Phase Separation Of Active Layer Research Articles

Suppressing Trap‐Assisted Nonradiative Recombination via Interface Modification for Achieving Efficient Organic Solar Cells

AbstractTrap states in organic solar cells (OSCs) can capture free charges, leading to a reduction in current density and significant energy loss. Since charge collection is primarily dependent on the interface layer, minimizing trap states at interfaces can effectively suppress energy losses, a topic that has been rarely explored. Herein, an interface strategy is proposed by combining Me‐4PACz and PEDOT:PSS to mitigate the trap‐assisted nonradiative recombination at the hole transport layer (HTL). OSCs based on the Me‐4PACz/PEDOT:PSS exhibit reduced trap densities and low energy losses compared to devices fabricated with a single‐layer HTL. This reduction can be attributed to a lower nonradiative recombination rate during hole transport at the interface. Changes in the work function of the two interlayers due to contact result in the existence of a built‐in potential inside the composite interlayer, promoting charge collection and reducing energy loss from charge recombination. Furthermore, the composite HTL interface induces vertical phase separation of active layer, leading to significant improvements of the fill factor for OSCs. As a result, high power conversion efficiencies (PCEs) of 18.70% and 19.02% are achieved for binary all‐polymer solar cells and polymer donor/small molecule acceptor solar cells, respectively.

Efficient Ternary Polymer Solar Cells with Tunable Crystallinity and Phase Separation of Active Layers via Incorporating GHK-Cu.

The crystallinity of a nonfullerene small-molecule acceptor plays an important function in the bimolecular recombination and carrier transfer of polymer solar cells (PSCs). However, because of the competition between the donor (PBDB-T) and acceptor (ITIC) in processes of phase separation and crystallization, the PBDB-T preferentially forms a crystalline network, which limits the molecular diffusion of ITIC and leads to the weak crystallinity of ITIC, eventually restricting the photoelectric conversion efficiency (PCE) of PSCs. Therefore, in our work, a small-molecule biomaterial, Gly-His-Lys-Cu (SMBM GHK-Cu), is incorporated into binary PBDB-T:ITIC to construct a PBDB-T:ITIC:GHK-Cu ternary system. The addition of GHK-Cu increases ITIC crystallinity and promotes the formation in continuous single-phase domains of PBDB-T and ITIC, which creates an optimized bicontinuous network path to increase and balance charge transmission in PSCs. Meanwhile, GHK-Cu makes energy transfer from GHK-Cu to PBDB-T appreciably efficient, improving the photon capture and exciton-generation rate of PBDB-T. Moreover, it can form a complementary absorption spectrum with PBDB-T and ITIC, which enhances the PCE of ternary devices. Excitingly, the PCE of PSC-based PBDB-T:ITIC is enhanced from 10.28% to 12.07% via incorporating 0.1 wt % GHK-Cu into PBDB-T:ITIC, in which the enhanced open voltage (VOC) is 0.92 V, the short-circuit current (JSC) is 17.87 mA/cm2, and the fill factor (FF) is 73.4%. Meanwhile, the PCE of PSC-based PM6:Y6 is also enhanced from 15.21% for a binary PSC to 17.11% for ternary PSC-based PM6:Y6:0.1 wt % GHK-Cu. This work shows that the cheap and environmentally friendly GHK-Cu has great potential for application in tuning the crystallinity and phase separation of the active layer.

Fullerene derivative layer induced phase separation and charge transport improvement for inverted polymer solar cells

The phase separation of donor and acceptor in bulk-heterojunction plays an important role on the exciton dissociation and charge carrier transport, which decides the performance of organic solar cells (OSCs). In this paper, the thin [6,6]-Phenyl-C71-butyric acid methyl ester (PC71BM) layer was incorporated as interlayer between active layer and the polyethylenemine electron transport layer of OSCs to realize high efficiency. Both a high short-circuit current density and fill factor were achieved, resulting in a power conversion efficiency up to 9.17% for the optimal device. The incorporation of PC71BM layer not only induced vertical phase separation of active layer to improve exciton dissociation and charge transfer but also modified surface morphology to increase light absorption of the active layer. This study offers a simple and lost cost strategy to improve performance of OSCs.

Efficient Polymer Solar Cells with Open-Circuit Voltage of 1.01 V and Power Conversion Efficiency of 8.09.

