This paper discusses a series of triphenylamine dibenzofulvene–based hole transporting materials (HTMs) featuring different numbers of MeO groups (none for YC‐1, four for YC‐2, and six for YC‐3) and their use in p‐i‐n perovskite solar cells (PSCs). We investigated the optoelectronic properties of these HTMs and found that the PSC devices incorporating YC‐1 as HTMs exhibited power conversion efficiencies (PCEs) of 15.78 ± 0.61%, which outperformed the corresponding PEDOT:PSS‐based device (12.80 ± 1.31%) under similar testing conditions. We then employed YC‐1 for the interfacial modified layer of a NiOx‐derived PSC having the structure ITO/NiOx/YC‐1/CH3NH3PbI3/PC61BM/bathocuproine/Ag. The presence of YC‐1 promoted the growth of micrometer‐sized grains of perovskite and induced a lower content of grain boundary defects, both of which improved the carrier extraction. Thereby, compared with conventional NiOx device, we observed a great increase in the PCE, from 17.16 ± 0.68% to 18.81 ± 0.42%, with a champion cell displaying a PCE of 19.37% (with negligible hysteresis). The corresponded device exhibited a stabilized efficiency of approximately 19% after storage in the dark at 25°C under argon for over 1000 hours. This study suggests a new approach for designing the high‐performance stable p‐i‐n PSCs.
Five organosoluble visible light benzophenone derivatives (BPs), incorporated different arylamine as electron donating groups have been synthesized and investigated for their roles as photoinitiating systems for free radical photopolymerization of acrylate monomer upon the UV and LED exposure. All the target compounds (BP-1-5) have confirmed through 1 H NMR, HR-MS/EI-MS spectra and elemental analysis. BPs displayed red-shifted absorption, higher molar extinction coefficient and better thermal properties as compared to reference benzophenone (BP) compound. BP and BPs in combination with hydrogen donor, triethylamine (TEA), are prepared and investigated their electron spin resonance (ESR) spectroscopy and photo-DSC (photo-differential scanning calorimetry). ESR spectra of BP-1/TEA package showed the highest radical intensity among the test photoinitiator packages. In addition, BP-1-based formulation exhibited the best double bond conversion efficiency than other BPs and comparable to the BP for the free radical polymerization (FRP) of TMPTA under similar UV light source. We then selected BP-1/TEA and BP/TEA package for FRP under LED light irradiation. Interesting, the BP-1/ TEA system exhibited better efficiency and shorter time at maximum heat flow than BP/TEA. This result indicates BP-1 photoinitiator not only displays good light harvesting, thermal property, but exhibits conversion efficiency under the irradiation of UV and LED.
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