5 research outputs found
Ni(OH)<sub>2</sub> Nanoflowers/Graphene Hydrogels: A New Assembly for Supercapacitors
A novel structure
of graphene-based hybrid hydrogels was constructed,
in which Ī±-NiĀ(OH)<sub>2</sub> nanoflowers with nanopetals thicknesses
of approximately 20 nm were uniformly anchored on a three-dimensional
graphene framework. Benefiting from the unique morphological nickel
hydroxide nanoflowers and hydrogels, the nickel hydroxide nanoflowers/graphene
hydrogels exhibited great specific capacitances (1 AĀ·g<sup>ā1</sup>; 1632 FĀ·g<sup>ā1</sup>), great rate capabilities, and
longer cycle life (after 1000 cycles, 95.2% capacitance retention)
when used as electrodes in supercapacitors
Solvothermal-Induced 3D Macroscopic SnO<sub>2</sub>/Nitrogen-Doped Graphene Aerogels for High Capacity and Long-Life Lithium Storage
3D macroscopic tin
oxide/nitrogen-doped graphene frameworks (SnO<sub>2</sub>/GN) were
constructed by a novel solvothermal-induced self-assembly
process, using SnO<sub>2</sub> colloid as precursor (crystal size
of 3ā7 nm). Solvothermal treatment played a key role as N,N-dimethylmethanamide
(DMF) acted both as reducing reagent and nitrogen source, requiring
no additional nitrogen-containing precursors or post-treatment. The
SnO<sub>2</sub>/GN exhibited a 3D hierarchical porous architecture
with a large surface area (336 m<sup>2</sup>g<sup>ā1</sup>),
which not only effectively prevented the agglomeration of SnO<sub>2</sub> but also facilitated fast ion and electron transport through
3D pathways. As a result, the optimized electrode with GN content
of 44.23% exhibited superior rate capability (1126, 855, and 614 mAh
g<sup>ā1</sup> at 1000, 3000, and 6000 mA g<sup>ā1</sup>, respectively) and extraordinary prolonged cycling stability at
high current densities (905 mAh g<sup>ā1</sup> after 1000 cycles
at 2000 mA g<sup>ā1</sup>). Electrochemical impedance spectroscopy
(EIS) and morphological study demonstrated the enhanced electrochemical
reactivity and good structural stability of the electrode
Development of Cobalt Hydroxide as a Bifunctional Catalyst for Oxygen Electrocatalysis in Alkaline Solution
CoĀ(OH)<sub>2</sub> in the form of
hexagonal nanoplates synthesized by a simple hydrothermal reaction
has shown even greater activity than cobalt oxides (CoO and Co<sub>3</sub>O<sub>4</sub>) in oxygen reduction and oxygen evolution reactions
(ORR and OER) under alkaline conditions. The bifunctionality for oxygen
electrocatalysis as shown by the OERāORR potential difference
(Ī<i>E</i>) could be reduced to as low as 0.87 V,
comparable to the state-of-the-art non-noble bifunctional catalysts,
when the CoĀ(OH)<sub>2</sub> nanoplates were compounded with nitrogen-doped
reduced graphene oxide (N-rGO). The good performance was attributed
to the nanosizing of CoĀ(OH)<sub>2</sub> and the synergistic interaction
between CoĀ(OH)<sub>2</sub> and N-rGO. A zincāair cell assembled
with a CoĀ(OH)<sub>2</sub>āair electrode also showed a performance
comparable to that of the state-of-the-art zincāair cells.
The combination of bifunctional activity and operational stability
establishes CoĀ(OH)<sub>2</sub> as an effective low-cost alternative
to the platinum group metal catalysts
High-Performance Aqueous Zinc-Ion Batteries Enabled by Binder-Free and Ultrathin V<sub>2</sub>O<sub>5ā<i>x</i></sub>@Graphene Aerogels with Intercalation Pseudocapacitance
As
a result of the absence of solid-state diffusion limitation,
intercalation pseudocapacitance behavior is emerging as an attractive
charge-storage mechanism that can greatly facilitate the ion kinetics
to boost the rate capability and cycle stability of batteries; however,
related research in the field of zinc-ion batteries (ZIBs) is still
in the initial stage and only found in limited cathode materials.
In this study, a novel V2O5āx@rGO hybrid aerogel consisting of ultrathin V2O5 nanosheets (ā¼1.26 nm) with abundant oxygen vacancies
(VoĢ) and a three-dimensional (3D) graphene conductive network
was specifically designed and used as a freestanding and binder-free
electrode for ZIBs. As expected, the ideal microstructure of both
the material and the electrode enable fast electron/ion diffusion
kinetics of the electrode, which realize a typical intercalation pseudocapacitance
behavior as demonstrated by the simulation calculation of cyclic voltammetry
(CV), ex situ X-ray diffraction (XRD), X-ray photoelectron spectroscopy
(XPS), and first-principles density functional theory (DFT) calculation.
Thanks to the elimination of solid-state diffusion limitation, the
V2O5āx@rGO electrode
delivers a high reversible rate capacity of 153.9 mAh gā1 at 15 A gā1 and 90.6% initial capacity retention
at 0.5 A gā1 after 1050 cycles in ZIBs. The intercalation
pseudocapacitance behavior is also realized in the assembled soft-pack
battery, showing promising practical application prospects
Fabricating 3D Macroscopic Graphene-Based Architectures with Outstanding Flexibility by the Novel Liquid Drop/Colloid Flocculation Approach for Energy Storage Applications
Inspired by āwater
ripplesā in nature and the flocculation phenomenon in colloid
chemistry, a novel liquid drop/colloid flocculation approach is developed
to fabricate an extremely flexible and compressible 3D macroscopic
graphene-based architecture (hydrogels or aerogels), via a new coagulation-induced
self-assembly mechanism. This facile and universal technique can be
achieved in a neutral, acidic, or basic coagulation bath, producing
microsized hydrogels with various structures, such as mushroom, circle,
disc shapes, etc. The method also allows us to introduce various guest
materials in the graphene matrix using transition metal salts as the
coagulating bath. A mushroom-shaped NiCo oxide/GS hybrid aerogel (diameter:
3 mm) is prepared as an example, with ultrathin NiCo oxide nanosheets
in situ grown onto the surface of graphene. By employing as binder-free
electrodes, these hybrid aerogels exhibit a specific capacitance of
858.3 F g<sup>ā1</sup> at 2 A g<sup>ā1</sup>, as well
as a good rate capability and cyclic stability. The asymmetric supercapacitor,
assembling with the hybrid aerogels as cathode and graphene hydrogels
as anode materials, could deliver an energy density of 21 Wh kg<sup>ā1</sup> at power density of 4500 W kg<sup>ā1</sup>. The ease of synthesis and the feasibility of obtaining highly flexible
aerogels with varied morphologies and compositions make this method
a promising one for use in the field of biotechnology, electrochemistry,
flexible electronics, and environment applications