A series of polymer solar cells (PSCs) were prepared with different solvent additive 1-chloronaphthalene (CN) doping volume ratio to adjust the phase separation of active layers. The optimized PSCs exhibit a power conversion efficiency (PCE) of 8.09%, along with an open-circuit voltage of 1.01 V, a short circuit current density of 13.64 mA cm–2, and a fill factor of 58.70%. All the key photovoltaic parameters of PSCs can be simultaneously increased by incorporating 1.0 vol % CN in blend solutions due to the optimized phase separation of active layers assisted by the volatilization of CN. Over 24% PCE improvement can be obtained by incorporating 1.0 vol % CN, indicating that the dynamic process of film forming should play the vital role in determining the performance of PSCs.

Electron transport layer-free polymer solar cells show 40% higher efficiency than using ZnO transparent cathode

The poor compatibility of inorganic materials (electron transport layer) with the active layer and an ultrathin film of conjugated polymers becomes the great obstacle to producing high-quality polymer solar cells with high-throughput roll-to-roll (R2R) method. Novel electron transport layer-free polymer solar cells have been constructed by integrating the conjugated aminoalkyl-functionalized polymer, poly[3-(5-(9,9-bis(3-(dimethylamino)propyl)-7-methyl-9H-fluoren-2-yl)thiophen-2-yl)-2,5-bis(2-butyloctyl)-6-(5-methylthiophen-2-yl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione] (PDTFN) into the active layer. PDTFN was synthesized by different Suzuki reaction conditions to gain different molecular weights- small molecular weight (PDTFN-L) and high molecular weight (PDTFN-H). It is noteworthy that PDTFN-H can significantly enhance the power conversion efficiency of the solar cells that incorporate a photoactive layer composed of poly[(3-hexylthiophene)-2,5-diyl] (P3HT) and the fullerene acceptor [6,6-phenyl-C71-butyric acid methyl ester] (PC71BM). The power conversion efficiency varies from 2.5% for ZnO transparent cathode based solar cells to 3.6% for PDTFN-H based electron transport layer-free solar cells. This improved performance can be attributed to the following reasons: the PDTFN-H can enhance cathode electron transporting by introducing the PDTFN-H into active layer without extra coating the cathode interfacial material; besides, a favorable vertical phase separation of active layer was formed due to the PDTFN-H excellent compatibility with the bulk-heterojunction. These experimental results revealed that the electron transport layer-free polymer solar cells based on PDTFN-H can be a promising novel effective fabrication with simplified manufacturing process and lower cost.

Ternary non-fullerene polymer solar cells with an efficiency of 11.6% by simultaneously optimizing photon harvesting and phase separation

A PCE of 11.6% is achieved in ternary PSCs by optimizing photon harvesting and phase separation of active layers.

A two-dimension-conjugated small molecule for efficient ternary organic solar cells

Ternary organic solar cells (OSCs) are burgeoning as one of the effective strategies to achieve high power conversion efficiencies (PCEs) by incorporating a third component with a complementary absorption into the binary blends. In this study, we presented a new two-dimension-conjugated small molecule denoted by DR3TBDTTVT, which alone gave rise to a best PCE of 5.71% with acceptor PC71BM as active layer. Given the complementary absorption with PTB7-Th, DR3TBDTTVT was doped into (PTB7-Th:PC71BM)-based binary blends, and ternary OSCs were developed. The ternary OSCs with 10 wt% of DR3TBDTTVT displayed improved hole-mobility, reduced device resistance and better phase separation of active layer, thus leading to an impressive PCE of 7.77% with open-circuit voltage of 0.77 V, short-circuit density of 14.52 mA cm−2 and fill factor of 70.3%. Ternary OSCs well make up for the light-harvesting insufficiency of binary OSCs, and this research provides a new material for the improvement of PCEs for single-junction OSCs.

