Hyungcheol Back

Efficient planar-heterojunction perovskite solar cells achieved via interfacial modification of a sol–gel ZnO electron collection layer

The importance of interfacial engineering as a new strategy for improving the power conversion efficiencies (PCEs) of planar-heterojunction (PHJ) perovskite solar cells is highlighted in this study. With our optimized interfacial modification, we demonstrated efficient PHJ perovskite solar cells with a high PCE of 12.2% using a sol–gel-processed ZnO ECL modified by [6,6]-phenyl C61 butyric acid methyl ester (PCBM).

Achieving long-term stable perovskite solar cells via ion neutralization

Despite recent reports of high power conversion efficiency (PCE) values of over 20%, the instability of perovskite solar cells (PSCs) has been considered the most serious obstacle toward their commercialization. By rigorously exploring the self-degradation process of planar-type PSCs using typical metal electrodes (Ag or Al), we found that the corrosion of the metal electrodes by inherent ionic defects in the perovskite layers is a major origin of intrinsic device degradation even under inert conditions. In this work, we have developed a new concept of a chemical inhibition in PSCs using amine-mediated metal oxide systems and succeeded in chemically neutralizing mobile ionic defects through mutual ionic interaction. As a consequence, we realized planar-type PSCs with long-term stability that maintain nearly 80% of their initial PCEs even after 1 year (9000 h) of storage under nitrogen and 80% of their initial PCEs after 200 h in ambient conditions without any encapsulation.

A series connection architecture for large-area organic photovoltaic modules with a 7.5% module efficiency

The fabrication of organic photovoltaic modules via printing techniques has been the greatest challenge for their commercial manufacture. Current module architecture, which is based on a monolithic geometry consisting of serially interconnecting stripe-patterned subcells with finite widths, requires highly sophisticated patterning processes that significantly increase the complexity of printing production lines and cause serious reductions in module efficiency due to so-called aperture loss in series connection regions. Herein we demonstrate an innovative module structure that can simultaneously reduce both patterning processes and aperture loss. By using a charge recombination feature that occurs at contacts between electron- and hole-transport layers, we devise a series connection method that facilitates module fabrication without patterning the charge transport layers. With the successive deposition of component layers using slot-die and doctor-blade printing techniques, we achieve a high module efficiency reaching 7.5% with area of 4.15 cm2.

High‐Performance Integrated Perovskite and Organic Solar Cells with Enhanced Fill Factors and Near‐Infrared Harvesting

Highly efficient P-I-N type perovskite/bulk-heterojunction (BHJ) integrated solar cells (ISCs) with enhanced fill factor (FF) (≈80%) and high near-infrared harvesting (>30%) are demonstrated by optimizing the BHJ morphology with a novel n-type polymer, N2200, and a new solvent-processing additive. This work proves the feasibility of highly efficient ISCs with panchromatic absorption as a new photovoltaic architecture and provides important design rules for optimizing ISCs.

Achieving Large‐Area Planar Perovskite Solar Cells by Introducing an Interfacial Compatibilizer

Despite the recent unprecedented increase in the power conversion efficiencies (PCEs) of small-area devices (≤0.1 cm2 ), the PCEs deteriorate drastically for PSCs of larger areas because of the incomplete film coverage caused by the dewetting of the hydrophilic perovskite precursor solutions on the hydrophobic organic charge-transport layers (CTLs). Here, an innovative method of fabricating scalable PSCs on all types of organic CTLs is reported. By introducing an amphiphilic conjugated polyelectrolyte as an interfacial compatibilizer, fabricating uniform perovskite films on large-area substrates (18.4 cm2 ) and PSCs with the total active area of 6 cm2 (1 cm2 × 6 unit cells) via a single-turn solution process is successfully demonstrated. All of the unit cells exhibit highly uniform PCEs of 16.1 ± 0.9% (best PCE of 17%), which is the highest value for printable PSCs with a total active area larger than 1 cm2 .

