| 1. |
- Li, Yongxi, et al.
(författare)
-
A fused-ring based electron acceptor for efficient non-fullerene polymer solar cells with small HOMO offset
- 2016
-
Ingår i: NANO ENERGY. - : ELSEVIER SCIENCE BV. - 2211-2855. ; 27, s. 430-438
-
Tidskriftsartikel (refereegranskat)abstract
- A non-fullerene electron acceptor bearing a novel backbone with fused 10-heterocyclic ring (in-dacenodithiopheno-indacenodiselenophene), denoted by IDTIDSe-IC is developed for fullerene free polymer solar cells. IDTIDSe-IC exhibits a low band gap (E-g=1.52 eV) and strong absorption in the 600850 nm region. Combining with a large band gap polymer J51 (E-g=1.91 eV) as donor, broad absorption coverage from 300 nm to 800 nm is obtained due to complementary absorption of J51 and IDTIDSe-IC, which enables a high PCE of 8.02% with a V-oc of 0.91 V, a J(SC) of 15.16 mA/cm(2) and a FF of 58.0% in the corresponding PSCs. Moreover, the EQE of 50-65% is achieved in the absorption range of IDTIDSe-IC with only about 0.1 eV HOMO difference between J51 and IDTIDSe-IC. (C) 2016 Elsevier Ltd. All rights reserved.
|
|
| 2. |
- Qian, Deping, et al.
(författare)
-
Design rules for minimizing voltage losses in high-efficiency organic solar cells
- 2018
-
Ingår i: Nature Materials. - : NATURE PUBLISHING GROUP. - 1476-1122 .- 1476-4660. ; 17:8, s. 703-
-
Tidskriftsartikel (refereegranskat)abstract
- The open-circuit voltage of organic solar cells is usually lower than the values achieved in inorganic or perovskite photovoltaic devices with comparable bandgaps. Energy losses during charge separation at the donor-acceptor interface and non-radiative recombination are among the main causes of such voltage losses. Here we combine spectroscopic and quantum-chemistry approaches to identify key rules for minimizing voltage losses: (1) a low energy offset between donor and acceptor molecular states and (2) high photoluminescence yield of the low-gap material in the blend. Following these rules, we present a range of existing and new donor-acceptor systems that combine efficient photocurrent generation with electroluminescence yield up to 0.03%, leading to non-radiative voltage losses as small as 0.21 V. This study provides a rationale to explain and further improve the performance of recently demonstrated high-open-circuit-voltage organic solar cells.
|
|
| 3. |
- Xu, Bo, et al.
(författare)
-
Integrated Design of Organic Hole Transport Materials for Efficient Solid-State Dye-Sensitized Solar Cells
- 2015
-
Ingår i: Advanced Energy Materials. - : Wiley. - 1614-6832 .- 1614-6840. ; 5:3
-
Tidskriftsartikel (refereegranskat)abstract
- A series of triphenylamine-based small molecule organic hole transport materials (HTMs) with low crystallinity and high hole mobility are systematically investigated in solid-state dye-sensitized solar cells (ssDSCs). By using the organic dye LEG4 as a photosensitizer, devices with X3 and X35 as the HTMs exhibit desirable power conversion efficiencies (PCEs) of 5.8% and 5.5%, respectively. These values are slightly higher than the PCE of 5.4% obtained by using the state-of-the-art HTM Spiro-OMeTAD. Meanwhile, transient photovoltage decay measurement is used to gain insight into the complex influences of the HTMs on the performance of devices. The results demonstrate that smaller HTMs induce faster electron recombination in the devices and suggest that the size of a HTM plays a crucial role in device performance, which is reported for the first time.
|
|
| 4. |
- Liu, Jing, et al.
