检测、生物成像、药物载体、光催化及电催化技术等领域具有很好的潜在应用价值。总结了碳点合成方法、结构与性能及应用面进展,剖析了目前制约碳点应用发展的瓶颈问题,并展望了其未来的研究发展重点方向。   相似文献   

9.
    
Mg batteries have the advantages of resource abundance, high volumetric energy density, and dendrite‐free plating/stripping of Mg anodes. However the injection of highly polar Mg2+ cannot maintain the structural integrity of intercalation‐type cathodes even for open framework prototypes. The lack of high‐voltage electrolytes and sluggish Mg2+ diffusion in lattices or through interfaces also limit the energy density of Mg batteries. Mg–S system based on moderate‐voltage conversion electrochemistry appears to be a promising solution to high‐energy Mg batteries. However, it still suffers from poor capacity and cycling performances so far. Here, a ZIF‐67 derivative carbon framework codoped by N and Co atoms is proposed as effective S host for highly reversible Mg–S batteries even under high rates. The discharge capacity is as high as ≈600 mA h g?1 at 1 C during the first cycle, and it is still preserved at ≈400 mA h g?1 after at least 200 cycles. Under a much higher rate of 5 C, a capacity of 300–400 mA h g?1 is still achievable. Such a superior performance is unprecedented among Mg–S systems and benefits from multiple factors, including heterogeneous doping, Li‐salt and Cl? addition, charge mode, and cut‐off capacity, as well as separator decoration, which enable the mitigation of electrode passivation and polysulfide loss.  相似文献   

10.
The metal–insulator transition (MIT) of vanadium dioxide (VO2) has been of great interest in materials science for both fundamental understanding of strongly correlated physics and a wide range of applications in optics, thermotics, spintronics, and electronics. Due to the merits of chemical interaction with accessibility, versatility, and tunability, chemical modification provides a new perspective to regulate the MIT of VO2, endowing VO2 with exciting properties and improved functionalities. In the past few years, plenty of efforts have been devoted to exploring innovative chemical approaches for the synthesis and MIT modulation of VO2 nanostructures, greatly contributing to the understanding of electronic correlations and development of MIT-driven functionalities. Here, this comprehensive review summarizes the recent achievements in chemical synthesis of VO2 and its MIT modulation involving hydrogen incorporation, composition engineering, surface modification, and electrochemical gating. The newly appearing phenomena, mechanism of electronic correlation, and structural instability are discussed. Furthermore, progresses related to MIT-driven applications are presented, such as the smart window, optoelectronic detector, thermal microactuator, thermal radiation coating, spintronic device, memristive, and neuromorphic device. Finally, the challenges and prospects in future research of chemical modulation and functional applications of VO2 MIT are also provided.  相似文献   

11.
    
Developing a facile and cost‐efficient method to synthesize carbon‐based nanomaterials possessing excellent structural and functional properties has become one of the most attractive topics in energy conversion and storage fields. In this study, density functional theory calculation results reveal the origin of high oxygen reduction reaction (ORR) activity predominantly derived from the synergistic effect of intrinsic defects and heteroatom dopants (e.g., N, S) that modulate the bandgap and charge density distribution of carbon matrix. Under the guidance of the first‐principle prediction, by using ultralight biomass waste as precursor of C, N, and S elements, a defect‐rich and N/S dual‐doped cheese‐like porous carbon nanomaterial is successfully designed and constructed. Herein, the intrinsic defects are artfully generated in terms of alkaline and ammonia activation. The electrochemical measurements display that such a material owns a comparable ORR activity (E1/2 = 0.835 V) to the commercial Pt/C catalyst, along with splendid durability and methanol tolerance in alkali media. Furthermore, as cathode catalyst, it displays a high Zn–air battery performance. The excellent ORR activity of the catalyst can be attributed to its unique 3D porous architecture, abundant intrinsic defects, and high‐content active heteroatom dopants in the carbon matrix.  相似文献   

12.
    
It is a serious challenge to develop photoanodes with fast charge separation efficiency and surface reaction kinetics. Herein, the N doped carbon dot modified WO3 nanoflake (NCDs/WO3) is constructed by impregnation method. The resulting NCDs/WO3 exhibits an excellent photocurrent density of 1.42 mA cm−2 (1.0 V vs saturated calomel electrode, SCE) in 1 m H2SO4 solution under AM 1.5 G irradiation, which is 2.25 times higher than that of the pristine WO3. In addition, the onset potential of NCDs/WO3 photoanode represents a cathodic shift of 70 mV, indicating the charge separation and transfer process are both promoted. These results demonstrate N doped CD modified WO3 can further enhance the conductivity and electrochemical activity surface area, which contributes to the higher photoelectrochemical (PEC) performance. This work provides an efficient strategy for the development of doping carbon material with heteroatoms to increase the charge transfer and charge separation efficiency in PEC water oxidation.  相似文献   

