Wuyue Liu

Bio: Wuyue Liu is an academic researcher from Chinese Academy of Sciences. The author has contributed to research in topics: Organic solar cell & Materials science. The author has an hindex of 5, co-authored 6 publications receiving 329 citations.

Organic Solar Cells with 18% Efficiency Enabled by an Alloy Acceptor: A Two-in-One Strategy

Abstract: The trade-off between the open-circuit voltage (Voc ) and short-circuit current density (Jsc ) has become the core of current organic photovoltaic research, and realizing the minimum energy offsets that can guarantee effective charge generation is strongly desired for high-performance systems. Herein, a high-performance ternary solar cell with a power conversion efficiency of over 18% using a large-bandgap polymer donor, PM6, and a small-bandgap alloy acceptor containing two structurally similar nonfullerene acceptors (Y6 and AQx-3) is reported. This system can take full advantage of solar irradiation and forms a favorable morphology. By varying the ratio of the two acceptors, delicate regulation of the energy levels of the alloy acceptor is achieved, thereby affecting the charge dynamics in the devices. The optimal ternary device exhibits more efficient hole transfer and exciton separation than the PM6:AQx-3-based system and reduced energy loss compared with the PM6:Y6-based system, contributing to better performance. Such a "two-in-one" alloy strategy, which synergizes two highly compatible acceptors, provides a promising path for boosting the photovoltaic performance of devices.

A Twisted Thieno[3,4-b]thiophene-Based Electron Acceptor Featuring a 14-π-Electron Indenoindene Core for High-Performance Organic Photovoltaics

Abstract: With an indenoindene core, a new thieno[3,4-b]thiophene-based small-molecule electron acceptor, 2,2'-((2Z,2'Z)-((6,6'-(5,5,10,10-tetrakis(2-ethylhexyl)-5,10-dihydroindeno[2,1-a]indene-2,7-diyl)bis(2-octylthieno[3,4-b]thiophene-6,4-diyl))bis(methanylylidene))bis(5,6-difluoro-3-oxo-2,3-dihydro-1H-indene-2,1-diylidene))dimalononitrile (NITI), is successfully designed and synthesized. Compared with 12-π-electron fluorene, a carbon-bridged biphenylene with an axial symmetry, indenoindene, a carbon-bridged E-stilbene with a centrosymmetry, shows elongated π-conjugation with 14 π-electrons and one more sp3 carbon bridge, which may increase the tunability of electronic structure and film morphology. Despite its twisted molecular framework, NITI shows a low optical bandgap of 1.49 eV in thin film and a high molar extinction coefficient of 1.90 × 105 m-1 cm-1 in solution. By matching NITI with a large-bandgap polymer donor, an extraordinary power conversion efficiency of 12.74% is achieved, which is among the best performance so far reported for fullerene-free organic photovoltaics and is inspiring for the design of new electron acceptors.

n-Type Molecular Photovoltaic Materials: Design Strategies and Device Applications.

Abstract: The use of photovoltaic technologies has been regarded as a promising approach for converting solar energy to electricity and mitigating the energy crisis, and among these, organic photovoltaics (O...

Design of All-Fused-Ring Electron Acceptors with High Thermal, Chemical, and Photochemical Stability for Organic Photovoltaics

Abstract: High-performance donor–acceptor electron acceptors containing 2-(3-oxo-2,3-dihydro-1H-inden-1-ylidene)malononitrile (INCN)-type terminals are labile toward photooxidation and basic conditions, and ...

Theory‐Guided Material Design Enabling High‐Performance Multifunctional Semitransparent Organic Photovoltaics without Optical Modulations

Abstract: Semitransparent organic photovoltaics (ST‐OPVs) have drawn great attention for promising applications in building‐integrated photovoltaics, providing additional power generation for daily use. A previously proposed strategy, “complementary NIR absorption,” is widely applied for high‐performance ST‐OPVs. However, rational material design toward high performance has not been achieved. In this work, an external quantum efficiency (EQE) model describing this strategy is developed to explore the full potential of material design on ST‐OPV performance. Guided by the model, a novel nonfullerene acceptor (NFA), ATT‐9, is designed and synthesized, which possesses optimal bandgap for ST‐OPVs, achieving a record short‐circuit current density of 30 mA cm−2 and a power conversion efficiency of 13.40%, the highest value among devices based on NFAs with bandgaps lower than 1.2 eV. It is notworthy that, at such a low bandgap, the energy loss of the device is only 0.58 eV, which is attributed to the low energetic disorder confirmed by an ultralow Urbach energy of 21.6 meV. Benefiting from the optimal bandgap and low energy loss, the ATT‐9‐based ST‐OPV achieves a high light utilization efficiency of 3.33% without optical modulations, and meanwhile shows excellent thermal insulation, exceeding the commercial 3M heat‐insulating window film, demonstrating the outstanding application prospects of multifunctional ST‐OPVs.

Over 14% Efficiency in Organic Solar Cells Enabled by Chlorinated Nonfullerene Small-Molecule Acceptors.

