RESUMO
The conversion of ubiquitous hygrothermal resources into renewable energy offers significant potential for cable-free, self-powered systems that can operate worldwide without regard to climatic or geographic limitations. Here, an all-printed flexible hygro-thermoelectric paper generator is demonstrated that uses bifunctional mobile ions and electrons to make the moist-diffusion effect, the Soret effect, and the Seebeck effect work synergistically. In the ordinary hygrothermal settings, it generates an unconventional hygro-thermoelectric output pattern and shows almost a dozen-fold increase in positive hygro-thermopower of 26.70 mV K-1 and also another negative hygro-thermopower of -15.71 mV K-1 compared to pure thermopower. A single paper generator can produce a giant 680 mV displaying typical cyclic sinusoidal waveform characters with volt-sized amplitudes. The ion-electron conductive ink is easily printable and consists primarily of a Bi2 Te3 /PEDOT:PSS thermoelectric matrix modulated with a hygroscopic glycerol that releases ion charges for moist-diffusion effect and Soret effect, as well as electron charges for Seebeck effect. The emerged hygro-thermoelectric harvesting strategy from surrounding hygrothermal resources offers a revolutionary approach to the next generation of hybrid energy with cost-efficiency, flexibility, and sustainability, and also enables large-scale roll-to-roll production.
RESUMO
P-doped graphitic carbon nitride tubes (P-CNTS) with different P concentrations were successfully fabricated via a pre-hydrothermal in combination with a calcination process under a nitrogen atmosphere. The as-prepared samples exhibited excellent photocatalytic performance with a hydrogen production rate (HPR) of 2749.3 µmol g-1 h-1, which was 17.5 and 6.6 times higher than that of the bulk graphitic carbon nitride (CNB) and graphitic carbon nitride tube (CNT). The structural and textural properties of the P-CNT samples were well-investigated via a series of characterization methods. Compared with the bulk g-C3N4, the tubular structure of the doped samples was provided with a larger specific surface area (SSA) and a relatively rough interior. Besides the above, surface defects were formed due to the doping, which could act as more active sites for the hydrogen production reaction. In addition, the introduction of the P element could effectively adjust the band-gap, strengthen the harvest of visible-light, and boost the effective separation of photogenerated charges. More interestingly, these findings can open up a novel prospect for the enhancement of the photocatalytic performance of the modified g-C3N4.
RESUMO
By the slight adjustment of oxides constituting thin film transistor-liquid crystal display (TFT-LCD) substrate glass, including equal mole fraction substitution of Al2O3, GeO2, B2O3, P2O5 and ZrO2 for SiO2, as well as the substitution of CaO for SrO with the total contents unchanged, the structural and physico-chemical properties of the glass was investigated by Raman spectroscopy and other measurements. The results showed that the short-range disorder brought by the substitution of GeO2, B2O3 and P2O5 for SiO2 could weaken the stability and compactness of the glass network, and the physico-chemical properties deteriorated, while the process of glass melting would become easier accordingly. The short-range disorder by the substitution of ZrO2 for SiO2 with 1% mole fraction showed a little difference with other samples. Finally, the substitution of modified cations, such as CaO and SrO, showed a smaller variation compared with the substitution of network formers. On the condition of 1% mole fraction substitution of oxides investigated, the variation of samples showed a reasonable change and the performance was basically all satisfied for the use of TFT-LCD substrate.
