Browse
Submit Data
Databases
API
Help

Dataset Information

19 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

A Self-supported Graphene/Carbon Nanotube Hollow Fiber for Integrated Energy Conversion and Storage.

ABSTRACT: Wearable fiber-shaped integrated energy conversion and storage devices have attracted increasing attention, but it remains a big challenge to achieve a common fiber electrode for both energy conversion and storage with high performance. Here, we grow aligned carbon nanotubes (CNTs) array on continuous graphene (G) tube, and their seamlessly connected structure provides the obtained G/CNTs composite fiber with a unique self-supported hollow structure. Taking advantage of the hollow structure, other active materials (e.g., polyaniline, PANI) could be easily functionalized on both inner and outer surfaces of the tube, and the obtained G/CNTs/PANI composite hollow fibers achieve a high mass loading (90%) of PANI. The G/CNTs/PANI composite hollow fibers can not only be used for high-performance fiber-shaped supercapacitor with large specific capacitance of 472 mF cm^-2, but also can replace platinum wire to build fiber-shaped dye-sensitized solar cell (DSSC) with a high power conversion efficiency of 4.20%. As desired, the integrated device of DSSC and supercapacitor with the G/CNTs/PANI composite hollow fiber used as the common electrode exhibits a total power conversion and storage efficiency as high as 2.1%. Furthermore, the self-supported G/CNTs hollow fiber could be further functionalized with other active materials for building other flexible and wearable electronics.

SUBMITTER: Liu K

PROVIDER: S-EPMC7770695 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

Elastic Carbon Aerogels Reconstructed from Electrospun Nanofibers and Graphene as Three-Dimensional Networked Matrix for Efficient Energy Storage/Conversion.

Project description:Three-dimensional (3D) all-carbon nanofibrous aerogels with good structural stability and elasticity are highly desirable in flexible energy storage/conversion devices. Hence, an efficient surface-induced co-assembly strategy is reported for the novel design and reconstruction of electrospun nanofibers into graphene/carbon nanofiber (CNF) composite aerogels (GCA) with hierarchical structures utilizing graphene flakes as cross-linkers. The as-obtained GCA monoliths possess interconnected macropores and integrated conductive networks, which exhibit high elasticity and great structural robustness. Benefitting from the largely increased surface area and charge-transfer efficiency derived from the multi-form firm interconnections (including pillaring, bridging and jointing) between graphene flakes and CNF ribs, GCA not only reveals prominent capacitive performance as supercapacitor electrode, but also shows excellent hydrogen evolution reaction activity in both acidic and alkaline solutions as a 3D template for decoration of few-layered MoSe2 nanosheets, holding great potentials for energy-related applications.

| S-EPMC4980659 | biostudies-literature

Flexible and Stretchable Bio-Integrated Electronics Based on Carbon Nanotube and Graphene.

Project description:Scientific and engineering progress associated with increased interest in healthcare monitoring, therapy, and human-machine interfaces has rapidly accelerated the development of bio-integrated multifunctional devices. Recently, compensation for the cons of existing materials on electronics for health care systems has been provided by carbon-based nanomaterials. Due to their excellent mechanical and electrical properties, these materials provide benefits such as improved flexibility and stretchability for conformal integration with the soft, curvilinear surfaces of human tissues or organs, while maintaining their own unique functions. This review summarizes the most recent advanced biomedical devices and technologies based on two most popular carbon based materials, carbon nanotubes (CNTs) and graphene. In the beginning, we discuss the biocompatibility of CNTs and graphene by examining their cytotoxicity and/or detrimental effects on the human body for application to bioelectronics. Then, we scrutinize the various types of flexible and/or stretchable substrates that are integrated with CNTs and graphene for the construction of high-quality active electrode arrays and sensors. The convergence of these carbon-based materials and bioelectronics ensures scalability and cooperativity in various fields. Finally, future works with challenges are presented in bio-integrated electronic applications with these carbon-based materials.

| S-EPMC6073353 | biostudies-literature

Carbon nanotube-reduced graphene oxide fiber with high torsional strength from rheological hierarchy control.