Soluble Transition Metal Oxide/Polymeric Acid Composites for Efficient Hole-Transport Layers in Polymer Solar Cells

We report a new method for developing a low-temperature solution processed vanadium oxide (s-VOx) and poly(4-styrene sulfonic acid) (PSS) composite to act as an efficient hole-transport layer (HTL) in polymer solar cells (PSCs). By compositing the s-VOx and PSS (s-VOx:PSS), the work function values of the s-VOx:PSS changed from 5.0 to 5.3 eV. Therefore, the energy level barrier between the HTL and organic active layer decreased, facilitating charge injection/extraction at the interfaces. In addition, the s-VOx:PSS films were denser and had more pin-hole-free surfaces than pristine s-VOx films, resulting in enhanced PSC performance due to significantly decreased leakage currents and excellent device stability in ambient condition. Because our approach of combining soluble transition metal oxide (TMO) and polymeric acid shows dramatically better performance than pristine TMO, we expect that it can provide useful guidelines for the synthesis and application of TMOs for organic electronics in the future.

Seamless polymer solar cell module architecture built upon self-aligned alternating interfacial layers

An efficient module cell architecture of a polymer solar cell built upon self-aligned alternating interfacial layers is presented. Alternating conventional and inverted subcells are serially connected on a single compound electrode with self-aligned interfacial layers. A high relative power conversion efficiency of 82% of the large-area module cell (4.24%) to the small-sized laboratory cells (5.19%) could be obtainable.

Long-Term Stable Recombination Layer for Tandem Polymer Solar Cells Using Self-Doped Conducting Polymers.

UNLABELLED Recently, the most efficient tandem polymer solar cells (PSCs) have used poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) ( PEDOT PSS) as a p-type component of recombination layer (RL). However, its undesirable acidic nature, originating from insulating PSS, of PEDOT PSS drastically reduces the lifetime of PSCs. Here, we demonstrate the efficient and stable tandem PSCs by introducing acid-free self-doped conducting polymer (SCP), combined with zinc oxide nanoparticles (ZnO NPs), as RL for PEDOT PSS-free tandem PSCs. Moreover, we introduce an innovative and versatile nanocomposite system containing photoactive and p-type conjugated polyelectrolyte (p-CPE) into the tandem fabrication of an ideal self-organized recombination layer. In our new RL, highly conductive SCP facilitates charge transport and recombination process, and p-CPE helps to achieve nearly loss-free charge collection by increasing effective work function of indium tin oxide (ITO) and SCP. Because of the synergistic effect of extremely low electrical resistance, ohmic contact, and pH neutrality, tandem devices with our novel RL performed well, exhibiting a high power conversion efficiency of 10.2% and a prolonged lifetime. These findings provide a new insight for strategic design of RLs using SCPs to achieve efficient and stable tandem PSCs and enable us to review and extend the usefulness of SCPs in various electronics research fields.

A New Architecture for Printable Photovoltaics Overcoming Conventional Module Limits

A new architecture for manufacturing large-area polymer solar cells that does not produce concomitant aperture and Ohmic losses is presented. By introducing the innovative concept of metal-filamentary nanoelectrodes, which are vertically formed inside the main active layers, loss-free, widely expandable solar cells with the highest relative power conversion efficiency (ca. 90%) in organic photovoltaic systems are demonstrated.

High-efficiency large-area perovskite photovoltaic modules achieved via electrochemically assembled metal-filamentary nanoelectrodes

We devised an electrochemical patterning process for large-area perovskite photovoltaic modules. Realizing industrial-scale, large-area photovoltaic modules without any considerable performance losses compared with the performance of laboratory-scale, small-area perovskite solar cells (PSCs) has been a challenge for practical applications of PSCs. Highly sophisticated patterning processes for achieving series connections, typically fabricated using printing or laser-scribing techniques, cause unexpected efficiency drops and require complicated manufacturing processes. We successfully fabricated high-efficiency, large-area PSC modules using a new electrochemical patterning process. The intrinsic ion-conducting features of perovskites enabled us to create metal-filamentary nanoelectrodes to facilitate the monolithic serial interconnections of PSC modules. By fabricating planar-type PSC modules through low-temperature annealing and all-solution processing, we demonstrated a notably high module efficiency of 14.0% for a total area of 9.06 cm2 with a high geometric fill factor of 94.1%.