Wikipedia

Polymer-fullerene bulk heterojunction solar cell

Polymer-fullerene bulk heterojunction solar cells are a type of solar cell researched in academic laboratories. Polymer-fullerene solar cells are a subset of organic solar cells, also known as organic photovoltaic (OPV) cells, which use organic materials as their active component to convert solar radiation into electrical energy. The polymer, which functions as the donor material in these solar cells, and fullerene derivatives, which function as the acceptor material (such as PCBM, or phenyl-C61-butyric acid methyl ester), are essential components.[2] Specifically, fullerene derivatives act as electron acceptors for donor materials like P3HT (poly-3-hexyl thiophene-2,5-diyl), creating a polymer-fullerene based photovoltaic cell.[3] The Polymer-fullerene BHJ forms two channels for transferring electrons and holes to the corresponding electrodes, as opposed to the planar architecture when the Acceptor (A) and Donor (D) materials were sequentially stacked on top of each other and could selectively touch the cathode and anode electrodes. Hence, the D and A domains are expected to form a bi-continuous network with Nano-scale morphology for efficient charge transport and collection after exciton dissociation. Therefore, in the BHJ device architecture, a mixture of D and A molecules in the same or different solvents was used to form a bi-continual layer, which serves as the active layer of the device that absorbs light for exciton generation. The bi-continuous three-dimensional interpenetrating network of the BHJ design generates a greater D-A interface, which is necessary for effective exciton dissociation in the BHJ due to short exciton diffusion.[4] When compared to the prior bilayer design, photo-generated excitons may dissociate into free holes and electrons more effectively, resulting in better charge separation for improved performance of the cell.

When electrons of donor molecules are photoexcited, they jump from the HOMO to LUMO energy level. The electrons now in the LUMO energy level can travel to nearby acceptor molecules, which are more electronegative and thus lower in energy. The driving force for the electron transfer between donor and acceptor is the difference in LUMO energy levels.[1]

Photovoltaic cells featuring a polymeric blend of organics have shown promise in a field largely dominated by inorganic (e.g. silicon) solar cells. Some of the improvements that organic solar cells have over inorganic solar cells are that they are flexible and therefore can be applied to a larger range of surfaces.[5] They can also be produced much more easily via inkjet printing or spray deposition, and therefore are vastly cheaper to manufacture.[6] A downside is that, because they are not crystalline (like silicon), but instead are produced in a purposely disordered blend of electron-acceptor and -donor materials (hence the name bulk heterojunction), they have a limited efficiency of charge transport.[7]

However, the efficiencies of these new types of photovoltaic cells have risen from 2.5% in 2001, to 5% in 2006, to greater than 10% in 2011.[8] This is because improved methods for solution processing of acceptor and donor materials led to more efficient blending of the two materials. Further research can lead to polymer-fullerene based photovoltaic cells that approach the efficiency of current inorganic photovoltaic cells.

Structure

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Three different schematic representations of blending electron donor and acceptor materials. (a) Bilayer representation, with efficient charge generation but poor charge transport.[10] (b) Solution processed representation, in which rapid drying leads to a randomized network of acceptor/donor blending, currently the most optimal way to blend. (c) Theoretical, ideal representation of acceptor/donor blending.[9]

Materials used in polymer-based photovoltaic cells are characterized by their total electron affinities and absorption power. The electron-rich, donor materials tend to be conjugated polymers with relatively high absorption power, whereas the acceptor in this case is a highly symmetric fullerene molecule with a strong affinity for electrons, ensuring sufficient electron mobility between the two.[5]

 
The typical structural layout of photovoltaic devices. Transparent, conductive ITO is applied onto glass, and a hole transport layer of PEDOT:PSS (poly(3,4-ethylenedioxythiophene)poly(styrenesulfonate)) on top of that. The photoactive layer is a blend of electron acceptor and donor atoms, and the cathode interlayer is a low work function metal used to lower the work function of the electrode on top to accept electrons.[10][11]

The arrangement of materials essentially determines the overall efficiency of the heterojunction solar cell. There are three donor-acceptor bulk morphologies: (a) the bilayer, (b) the bulk heterojunction, and (c) the "comb" structure. Typically, a polymer-fullerene bulk heterojunction solar cell has a layered structure.

