Zhengke Li

Aggregation and morphology control enables multiple cases of high-efficiency polymer solar cells

Although the field of polymer solar cell has seen much progress in device performance in the past few years, several limitations are holding back its further development. For instance, current high-efficiency (>9.0%) cells are restricted to material combinations that are based on limited donor polymers and only one specific fullerene acceptor. Here we report the achievement of high-performance (efficiencies up to 10.8%, fill factors up to 77%) thick-film polymer solar cells for multiple polymer:fullerene combinations via the formation of a near-ideal polymer:fullerene morphology that contains highly crystalline yet reasonably small polymer domains. This morphology is controlled by the temperature-dependent aggregation behaviour of the donor polymers and is insensitive to the choice of fullerenes. The uncovered aggregation and design rules yield three high-efficiency (>10%) donor polymers and will allow further synthetic advances and matching of both the polymer and fullerene materials, potentially leading to significantly improved performance and increased design flexibility.

A Tetraphenylethylene Core‐Based 3D Structure Small Molecular Acceptor Enabling Efficient Non‐Fullerene Organic Solar Cells

A tetraphenylethylene core-based small molecular acceptor with a unique 3D molecular structure is developed. Bulk-heterojunction blend films with a small feature size (≈20 nm) are obtained, which lead to non-fullerene organic solar cells (OSCs) with 5.5% power conversion efficiency. The work provides a new molecular design approach to efficient non-fullerene OSCs based on 3D-structured small-molecule acceptors.

High-Performance Non-Fullerene Polymer Solar Cells Based on a Pair of Donor-Acceptor Materials with Complementary Absorption Properties.

A 7.3% efficiency non-fullerene polymer solar cell is realized by combining a large-bandgap polymer PffT2-FTAZ-2DT with a small-bandgap acceptor IEIC. The complementary absorption of donor polymer and small-molecule acceptor is responsible for the high-performance of the solar-cell device. This work provides important guidance to improve the performance of non-fullerene polymer solar cells.

Donor polymer design enables efficient non-fullerene organic solar cells.

To achieve efficient organic solar cells, the design of suitable donor–acceptor couples is crucially important. State-of-the-art donor polymers used in fullerene cells may not perform well when they are combined with non-fullerene acceptors, thus new donor polymers need to be developed. Here we report non-fullerene organic solar cells with efficiencies up to 10.9%, enabled by a novel donor polymer that exhibits strong temperature-dependent aggregation but with intentionally reduced polymer crystallinity due to the introduction of a less symmetric monomer unit. Our comparative study shows that an analogue polymer with a C2 symmetric monomer unit yields highly crystalline polymer films but less efficient non-fullerene cells. Based on a monomer with a mirror symmetry, our best donor polymer exhibits reduced crystallinity, yet such a polymer matches better with small molecular acceptors. This study provides important insights to the design of donor polymers for non-fullerene organic solar cells.

A Difluorobenzoxadiazole Building Block for Efficient Polymer Solar Cells

A difluorobenzoxadiazole building block is synthesized and utilized to construct a conjugated polymer leading to high-performance thick-film polymer solar cells with a V(OC) of 0.88 V and a power conversion efficiency of 9.4%. This new building block can be used in many possible polymer structures for various organic electro-nic applications.

Efficient non-fullerene polymer solar cells enabled by tetrahedron-shaped core based 3D-structure small-molecular electron acceptors

Here we report a series of tetraphenyl carbon-group (tetraphenylmethane (TPC), tetraphenylsilane (TPSi) and tetraphenylgermane (TPGe)) core based 3D-structure non-fullerene electron acceptors, enabling efficient polymer solar cells with a power conversion efficiency (PCE) of up to ∼4.3%. The results show that TPC and TPSi core-based polymer solar cells (PSCs) perform significantly better than that based on TPGe. Our study provides a new approach for designing small molecular acceptor materials for polymer solar cells.

Reduced Intramolecular Twisting Improves the Performance of 3D Molecular Acceptors in Non‐Fullerene Organic Solar Cells

A small-molecular acceptor, tetraphenylpyrazine-perylenediimide tetramer (TPPz-PDI4 ), which has a reduced extent of intramolecular twisting compared to two other small-molecular acceptors is designed. Benefiting from the lowest extent of intramolecular twisting, TPPz-PDI4 exhibits the highest aggregation tendency and electron mobility, and therefore achieves a highest power conversion efficiency of 7.1%.

Photonic bandgaps in disordered inverse-opal photonic crystals

Three-dimensional photonic crystals with full bandgaps at optical wavelengths can be fabricated with inverse-opal techniques. We have shown that the bandgap is extremely sensitive to the presence of geometric disorder in the crystals (see Figure). The bandgap closes completely with a disorder strength as small as under two percent of the lattice constant. This fragility persists even at very high refractive index contrasts and is attributed to the creation of a bandgap at high frequency bands (8–9 bands) in inverse-opal crystals. This should impose severe demand on the quality of lattice uniformity.

An All-Solution Processed Recombination Layer with Mild Post-Treatment Enabling Efficient Homo-Tandem Non-fullerene Organic Solar Cells.

The first homo-tandem non-fullerene organic solar cell enabled by a novel recombination layer which only requires a very mild thermal annealing treatment is reported. The best efficiency achieved is 10.8% with a Voc over 2.1 V, which is the highest Voc for double-junction organic solar cells reported to date.

Quantitative relations between interaction parameter, miscibility and function in organic solar cells

Although it is known that molecular interactions govern morphology formation and purity of mixed domains of conjugated polymer donors and small-molecule acceptors, and thus largely control the achievable performance of organic solar cells, quantifying interaction–function relations has remained elusive. Here, we first determine the temperature-dependent effective amorphous–amorphous interaction parameter, χaa(T), by mapping out the phase diagram of a model amorphous polymer:fullerene material system. We then establish a quantitative ‘constant-kink-saturation’ relation between χaa and the fill factor in organic solar cells that is verified in detail in a model system and delineated across numerous high- and low-performing materials systems, including fullerene and non-fullerene acceptors. Our experimental and computational data reveal that a high fill factor is obtained only when χaa is large enough to lead to strong phase separation. Our work outlines a basis for using various miscibility tests and future simulation methods that will significantly reduce or eliminate trial-and-error approaches to material synthesis and device fabrication of functional semiconducting blends and organic blends in general.This work reports a quantitative investigation of the interaction parameter and miscibility of donor and acceptor organic molecules and their relationship with the fill factor and photovoltaic performance of bulk-heterojunction organic solar cells.