Project description:High torsional strength fibers are of practical interest for applications such as artificial muscles, electric generators, and actuators. Herein, we maximize torsional strength by understanding, measuring, and overcoming rheological thresholds of nanocarbon (nanotube/graphene oxide) dopes. The formed fibers show enhanced structure across multiple length scales, modified hierarchy, and improved mechanical properties. In particular, the torsional properties were examined, with high shear strength (914 MPa) attributed to nanotubes but magnified by their structure, intercalating graphene sheets. This design approach has the potential to realize the hierarchical dimensional hybrids, and may also be useful to build the effective network structure of heterogeneous materials.

| S-EPMC7810860 | biostudies-literature

Carbothermal Synthesis of Nitrogen-Doped Graphene Composites for Energy Conversion and Storage Devices.

Project description:Metal oxides and carbonaceous composites are both promising materials for electrochemical energy conversion and storage devices, such as secondary rechargeable batteries, fuel cells and electrochemical capacitors. In this study, Fe3O4 nanoparticles wrapped in nitrogen-doped (N-doped) graphene nanosheets (Fe3O4@G) were fabricated by a facile one-step carbothermal reduction method derived from Fe2O3 and liquid-polyacrylonitrile (LPAN). The unique two-dimensional structure of N-doped graphene nanosheets, can not only accommodate the volume changes during lithium intercalation/extraction processes and suppress the particles aggregation but also act as an electronically conductive matrix to improve the electrochemical performance of Fe3O4 anode, especially the rate capability. What's more, by etching Fe3O4@G to remove the iron-based oxide template, porous N-doped graphene composites (NGCs) were prepared and presented abundant pore structure with high specific surface area, delivering a specific capacitance of 172 F·g-1 at 0.5 A·g-1. In this way, Fe2O3 was both template and activator to adjust the pore size of graphene. And the effect of specific surface area and pore size tuned by the Fe2O3 activator were also revealed.

| S-EPMC6204351 | biostudies-literature

Investigation of thermal energy transport interface of hybrid graphene-carbon nanotube/polyethylene nanocomposites.

Project description:It is well known the thermal properties of three-dimensional (3-D) hybrid graphene (GR)-carbon nanotube (CNT) structures are not superior to that of the individual GR and CNT, however, the 3-D hybrid GR-CNT structures can effectively improve the thermal properties of polymer matrix. Therefore, understanding the thermal energy transport in the interface between polymer matrix and 3-D hybrid GR-CNT structure is essential. Here, the enhancement mechanism of interfacial thermal transport of hybrid GR-CNT structure was explored by applying non-equilibrium molecular dynamics (NEMD) simulations. Three different types of hybrid GR-CNT structures were built. The influences of CNT radius and CNT type for the hybrid GR-CNT on the interfacial thermal properties were also analyzed. Computational results show that among the three different types of hybrid GR-CNT structures, the Model-I, i.e., the covalent bond hybrid GR-CNT structures are of the best interfacial thermal properties. Meanwhile, the CNT radius of hybrid GR-CNT structure has a great influence on the interfacial thermal properties.

| S-EPMC5666017 | biostudies-literature

Facile synthesis of ultrahigh-surface-area hollow carbon nanospheres for enhanced adsorption and energy storage.

Project description:Exceptionally large surface area and well-defined nanostructure are both critical in the field of nanoporous carbons for challenging energy and environmental issues. The pursuit of ultrahigh surface area while maintaining definite nanostructure remains a formidable challenge because extensive creation of pores will undoubtedly give rise to the damage of nanostructures, especially below 100?nm. Here we report that high surface area of up to 3,022?m(2)?g(-1) can be achieved for hollow carbon nanospheres with an outer diameter of 69?nm by a simple carbonization procedure with carefully selected carbon precursors and carbonization conditions. The tailor-made pore structure of hollow carbon nanospheres enables target-oriented applications, as exemplified by their enhanced adsorption capability towards organic vapours, and electrochemical performances as electrodes for supercapacitors and sulphur host materials for lithium-sulphur batteries. The facile approach may open the doors for preparation of highly porous carbons with desired nanostructure for numerous applications.

| S-EPMC4490369 | biostudies-literature

PAF-derived nitrogen-doped 3D Carbon Materials for Efficient Energy Conversion and Storage.