Working Principle

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Working principle of the Fullerene based BHJ OPVs device involves four fundamental steps namely (i) photons absorption and exciton creation, (ii) exciton diffusion and splitting at the D-A interface, (iii) charge transportation, and, (iv) charge collection.[12] In a BHJ OPV device, the donor material is the one that absorbs the incoming light. Due to a substantial potential energy drop, the excitons must diffuse to the D-A interface, where they will be split into free charge carriers such as electrons and holes.[13] There can be some limitations and losses during the device operation steps discussed above, which include absorption loss due to spectral mismatch, thermalization loss, the energy required for exciton splitting might be inefficient, charge recombination loss, etc.[14]

Device Architecture

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For Fullerene-based OPV, there are two device architectures in use today: traditional (conventional) and inverted. The BHJ conventional architecture has set a significant milestone in terms of improving efficiencies in OPVs in order to commercialize them. However, due to oxygen and moisture intrusion into the electrodes, as well as damage caused by air or oxidation of the electrodes, the environmental stability of these OPVs remains the most difficult challenge to overcome. To overcome this challenge researchers had established inverted device architecture for BHJ PSCs. In an inverted device, the bottom transparent electrode serves as the cathode while the top electrode is an anode. The inverted devices exhibited higher environmental stability,[15] and higher efficiencies in most cases in comparison with the conventional architecture of OPVs, which is achieved by using high work function metal or metal oxides as a cathode and the low work function metal as an anode. In the normal architecture the low work function cathode would easily get oxidized in the air by oxygen and moisture, thus using a higher work function cathode minimizes this tendency and improves efficiency and stability.

Functions/Applications

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The primary function of a solar cell is the conversion of light energy into electrical energy by means of the photovoltaic effect.[16] In particular, polymer-fullerene bulk heterojunction solar cells are promising because of their potential in low processing costs and mechanical flexibility in comparison to conventional inorganic solar cells.[17][18] Solution processing potentially allows reductions in manufacturing costs through screen printing, doctor blading, inkjet printing, and spray deposition at low temperatures.[19][20] To overcome the narrow spectral overlap of organic polymer absorption bands, experiments have blended conjugated polymer donors with high electron affinity fullerene derivatives as acceptors to extend the spectral sensitivity. Ternary solar cells are a promising approach to increased efficiency and light harvesting properties of organic photovoltaic cells (OPV).[21]

Challenges in Fullerene based BHJ OPV

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The Fullerene based BHJ OPV Devices are expected to possess the following characteristics for successful commercialization: high performance, environmentally friendly, simple fabrication process, high stability, and low cost. However, efficiency and stability are the major challenges faced by PSC for its successful commercialization.[22][23][24] Shorter diffusion lengths of excitons in conjugated polymers are limited to a few nanometers (less than 20 nm), which is shorter than the optical absorption path length (~ 100–200 nm),[25] contributes to lower power conversion efficiencies in PSCs. Another factor that limits device efficiencies is lower charge carrier mobility in the conjugated polymers causing, their recombination before reaching their respective electrodes.[26] Consequently, the solar cell experiences a significant loss in photo generated current, and hence poor device performance. Poor charge carrier collection at the electrodes due to bad mismatch is also another factor that limits device performance. If there is a mismatch between the anode and cathode with that of donor HOMO or acceptor LUMO, respectively, then no Ohmic contacts would be established, which ultimately, results in poor performance of the solar cell. In most Fullerene based BHJ OPVs, there is a mismatch between the anode and cathode with that of donor HOMO and acceptor LUMO respectively, which poses a great challenge in charge carrier collection in the respective electrodes, and overall device performance.