Abstract: To make organic solar cells (OSCs) more competitive in the diverse photovoltaic cell technologies, it is very important to demonstrate that OSCs can achieve very good efficiencies and that their cost can be reduced. Here, a pair of nonfullerene small-molecule acceptors, IT-2Cl and IT-4Cl, is designed and synthesized by introducing easy-synthesis chlorine substituents onto the indacenodithieno[3,2-b]thiophene units. The unique feature of the large dipole moment of the C-Cl bond enhances the intermolecular charge-transfer effect between the donor-acceptor structures, and thus expands the absorption and down shifts the molecular energy levels. Meanwhile, the introduction of C-Cl also causes more pronounced molecular stacking, which also helps to expand the absorption spectrum. Both of the designed OSCs devices based on two acceptors can deliver a power conversion efficiency (PCE) greater than 13% when blended with a polymer donor with a low-lying highest occupied molecular orbital level. In addition, since IT-2Cl and IT-4Cl have very good compatibility, a ternary OSC device integrating these two acceptors is also fabricated and obtains a PCE greater than 14%. Chlorination demonstrates effective ability in enhancing the device performance and facile synthesis route, which both deserve further exploitation in the modification of photovoltaic materials.

A Wide Band Gap Polymer with a Deep Highest Occupied Molecular Orbital Level Enables 14.2% Efficiency in Polymer Solar Cells.

Abstract: To simultaneously achieve low photon energy loss (Eloss) and broad spectral response, the molecular design of the wide band gap (WBG) donor polymer with a deep HOMO level is of critical importance in fullerene-free polymer solar cells (PSCs). Herein, we developed a new benzodithiophene unit, i.e., DTBDT-EF, and conducted systematic investigations on a WBG DTBDT-EF-based donor polymer, namely, PDTB-EF-T. Due to the synergistic electron-withdrawing effect of the fluorine atom and ester group, PDTB-EF-T exhibits a higher oxidation potential, i.e., a deeper HOMO level (ca. −5.5 eV) than most well-known donor polymers. Hence, a high open-circuit voltage of 0.90 V was obtained when paired with a fluorinated small molecule acceptor (IT-4F), corresponding to a low Eloss of 0.62 eV. Furthermore, side-chain engineering demonstrated that subtle side-chain modulation of the ester greatly influences the aggregation effects and molecular packing of polymer PDTB-EF-T. With the benefits of the stronger interchain π–π int...

High-efficiency small-molecule ternary solar cells with a hierarchical morphology enabled by synergizing fullerene and non-fullerene acceptors

Abstract: Using combinatory photoactive blends is a promising approach to achieve high power conversion efficiency in ternary organic photovoltaics However, the fundamental challenge of how to manipulate th

Dithieno[3,2-b:2',3'-d]pyrrol Fused Nonfullerene Acceptors Enabling Over 13% Efficiency for Organic Solar Cells.

Abstract: A new electron-rich central building block, 5,5,12,12-tetrakis(4-hexylphenyl)-indacenobis-(dithieno[3,2-b:2',3'-d]pyrrol) (INP), and two derivative nonfullerene acceptors (INPIC and INPIC-4F) are designed and synthesized. The two molecules reveal broad (600-900 nm) and strong absorption due to the satisfactory electron-donating ability of INP. Compared with its counterpart INPIC, fluorinated nonfullerene acceptor INPIC-4F exhibits a stronger near-infrared absorption with a narrower optical bandgap of 1.39 eV, an improved crystallinity with higher electron mobility, and down-shifted highest occupied molecular orbital and lowest unoccupied molecular orbital energy levels. Organic solar cells (OSCs) based on INPIC-4F exhibit a high power conversion efficiency (PCE) of 13.13% and a relatively low energy loss of 0.54 eV, which is among the highest efficiencies reported for binary OSCs in the literature. The results demonstrate the great potential of the new INP as an electron-donating building block for constructing high-performance nonfullerene acceptors for OSCs.

Layer-by-Layer Processed Ternary Organic Photovoltaics with Efficiency over 18.

Abstract: Obtaining a finely tuned morphology of the active layer to facilitate both charge generation and charge extraction has long been the goal in the field of organic photovoltaics (OPVs). Here, a solution to resolve the above challenge via synergistically combining the layer-by-layer (LbL) procedure and the ternary strategy is proposed and demonstrated. By adding an asymmetric electron acceptor, BTP-S2, with lower miscibility to the binary donor:acceptor host of PM6:BO-4Cl, vertical phase distribution can be formed with donor-enrichment at the anode and acceptor-enrichment at the cathode in OPV devices during the LbL processing. In contrast, LbL-type binary OPVs based on PM6:BO-4Cl still show bulk-heterojunction like morphology. The formation of the vertical phase distribution can not only reduce charge recombination but also promote charge collection, thus enhancing the photocurrent and fill factor in LbL-type ternary OPVs. Consequently, LbL-type ternary OPVs exhibit the best efficiency of 18.16% (certified: 17.8%), which is among the highest values reported to date for OPVs. The work provides a facile and effective approach for achieving high-efficiency OPVs with expected morphologies, and demonstrates the LbL-type ternary strategy as being a promising procedure in fabricating OPV devices from the present laboratory study to future industrial production.