Tailored interfaces of unencapsulated perovskite solar cells for &gt;1,000 hour operational stability

Christians, Jeffrey A.; Schulz, Philip; Tinkham, Jonathan S.; Schloemer, Tracy H.; Harvey, Steven P.; Villers, Bertrand J. Tremolet de; Sellinger, Alan; Berry, Joseph J.; Luther, Joseph M.

doi:10.1038/s41560-017-0067-y

Cited by 747 publications

(739 citation statements)

References 45 publications

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“…[1][2][3][4][5] Even though other optoelectronic devices like light emitting diodes and lasers are being researched, [6][7][8][9][10][11][12][13] perovskite-based photovoltaics (PV) is the key technology driving the fast emergence of perovskitebased optoelectronics. [21][22][23] Most reported record PCEs are still based on highly expensive organic hole transport layer (HTL) materials like 2,2′,7,7′-tetrakis[N,N-di (4methoxyphenyl)amino]-9,9′-spirobifluorene (spiro-MeOTAD) or poly[bis(4-phenyl)(2,4,6-trimethylphenyl)amine] (PTAA). [14] Despite the rapid progress in terms of PCE, one key challenge of perovskite-based PV is still its low stability under realistic outdoor stress conditions-temperature, humidity, and ultraviolet (UV) radiation.…”

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confidence: 99%

Electron‐Beam‐Evaporated Nickel Oxide Hole Transport Layers for Perovskite‐Based Photovoltaics

Abzieher

Moghadamzadeh

Schackmar

et al. 2019

Advanced Energy Materials

137

149

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application-oriented research like process engineering and upscaling is observed. [1][2][3][4][5] Even though other optoelectronic devices like light emitting diodes and lasers are being researched, [6][7][8][9][10][11][12][13] perovskite-based photovoltaics (PV) is the key technology driving the fast emergence of perovskitebased optoelectronics. Recently, power conversion efficiencies (PCEs) close to 24% were demonstrated for perovskite PV, exceeding the PCEs of established thinfilm technologies. [14] Despite the rapid progress in terms of PCE, one key challenge of perovskite-based PV is still its low stability under realistic outdoor stress conditions-temperature, humidity, and ultraviolet (UV) radiation. A significant advance toward more stable devices was demonstrated by engineering the composition of the large cation site of the perovskite crystal structure and by including low-dimensional perovskite interlayers and passivation layers. [15][16][17][18][19][20] Further advances in stability are based on the charge extracting materials and their interfaces with the perovskite absorber layers. [21][22][23] Most reported record PCEs are still based on highly expensive organic hole transport layer (HTL) materials like 2,2′,7,7′-tetrakis[N,N-di (4methoxyphenyl)amino]-9,9′-spirobifluorene (spiro-MeOTAD) or poly[bis(4-phenyl)(2,4,6-trimethylphenyl)amine] (PTAA). [20,24,25] Although these materials result in good performance on short High-quality charge carrier transport materials are of key importance for stable and efficient perovskite-based photovoltaics. This work reports on electron-beam-evaporated nickel oxide (NiO x ) layers, resulting in stable power conversion efficiencies (PCEs) of up to 18.5% when integrated into solar cells employing inkjet-printed perovskite absorbers. By adding oxygen as a process gas and optimizing the layer thickness, transparent and efficient NiOx hole transport layers (HTLs) are fabricated, exhibiting an average absorptance of only 1%. The versatility of the material is demonstrated for different absorber compositions and deposition techniques. As another highlight of this work, all-evaporated perovskite solar cells employing an inorganic NiO x HTL are presented, achieving stable PCEs of up to 15.4%. Along with good PCEs, devices with electron-beam-evaporated NiO x show improved stability under realistic operating conditions with negligible degradation after 40 h of maximum power point tracking at 75 °C. Additionally, a strong improvement in device stability under ultraviolet radiation is found if compared to conventional perovskite solar cell architectures employing other metal oxide charge transport layers (e.g., titanium dioxide). Finally, an all-evaporated perovskite solar mini-module with a NiO x HTL is presented, reaching a PCE of 12.4% on an active device area of 2.3 cm 2 .

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mentioning

confidence: 99%

Electron‐Beam‐Evaporated Nickel Oxide Hole Transport Layers for Perovskite‐Based Photovoltaics

