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Massimiliano Righi

Publications and source records attributed to Massimiliano Righi.

3 recordsLinked to original sources

Low-density functionalized amorphous carbon nanofoam as binder-free Supercapacitor electrode

Nanoporous carbon materials containing small domains of sp2-carbon with highly disordered structures are promising for supercapacitor applications. Herein, we synthesize amorphous carbon nanofoam with 98% volumetric void fraction and low mass density of around 30 mg/cm3 by pulsed laser deposition at room temperature. With the unavoidable oxygen functional groups on the nanoporous surface, carbon nanofoam and nitrogen-functionalized carbon nanofoams are directly grown on the desired substrate under different background gases (Ar, N2, N2-H2), and employed as supercapacitor electrodes. Among the background gases used in synthesis, the use of nitrogen yields nanofoam with higher thickness and more N-content with higher graphitic-N. From the test of amorphous carbon nanofoam supercapacitor device, nitrogenated amorphous carbon electrode shows a higher areal capacitance of 4.1 mF/cm2 at 20 mV/s in aqueous electrolyte, a better capacitance retention at higher current, and excellent cycle stability (98%) over 10000 charge-discharge cycles are achieved compared to not-functionalized counterpart prepared under Ar background gas (2.7 mF/cm2 and cycle stability of 88%).

physics.app-ph↗

Cumulenic sp-carbon Atomic Wires Wrapped Polymers for Supercapacitor Application

Carbon atomic wires, a linear atomic chain of sp-carbon, is theoretically predicted to have around five times higher surface area than graphene, notable charge mobilities, as well as excellent optical and thermal properties. Despite these impressive properties, the properties of sp-carbon as an electrochemical energy-storage electrode have not been reported so far. Herein, we prepare solution processed thin films of tetraphenyl[3]cumulenic sp-carbon atomic wires embedded in a polymer matrix, in which sp-carbon atomic wires feature three cumulated carbon-carbon double bonds terminated at each end by two phenyl groups. Raman and UV-visible spectroscopy are used to confirm the presence and possible degradation of sp-carbons inside the polymeric matrix. Finally, we investigate the supercapacitor performance of cumulenic sp-carbon atomic wires embedded polymer in three aqueous mediums, namely 1M Na2SO4 (neutral), 1M H2SO4 (acidic), and 6M KOH (basic). The results suggest 6M KOH is the best electrolyte to obtain high charge-storage performance of device with areal capacitance of 2.4 mF/cm2 at 20 mV/s, 85% cycle stability after 10000 charge-discharge cycles, and excellent frequency response.

physics.app-ph↗

Ballistic-aggregated Carbon Nanofoam in Target-side of Pulsed Laser Deposition for Energy Storage Applications

In pulsed laser deposition, along the traditionally exploited deposition on the front-side of the plasma-plume, a coating forms on the surface of the target as well. For reproducibility, this residue is usually cleaned and discarded. Here we instead investigate the target-side coated materials and employ them as a binder-free supercapacitor electrode. The ballistic-aggregated, target-side nanofoam is compact and features a larger fraction of sp2-carbon, higher nitrogen content with higher graphitic-N and lower oxygen content with fewer COOH groups than that of diffusive-aggregated conventional nanofoams. They are highly hydrogenated graphite-like amorphous carbon and superhydrophilic. The resulting symmetric micro-supercapacitor delivers higher volumetric capacitance of 522 mF/cm3 at 100 mV/s and 104% retention after 10000 charge-discharge cycles over conventional nanofoam (215 mF/cm3 and 85% retention) with an areal capacitance of 134 μF/cm2 at 120 Hz and ultrafast frequency response. Utilizing the normally discarded target-side material can therefore enable high performing devices while reducing waste, cost and energy input per usable product. leading towards a greater sustainability on nanomaterials synthesis and deposition techniques.

physics.app-ph↗