Due to their low thermal conductivity, non-toxicity and low cost, conductive polymer materials are potential candidates for thermoelectric applications. Here, a detailed investigation into the thermoelectric properties of P3HT films is reported. A thermoelectric power factor over 20 mW m À1 K À2 at room temperature was obtained by employing a ferric salt of triflimide (TFSI À ) anions as a dopant. Flexible films of P3HT-TFSI were characterized by X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD) and scanning electron microscopy (SEM), along with temperature-variant electrical measurements. Given the promising results obtained from ordinary P3HT films by a simple doping treatment, this work suggests the significance of the appropriate choice of dopants and/or counterions, as well as the polymers themselves.
We investigated rechargeable aluminum (Al) batteries composed of an Al negative electrode, a graphite positive electrode, and an ionic liquid (IL) electrolyte at temperatures down to -40 °C. The reversible battery discharge capacity at low temperatures could be superior to that at room temperature. In situ/operando electrochemical and synchrotron X-ray diffraction experiments combined with theoretical modeling revealed stable AlCl/graphite intercalation up to stage 3 at low temperatures, whereas intercalation was reversible up to stage 4 at room temperature (RT). The higher-degree anion/graphite intercalation at low temperatures affords rechargeable Al battery with higher discharge voltage (up to 2.5 V, a record for Al battery) and energy density. A remarkable cycle life of >20,000 cycles at a rate of 6C (10 minutes charge time) was achievable for Al battery operating at low temperatures, corresponding to a >50-year battery life if charged/discharged once daily.
A recyclable and green triboelectronic nanogenerator (TENG) is developed based on triboelectrification and designed cascade reactions. Once triggered by water, the TENG can fully dissolve and degrade into environmentally benign end products. With features of rapid dissolution, reproductivity, and green electronic, the TENG has potential of serving as clearable energy harvester and nanosensor for health monitoring and motion sensing.
Harnessing inexhaustible solar energy for photocatalytic disposal of nitrogen oxides is of great significance nowadays. In this study, Ag-SrTiO3 nanocomposites (Ag-STO) were synthesized via one-pot solvothermal method for the first time. The deposition of Ag nanoparticles incurs a broad plasmonic resonance absorption in the visible light range, resulting in enhanced visible light driven activity on NO removal in comparison with pristine SrTiO3. The Ag loading amount has a significant influence on light absorption properties of Ag-STO, which further affects the photocatalytic efficiency. It was shown that 0.5% Ag loading onto SrTiO3 (in mass ratio) could remove 30% of NO in a single reaction path under visible light irradiation, which is twice higher than that achieved on pristine SrTiO3. Most importantly, the generation of harmful intermediate (NO2) is largely inhibited over SrTiO3 and Ag-STO nanocomposites, which can be ascribed to the basic surface property of strontium sites. As identified by electron spin resonance (ESR) spectra,·O2(-) and ·OH radicals are the major reactive species for NO oxidation. Essentially speaking, the abundance of reactive oxygen radicals produced over Ag-STO nanocomposites are responsible for the improved photocatalytic activity. This work provides a facile and controllable route to fabricate plasmonic Ag-SrTiO3 nanocomposite photocatalyst featuring high visible light activity and selectivity for NO abatement.
Polysulfides are immobilized not only by electron-rich functional groups through coordination interaction but also by cations through electrostatic attraction.
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