Search

Quantum dots (QDs) exhibit size-tunable optical properties, making them suitable for efficient light-sensing and light-emitting devices. Tandem devices that can convert near-infrared (NIR) to visible (Vis) signals can be fabricated by integrating an NIR-sensing QD device with a Vis electroluminescence (EL) QD device. However, these devices require delicate control of the QD layer during processing to prevent damage to the predeposited QD layers in tandem devices during the subsequent deposition of other functional layers. This has restricted attainable device structures for QD-based upconversion devices. Herein, we present a modular approach for fabricating QD-based optoelectric upconversion devices. This approach involves using NIR QD-absorbing (Abs) and Vis QD-EL units as building modules, both of which feature cross-linked functional layers that exhibit structural tolerance to dissolution during subsequent solution-based processes. Tandem devices are fabricated in both normal (EL unit on Abs unit) and inverted (Abs unit on EL unit) structures using the same set of NIR QD-Abs and Vis QD-EL units stacked in opposite sequences. The tandem device in the normal structure exhibits a high NIR photon-to-Vis-photon conversion efficiency of up to 1.9% in a practical transmissive mode. By extending our modular approach, we also demonstrate a three-stack tandem device that incorporates a single NIR-absorbing unit coupled with two EL units, achieving an even higher conversion efficiency of up to 3.2%.

While multi-junction geometries have the potential to boost the efficiency of organic solar cells, the experimental gains yet obtained are still very modest. This work proposes an alternative spectral splitting device concept in which various individual semiconducting junctions with cascading bandgaps are laid side by side, thus the name RAINBOW. Each lateral sub-cell receives a fraction of the spectrum that closely matches the main absorption band of the given semiconductor. Here, simulations are used to identify the important material and device properties of each RAINBOW sub-cell. Using the resulting design rules, three systems are selected, with narrow, medium, and wide effective bandgaps, and their potential as sub-cells in this geometry is experimentally investigated. With the aid of a custom-built setup that generates spectrally spread sunlight on demand, the simulations are experimentally validated, showing that this geometry can lead to a reduction in thermalization losses and an improvement in light harvesting, which results in a relative improvement in efficiency of 46.6% with respect to the best sub-cell. Finally, a working proof-of-concept monolithic device consisting of two sub-cells deposited from solution on the same substrate is fabricated, thus demonstrating the feasibility and the potential of the RAINBOW solar cell concept., (© 2023 The Authors. Advanced Materials published by Wiley‐VCH GmbH.)

Perovskite solar cells (PSCs) are gaining popularity due to their high efficiency and low-cost fabrication. In recent decades, noticeable research efforts have been devoted to improving the stability of these cells under ambient conditions. Moreover, researchers are exploring new materials and fabrication techniques to enhance the performance of PSCs under various environmental conditions. The mechanical stability of flexible PSCs is another area of research that has gained significant attention. The latest research also focuses on developing tin-based PSCs that can overcome the challenges associated with lead-based perovskites. This review article provides a comprehensive overview of the latest advances in materials, fabrication techniques, and stability enhancement strategies for PSCs. It discusses the recent progress in perovskite crystal structure engineering, device construction, and fabrication procedures that has led to significant improvements in the photo conversion efficiency of these solar devices. The article also highlights the challenges associated with PSCs such as their poor stability under ambient conditions and discusses various strategies employed to enhance their stability. These strategies include the use of novel materials for charge transport layers and encapsulation techniques to protect PSCs from moisture and oxygen. Finally, this article provides a critical assessment of the current state of the art in PSC research and discusses future prospects for this technology. This review concludes that PSCs have great potential as a low-cost alternative to conventional silicon-based solar cells but require further research to improve their stability under ambient conditions in view of their definitive commercialization.

Printing a large-area bismuth vanadate photoanode offers a promising approach for cost-effective photoelectrochemical (PEC) water splitting. However, the light absorption trade-off with charge transfer, as well as stability issues always lead to poor PEC efficiency. Here, the solution-processed recipe is advanced with BiI 3 dopant for the printed deposition with controllable crystal growth. The resultant BiVO 4 films prefer (001) orientation with nanorod feature on substrate, allowing a faster charge transfer and improved photocurrent. The BiVO 4 photoanode in tandem with perovskite solar module delivers an operating photocurrent density of 5.88 mA cm -2 at zero bias in 3.11 cm 2 active area under AM 1.5 G illumination, yielding a solar-to-hydrogen efficiency as high as 7.02% for unbiased water splitting. Equally important, the stability of the aged BiVO 4 rods has been addressed to distinguish phase segregation at surface. The photocatalysis degradation composes of vanadium loss and Bi 2 O 3 enriching at the surface, opening a lid on the long-term stability of BiVO 4 photoanodes., (© 2023 Wiley-VCH GmbH.)

