The arch-shaped single electrode based triboelectric nanogenerator (TENG) is fabricated using thin film of reduced graphene oxide nanoribbons (rGONRs) with polyvinylidene fluoride (PVDF) polymer used as binder to effectively convert mechanical energy into electrical energy. The incorporation of rGONRs in PVDF polymer enhances average surface roughness of rGONRs/PVDF thin film. With the combination of the enhancement of average roughness and production of functional groups, which indicate improve charge storage capacity of prepared film. Furthermore, the redox peaks obtained through cyclic voltammetry were identified more in rGONRs/PVDF composite in comparison to pristine rGONRs to confirm charge transfer capability of film. Herein, the output performance was discussed experimentally as well as theoretically, maximum voltage was obtained to be 0.35 V. The newly designed TENG to harvest mechanical energy and opens up many new avenues of research in the energy harvesting applications.
The utilization of wide bandgap (WBG) tin halide perovskites (Sn‐HPs) offers an environmentally friendly alternative for multi‐junction Sn‐HP photovoltaics. Nonetheless, rapid crystallization leads to suboptimal film morphology and substantial creation of defect states, which undermine device efficiency. This study introduces 4‐Phenylthiosemicarbazide (4PTSC) as an additive to achieve a densely packed Sn‐HP film with fewer imperfections. The strong chemical coordination between SnI2 and the functional groups S═C─N (Sn···S═C─N), NH2, and phenyl conjugation enhances solution stability and supports the delay of perovskite crystallization through adduct formation. This process yields pinhole‐free films with preferred grain growth. 4PTSC acts as a strong coordination complex and a reducing agent to passivate uncoordinated Sn2+ and halide ions and reduce the formation of SnI4, thereby reducing defect formation. The π‐conjugated phenyl ring in the 4PTSC facilitates the preferred crystal growth orientation of perovskite grains. Furthermore, the hydrophobic nature of 4PTSC mitigates Sn2+ oxidation by repelling moisture, enhancing stability. The open circuit voltage significantly increased from 0.78 to 0.94 V, resulting in achieving the champion efficiency of 12.22% (certified 11.70%), surpassing all previously reported efficiencies for WBG Sn halide perovskite solar cells. Additionally, the unencapsulated 4PTSC‐1.0 device maintained outstanding stability over 1200 h under ambient atmospheric conditions.
The PEAI additive helps in the crystal growth regulation of CsPbI 2 Br perovskite, which contributes to indoor/outdoor photovoltaic implementation with exceptional conversion efficiency.
1 June 2017 in Physica E: Low-dimensional Systems and Nanostructures