Wei-Hsuan Chang

Improved air stability of perovskite solar cells via solution-processed metal oxide transport layers

Lead halide perovskite solar cells have recently attracted tremendous attention because of their excellent photovoltaic efficiencies. However, the poor stability of both the perovskite material and the charge transport layers has so far prevented the fabrication of devices that can withstand sustained operation under normal conditions. Here, we report a solution-processed lead halide perovskite solar cell that has p-type NiO(x) and n-type ZnO nanoparticles as hole and electron transport layers, respectively, and shows improved stability against water and oxygen degradation when compared with devices with organic charge transport layers. Our cells have a p-i-n structure (glass/indium tin oxide/NiO(x)/perovskite/ZnO/Al), in which the ZnO layer isolates the perovskite and Al layers, thus preventing degradation. After 60 days storage in air at room temperature, our all-metal-oxide devices retain about 90% of their original efficiency, unlike control devices made with organic transport layers, which undergo a complete degradation after just 5 days. The initial power conversion efficiency of our devices is 14.6 ± 1.5%, with an uncertified maximum value of 16.1%.

An Efficient Triple‐Junction Polymer Solar Cell Having a Power Conversion Efficiency Exceeding 11%

Tandem solar cells have the potential to improve photon conversion efficiencies (PCEs) beyond the limits of single-junction devices. In this study, a triple-junction tandem design is demonstrated by employing three distinct organic donor materials having bandgap energies ranging from 1.4 to 1.9 eV. Through optical modeling, balanced photon absorption rates are achieved and, thereby, the photo-currents are matched among the three subcells. Accordingly, an efficient triple-junction tandem organic solar cell can exhibit a record-high PCE of 11.5%.

Solution-processed hybrid perovskite photodetectors with high detectivity

Photodetectors capture optical signals with a wide range of incident photon flux density and convert them to electrical signals instantaneously. They have many important applications including imaging, optical communication, remote control, chemical/biological sensing and so on. Currently, GaN, Si and InGaAs photodetectors are used in commercially available products. Here we demonstrate a novel solution-processed photodetector based on an organic-inorganic hybrid perovskite material. Operating at room temperature, the photodetectors exhibit a large detectivity (the ability to detect weak signals) approaching 10(14) Jones, a linear dynamic range over 100 decibels (dB) and a fast photoresponse with 3-dB bandwidth up to 3 MHz. The performance is significantly better than most of the organic, quantum dot and hybrid photodetectors reported so far; and is comparable, or even better than, the traditional inorganic semiconductor-based photodetectors. Our results indicate that with proper device interface design, perovskite materials are promising candidates for low-cost, high-performance photodetectors.

Moisture assisted perovskite film growth for high performance solar cells

Moisture is assumed to be detrimental to organometal trihalide perovskite, as excess water can damage the crystallinity of the perovskite structure. Here, we report a growth mode for via thermal annealing of the perovskite precursor film in a humid environment (e.g., ambient air) to greatly improve the film quality, grain size, carrier mobility, and lifetime. Our method produces devices with maximum power conversion efficiency of 17.1% and a fill factor of 80%, revealing a promising route to achieve high quality perovskite polycrystalline films with superior optoelectronic properties that can pave the way towards efficient photovoltaic conversion.

A Selenium‐Substituted Low‐Bandgap Polymer with Versatile Photovoltaic Applications

IO N Organic photovoltaic (OPV) devices provide an opportunity to utilize the solar energy effi ciently while maintaining low cost. [ 1 ] To harvest a greater part of the solar spectrum, lowering the energy bandgap of the active material is a major task for materials scientists. The design and synthesis of low-bandgap (LBG) conjugated polymers for use as electron donor materials for bulk heterojuction (BHJ) polymer solar cell (PSC) applications have attracted remarkable attention during the last decade. [ 2 ] The reasons for pursuing LBG polymers include: 1) The Shockley-Quiesser equation indicates a bandgap of around 1.4 eV is ideal for a single junction solar cell device. [ 3 ]

Synthesis of 5H-Dithieno[3,2-b:2′,3′-d]pyran as an Electron-Rich Building Block for Donor–Acceptor Type Low-Bandgap Polymers