(författare)
-
Fast charge separation in a non-fullerene organic solar cell with a small driving force
- 2016
-
Ingår i: NATURE ENERGY. - : NATURE PUBLISHING GROUP. - 2058-7546. ; 1
-
Tidskriftsartikel (refereegranskat)abstract
- Fast and efficient charge separation is essential to achieve high power conversion efficiency in organic solar cells (OSCs). In state-of-the-art OSCs, this is usually achieved by a significant driving force, defined as the offset between the bandgap (E-gap) of the donor/acceptor materials and the energy of the charge transfer (CT) state (E-CT), which is typically greater than 0.3 eV. The large driving force causes a relatively large voltage loss that hinders performance. Here, we report non-fullerene OSCs that exhibit ultrafast and efficient charge separation despite a negligible driving force, as E-CT is nearly identical to E-gap. Moreover, the small driving force is found to have minimal detrimental effects on charge transfer dynamics of the OSCs. We demonstrate a non-fullerene OSC with 9.5% efficiency and nearly 90% internal quantum efficiency despite a low voltage loss of 0.61V. This creates a path towards highly efficient OSCs with a low voltage loss.
|
|
| 5. |
- Planes, Emilie, et al.
(författare)
-
Encapsulation Effect on Performance and Stability of Organic Solar Cells
- 2020
-
Ingår i: Advanced Materials Interfaces. - : WILEY. - 2196-7350. ; 7:15
-
Tidskriftsartikel (refereegranskat)abstract
- To increase the lifetime of organic photovoltaic (OPV) devices and pass European lifetime standards, some encapsulation systems are often used to limit the exposition to oxygen and humidity of solar cells. Despite this progress, the damages induced by the encapsulation process are scarcely studied in literature. In this article, the consequences of the common roll-to-roll and vacuum lamination approaches are investigated and compared. The losses of performances are first followed induced by both the encapsulation itself and in a damp heat ageing. The vacuum lamination seems harmless for the solar cells. However, a significant damage is evidenced, even with a relatively mild roll-to-roll encapsulation. The degradation mechanisms are further investigated by complementary imaging characterization tools: photoluminescence/electroluminescence imaging and spectroscopy, laser-beam-induced current mapping, and correlated toJ(V) curves. The recent advancements in the optoelectronic domain may allow linking cell performance to localized flaws. It appears that, although the processing conditions are rather homogeneous, the resulting degradation ends up with a strong localization feature.
|
|
| 6. |
- Qian, Deping
(författare)
-
Studies of Voltage Losses in Organic Solar Cells
- 2017
-
Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Organic photovoltaic (OPV) devices based on semiconducting polymers and small molecules are potential alternatives to inorganic solar cells, owing to their advantages of being inexpensive, lightweight, flexible and suitable for roll-to-roll production. The state of art organic solar cells (OSCs) performed power conversion efficiencies (PCEs) over 13%.The quantum efficiency losses in OSCs have been significantly reduced within the charge generation and extraction processes, resulting in high EQEPV (70-90%) and high FF (70-80%). Whereas, large voltage losses (Δ? = ??/? − ???) were observed in conventional fullerene based solar cells, and it has been the main limiting factor for further OPV advancement. Therefore, strategies to reduce the voltage losses are required.In this thesis, newly designed non-fullerene (NF) acceptors are used to construct novel material systems for high efficiency solar cells. In particular, we studied the hole transfer in these fullerene free systems. We also reported a NF system that exhibit ultrafast and efficient charge separation despite a negligible driving force, as ECT is nearly identical to ??. Moreover, the small driving force is found to have minimal detrimental effects on charge transfer dynamics of the OSCs. We demonstrate a NF based OSC with efficiency of 9.5% and internal quantum efficiency nearly 90% despite a low voltage loss of 0.61 V. This creates a path towards highly efficient OSCs with a low voltage loss.CT states in OSCs are also investigated, since VOC is governed by the CT energy (ECT), which is found as ???? = ??? − 0.6 in a large set of fullerene based solar cells. In order to reduce these recombination losses from CT states, we explored polymer-diPDI systems which exhibited weakened D-A coupling strength, due to the steric hindrance effect. The radiative recombination losses at D/A interface in these NF devices are all reduced to less than 0.18 eV. In particular, in some cases, the additional emission from pure material is favorable for suppressing the non-radiative CT states decay. Consequently, the recombination losses in these NF systems are reduced to 0.5 eV, while the charge generation is still efficient as confirmed by PL quenching and EQEPV.Novel material systems based on non-fullerene acceptors are investigated. The systems performed energy offsets (ΔHOMO or ΔLUMO) less than 0.15eV, resulting in the same energy of CT states and bulk excitons. In this regard, the charge transfer energy loss is minimized. We also found that the EL spectra as well as the EQEEL of the blend solar cells are similar with that of lower gap components in blends. Thus the non-radiative voltage losses are reduced to < 0.3V and small voltage loss of 0.5-0.7V are obtained. Meanwhile, the charge generation in systems are still efficient and high EQEPV of 50-70% can be achieved. It confirms that there is no intrinsic limit for the VOC and efficiency of OPVs as compared with other photovoltaic technologies.
