Joule, Journal Year: 2024, Volume and Issue: 8(8), P. 2208 - 2219
Published: July 24, 2024
Language: Английский
Joule, Journal Year: 2024, Volume and Issue: 8(8), P. 2208 - 2219
Published: July 24, 2024
Language: Английский
Angewandte Chemie International Edition, Journal Year: 2024, Volume and Issue: 63(21)
Published: Feb. 22, 2024
All-polymer solar cells (all-PSCs) have been regarded as one of the most promising candidates for commercial applications owing to their outstanding advantages such mechanical flexibility, light weight and stable film morphology. However, compared large amount new-emerging excellent polymer acceptors, development high-performance donor lags behind. Herein, a new D-π-A type donor, namely QQ1, was developed based on dithienoquinoxalineimide (DTQI) A unit, benzodithiophene with thiophene-conjugated side chains (BDTT) D alkyl-thiophene π-bridge, respectively. QQ1 not only possesses strong dipole moment, but also shows wide band gap 1.80 eV deep HOMO energy level -5.47 eV, even without halogen substituents that are commonly indispensable donors. When blended classic acceptor PY-IT, QQ1-based all-PSC delivers an PCE 18.81 %. After introduction F-BTA3 third component, record 19.20 % obtained, highest value reported so far all-PSCs. The impressive photovoltaic performance originates from broad absorption range, reduced loss, compact π-π stacking. These results provide insight in rational design novel nonhalogenated donors further
Language: Английский
Citations
61Chemical Society Reviews, Journal Year: 2024, Volume and Issue: 53(9), P. 4674 - 4706
Published: Jan. 1, 2024
This review summarizes the recent progress, key design principles and prospects of dimer multimer acceptors for developing polymer solar cells (PSCs) with high efficiency long-term stability.
Language: Английский
Citations
42Energy & Environmental Science, Journal Year: 2024, Volume and Issue: 17(10), P. 3365 - 3374
Published: Jan. 1, 2024
A strong electron-deficient unit CNPz as a solid additive was developed in PTQ10/ m -BTP-PhC6 binary organic solar cells. high PCE of 19.67% achieved with significant increase the J SC and FF (81.8%).
Language: Английский
Citations
37Advanced Energy Materials, Journal Year: 2024, Volume and Issue: 14(22)
Published: March 8, 2024
Abstract Herein, two emerging device optimization methods, solid additive and layer‐by‐layer (LBL) process, for organic solar cells (OSCs) are simultaneously studied. Through traditional blend cast recently proposed identical solvent LBL cast, BDCB (2‐monobromo‐1,3‐dichloro‐bezene), a benzene derivative, is used to improve the performance based on celebrity combination PM6:L8‐BO. The results reveal that finely optimized concentration in PM6 solution can push efficiency of 19.03% compared with only 18.12% while power conversion (PCE) changing trend determined by BDCB's ratio L8‐BO's precursor. morphology characterizations confirm there exists no significant stratification LBL‐processed devices, supported previously reported swelling‐intercalation‐phase separation (SIPS) model. Thereby, additive's 2D considered smart strategy tuning SIPS which various final states. This work not reports cutting‐edge binary OSCs, but also new insight deep understanding method‐based development.
Language: Английский
Citations
32Advanced Materials, Journal Year: 2024, Volume and Issue: unknown
Published: July 16, 2024
Double-fibril network morphology (DFNM), in which the donor and acceptor can self-assemble into a double-fibril structure, is beneficial for exciton dissociation charge transport organic solar cells. Herein, it demonstrated that such DFNM be constructed optimized all-polymer cells (all-PSCs) with assistance of 2-alkoxynaphthalene volatile solid additives. It revealed incorporation induce stepwise regulation aggregation molecules during film casting thermal annealing processes. Through altering alkoxy additives, both intermolecular interactions molecular miscibility host materials precisely tuned, allows optimization process facilitation self-assembly, thus leading to reinforced packing DFNM. As result, an unprecedented efficiency 19.50% (certified as 19.1%) obtained 2-ethoxynaphthalene-processed PM6:PY-DT-X all-PSCs excellent photostability (T
Language: Английский
Citations
29Advanced Materials, Journal Year: 2024, Volume and Issue: 36(41)
Published: Aug. 13, 2024
Abstract High‐performance organic solar cells often rely on halogen‐containing solvents, which restrict the photovoltaic industry. Therefore, it is imperative to develop efficient materials compatible with halogen‐free solvents. Herein, a series of benzo[ ]phenazine (BP)‐core‐based small‐molecule acceptors (SMAs) achieved through an isomerization chlorination strategy presented, comprising unchlorinated NA1, 10‐chlorine substituted NA2, 8‐chlorine NA3, and 7‐chlorine NA4. Theoretical simulations highlight NA3's superior orbit overlap length tight molecular packing, attributed interactions between end group BP unit. Furthermore, NA3 demonstrates dense 3D network structures record electronic coupling 104.5 meV. These characteristics empower ortho‐xylene ( o ‐XY) processed PM6:NA3 device power conversion efficiency (PCE) 18.94%, surpassing PM6:NA1 (15.34%), PM6:NA2 (7.18%), PM6:NA4 (16.02%). Notably, significantly lower PCE in excessive self‐aggregation NA2 ‐XY. Importantly, incorporation D18‐Cl into binary blend enhances crystallographic ordering increases exciton diffusion donor phase, resulting ternary 19.75% (certified as 19.39%). findings underscore significance incorporating new electron‐deficient units design SMAs tailored for environmentally benign solvent processing OSCs.
