Explore the vast range of titles available.

In general, mixed cations and anions containing formamidinium (FA), methylammonium (MA), caesium, iodine, and bromine ions are used to stabilize the black α-phase of the FA-based lead triiodide (FAPbI₃) in perovskite solar cells. However, additives such as MA, caesium, and bromine widen its bandgap and reduce the thermal stability. We stabilized the α-FAPbI₃ phase by doping with methylenediammonium dichloride (MDACl₂) and achieved a certified short-circuit current density of between 26.1 and 26.7 milliamperes per square centimeter. With certified power conversion efficiencies (PCEs) of 23.7%, more than 90% of the initial efficiency was maintained after 600 hours of operation with maximum power point tracking under full sunlight illumination in ambient conditions including ultraviolet light. Unencapsulated devices retained more than 90% of their initial PCE even after annealing for 20 hours at 150°C in air and exhibited superior thermal and humidity stability over a control device in which FAPbI₃ was stabilized by MAPbBr₃.

The formation of a dense and uniform thin layer on the substrates is crucial for the fabrication of high-performance perovskite solar cells (PSCs) containing formamidinium with multiple cations and mixed halide anions. The concentration of defect states, which reduce a cell’s performance by decreasing the open-circuit voltage and short-circuit current density, needs to be as low as possible. We show that the introduction of additional iodide ions into the organic cation solution, which are used to form the perovskite layers through an intramolecular exchanging process, decreases the concentration of deep-level defects. The defect-engineered thin perovskite layers enable the fabrication of PSCs with a certified power conversion efficiency of 22.1% in small cells and 19.7% in 1-square-centimeter cells.

Broadening the optical absorption of organic photovoltaic (OPV) materials by enhancing the intramolecular push-pull effect is a general and effective method to improve the power conversion efficiencies of OPV cells. However, in terms of the electron acceptors, the most common molecular design strategy of halogenation usually results in down-shifted molecular energy levels, thereby leading to decreased open-circuit voltages in the devices. Herein, we report a chlorinated non-fullerene acceptor, which exhibits an extended optical absorption and meanwhile displays a higher voltage than its fluorinated counterpart in the devices. This unexpected phenomenon can be ascribed to the reduced non-radiative energy loss (0.206 eV). Due to the simultaneously improved short-circuit current density and open-circuit voltage, a high efficiency of 16.5% is achieved. This study demonstrates that finely tuning the OPV materials to reduce the bandgap-voltage offset has great potential for boosting the efficiency. Halogenation has proved an effective strategy to improve the power conversion efficiencies of organic solar cells but it usually leads to lower open-circuit voltages. Here, Cui et al. unexpectedly obtain higher open-circuit voltages and achieve a record high PCE of 16.5% by chlorination.

Perovskite/CIGS tandem cellsTandem solar cells can boost efficiency by using more of the available solar spectrum. Han et al. fabricated a two-terminal tandem cell with an inorganicorganic hybrid perovskite top layer and a Cu(In,Ga)Se2 (CIGS) bottom layer. Control of the roughness of the CIGS surface and the use of a heavily doped organic hole transport layer were crucial to achieve a 22.4% power conversion efficiency. The unencapsulated tandem cells maintained almost 90% of their efficiency after 500 hours of operation under ambient conditions.Science, this issue p. 904The combination of hybrid perovskite and Cu(In,Ga)Se2 (CIGS) has the potential for realizing high-efficiency thin-film tandem solar cells because of the complementary tunable bandgaps and excellent photovoltaic properties of these materials. In tandem solar device architectures, the interconnecting layer plays a critical role in determining the overall cell performance, requiring both an effective electrical connection and high optical transparency. We used nanoscale interface engineering of the CIGS surface and a heavily doped poly[bis(4-phenyl)(2,4,6-trimethylphenyl)amine] (PTAA) hole transport layer between the subcells that preserves open-circuit voltage and enhances both the fill factor and short-circuit current. A monolithic perovskite/CIGS tandem solar cell achieved a 22.43% efficiency, and unencapsulated devices under ambient conditions maintained 88% of their initial efficiency after 500 hours of aging under continuous 1-sun illumination.

The development of organic solar cells (OSCs) with thick active layers is of crucial importance for the roll-to-roll printing of large-area solar panels. Unfortunately, increasing the active layer thickness usually results in a significant reduction in efficiency. Herein, we fabricated efficient thick-film OSCs with an active layer consisting of one polymer donor and two non-fullerene acceptors. The two acceptors were found to possess enlarged exciton diffusion length in the mixed phase, which is beneficial to exciton generation and dissociation. Additionally, layer by layer approach was employed to optimize the vertical phase separation. Benefiting from the synergetic effects of enlarged exciton diffusion length and graded vertical phase separation, an efficiency of 17.31% (certified value of 16.9%) is obtained for the 300 nm-thick OSC, with a short-circuit current density of 28.36 mA cm −2 , and a high fill factor of 73.0%. Moreover, the device with an active layer thickness of 500 nm also shows an efficiency of 15.21%. This work provides valuable insights into the fabrication of OSCs with thick active layers. Exciton diffusion length and graded vertical phase separation of the active layer play a critical role in the realization of high-performance thick-film organic solar cells (OSCs). Here, authors demonstrated OSCs with an efficiency of 17.31%, with an active layer thickness of around 300 nm.