Semitransparent solar cells (ST-SCs) have received great attention due to their promising application in many areas, such as building integrated photovoltaics (BIPVs), tandem devices, and wearable electronics. In the past decade, perovskite solar cells (PSCs) have revolutionized the field of photovoltaics (PVs) with their high efficiencies and facile preparation processes. Due to their large absorption coefficient and bandgap tunability, perovskites offer new opportunities to ST-SCs. Here, a general overview is provided on the recent advances in ST-PSCs from materials and devices to applications and some personal perspectives on the future development of ST-PSCs., (© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

The tandem structure is an efficient way to simultaneously tackle absorption and thermalization losses of the single junction solar cells. In this work, a high-performance tandem organic solar cell (OSC) using two subcells with the same donor poly[(2,6-(4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)-benzo[1,2-b:4,5-b']dithiophene))-alt-(5,5-(1',3'-di-2-thienyl-5',7'-bis(2-ethylhexyl)benzo[1',2'-c:4',5'-c']dithiophene-4,8-dione))] (PBDB-T) and two acceptors, F-M and 2,9-bis(2-methylene-(3(1,1-dicyanomethylene)benz[f ]indanone))7,12-dihydro-(4,4,10,10-tetrakis(4-hexylphenyl)-5,11-diocthylthieno[3',2':4,5]cyclopenta[1,2-b]thieno[2″,3″:3',4']cyclopenta[1',2':4,5]thieno[2,3-f][1]benzothiophene (NNBDT), with complementary absorptions is demonstrated. The two subcells show high V oc with value of 0.99 V for the front cell and 0.86 V for the rear cell, which is the prerequisite for obtaining high V oc of their series-connected tandem device. Although there is much absorption overlap for the subcells, a decent J sc of the tandem cell is still obtained owing to the complementary absorption of the two acceptors in a wide range. With systematic device optimizations, a best power conversion efficiency of 14.52% is achieved for the tandem device, with a high V oc of 1.82 V, a notable FF of 74.7%, and a decent J sc of 10.68 mA cm -2 . This work demonstrates a promising strategy of fabricating high-efficiency tandem OSCs through elaborate selection of the active layer materials in each subcell and tradeoff of the V oc and J sc of the tandem cells., (© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

The concept of hybrid tandem device structures that combine metal oxides with thin-film semiconducting photoabsorbers holds great promise for large-scale, robust, and cost-effective bias-free photoelectrochemical water splitting (PEC-WS). This work highlights important steps toward the efficient coupling of high-performance hematite photoanodes with multijunction thin-film silicon photocathodes providing high bias-free photocurrent density. The hybrid PEC-WS device is optimized by testing three types of multijunction silicon photocathodes with the hematite photoanode: amorphous silicon (a-Si:H) tandem: a-Si:H/a-Si:H and triple junction with microcrystalline silicon (μc-Si:H): a-Si:H/a-Si:H/μc-Si:H and a-Si:H/μc-Si:H/μc-Si:H. The results provide evidence that the multijunction structures offer high flexibility for hybrid tandem devices with regard to tunable photovoltages and spectral matching. Furthermore, both photoanode and photocathode are tested under various electrolyte and light concentration conditions, respectively, with respect to their photoelectrochemical performance and stability. A 27 % enhancement in the solar-to-hydrogen conversion efficiency is observed upon concentrating light from 100 to 300 mW cm -2 . Ultimately, bias-free water splitting is demonstrated, with a photocurrent density of 4.6 mA cm -2 (under concentrated illumination) paired with excellent operation stability for more than 24 h of the all-earth-abundant and low-cost hematite/silicon tandem PEC-WS device., (© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

The reported power conversion efficiencies (PCEs) of nonfullerene acceptor (NFA) based organic photovoltaics (OPVs) now exceed 14% and 17% for single-junction and two-terminal tandem cells, respectively. However, increasing the PCE further requires an improved understanding of the factors limiting the device efficiency. Here, the efficiency limits of single-junction and two-terminal tandem NFA-based OPV cells are examined with the aid of a numerical device simulator that takes into account the optical properties of the active material(s), charge recombination effects, and the hole and electron mobilities in the active layer of the device. The simulations reveal that single-junction NFA OPVs can potentially reach PCE values in excess of 18% with mobility values readily achievable in existing material systems. Furthermore, it is found that balanced electron and hole mobilities of >10 -3 cm 2 V -1 s -1 in combination with low nongeminate recombination rate constants of 10 -12 cm 3 s -1 could lead to PCE values in excess of 20% and 25% for single-junction and two-terminal tandem OPV cells, respectively. This analysis provides the first tangible description of the practical performance targets and useful design rules for single-junction and tandem OPVs based on NFA materials, emphasizing the need for developing new material systems that combine these desired characteristics., Competing Interests: The authors declare no conflict of interest.

Solar photon-to-electron conversion with polymer solar cells (PSCs) has experienced rapid development in the recent few years. Even so, the exploration of molecules and devices in efficiently converting near-infrared (NIR) photons into electrons remains critical, yet challenging. Herein presented is a family of near-infrared nonfullerene acceptors (NIR NFAs, T1-T4) with fluorinated regioisomeric A-Aπ-D-Aπ-A backbones for constructing efficient single-junction and tandem PSCs with photon response up to 1000 nm. It is found that the tuning of the regioisomeric bridge (Aπ) and fluoro (F)-substituents on a molecular skeleton strongly influences the backbone conformation and conjugation, leading to the optimized optoelectronic and stable stacking of resultant NFAs, which eventually impacts the performance of derived PSCs. In PSCs, the proximal NFAs with varied F-atoms (T1-T3) mostly outperform than that of distal NFA (T4). Notably, single-junction PSC with PTB7-Th:T2 blend can reach 10.87% power conversion efficiency (PCE), after implementing a solvent additive to improve blend morphology. Moreover, efficient tandem PSCs are fabricated through integrating such NIR cells with mediate bandgap nonfullerene-based subcells, to achieve a PCE of 14.64%. The results reveal the structural design of organic semiconductor and device with improved photovoltaic performance., (© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Highly efficient polymer solar cells with a tandem structure are fabricated by using two excellent photovoltaic polymers and a highly transparent intermediate recombination layer. Power conversion -efficiencies over 10% can be realized with a photovoltaic response within 800 nm., (© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)