Language: Английский
Citations
28Materials Science and Engineering R Reports, Journal Year: 2024, Volume and Issue: 159, P. 100794 - 100794
Published: April 13, 2024
Language: Английский
Citations
17Advanced Energy Materials, Journal Year: 2024, Volume and Issue: 14(19)
Published: March 10, 2024
Abstract Se‐functionalized small molecule acceptors (SMAs) exhibit unique advantages in constructing materials with near‐infrared absorption, but their photovoltaic performance lags behind that of S‐containing analogs organic solar cells (OSCs). Herein, two new Se‐containing SMAs, namely Se‐EH and Se‐EHp, are designed synthesized by regulating bifurcation site outer alkyl chain, which enables Se‐EHp to form different 3D crystal frameworks from CH1007. displays tighter π–π stacking denser packing framework smaller‐sized pore structure induced larger steric hindrance effect chain branched at 2‐position, a higher dielectric constant PM6:Se‐EH active layer can be obtained. OSCs based on achieved very high PCEs 18.58% binary 19.03% ternary devices FF approaching 80% for SMAs. A more significant adjusts the molecular crystallization favorable nanofiber interpenetrating network an appropriate domain size reduce rate sub‐ns recombination promote balanced transport carriers. This work provides references further design development highly efficient
Language: Английский
Citations
16Advanced Energy Materials, Journal Year: 2024, Volume and Issue: 14(26)
Published: May 13, 2024
Abstract High power conversion efficiency (PCE) and mechanical robustness are prerequisites for wearable applications of organic solar cells (OSCs). However, stretchability present active systems (i.e., crack‐onset strain (COS) < 30%) should be improved. While introducing elastomers into is considered a simple method improving stretchability, the inclusion typically results in decrease PCE OSC with limited enhancement due to lack interconnected electrical pathways. In this study, it developed efficient intrinsically stretchable (IS)‐OSCs exceptional robustness, by constructing co‐continuous networks conjugated polymers (D18) (SEBS) within layers. It demonstrated that blend film specific ratio (40:60 w/w) D18:SEBS crucial forming structures, establishing well‐connected channels. Consequently, D18 0.4 :SEBS 0.6 /L8‐BO OSCs achieve 16‐times higher (COS = 126%) than based on D18/L8‐BO 8%), while achieving 4‐times (12.13%) compared SEBS‐rich layers (D18 0.2 0.8 /L8‐BO, 3.15%). Furthermore, ‐based IS‐OSCs preserve 86 90% original PCEs at 50% after 200 stretching/releasing cycles 15% strain, respectively, demonstrating highest among reported IS‐OSCs.
Language: Английский
Citations
15Advanced Materials, Journal Year: 2024, Volume and Issue: 36(30)
Published: June 5, 2024
Abstract Leveraging breakthroughs in Y‐series nonfullerene acceptors (NFAs), organic solar cells (OSCs) have achieved impressive power conversion efficiencies (PCEs) exceeding 19%. However, progress advancing OSCs has decelerated due to constraints realizing the full potential of NFAs. Herein, a simple yet effective solid additive‐induced preaggregation control method employing 2‐chloro‐5‐iodopyridine (PDCI) is reported unlock Specifically, PDCI interacts predominantly with NFAs enabling enhanced and ordered phase‐aggregation solution. This leads notable improvement redshifted absorption acceptor phase during film formation, along improved crystallinity. Moreover, PDCI‐induced solution enables molecule packing film‐formation process through delicate intermediate states transition. Consequently, preaggregated significantly improves PCE PM6:Y6 from 16.12% 18.12%, among best values for OSCs. Importantly, this approach universally applicable other NFA‐based OSCs, achieving champion 19.02% PM6:BTP‐eC9 system. Thus, strategy further unlocks NFAs, offering promising avenue enhancing photovoltaic performance
Language: Английский
Citations
15