ABSTRACT
Organic photovoltaics (OPVs) with nonfullerene acceptors (NFAs) feature excellent device performance and device stability. However, they are facing problems when the amine-rich polyelectrolytes are used as cathode interfacial layers. In this work, a small molecule, ethanedithiol (EDT) at the polyethyleneimine ethoxylated (PEIE)/active layer interface is inserted for mitigating the undesirable reaction between amine-rich groups and electron-acceptor moieties in NFA. The main role of EDT is to passivate the PEIE surface and prevent electron flow to NFA and the unwanted reaction can be mitigated. It improves the performance of OPV devices by reducing the work function, decreasing trap-assisted recombination, and improving electron-mobility. As a result, the flexible device with the PEIE interfacial layer with a power conversion efficiency (PCE) of 7.20% can be improved to 10.11% after the inclusion of EDT. Moreover, EDT-modified device can retain 98.18% after it is bent for 200 cycles and can maintain 80.83% of its initial PCE under continuous light illuminated in ambient conditions without any encapsulation. Based on these findings, the proposed strategy constitutes a crucial step toward highly efficient flexible OPVs.
ABSTRACT
Indoor photovoltaics (IPVs) have great potential to provide a self-sustaining power source for Internet-of-Things (IoT) devices. The rapid growth in demand for low-power IoT devices for indoor application not only boosts the development of high-performance IPVs, but also promotes the electronics and semiconductor industry for the design and development of ultra-low-power IoT systems. In this Review, the recent progress in IPV technologies, design rules, market trends, and future prospects for highly efficient indoor photovoltaics are discussed. Special attention is given to the progress and development of organic photovoltaics (OPVs), which demonstrate great possibilities for IPVs, owing to their bandgap tunability, high absorbance coefficient, semitransparency, solution processability, and easy large-area manufacturing on flexible substrates. Highly efficient indoor organic photovoltaics (IOPVs) can be realized through designing efficient donor and acceptor absorber materials that have good spectral responses in the visible region and better energy-aligned interfacial layers, and through modulation of optical properties. Interfacial engineering, photovoltage losses, device stability, and large-area organic photovoltaic modules are surveyed to understand the mechanisms of efficient power conversion and challenges for IOPVs under indoor conditions as a self-sustaining power source for IoT devices. Finally, the prospects for further improve in IOPV device performance and practical aspects of integrating IOPVs in low-power IoT devices are discussed.
ABSTRACT
Photoelectrochemical (PEC) water splitting is an alternative to fossil fuel combustion involving the generation of renewable hydrogen without environmental pollution or greenhouse gas emissions. Cuprous oxide (Cu2O) is a promising semiconducting material for the simple reduction of hydrogen from water, in which the conduction band edge is slightly negative compared to the water reduction potential. However, the solar-to-hydrogen conversion efficiency of Cu2O is lower than the theoretical value due to a short carrier-diffusion length under the effective light absorption depth. Thus, increasing light absorption in the electrode-electrolyte interfacial layer of a Cu2O photoelectrode can enhance PEC performance. In this study, a Cu2O 3D photoelectrode comprised of pyramid arrays was fabricated using a two-step method involving direct-ink-writing of graphene structures. This was followed by the electrodeposition of a Cu current-collecting layer and a p-n homojunction Cu2O photocatalyst layer onto the printed structures. The performance for PEC water splitting was enhanced by increasing the total light absorption area (A a) of the photoelectrode via controlling the electrode topography. The 3D photoelectrode (A a = 3.2 cm2) printed on the substrate area of 1.0 cm2 exhibited a photocurrent (I ph) of -3.01 mA at 0.02 V (vs. RHE), which is approximately three times higher than that of a planar photoelectrode with an A a = 1.0 cm2 (I ph = -0.91 mA). Our 3D printing strategy provides a flexible approach for the design and the fabrication of highly efficient PEC photoelectrodes.