Abzieher

Moghadamzadeh

Schackmar

et al. 2019

Advanced Energy Materials

137

149

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“…[9,10] This technology is expected to successfully contribute to the enormous challenge of future power supply from sustainable energy sources. Nitrogen has been also exploited as inert species [20][21][22][23][24] but its role is still unfocused. Solutions to guarantee the durability of products are mandatory and can be numerous, if the problem is addressed from different perspectives.…”

mentioning

confidence: 99%

Nitrogen Soaking Promotes Lattice Recovery in Polycrystalline Hybrid Perovskites

Alberti

Deretzis

Mannino

et al. 2019

Advanced Energy Materials

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wide dissemination, and high technological throughput. [8] As a unique event in the landscape of solar energy harvesting, perovskite solar cells have experienced an increment of their power conversion efficiency by ≈8% (from 13.4% to 23.7%) in the last 5 years. [9,10] This technology is expected to successfully contribute to the enormous challenge of future power supply from sustainable energy sources. However, the well-known structural instability of hybrid perovskites under working conditions limits a real market uptake of all the related technologies. Solutions to guarantee the durability of products are mandatory and can be numerous, if the problem is addressed from different perspectives.Within the possible approaches to stabilize the perovskite lattice and its behavior under illumination, recent efforts have focused on introducing various treatments, [11,12] molecules, or additives, [13][14][15][16][17][18][19] through different procedures. Nitrogen has been also exploited as inert species [20][21][22][23][24] but its role is still unfocused. The existing (direct or indirect) findings in the literature stimulate the idea of beneficially using N 2 molecules in technological solutions, if their role is persuasively afforded. [25] N 2 molecules are small, safe, and easy to apply.Related to the material stability, we emphasize that the plethora of perovskites produced in different laboratories, with preparation procedures changing from lab to lab and from time to time, ask for treatments that take care and, in a certain extent, reset the starting conditions in a convenient and reproducible manner. This is particularly needed for small grained perovskite layers, on one hand used to implement pinhole-free coverages, but, on the other hand, offering extended lattice discontinuities due to the high surface to volume ratio. In addition to morphology and environment, temperature-related effects are unavoidable during device operation. [24,26] A rationalization of the phenomena needs to embody heating and thermal cycles to preserve the material integrity and/or the structural reversibility versus temperature.In this framework, we argue that nitrogen species have an active role in the stabilization of all the exposed methylammonium lead iodide (MAPbI 3 ) surfaces via their action at grain shells. This conclusion is independent of the particular On the basis of experiment and theory, a general paradigm is drawn that reconsiders N 2 not simply being an inert species but rather an effective healing gas molecule if entering a methylammonium lead iodide (MAPbI 3 ) layer. Nitrogen is soaked into polycrystalline MAPbI 3 via a postdeposition mild thermal treatment under slightly overpressure conditions to promote its diffusion across the whole layer. A significant reduction of radiative recombination and a concurrent increase of light absorption, with a maximum benefit at 80 °C, are observed. Concomitantly, the current of holes drawn from the surfaces with nanometer resolution through a biased tip is raised by a factor of 3 un...

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“…[3][4][5] However, in order to produce them at a large scale, stability and reproducibility issues must be overcome. [6][7][8][9] Thus far, much research on PSCs has been oriented towards compositional engineering. [3][4][5]10 Perovskites with outstanding photovoltaic properties have a distinctive structure, composed by three atoms according to the formula ABX 3 , where A corresponds to a monovalent organic/inorganic cation, B corresponds to a divalent inorganic cation (commonly Pb) and X corresponds to a halide anion (Cl, Br and I).…”

Section: Introductionmentioning

confidence: 99%

Evaluation of multiple cation/anion perovskite solar cells through life cycle assessment

Alberola-Borràs

Vidal

Mora‐Seró

2018

Sustainable Energy Fuels

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After the great initiation of perovskite as a photovoltaic material, laboratory efficiencies similar to other photovoltaic technologies already commercialised have been reached. Consequently, recent research interests on perovskite solar cells try to address the stability improvement as well as make its industrialisation possible. Record efficiencies in perovskite solar cells (PSCs) have been achieved using as active material a multiple cation/anion perovskite by combining methylammonium (MA) and formamidinium (FA), but also Cs cation and I and Br as anions, materials that also have demonstrated a superior stability. Herein, the environmental performance of the production of such perovskite films was evaluated via life cycle assessment. Our study points out that multiple cation/anion perovskite films show major detrimental environmental impacts for all categories assessed, except for abiotic depletion potential, when they are compared with a canonical perovskite MAPbI 3 . In addition, a closer analysis of the materials utilised for the synthesis of the different multiple cation perovskites compositions revealed that lead halide reagents and chlorobenzene were the most adverse compounds in terms of impact. However, the former is used in all the perovskite compositions and the later can be avoided by the use of alternative fabrication methods to anti-solvent. To this extent, FAI, with the current synthesis procedures, is the most determining compound as it increases significantly the impacts and the cost in comparison with MAI. A further economic analysis, exposed that multiple cation perovskites need a significantly higher photoconversion efficiency to produce the same payback times than canonical perovskite.2

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Tailored interfaces of unencapsulated perovskite solar cells for >1,000 hour operational stability

Cited by 747 publications

References 45 publications

Electron‐Beam‐Evaporated Nickel Oxide Hole Transport Layers for Perovskite‐Based Photovoltaics

Electron‐Beam‐Evaporated Nickel Oxide Hole Transport Layers for Perovskite‐Based Photovoltaics

Nitrogen Soaking Promotes Lattice Recovery in Polycrystalline Hybrid Perovskites

Evaluation of multiple cation/anion perovskite solar cells through life cycle assessment

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