Eliminating the solvent blocking requirement of interconnection layers in polymer tandem solar cells by thin-film transfer technique.

Interconnection layers (ICLs) for polymer tandem solar cells reported so far are limited in materials' choice and layer structure, because of a requirement that the ICLs must prevent the penetration of solvents used for the top cells. In this research, it is demonstrated that depositing the active layer of the top subcell using a dry thin-film transfer technique allows for incorporation of an ICL composed of vacuum deposited materials in a polymer tandem cell, providing a large degree of freedom in ICL design. Specifically, a polymer tandem solar cell was fabricated using an ICL composed of bathocuproine:silver/silver islands/1,4,5,8,9,11-hexaazatriphenylene hexacarbonitrile (BCP:Ag/Ag islands/HAT-CN), where the thicknesses of the BCP:Ag and Ag island layers are precisely controlled at the nanoscale to facilitate the transport of electrons generated in the bottom subcell and to ensure their efficient recombination with holes generated in the top subcell. Consequently, the tandem device featuring the optimized ICL, whose active layers are composed of poly(3-hexylthiophene):[6,6]-phenyl-C61-butyric acid methyl ester (P3HT:PC61BM) and poly[2,6-(4,4-bis-(2-ethylhexyl)-4H-cyclopenta[2,1-b;3,4-b']dithiophene)-alt-4,7-(2,1,3-benzothiadiazole)]:[6,6]-phenyl-C71-butyric acid methyl ester (PCPDTBT:PC71BM), exhibits an open-circuit voltage of 1.20 V, which is equal to the sum of the open-circuit voltages of the two subcells, with a fill factor (FF) of 0.60 almost identical to the FFs of the subcells.

Hybrid Organic Tandem Solar Cell Comprising Small-Molecule Bottom and Polymer:Fullerene Top Subcells Fabricated by Thin-Film Transfer.

Multilayer structures involving solution-deposited polymer films are difficult to fabricate, not allowing for unrestricted designs of polymer-based optoelectronic devices required for maximizing their performance. Here, we fabricate a hybrid organic tandem solar cell whose top and bottom subcells have polymer:fullerene and small molecules active layers, respectively, by a solvent-free process based on transferring the polymer:fullerene layer from an elastomeric stamp onto a vacuum-deposited bottom subcell. The interface between small-molecule and transferred polymer:fullerene layers is void-free at the nanoscale, allowing for efficient charge transport across the interface. Consequently, the transfer-fabricated tandem cell has an open-circuit voltage (V OC) almost identical to the sum of V OC values for the single-junction devices. The short-circuit current density (J SC) of the tandem cell is maximized by current matching achieved by varying the thickness of the small-molecule active layer in the bottom subcell, which is verified by numerical simulations. The optimized transfer-fabricated tandem cell, whose active layers are composed of poly[2,1,3-benzothiadiazole-4,7-diyl[4,4-bis(2-ethylhexyl)-4H-cyclopenta[2,1-b:3,4-b']dithiophene-2,6-diyl]]:[6,6]-Phenyl-C71-butyric acid methyl ester and Di-[4-(N,N-di-p-tolyl-amino)-phenyl]cyclohexane:C70, has V OC = 1.46 V, J SC = 8.48 mA/cm2, a fill factor of 0.51, leading to the power-conversion efficiency of 6.26%, the highest among small molecule-polymer:fullerene hybrid tandem solar cells demonstrated so far.

A dual-scale metal nanowire network transparent conductor for highly efficient and flexible organic light emitting diodes.

Although solution processed metal nanowire (NW) percolation networks are a strong candidate to replace commercial indium tin oxide, their performance is limited in thin film device applications due to reduced effective electrical areas arising from the dimple structure and percolative voids that single size metal NW percolation networks inevitably possess. Here, we present a transparent electrode based on a dual-scale silver nanowire (AgNW) percolation network embedded in a flexible substrate to demonstrate a significant enhancement in the effective electrical area by filling the large percolative voids present in a long/thick AgNW network with short/thin AgNWs. As a proof of concept, the performance enhancement of a flexible phosphorescent OLED is demonstrated with the dual-scale AgNW percolation network compared to the previous mono-scale AgNWs. Moreover, we report that mechanical and oxidative robustness, which are critical for flexible OLEDs, are greatly increased by embedding the dual-scale AgNW network in a resin layer.