ABSTRACT
The data provided in this data set is the study of organic-inorganic hybrid perovskite solar cells fabricated through incorporating the small amounts of ammonium halide NH4X (X = F, Cl, Br, I) additives into a CH3NH3PbI3 (MAPbI3) perovskite solution and is published as "High-Performance CH3NH3PbI3 Inverted Planar Perovskite Solar Cells via Ammonium Halide Additives", available in Journal of Industrial and Engineering Chemistry [1]. A compact and uniform perovskite absorber layer with large perovskite crystalline grains, is realized by simply incorporating small amounts of additives into precursor solutions, and utilizing the anti-solvent engineering technique to control the nucleation and growth of perovskite crystal, turning out the enhanced device efficiency (NH4F: 14.88 ± 0.33%, NH4Cl: 16.63 ± 0.21%, NH4Br: 16.64 ± 0.35%, and NH4I: 17.28 ± 0.15%) compared to that of a reference MAPbI3 device (Ref.: 12.95 ± 0.48%). In addition, this simple technique of ammonium halide addition to precursor solutions increase the device reproducibility as well as long term stability.
ABSTRACT
Doping is a widely-implemented strategy for enhancing the inherent electronic properties of charge transport layers in photovoltaic devices. A facile solution-processed zinc oxide (ZnO) and various cation and anion-doped ZnO layers were synthesized via the sol-gel method and employed as electron transport layers (ETLs) for inverted polymer solar cells (PSCs). The results indicated that all PSCs with doped ZnO ETLs exhibited better photovoltaic performance compared with the PSCs with a pristine ZnO ETL. By exploring the role of various anion and cation dopants (three compounds with the same Al3+ cation: Al(acac)3, Al(NO3)3, AlCl3 and three compounds with the same Cl- anion: NH4Cl, MgCl2, AlCl3), we found that the work function changed to favor electronic extraction only when the Cl anion was involved. In addition, the conductivity of ZnO was enhanced more with the Al3+ cation. Therefore, in inverted solar cells, doping with Al3+ and Cl- delivered the best power conversion efficiency (PCE). The maximum PCE of 10.38% was achieved from the device with ZnO doped with Al+ and Cl-.
ABSTRACT
The reduction of charge carrier recombination and intrinsic defect density in organic-inorganic halide perovskite absorber materials is a prerequisite to achieving high-performance perovskite solar cells with good efficiency and stability. Here, we fabricated inverted planar perovskite solar cells by incorporation of a small amount of excess organic/inorganic halide (methylammonium iodide (CH3NH3I; MAI), formamidinium iodide (CH(NH2)2I; FAI), and cesium iodide (CsI)) in CH3NH3PbI3 perovskite film. Larger crystalline grains and enhanced crystallinity in CH3NH3PbI3 perovskite films with excess organic/inorganic halide reduce the charge carrier recombination and defect density, leading to enhanced device efficiency (MAI+: 14.49 ± 0.30%, FAI+: 16.22 ± 0.38% and CsI+: 17.52 ± 0.56%) compared to the efficiency of a control MAPbI3 device (MAI: 12.63 ± 0.64%) and device stability. Especially, the incorporation of a small amount of excess CsI in MAPbI3 perovskite film leads to a highly reproducible fill factor of over 83%, increased open-circuit voltage (from 0.946 to 1.042 V), and short-circuit current density (from 18.43 to 20.89 mA/cm2).
ABSTRACT
A series of four donor-acceptor alternating copolymers based on dialkyloxy-benzothiadiazole (ROBT) as an acceptor and thienoacenes as donor units were synthesized and tested for polymer solar cells (PSCs). These new polymers had different donor units with varied electron-donating ability (thieno[3,2-b]thiophene (TT), dithieno[3,2-b:2',3'-d]thiophene (DTT), benzo[1,2-b:4,5-b']dithiophene (BDT), and naphtha[1,2-b:5,6-b']dithiophene (NDT)) in the polymer backbone. To understand the effect of these thienoacenes on the optoelectronic and photovoltaic properties of the copolymers, we systematically analyzed and compared the energy levels, crystallinity, morphology, charge recombination, and charge carrier mobility in the resulting polymers. In this series, optimized photovoltaic cells yielded power conversion efficiency (PCE) values of 6.25% (TT), 9.02% (DTT), 6.34% (BDT), and 2.29% (NDT) with different thienoacene donors. The introduction of DTT into the thienoacene-ROBT polymer enabled the generation of well-ordered molecular packings with a π-π stacking distance of 3.72 Å, high charge mobilities, and an interconnected nanofibrillar morphology in blend films. As a result, the PSC employing the polymer with DTT exhibited the highest PCE of 9.02%. Thus, our structure-property relationship studies of thienoacene-ROBT-based polymers emphasize that the molecular design of the polymers must be carefully optimized to develop high efficient PSCs. These findings will help us to understand the impact of the donor thienoacene on the optoelectronic and photovoltaic performance of polymers.