The stability of PSC device is the most important factor that should be given great attention to realize their commercialization, though there have been limited literature on the stability of PSCs compared to the literature on the efficiency of PSCs. A study on the stability of PSCs helps in understanding how a device degrades during its operation.[27] Device instability occurs due to a range of complex phenomena that are in play simultaneously.[23] These degradation factors include mechanical stress, irradiation (time & intensity), water, oxygen, heating, etc. (Fig 2.6), and may affect the active layer, the transport layers, the contacts, and the interface of every layer with the adjacent layers.

References

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  1. ^ Dennler, Gilles; Scharber, Markus C.; Brabec, Christoph J. (6 April 2009). "Polymer-Fullerene Bulk-Heterojunction Solar Cells". Advanced Materials. 21 (13): 1323–1338. Bibcode:2009AdM....21.1323D. doi:10.1002/adma.200801283.
  2. ^ Thompson, Barry C.; Fréchet, Jean M. J. (January 2008). "Polymer–Fullerene Composite Solar Cells". Angewandte Chemie International Edition. 47 (1): 58–77. doi:10.1002/anie.200702506. ISSN 1433-7851. PMID 18041798.
  3. ^ Kennedy, Robert D.; Ayzner, Alexander L.; Wanger, Darcy D.; Day, Christopher T; Halim, Merissa; Khan, Saeed I.; Tolbert, Sarah H.; Schwartz, Benjamin J.; Rubin, Yves (24 December 2008). "Self-Assembling Fullerenes for Improved Bulk-Heterojunction Photovoltaic Devices". Journal of the American Chemical Society. 130 (51): 17290–17292. doi:10.1021/ja807627u. PMID 19053441.
  4. ^ Xia, Tian; Cai, Yunhao; Fu, Huiting; Sun, Yanming (2019-06-01). "Optimal bulk-heterojunction morphology enabled by fibril network strategy for high-performance organic solar cells". Science China Chemistry. 62 (6): 662–668. doi:10.1007/s11426-019-9478-2. ISSN 1869-1870.
  5. ^ a b Mayer, Alex C.; Scully, Shawn R.; Hardin, Brian E.; Rowell, Michael W.; McGehee, Michael D. (November 2007). "Polymer-based solar cells". Materials Today. 10 (11): 28–33. doi:10.1016/S1369-7021(07)70276-6.
  6. ^ Nelson, Jenny (October 2011). "Polymer:fullerene bulk heterojunction solar cells". Materials Today. 14 (10): 462–470. doi:10.1016/S1369-7021(11)70210-3.
  7. ^ Deibel, Carsten; Dyakonov, Vladimir (1 September 2010). "Polymer–fullerene bulk heterojunction solar cells". Reports on Progress in Physics. 73 (9): 096401. arXiv:1003.0359. Bibcode:2010RPPh...73i6401D. doi:10.1088/0034-4885/73/9/096401. S2CID 118855668.
  8. ^ Scharber, M.C.; Sariciftci, N.S. (December 2013). "Efficiency of bulk-heterojunction organic solar cells". Progress in Polymer Science. 38 (12): 1929–1940. doi:10.1016/j.progpolymsci.2013.05.001. PMC 3837184. PMID 24302787.
  9. ^ Yang, Xiaoniu; Loos, Joachim; Veenstra, Sjoerd C.; Verhees, Wiljan J. H.; Wienk, Martijn M.; Kroon, Jan M.; Michels, Matthias A. J.; Janssen, René A. J. (April 2005). "Nanoscale Morphology of High-Performance Polymer Solar Cells". Nano Letters. 5 (4): 579–583. Bibcode:2005NanoL...5..579Y. doi:10.1021/nl048120i. PMID 15826090.
