Abstract:With the battery-type anode and capacitor-type cathode, lithium-ion capacitors (LICs) are expected to exhibit both high energy and high power density but suffer from the mismatch of the electrode reaction kinetics and capacity. Herein, to alleviate the mismatch between the two electrodes and synergistically enhance the energy/power density, we design a method of microwave irradiation reduction to prepare graphene-based electrode material (MRPG/CNT) with fast ion/electron pathway. The threedimensional structure… Show more
“…CNT yarn is a one-dimensional, high bulk CNT assembly composed of CNT bundles and threads with a porous and hierarchical structure. Due to the excellent strength (∼100 GPa), large elastic modulus (∼1 TPa), and high conductivity (2 × 10 7 S m −1 ) of CNTs, the macro-scale CNT assemblies of a CNT yarn attracts tremendous attention, such as in wearable electronic textiles, 1–3 advanced materials, 4 energy storage, 5,6 nanotechnology. 7,8 In the past, various promising post-treatment methods have been used to improve the mechanical and electrical properties of CNT yarn.…”
Carbon nanotube yarn (CNTY) with large size and excellent mechanical property would have wider technological influences for fields ranging from electrical devices to wearable textiles; however, inventing such CNTY has...
“…CNT yarn is a one-dimensional, high bulk CNT assembly composed of CNT bundles and threads with a porous and hierarchical structure. Due to the excellent strength (∼100 GPa), large elastic modulus (∼1 TPa), and high conductivity (2 × 10 7 S m −1 ) of CNTs, the macro-scale CNT assemblies of a CNT yarn attracts tremendous attention, such as in wearable electronic textiles, 1–3 advanced materials, 4 energy storage, 5,6 nanotechnology. 7,8 In the past, various promising post-treatment methods have been used to improve the mechanical and electrical properties of CNT yarn.…”
Carbon nanotube yarn (CNTY) with large size and excellent mechanical property would have wider technological influences for fields ranging from electrical devices to wearable textiles; however, inventing such CNTY has...
“…The electrochemical performances of the assembled LIC device were measured, as illustrated in Figure . In order to obtain the matched kinetics, it is necessary to optimize the mass ratio of anode and cathode. , When the mass ratio of Ca-LSCM anode and YP-80F cathode is 1:6, the assembled Ca-LSCM//YP-80F LIC achieves the optimal performance (Figure a). Among all assembled LIC devices (Figure S22–24), the CV curves of optimal Ca-LSCM//YP-80F LIC at different scan rates exhibit a quasi-rectangular shape (Figure b), which is ascribed to the hybrid energy storage mechanisms of the anode and cathode.…”
Section: Resultsmentioning
confidence: 99%
“…The long-term cycling performance for LIC was tested on the NEWARE system. The energy and power densities of LIC were calculated by numerically integrating the galvanostatic discharge curves using eqs and : ,− E=prefixtrue∫t1t2UImnormaldtP=Etwhere m (g) represents the total mass of active materials in the anode and cathode, U (V) and I (A) represent the discharge current and operating voltage, respectively, and t (s) are the initial time of the discharge process ( t 1 ) and terminal time of the discharge process ( t 2 ).…”
Amorphous carbon monoliths with tunable microstructures
are candidate
anodes for future lithium-based energy storage. Enhancing lithium
storage capability and solid-state diffusion kinetics are the precondition
for practical applications. Transforming intrinsic oxygen-rich defects
into active sites and engineering enlarged interlayer spacing are
of great importance. Herein, a novel explosion strategy is designed
based on oxalate pyrolysis producing CO and CO2 to successfully
prepare lignin-derived carbon monolith (LSCM) with active carbonyl
(CO) groups and enlarged interlayer spacing. Explosion promotes
the demethylation of methoxyl groups and cleavage of carboxyl groups
to form CO groups. CO2 etches carbon atoms in a
short time to improve the heteroatom level, expanding the interlayer
spacing. ZnC2O4 is decomposed at 400 °C,
simultaneously producing CO and CO2, which constructs less
CO groups and large interlayer spacing. MgC2O4 is decomposed at 450 and 480 °C, staged-weakly producing
CO and CO2, which constructs more CO groups and
larger interlayer spacing. CaC2O4 is decomposed
at 480 and 700 °C, staged-uniformly producing CO and CO2, which constructs abundant CO groups and largest interlayer
spacing. The LSCM prepared by staged-uniform explosion exhibits high
lithium storage capacity, superior rate capability, and cycling performance.
The assembled lithium ion capacitor device achieves excellent energy/power
densities of 78 Wh kg–1/100 W kg–1 and superior durability (capacitance retention of 8 4.6% after 20,000
cycles). This work gives a novel insight to engineer advanced oxygen-functionalized
carbons for enhanced lithium storage.
“…To investigate the kinetic effect of P-doping on the Li + intercalation/deintercalation process, the galvanostatic intermittent titration technique (GITT) was used to evaluate the diffusion coefficient of Li + in the bulk phase of the electrode material during charging and discharging (details are explained in Supporting Information Figure S17). 40 Figures 3e and S18 show that the 8-PNC anode has a higher Li + diffusion coefficient of approximately 10 −8 to 10 −10 cm 2 s −1 compared to 8-NC (10 −9 to 10 −12 cm 2 s −1 ), 6-PNC (10 −9 to 10 −11 cm 2 s −1 ), and 4-PNC (10 −9 to 10 −11 cm 2 s −1 ) anodes, demonstrating the faster electrode process based on Li + intercalation/deintercalation mechanism in the 8-PNC anode. The favorable kinetic properties of the 8-PNC anode indicate that the increased interlayer spacing of the graphitized carbon microstructure by abundant P-doping effectively reduces the barrier of Li + diffusion in the interlayers.…”
The
development of high-performance electrode materials
is one
of the effective strategies to enable Li-ion capacitors (LICs) to
achieve a high energy density at a high power density. Herein, we
present the preparation of high-level pyrrolic-N-doped porous carbon
nanomaterials and high-content P and N codoped porous carbon nanomaterials
for the cathode and anode of high-performance LICs, respectively.
Both materials were derived from the polypyrrole precursor, and the
configurations of N-doping and P-doping were regulated only by adjusting
the carbonization temperature. For the cathode, the high-level pyrrolic-N-doping
can effectively improve the specific capacity by enhancing the storage
of the PF6
– anion on the surface of the
electrode material. However, for the anode, the high-content P-doping
can not only improve the specific capacity by enhancing the storage
of Li+ cation in the electrode material but also boost
the kinetics by increasing the diffusion rate of Li+ cation
in the electrode material. With rational design, the asymmetric dual-carbon
LIC achieves a high energy density of 214.7 W h kg–1 at 0.18 kW kg–1 and still maintains a high energy
density of 65.0 W h kg–1 at a high power density
of 19.5 kW kg–1 with excellent cycling stability
(75.1% retention after 5000 cycles at 3.2 kW kg–1).
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