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The medium-bandgap polymerized small molecule acceptors (PSMAs) have broad application scenarios. However, the effort in the molecular design of the high-performance medium-bandgap PSMAs is limited. In this article, we introduce alkoxy groups as outer side chains and as substituents of the thiophene π-bridges of the high-performance PSMA PY-IT to synthesize a medium-bandgap PSMA PO-TO. Due to that the non-covalent interaction between the alkoxy groups and the terminal groups of the small molecule acceptor (SMA) unit can weaken the intramolecular charge transfer (ICT) effect, the bandgap of PO-TO is enlarged and its absorption is blue-shifted compared with PY-IT, while the absorbance of PO-TO solution and film is enhanced significantly compare with that of PY-IT. When blended PO-TO with the polymer donor PBQx-TF, the corresponding all-polymer solar cells (all-PSCs) exhibit an open-circuit voltage (Voc) exceeding 1.04 V with a power conversion efficiency (PCE) of 13.75%. Furthermore, PO-TO was used as the third component to fabricate ternary all-PSCs with PBQx-TF as the polymer donor and PY-IT as the main polymer acceptor, and the ternary all-PSCs based on PBQx-TF:PY-IT:PO-TO (1:1:0.2, w/w/w) demonstrated a high PCE of 17.71% with simultaneously improved Voc of 0.940 V, short-circuit current density (Jsc) of 24.60 mA cm−2 and fill factor (FF) of 76.81%. In comparison, the binary all-PSCs based on PBQx-TF:PY-IT showed a PCE of 16.77%. This result indicates that introducing alkoxy groups is a promising strategy for synthesizing high-performance medium-bandgap PSMAs. [ABSTRACT FROM AUTHOR]

Reducing the energy loss of sub-cells is critical for high performance tandem organic solar cells, while it is limited by the severe non-radiative voltage loss via the formation of non-emissive triplet excitons. Herein, we develop an ultra-narrow bandgap acceptor BTPSeV-4F through replacement of terminal thiophene by selenophene in the central fused ring of BTPSV-4F, for constructing efficient tandem organic solar cells. The selenophene substitution further decrease the optical bandgap of BTPSV-4F to 1.17 eV and suppress the formation of triplet exciton in the BTPSV-4F-based devices. The organic solar cells with BTPSeV-4F as acceptor demonstrate a higher power conversion efficiency of 14.2% with a record high short-circuit current density of 30.1 mA cm−2 and low energy loss of 0.55 eV benefitted from the low non-radiative energy loss due to the suppression of triplet exciton formation. We also develop a high-performance medium bandgap acceptor O1-Br for front cells. By integrating the PM6:O1-Br based front cells with the PTB7-Th:BTPSeV-4F based rear cells, the tandem organic solar cell demonstrates a power conversion efficiency of 19%. The results indicate that the suppression of triplet excitons formation in the near-infrared-absorbing acceptor by molecular design is an effective way to improve the photovoltaic performance of the tandem organic solar cells. Reducing energy loss of sub-cells is critical for high performance tandem organic solar cells. Here, the authors design and synthesize an ultra-narrow bandgap acceptor through replacement of terminal thiophene by selenophene in the central fused ring, achieving efficiency of 19% for tandem cells. [ABSTRACT FROM AUTHOR]

The polymerized small-molecule acceptors have attracted great attention for application as polymer acceptor in all-polymer solar cells recently. The modification of small molecule acceptor building block and the π-bridge linker is an effective strategy to improve the photovoltaic performance of the polymer acceptors. In this work, we synthesized a new polymer acceptor PG-IT2F which is a modification of the representative polymer acceptor PY-IT by replacing its upper linear alkyl side chains on the small molecule building block with branched alkyl chains and attaching difluorene substituents on its thiophene π-bridge linker. Through this synergistic optimization, PG-IT2F possesses more suitable phase separation, increased charge transportation, better exciton dissociation, lower bimolecular recombination, and longer charge transfer state lifetime than PY-IT in their polymer solar cells with PM6 as polymer donor. Therefore, the devices based on PM6:PG-IT2F demonstrated a high power conversion efficiency of 17.24%, which is one of the highest efficiency reported for the binary all polymer solar cells to date. This work indicates that the synergistic regulation of small molecule acceptor building block and π-bridge linker plays a key role in designing and developing highly efficient polymer acceptors. The modification of small molecule acceptor building block and π−bridge linker is effective to improve photovoltaic performance. Here, the authors replace linear with branched alkyl chains and introduce difluorene-substituted linker to realise all-polymer solar cells with efficiency of 17.24%. [ABSTRACT FROM AUTHOR]