  10. ^ Zheng, Liping; Zhou, Qingmei; Deng, Xianyu; Yuan, Min; Yu, Gang; Cao, Yong (August 2004). "Methanofullerenes Used as Electron Acceptors in Polymer Photovoltaic Devices". The Journal of Physical Chemistry B. 108 (32): 11921–11926. doi:10.1021/jp048890i.
  11. ^ Kooistra, Floris B.; Knol, Joop; Kastenberg, Fredrik; Popescu, Lacramioara M.; Verhees, Wiljan J. H.; Kroon, Jan M.; Hummelen, Jan C. (February 2007). "Increasing the Open Circuit Voltage of Bulk-Heterojunction Solar Cells by Raising the LUMO Level of the Acceptor". Organic Letters. 9 (4): 551–554. doi:10.1021/ol062666p. PMID 17253699.
  12. ^ Ganesamoorthy, Ramasamy; Sathiyan, Govindasamy; Sakthivel, Pachagounder (2017-03-01). "Review: Fullerene based acceptors for efficient bulk heterojunction organic solar cell applications". Solar Energy Materials and Solar Cells. 161: 102–148. doi:10.1016/j.solmat.2016.11.024. ISSN 0927-0248.
  13. ^ Zhang, Yiwei; Sajjad, Muhammad T.; Blaszczyk, Oskar; Ruseckas, Arvydas; Serrano, Luis A.; Cooke, Graeme; Samuel, Ifor D. W. (2019-07-01). "Enhanced exciton harvesting in a planar heterojunction organic photovoltaic device by solvent vapor annealing". Organic Electronics. 70: 162–166. doi:10.1016/j.orgel.2019.03.014. hdl:10023/19644. ISSN 1566-1199.
  14. ^ Siddiki, Mahbube Khoda; Li, Jing; Galipeau, David; Qiao, Qiquan (2010-06-29). "A review of polymer multijunction solar cells". Energy & Environmental Science. 3 (7): 867–883. doi:10.1039/B926255P. ISSN 1754-5706.
  15. ^ Han, Donggeon; Yoo, Seunghyup (2014-09-01). "The stability of normal vs. inverted organic solar cells under highly damp conditions: Comparison with the same interfacial layers". Solar Energy Materials and Solar Cells. 128: 41–47. doi:10.1016/j.solmat.2014.04.036. ISSN 0927-0248.
  16. ^ Scharber, M. C.; Mühlbacher, D.; Koppe, M.; Denk, P.; Waldauf, C.; Heeger, A. J.; Brabec, C. J. (17 March 2006). "Design Rules for Donors in Bulk-Heterojunction Solar Cells—Towards 10 % Energy-Conversion Efficiency". Advanced Materials. 18 (6): 789–794. Bibcode:2006AdM....18..789S. doi:10.1002/adma.200501717. S2CID 13842344.
  17. ^ Robaeys, Pieter; Bonaccorso, Francesco; Bourgeois, Emilie; D'Haen, Jan; Dierckx, Wouter; Dexters, Wim; Spoltore, Donato; Drijkoningen, Jeroen; Liesenborgs, Jori; Lombardo, Antonio; Ferrari, Andrea C.; Van Reeth, Frank; Haenen, Ken; Manca, Jean V.; Nesladek, Milos (25 August 2014). "Enhanced performance of polymer:fullerene bulk heterojunction solar cells upon graphene addition". Applied Physics Letters. 105 (8): 083306. Bibcode:2014ApPhL.105h3306R. doi:10.1063/1.4893777.
  18. ^ Cates, Nichole C.; Gysel, Roman; Beiley, Zach; Miller, Chad E.; Toney, Michael F.; Heeney, Martin; McCulloch, Iain; McGehee, Michael D. (9 December 2009). "Tuning the Properties of Polymer Bulk Heterojunction Solar Cells by Adjusting Fullerene Size to Control Intercalation". Nano Letters. 9 (12): 4153–4157. Bibcode:2009NanoL...9.4153C. doi:10.1021/nl9023808. PMID 19780570.