Project description:Owing to the shortage of the traditional fossil fuels caused by fast consumption, it is an urgent task to develop the renewable and clean energy sources. Thus, advanced technologies for both energy conversion (e.g., solar cells and fuel cells) and storage (e.g., supercapacitors and batteries) are being studied extensively. In this work, we use porous aromatic framework (PAF) as precursor to produce nitrogen-doped 3D carbon materials, i.e., N-PAF-Carbon, by exposing NH3 media. The "graphitic" and "pyridinic" N species, large surface area, and similar pore size as electrolyte ions endow the nitrogen-doped PAF-Carbon with outstanding electronic performance. Our results suggest the N-doping enhance not only the ORR electronic catalysis but also the supercapacitive performance. Actually, the N-PAF-Carbon obtains ~70?mV half-wave potential enhancement and 80% increase as to the limiting current after N doping. Moreover, the N-PAF-Carbon displays free from the CO and methanol crossover effect and better long-term durability compared with the commercial Pt/C benchmark. Moreover, N-PAF-Carbon also possesses large capacitance (385?F g(-1)) and excellent performance stability without any loss in capacitance after 9000 charge-discharge cycles. These results clearly suggest that PAF-derived N-doped carbon material is promising metal-free ORR catalyst for fuel cells and capacitor electrode materials.

| S-EPMC4456730 | biostudies-literature

Highly N-doped microporous carbon nanospheres with high energy storage and conversion efficiency.

Project description:Porous carbon spheres (CSs) have distinct advantages in energy storage and conversion applications. We report the preparation of highly monodisperse N-doped microporous CSs through the carbonization of polystyrene-based polymer spheres and subsequent activation. The N-doped microporous CSs have a remarkably high N-doping content, over 10%, and high BET surface area of 884.9 m2 g-1. We characterize the synergistic effects of the micropores and N doping on the energy storage performance of a supercapacitor electrode consisting of the CSs and on the performance in an electrocatalytic reaction of a CS counter electrode in a photovoltaic cell. The N-doped microporous CSs exhibit a maximum capacitance of 373 F g-1 at a current density of 0.2 Ag-1, a high capacitance retention up to 62% with a 10-fold increase in current density, and excellent stability over 10,000 charge/discharge cycles. A counter electrode consisting of N-doped microporous CSs was found to exhibit superior electrocatalytic behavior to an electrode consisting of conventional Pt nanoparticles. These CSs derived from polymer spheres synthesized by addition polymerization will be new platform materials with high electrochemical performance.

| S-EPMC5663965 | biostudies-literature

High-Purity Graphitic Carbon for Energy Storage: Sustainable Electrochemical Conversion from Petroleum Coke.

Project description:The petroleum coke (PC) has been widely used as raw materials for the preparation of electrodes in aluminium electrolysis and lithium-ion batteries (LIB), during which massive CO2 gases are produced. To meet global CO2 reduction, an environmentally friendly route for utilizing PC is highly required. Here, a simple, scalable, catalyst-free process that can directly convert high-sulfur PC into graphitic nanomaterials under cathodic polarization in molten CaCl2 -LiCl at mild temperatures is proposed. The energy consumption of the proposed process is calculated to be 3 627.08 kWh t-1 , half that of the traditional graphitization process (≈7,825.21 kWh t-1 graphite). When applied as a negative electrode for LIBs, the as-converted graphite materials deliver a competitive specific capacity of ≈360 mAh g-1 (0.2 C) compared with commercial graphite. This approach has great potential to scale up for sustainably converting low-value PC into high-quality graphite for energy storage.

| S-EPMC10015905 | biostudies-literature

Designing of Carbon Nitride Supported ZnCo2O4 Hybrid Electrode for High-Performance Energy Storage Applications.

Project description:This study reports a unique graphitic-C3N4 supported ZnCo2O4 composite, synthesized through a facile hydrothermal method to enhance the electrochemical performance of the electrode. The g-C3N4@ZnCo2O4 hybrid composite based electrode exhibits a significant increase in specific surface area and maximum specific capacity of 157 mAhg-1 at 4 Ag-1. Moreover, g-C3N4@ZnCo2O4 electrode maintained significant capacity retention of 90% up to 2500 cycles. Utilizing this composite in the development of the symmetric device, g-C3N4@ZnCo2O4//g-C3N4@ZnCo2O4 displays a specific capacity of 121 mAhg-1. The device exhibits an energy density of 39 Whkg-1 with an equivalent power density of 1478 Wkg-1. A good cycling stability performance with an energy efficiency of 75% and capacity retention of 71% was observed up to 10,000 cycles. The superior performance of g-C3N4@ZnCo2O4 is attributed to the support of the g-C3N4 which increases the surface area, electroactive sites and provides chemical stability for electrochemical performance. The outstanding performance of this exclusive device symbolizes remarkable progress in the direction of high-performance energy storage applications.

| S-EPMC7005029 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data