Doping a D-A structural polymer based on benzodithiophene and triazoloquinoxaline for efficiency improvement of ternary solar cells

A novel donor-acceptor (D-A) structural polymer PBDT-BTzQx-C12 consisting of benzodithiophene and triazoloquinoxaline units as donor and acceptor building blocks was synthesized. The PBDT-BTzQx-C12 was evaluated as complementary electron donor in polymer solar cells (PSCs) with poly(3-hexylthiophene) (P3HT) as electron donor and [6,6]-phenyl-C71-butyric acid methyl ester (PC71BM) as electron acceptor. The power conversion efficiencies (PCEs) of PSCs were improved from 3.18% to 3.54% by doping 2 wt. % PBDT-BTzQx-C12, corresponding to an approximately 11% PCE improvement. The performance improvement of ternary PSCs should be attributed to the increase of photon harvesting and the optimized phase separation of active layers by doping D-A structural PBDT-BTzQx-C12.

Preparation of Organic Photovoltaics Using the Sensitizing Effect of Quantum Dots

Organic photovoltaic is one of the solar cell consists of fullerene derivative which is an n-type semiconductor and the conductive polymer as p-type semiconductor. In my research, silicon quantum dots was introduced to the active layer consisting of fullerene derivative (PCBM) and a conductive polymer (PCPDTBT), to prepare the hybrid photovoltaic. The prepared hybrid solar cell with Si quantum dots achieved better cell performance compared with controlled solar cell without quantum dots. The hybrid solar cell showed larger value of Incident photon-to-current conversion efficiencies and lower photoluminescence intensity. This indicated that domain size among phase separation in active layer was made smaller than the active layer of controlled solar cell, by introducing Si quantum dots. This change of aggregation structure by quantum dots was contributed to the improvement of cell characteristics.

Cooperative effects of solvent and polymer acceptor co-additives in P3HT:PDI solar cells: simultaneous optimization in lateral and vertical phase separation

In this work, solvent chloronaphthalene (CN) and polymer acceptor an alternating copolymer of perylene diimide and carbazole (PCPDI) were utilized as co-additives to optimize the nanoscale phase-separated morphology and photovoltaic properties of bulk-heterojunction (BHJ) polymer solar cells based on the poly(3-hexyl thiophene) (P3HT)/N,N'-bis(1-ethylpropyl)-perylene-3,4,9,10-tetracarboxylic diimide (EP-PDI) system. The domain size of EP-PDI molecules together with that of P3HT distinctly decreased by adding a 0.75 vol% CN additive. The optimized lateral phase separation increased the donor-acceptor interfacial area and facilitated the exciton dissociation process, leading to 5-fold enhancement of short-circuit current (JSC). Furthermore, when PCPDI was employed as a co-additive, acceptor materials (including PCPDI and EP-PDI) were prone to aggregation towards the top surface of blend films, improving vertical phase separation of active layers. PCPDI incorporation, which improved the percolation pathways for electron carriers, suppressed the crystallinity of P3HT distinctly. Thus, much more balanced charge transport was achieved by PCPDI addition, which resulted in almost 1-fold enhancement of open-circuit voltage (VOC) by reducing nongeminate recombination. As a consequence, cooperative effects of CN and PCPDI additives improved the nanoscale phase-separated morphology in lateral and vertical directions simultaneously, achieving the enhancement in both VOC and JSC.

Effect of Solvent and Subsequent Thermal Annealing on the Performance of Phenylenevinylene Copolymer:PCBM Solar Cells

The morphology of the photoactive layer used in the bulk heterojunction photovoltaic devices is crucial for efficient charge generation and their collection at the electrodes. We investigated the solvent vapor annealing and thermal annealing effect of an alternating phenylenevinylene copolymer P:PCBM blend on its morphology and optical properties. The UV-visible absorption spectroscopy shows that both solvent and thermal annealing can result in self-assembling of copolymer P to form an ordered structure, leading to enhanced absorption in the red region and hole transport enhancement. By combining the solvent and thermal annealing of the devices, the power conversion efficiency is improved. This feature was attributed to the fact that the PCBM molecules begin to diffuse into aggregates and together with the ordered copolymer P phase form bicontinuous pathways in the entire layer for efficient charge separation and transport. Furthermore, the measured photocurrent also suggests that the space charges no longer limit the values of the short circuit current (J(sc)) and fill factor (FF) for solvent-treated and thermally annealed devices. These results indicate that the higher J(sc) and PCE for the solvent-treated and thermally annealed devices can be attributed to the phase separation of active layers, which leads to a balanced carrier mobility. The overall PCE of the device based on the combination of solvent annealing and thermal annealing is about 3.7 %.