Poor stability of spiro-OMeTAD hole transport materials (HTM) with dopant is a major obstacle for the commercialization of perovskite solar cell (pero-SC). Herein, we demonstrate a series of quinoxaline-based D-A copolymers PBQ5, PBQ6 and PBQ10 as the dopant-free polymer HTMs for high performance pero-SCs. The D-A copolymers are composed of fluorothienyl benzodithiophene (BDTT) as D-unit, difluoroquinoxaline (DFQ) with different side chains as A-unit, and thiophene as π-bridge, where the side chains on the DFQ unit are bi-alkyl for PBQ5, bi-alkyl-fluorothienyl for PBQ6, and alkoxyl for PBQ10. All the three copolymers are adopted as the dopant-free HTM in the pero-SCs. The planar n-i-p structured pero-SCs based on (FAP-bI3)0.98(MAPbBr3)0.02 with PBQ6 HTM demonstrated the high power conversion efficiency (PCE) of 22.6% with Voc of 1.13 V and FF of 80.8%, which is benefitted from the suitable energy level and high hole mobility of PBQ6. The PCE of 22.6% is the highest efficiency reported in the n-i-p structured pero-SCs based on dopant-free D-A copolymer HTM. In addition, the pero-SCs show significantly enhanced ambient, thermal and light-soaking stability compared with the devices with traditional spiro-OMeTAD HTM. [ABSTRACT FROM AUTHOR]

All-polymer solar cells (all-PSCs) based on polymerized small molecular acceptors (PSMAs) have made significant progress recently. Here, we synthesize two A-DA'D-A small molecule acceptor based PSMAs of PS-Se with benzo[c][1,2,5]thiadiazole A'-core and PN-Se with benzotriazole A'-core, for the studies of the effect of molecular structure on the photovoltaic performance of the PSMAs. The two PSMAs possess broad absorption with PN-Se showing more red-shifted absorption than PS-Se and suitable electronic energy levels for the application as polymer acceptors in the all-PSCs with PBDB-T as polymer donor. Cryogenic transmission electron microscopy visualizes the aggregation behavior of the PBDB-T donor and the PSMA in their solutions. In addition, a bicontinuous-interpenetrating network in the PBDB-T:PN-Se blend film with aggregation size of 10~20 nm is clearly observed by the photoinduced force microscopy. The desirable morphology of the PBDB-T:PN-Se active layer leads its all-PSC showing higher power conversion efficiency of 16.16%. Through development of non-fullerene acceptors, OPVs have reached efficiencies of 18%, yet the inadequate operational lifetime still poses a challenge for the commercialisation. Here, the authors investigate the origin of instability of NFA solar cells, and propose some strategies to mitigate this issue. [ABSTRACT FROM AUTHOR]

Tandem organic solar cells are based on the device structure monolithically connecting two solar cells to broaden overall absorption spectrum and utilize the photon energy more efficiently. Herein, we demonstrate a simple strategy of inserting a double bond between the central core and end groups of the small molecule acceptor Y6 to extend its conjugation length and absorption range. As a result, a new narrow bandgap acceptor BTPV-4F was synthesized with an optical bandgap of 1.21 eV. The single-junction devices based on BTPV-4F as acceptor achieved a power conversion efficiency of over 13.4% with a high short-circuit current density of 28.9 mA cm−2. With adopting BTPV-4F as the rear cell acceptor material, the resulting tandem devices reached a high power conversion efficiency of over 16.4% with good photostability. The results indicate that BTPV-4F is an efficient infrared-absorbing narrow bandgap acceptor and has great potential to be applied into tandem organic solar cells. Development of tandem organic solar cells has been limited by the choice of near-infrared absorbing materials for the rear cell. Here, the authors report a simple strategy to extend the conjugation length of acceptor Y6 and broaden its absorption range to near-infrared region. A tandem organic solar cell with efficiency of 16.4% was achieved. [ABSTRACT FROM AUTHOR]