  19. ^ Li, G.; Yao, Y.; Yang, H.; Shrotriya, V.; Yang, G.; Yang, Y. (9 July 2007). ""Solvent Annealing" Effect in Polymer Solar Cells Based on Poly(3-hexylthiophene) and Methanofullerenes". Advanced Functional Materials. 17 (10): 1636–1644. doi:10.1002/adfm.200600624. S2CID 30133192.
  20. ^ Ma, W.; Yang, C.; Gong, X.; Lee, K.; Heeger, A. J. (October 2005). "Thermally Stable, Efficient Polymer Solar Cells with Nanoscale Control of the Interpenetrating Network Morphology". Advanced Functional Materials. 15 (10): 1617–1622. doi:10.1002/adfm.200500211. S2CID 135626155.
  21. ^ Lee, Jae Kwan; Ma, Wan Li; Brabec, Christoph J.; Yuen, Jonathan; Moon, Ji Sun; Kim, Jin Young; Lee, Kwanghee; Bazan, Guillermo C.; Heeger, Alan J. (March 2008). "Processing Additives for Improved Efficiency from Bulk Heterojunction Solar Cells". Journal of the American Chemical Society. 130 (11): 3619–3623. doi:10.1021/ja710079w. PMID 18288842.
  22. ^ Baran, Derya; Ashraf, Raja Shahid; Hanifi, David A.; Abdelsamie, Maged; Gasparini, Nicola; Röhr, Jason A.; Holliday, Sarah; Wadsworth, Andrew; Lockett, Sarah; Neophytou, Marios; Emmott, Christopher J. M.; Nelson, Jenny; Brabec, Christoph J.; Amassian, Aram; Salleo, Alberto (March 2017). "Reducing the efficiency–stability–cost gap of organic photovoltaics with highly efficient and stable small molecule acceptor ternary solar cells". Nature Materials. 16 (3): 363–369. doi:10.1038/nmat4797. hdl:10754/622456. ISSN 1476-4660. PMID 27869824.
  23. ^ a b Cheng, Pei; Zhan, Xiaowei (2016-05-03). "Stability of organic solar cells: challenges and strategies". Chemical Society Reviews. 45 (9): 2544–2582. doi:10.1039/C5CS00593K. ISSN 1460-4744. PMID 26890341.
  24. ^ Li, Ning; McCulloch, Iain; Brabec, Christoph J. (2018-06-13). "Analyzing the efficiency, stability and cost potential for fullerene-free organic photovoltaics in one figure of merit". Energy & Environmental Science. 11 (6): 1355–1361. doi:10.1039/C8EE00151K. hdl:10754/627384. ISSN 1754-5706.
  25. ^ Yeboah, Douglas; Singh, Jai (November 2017). "Dependence of Exciton Diffusion Length and Diffusion Coefficient on Photophysical Parameters in Bulk Heterojunction Organic Solar Cells". Journal of Electronic Materials. 46 (11): 6451–6460. doi:10.1007/s11664-017-5679-2. ISSN 0361-5235.
  26. ^ Sharma, Abhishek; Chauhan, Mihirsinh; Bharti, Vishal; Kumar, Manoj; Chand, Suresh; Tripathi, Brijesh; Tiwari, J. P. (2017-10-04). "Revealing the correlation between charge carrier recombination and extraction in an organic solar cell under varying illumination intensity". Physical Chemistry Chemical Physics. 19 (38): 26169–26178. doi:10.1039/C7CP05235A. ISSN 1463-9084. PMID 28930319.
  27. ^ Rafique, Saqib; Abdullah, Shahino Mah; Sulaiman, Khaulah; Iwamoto, Mitsumasa (2018-03-01). "Fundamentals of bulk heterojunction organic solar cells: An overview of stability/degradation issues and strategies for improvement". Renewable and Sustainable Energy Reviews. 84: 43–53. doi:10.1016/j.rser.2017.12.008. ISSN 1364-0321.
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