13.
The sluggish redox kinetics and shuttle effect seriously impede the large application of room-temperature sodium–sulfur (RT Na–S) batteries. Designing effective catalysts into cathode material is a promising approach to overcome the above issues. However, considering the multistep and multiphase transformations of sulfur redox process, it is impractical to achieve the effective catalysis of the entire S8→Na2Sx→Na2S conversion through applying a single catalyst. Herein, this work fabricates a nitrogen-doped core–shell carbon nanosphere integrated with two different catalysts (ZnS-NC@Ni-N4), where isolated Ni–N4 sites and ZnS nanocrystals are distributed in the shell and core, respectively. ZnS nanocrystals ensure the rapid reduction of S8 into Na2Sx (4 < x ≤ 8), while Ni–N4 sites realize the efficient conversion of Na2Sx into Na2S, bridged by the diffusion of Na2Sx from the core to shell. Besides, Ni–N4 sites on the shell can also induce an inorganic-rich cathode–electrolyte interface (CEI) on ZnS-NC@Ni-N4 to further inhibit the shuttle effect. As a result, ZnS-NC@Ni-N4/S cathode exhibits an excellent rate-performance (650 mAh g−1 at 5 A g−1) and ultralong cycling stability for 2000 cycles with a low capacity-decay rate of 0.011% per cycle. This work will guide the rational design of multicatalysts for high-performance RT Na–S batteries.  相似文献   

14.
    
Boron/oxygen co‐doped carbons (BOC) have great potentials as sulfur host materials for lithium–sulfur batteries, because they can increase electronic conductivity and anchor polysulfides. However, the doping interface as a key chemically active site still lacks in‐depth understanding owing to the difficulty in design at the molecular scale. Herein, the BOC network derived from covalent organic framework (COF) is prepared on the surface of CNTs via rational design of the organic condensation reaction. This strategy enables boron and oxygen heteroatoms to be uniformly doped throughout porous carbon because of the uniformly‐distributed two elements in the COF precursor. Thereby, the BOC matrix is demonstrated to play a pivotal role in promoting the chemical absorption of polysulfides and enhancing cycling stability. The BOC@CNT with 68.5% sulfur shows superior lithium polysulfides absorptivity and displays superior electrochemical performances as a cathode for Li–S batteries, including a large reversible capacity (1077 mA h g−1 after 200 cycles at 0.2 C), and outstanding cycling stability (794 mA h g−1 after 500 cycles at 1 C). The demonstrated strategy for fabricating BOC network by COF precursor for Li–S batteries provides a new approach to rationally design uniform heteroatom interfaces for good electrochemical performances.  相似文献   

15.
Developing efficient and robust metal–nitrogen–carbon electrocatalysts for oxygen reduction reaction (ORR) is of great significance for the application of hydrogen–oxygen fuel cells and metal–air batteries. Herein, a coordination engineering strategy is developed to improve the ORR kinetics and stability of cobalt–nitrogen–carbon (Co–N–C) electrocatalysts by grafting the oxygen-rich graphene quantum dots (GQDs) onto the zeolite imidazole frameworks (ZIFs) precursors. The optimized oxygen-rich GQDs-functionalized Co–N–C (G-CoNOC) electrocatalyst demonstrates an increased mass activity, nearly two times higher than that of pristine defective Co–N–C electrocatalyst, and retains a stability of 90.0% after 200 h, even superior to the commercial Pt/C. Comprehensive investigations demonstrate that the GQDs coordination can not only decrease carbon defects of Co–N–C electrocatalysts, improving the electron transfer efficiency and resistance to the destructive free radicals from H2O2, but also optimize the electronic structure of atomic Co active site to achieve a desired adsorption energy of OOH, leading to enhanced ORR kinetics and stability by promoting further H2O2 reduction, as confirmed by theoretical calculations and experimental results. Such a coordination engineering strategy provides a new perspective for the development of highly active noble-metal-free electrocatalysts for ORR.  相似文献   

16.
    
Metal nanoclusters providing maximized atomic surface exposure offer outstanding hydrogen evolution activities but their stability is compromised as they are prone to grow and agglomerate. Herein, a possibility of blocking metal ion diffusion at the core of cluster growth and aggregation to produce highly active Ru nanoclusters supported on an N, S co-doped carbon matrix (Ru/NSC) is demonstrated. To stabilize the nanocluster dispersion, Ru species are initially coordinated through multiple Ru─N bonds with N-rich 4′-(4-aminophenyl)-2,2:6′,2′′-terpyridine (TPY-NH2) ligands that are subsequently polymerized using a Schiff base. After the pyrolysis of the hybrid composite, highly dispersed ultrafine Ru nanoclusters with an average size of 1.55 nm are obtained. The optimized Ru/NSC displays minimal overpotentials and high turnover frequencies, as well as robust durability both in alkaline and acidic electrolytes. Besides, outstanding mass activities of 3.85 A mg−1Ru at 50 mV, i.e., 16 fold higher than 20 wt.% Pt/C are reached. Density functional theory calculations rationalize the outstanding performance by revealing that the low d-band center of Ru/NSC allows the desorption of *H intermediates, thereby enhancing the alkaline HER activity. Overall, this work provides a feasible approach to engineering cost-effective and robust electrocatalysts based on carbon-supported transition metal nanoclusters for future energy technologies.  相似文献   

