RESUMEN
Manipulating the separation and transfer behaviors of charges has long been pursued for promoting the photoelectrochemical (PEC) hydrogen generation based on II-VI quantum dot (QDs), but remains challenging due to the lack of effective strategies. Herein, a facile strategy is reported to regulate the recombination and transfer of interfacial charges through tuning the surface stoichiometry of heterostructured QDs. Using this method, it is demonstrated that the PEC cells based on CdSe-(Sex S1- x )4 -(CdS)2 core/shell QDs with a proper Ssurface /Cdsurface ratio exhibits a remarkably improved photocurrent density (≈18.4 mA cm-2 under one sun illumination), superior to the PEC cells based on QDs with Cd-rich or excessive S-rich surface. In-depth electrochemical and spectroscopic characterizations reveal the critical role (hole traps) of surface S atoms in suppressing the recombination of photogenerated charges, and further attribute the inferior performance of excessive S-rich QDs to the impeded charge transfer from QDs to TiO2 and electrolyte. This work puts forward a simple surface engineering strategy for improving the performance of QDs PEC cells, providing an efficient method to guide the surface design of QDs for their applications in other optoelectronic devices.
RESUMEN
In this communication, we assembled ordered polystyrene (PS) microsphere array as a template with the drop-coating method, and the oxygen plasma was used to etch the template to adjust the spacing between the PS microspheres. Nano-triangular gold array and silver nano-pyramid array were obtained by ion beam sputtering to deposit precious metal gold and silver. We observed the surface morphology of Au and Au/Ag composite films by scanning electron microscope and characterized the films by X-ray diffraction and ultraviolet/visible light spectrophotometer. The results show that the etching time of oxygen plasma has an obvious effect in adjusting the spacing between PSs and has a significant effect on the morphology of Au structure.
RESUMEN
The rapid development of wearable electronics has led to an enormous demand for power sources that are wearable, small-scale, flexible and compatible. In this work, poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS) as the liquid electrode and silicone rubber as the triboelectric/encapsulation layer were introduced to design a stretchable PEDOT:PSS liquid electrode-based triboelectric nanogenerator (PL-TENG). The elastic silicone rubber and PEDOT:PSS liquid electrode with a special macromolecular structure endowed PL-TENG with extraordinary flexibility and conductivity simultaneously. Working under the single-electrode mode with different motion frequencies from 0.5 to 2.5 Hz, PL-TENG generated open-circuit voltage of 265 V, short-circuit current of 24.9 µA and short-circuit charge quantity of 85 nC. The output performances still maintained the original values after washing in saline, storing for one month and stretching 10 000 times. At the same time, PL-TENG could also produce stable electrical outputs even when deformed into a variety of shapes including stretching in different directions, bending and twisting. All of these features demonstrated the excellent resistance of PL-TENG to sweat, time and deformation. When attached to a human body, PL-TENG could provide a sufficiently stable power output to drive wearable electronics sustainably.