RESUMEN
Hydrogels are an attractive category of biointerfacing materials with adjustable mechanical properties, diverse biochemical functions, and good ionic conductivity. Despite these advantages, their application in electronics has been restricted because of their lack of semiconducting properties, and they have traditionally only served as insulators or conductors. We developed single- and multiple-network hydrogels based on a water-soluble n-type semiconducting polymer, endowing conventional hydrogels with semiconducting capabilities. These hydrogels show good electron mobilities and high on/off ratios, enabling the fabrication of complementary logic circuits and signal amplifiers with low power consumption and high gains. We demonstrate that hydrogel electronics with good bioadhesive and biocompatible interface can sense and amplify electrophysiological signals with enhanced signal-to-noise ratios.
RESUMEN
Highly dispersed Pt, such as Pt single atoms and atomic clusters, has great potential in the electrocatalytic hydrogen evolution reaction (HER) due to the high atomic efficiency and unique electronic configuration. Rationally regrating the electronic structure of Pt catalysts is desirable for promoting the HER performance. Herein, a 3D self-supported monolithic electrode consisting of Pt single atoms (PtSAs ) and Pt atomic clusters (PtACs ) anchored on sulfur-doped titanium nitride nanotubes (S-TiN NTs) encapsulated in polyaniline (PANI) on Ti mesh (PANI@Pt/S-TiN NTs/Ti) via a facile electrochemical strategy for efficient HER is designed and synthesized. Contributed by the unique structure and composition and the synergy of PtSAs , PtACs and S-TiN NTs, the PANI@Pt/S-TiN NTs/Ti electrode exhibits ultrahigh HER activities with only 12, 25 and 39 mV overpotentials at -10 mA cm-2 in acidic, alkaline and neutral media, respectively, and can maintain a stable performance for 25 h. Impressively, the mass activities are respectively up to 26.1, 22.4, and 17.7 times as that of Pt/C/CC electrode. Theoretical calculation results show that the synergistic effect of PtSAs , PtACs , and S-TiN NTs can optimize the electronic structure of Pt and generate multiple active sites with a thermodynamically favorable hydrogen adsorption free energy (ΔGH* ), thereby resulting in an enhanced HER activity.