We describe the detailed synthesis and characterization of an electron-rich building block, dithienopyran (DTP), and its application as a donor unit in lowbandgap conjugated polymers. The electron-donating property of the DTP unit was found to be the strongest among the most frequently used donor units such as benzodithiophene (BDT) or cyclopentadithiophene (CPDT) units. When the DTP unit was polymerized with the strongly electron-deficient difluorobenzothiadiazole (DFBT) unit, a regiorandom polymer (PDTP−DFBT, bandgap = 1.38 eV) was obtained. For comparison with the DTP unit, polymers containing alternating benzodithiophene (BDT) or cyclopentadithiophene (CPDT) units and the DFBT unit were synthesized (PBDT−DFBT and PCPDT−DFBT). We found that the DTP based polymer PDTP−DFBT shows significantly improved solubility and processability compared to the BDT or CPDT based polymers. Consequently, very high molecular weight and soluble PDTP−DFBT can be obtained with less bulky side chains. Interestingly, PDTP−DFBT shows excellent performance in bulk-heterojunction solar cells with power conversion efficiencies reaching 8.0%, which is significantly higher than PBDT−DFBT and PCPDT−DFBT based devices. This study demonstrates that DTP is a promising building block for high-performance solar cell materials.

Perovskite Solar Cells Employing Dopant‐Free Organic Hole Transport Materials with Tunable Energy Levels

Conjugated small-molecule hole-transport materials (HTMs) with tunable energy levels are designed and synthesized for efficient perovskite solar cells. A champion device with efficiency of 16.2% is demonstrated using a dopant-free DERDTS-TBDT HTM, while the DORDTS-DFBT-HTM-based device shows an inferior performance of 6.2% due to its low hole mobility and unmatched HOMO level with the valence band of perovskite film.

High-performance semi-transparent polymer solar cells possessing tandem structures

In this study we employed tandem device architectures to tune the external appearance and light-conversion properties of polymer solar cells (PSCs) from visibly transparent to semi-transparent, making them more versatile for integrated photovoltaic applications and more efficient under solar illumination. Our best transparent solar cell was a tandem PSC exhibiting an efficiency of 6.4% and a maximum transmission of 51% at 550 nm; in contrast, a semi-transparent tandem PSC having an average transmission of 30% in the visible range exhibited an efficiency greater than 7%.

Perovskite/polymer monolithic hybrid tandem solar cells utilizing a low-temperature, full solution process†

In the current study, a monolithic integration of perovskite and polymer subcells into a tandem structure is realized through a full solution process. The wide bandgap perovskite absorber (CH3NH3PbI3) is processed via a one-step deposition employing an additive-assisted solvent wash method. In particular, a small molecule additive, BmPyPhB, is added into the precursor solution to improve the uniformity of the initial nucleation process of the crystal by providing heterogeneous nucleation sites throughout the solution space. Next, a solvent wash method is employed to induce the fast crystallization of uniform and well-defined grains in the absorber layer as well as to reduce the requirement for thermal annealing. Thus, the highest power conversion efficiency (PCE) of 9.1% is obtained for a single junction, planar-structured CH3NH3PbI3 solar cell. For the polymer absorber, a new IR-sensitive block copolymer, PBSeDTEG8, with photosensitivity up to 950 nm is utilized to broaden the photoresponse of the tandem solar cell. More importantly, this polymer:PCBM blend exhibits improved thermal stability, which can endure thermal annealing process while fabricating the perovskite subcell. Subsequently, this hybrid tandem solar cell based on perovskite/polymer subcells achieves the highest efficiency of 10.2%.

Integrated perovskite/bulk-heterojunction toward efficient solar cells.

We successfully demonstrated an integrated perovskite/bulk-heterojunction (BHJ) photovoltaic device for efficient light harvesting and energy conversion. Our device efficiently integrated two photovoltaic layers, namely a perovskite film and organic BHJ film, into the device. The device structure is ITO/TiO2/perovskite/BHJ/MoO3/Ag. A wide bandgap small molecule DOR3T-TBDT was used as donor in the BHJ film, and a power conversion efficiency (PCE) of 14.3% was achieved in the integrated device with a high short circuit current density (JSC) of 21.2 mA cm(-2). The higher JSC as compared to that of the traditional perovskite/HTL (hole transporting layer) device (19.3 mA cm(-2)) indicates that the BHJ film absorbs light and contributes to the current density of the device. Our result further suggests that the HTL in traditional perovskite solar cell, even with good light absorption capability, cannot contribute to the overall device photocurrent, unless this HTL becomes a BHJ layer (by adding electron transporting material like PC71BM).