17.
To realize the potential benefits of additive manufacturing technology in airframe and ground vehicle applications, the fatigue performance of load bearing additively manufactured materials must be understood. Due to the novelty of this rapidly developing technology, a very limited, yet swiftly evolving literature exists on the topic. Motivated by these two points, we have attempted to catalog and analyze the published fatigue performance data of an additively manufactured alloy of significant technological interest, Ti–6Al–4V. Focusing on uniaxial fatigue performance, we compare to traditionally manufactured Ti–6Al–4V, discussing failure mechanisms, defects, microstructure, and processing parameters. We then attempt to identify key knowledge gaps that must be addressed before AM technology can safely and effectively be employed in critical load bearing applications.  相似文献   

18.
    
Responsive thermochromic fiber materials capable of miniaturization and integrating comfortably and compliantly onto the soft and dynamically deforming human body are promising materials for visualized personal health monitoring. However, their development is hindered by monotonous colors, low-contrast color changes, and poor reversibility. Herein, full-color “off–on” thermochromic fluorescent fibers are prepared based on self-crystallinity phase change and Förster resonance energy transfer for long-term and passive body-temperature monitoring, especially for various personalized customization purposes. The off–on switching luminescence characteristic is derived from the reversible conversion of the dispersion state and fluorescent emission by fluorophores and quencher molecules, which are embedded in the matrix of a phase-change material, during the crystallizing/melting processes. The achievement of full-color fluorescence is attributed to the large modulation range of fluorescence colors according to primary color additive theory. These thermochromic fluorescent fibers exhibit good mechanical properties, fluorescent emission contrast, and reversibility, showing their great potential in flexible smart display devices. Moreover, the response temperature of the thermochromic fibers is controllable by adjusting the phase-change material, enabling body-temperature-triggered luminescence; this property highlights their potential for human body-temperature monitoring and personalized customization. This work presents a new strategy for designing and exploring flexible sensors with higher comprehensive performances.  相似文献   

19.
The fatigue strength and failure mechanisms of defect-free (“sound”) and flaw bearing friction stir butt-welds of 3.1 mm-thick AA2198-T8 Al–Li–Cu alloy have been investigated via S–N curves at R = 0.1 using cross weld specimens. The fatigue strength of sound welds is only reduced by 10–15% at the aimed lifetime of 105 cycles compared to the base material. Joint Line Remnant (JLR) bearing welds have a similar fatigue strength as sound welds and the JLR is not the crack initiation site. Kissing Bond (KB) bearing welds that have undergone a weld root polishing show a reduction in fatigue strength by 17% compared to sound welds. For specimens loaded at or above yield strength of the weld nugget the crack systematically initiates from the KB during the first cycle, which is interpreted further using fracture mechanics. The strongest reduction, about 28% in fatigue strength, is found for welds with an initial gap between the parent sheets (GAP welds) along with initiation at intergranular surface microcracks. Kahn tear tests show a reduction in tearing resistance for the flaw bearing welds with a similar ranking as for the fatigue strength.  相似文献   

20.
    
With a high theoretical capacity, the MnS anode, however, exhibits a rather complex sodium diffusion kinetics and poor mechanical stability that hinder its application in sodium-ion batteries (SIBs). In this work, a simple, economical, and scalable strategy is developed to inherently coat nanoporous MnS with a 3D N, S co-doped thin carbon layer by using commercially available MnCO3 as precursors. Specifically, the strategy involves a two-step annealing process, which converts the MnCO3 microparticles into nanoporous Mn2O3 and MnS step by step. The 3D N, S codoped carbon layer is in situ formed during the second annealing process by first coating the nanoporous Mn2O3 with a polyaniline layer. Due to the inherent 3D carbon protection and the strong electronic interaction between N, S dopants and MnS, the N, S codoped carbon protected MnS obtained at 900 °C (NS-C@MnS-900) anode displays a high specific capacity of 845 mAh g−1 at 0.1 A g−1, which is higher than all reported MnS-based SIB anodes. It also shows an outstanding cyclability and rate performance, maintaining a stable capacity of ≈493 mAh g−1 after 1300 cycles at 10 A g−1, which is also the best according to knowledge. These exceptional electrochemical performances and the scalable/simple/low-cost synthesis make the NS-C@MnS-900 attractive for industry application.  相似文献   

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