|
|
| 7. |
|
|
| 8. |
- Wang, Yuming, et al.
(författare)
-
Light-induced degradation of fullerenes in organic solar cells : a case study on TQ1:PC71BM
- 2018
-
Ingår i: Journal of Materials Chemistry A. - : Royal Society of Chemistry. - 2050-7488 .- 2050-7496. ; 6:25, s. 11884-11889
-
Tidskriftsartikel (refereegranskat)abstract
- The stability of organic solar cells (OSCs) is critical for practical applications of this emerging technology. Unfortunately, in spite of intensive investigations, the degradation mechanisms in OSCs have not been clearly understood yet. In this report, we employ a range of spectroscopic and transport measurements, coupled with drift-diffusion modelling, to investigate the light-induced degradation mechanisms of fullerene-based OSCs. We find that trap states formed in the fullerene phase under illumination play a critical role in the degradation of the open-circuit voltage (V-OC) in OSCs. Our results indicate that the degradation is intrinsic to the fullerenes in OSCs and that alternative acceptor materials are desired for the development of stable OSCs.
|
|
| 9. |
- Yang, Fan, et al.
(författare)
-
Performance limitations in thieno[3,4-c] pyrrole4,6-dione-based polymer: ITIC solar cells
- 2017
-
Ingår i: Physical Chemistry, Chemical Physics - PCCP. - : ROYAL SOC CHEMISTRY. - 1463-9076 .- 1463-9084. ; 19:35, s. 23990-23998
-
Tidskriftsartikel (refereegranskat)abstract
- We report a systematic study of the efficiency limitations of non-fullerene organic solar cells that exhibit a small energy loss (E-loss) between the polymer donor and the non-fullerene acceptor. To clarify the impact of Eloss on the performance of the solar cells, three thieno[3,4-c] pyrrole-4,6-dione-based conjugated polymers (PTPD3T, PTPD2T, and PTPDBDT) are employed as the electron donor, which all have complementary absorption spectra compared with the ITIC acceptor. The corresponding photovoltaic devices show that low Eloss (0.54 eV) in PTPDBDT: ITIC leads to a high open-circuit voltage (Voc) of 1.05 V, but also to a small quantum efficiency, and in turn photocurrent. The high Voc or small energy loss in the PTPDBDT-based solar cells is a consequence of less non-radiative recombination, whereas the low quantum efficiency is attributed to the unfavorable micro-phase separation, as confirmed by the steady-state and time-resolved photoluminescence experiments, grazing-incidence wide-angle X-ray scattering, and resonant soft X-ray scattering (R-SoXS) measurements. We conclude that to achieve high performance non-fullerene solar cells, it is essential to realize a large Voc with small Eloss while simultaneously maintaining a high quantum efficiency by manipulating the molecular interaction in the bulk-heterojunction.
|
|