Strong optical absorption by a semiconductor is a highly desirable property for many optoelectronic and photovoltaic applications. The optimal thickness of a semiconductor absorber is primarily determined by its absorption coefficient. To date, this parameter has been considered as a fundamental material property, and efforts to realize thinner photovoltaics have relied on light-trapping structures that add complexity and cost. Here we demonstrate that engineering cation disorder in a ternary chalcogenide semiconductor leads to considerable absorption increase due to enhancement of the optical transition matrix elements. We show that cation-disorder-engineered AgBiS2 colloidal nanocrystals offer an absorption coefficient that is higher than other photovoltaic materials, enabling highly efficient extremely thin absorber photovoltaic devices. We report solution-processed, environmentally friendly, 30-nm-thick solar cells with short-circuit current density of 27 mA cm−2, a power conversion efficiency of 9.17% (8.85% certified) and high stability under ambient conditions.AgBiS2 nanocrystals with enhanced optical absorption yield efficient ultrathin solar cells.

Despite significant development recently, improving the power conversion efficiency of organic photovoltaics (OPVs) is still an ongoing challenge to overcome. One of the prerequisites to achieving this goal is to enable efficient charge separation and small voltage losses at the same time. In this work, a facile synthetic strategy is reported, where optoelectronic properties are delicately tuned by the introduction of electron-deficient-core-based fused structure into non-fullerene acceptors. Both devices exhibited a low voltage loss of 0.57 V and high short-circuit current density of 22.0 mA cm −2 , resulting in high power conversion efficiencies of over 13.4%. These unconventional electron-deficient-core-based non-fullerene acceptors with near-infrared absorption lead to low non-radiative recombination losses in the resulting organic photovoltaics, contributing to a certified high power conversion efficiency of 12.6%. Improving the power conversion efficiency is the main target of the organic solar cell research. Here Yuan et al. develop unconventional electron-deficient-core-based non-fullerene acceptors to achieve both low voltage loss and high current density, leading to a certified high efficiency of 12.6%.

The chemical structure of donors and acceptors limit the power conversion efficiencies achievable with active layers of binary donor-acceptor mixtures. Here, using quaternary blends, double cascading energy level alignment in bulk heterojunction organic photovoltaic active layers are realized, enabling efficient carrier splitting and transport. Numerous avenues to optimize light absorption, carrier transport, and charge-transfer state energy levels are opened by the chemical constitution of the components. Record-breaking PCEs of 18.07% are achieved where, by electronic structure and morphology optimization, simultaneous improvements of the open-circuit voltage, short-circuit current and fill factor occur. The donor and acceptor chemical structures afford control over electronic structure and charge-transfer state energy levels, enabling manipulation of hole-transfer rates, carrier transport, and non-radiative recombination losses. Efficiency of organic solar cells is determined by the physical properties of donors and acceptors in bulk heterojunction film. The authors optimise quaternary blends to realize a double cascading energy level alignment enabling efficient carrier dissociation and transport, achieving 18% efficiency.

The low output current density of piezoelectric nanogenerators (PENGs) severely restricts their application for ambient mechanical energy harvest. This has been a key challenge in the development of PENG. Here, to conquer this, based on a piezoelectric material with high piezoelectric coefficient (Sm-PMN-PT), a new design of PENG with a three-dimensional intercalation electrode (IENG) is proposed. By creating many boundary interfaces inside the piezoelectric material, the total amount of surface polarization charges increased, which contributes to an increased current density. The IENG can output a maximum peak short-circuit current of 320 μA, and the corresponding current density 290 μA cm −2 is 1.93 and 1.61 times the record values of PENG and triboelectric nanogenerator (TENG), respectively. It can also charge a 1 μF capacitor from 0 V to 8 V in 21 cycles, and the equivalent surface charge density 1690 μC m −2 is 1.35 times the record value of TENG. Increasing the output current density is the key challenge for nanogenerators. Here, a new piezoelectric nanogenerator with a three-dimensional intercalation electrode is developed to reach 290 μA cm −2 by creating and utilizing many boundary interfaces.

Copper Indium Gallium Sulfide Selenide (CIGSSe)-based solar cells, featuring Al/ZnO/ZnMnO/CIGSSe/Cu 2 O/Ni layers, are optimized using the solar cell capacitance simulator (SCAPS) for enhanced photovoltaic (PV) performance. The solar cell design incorporates a CIGSSe absorber layer, a zinc manganese oxide (ZnMnO) buffer layer, and a zinc oxide (ZnO) window layer. The upper/top and back contacts are made of aluminum (Al) and nickel (Ni), respectively, with an electron-reflected-hole transport layer (ER-HTL) of cuprous oxide (Cu 2 O). The performance of the proposed structure can be improved by adjusting the thicknesses of the absorber, buffer, and window layers, along with the acceptor and donor concentrations of the absorber and buffer layers, series and shunt resistance, and temperature. The configuration improves the cell structure’s open-circuit voltage ( V OC ), short-circuit current ( J SC ), fill factor (FF), and power conversion efficiency (PCE). For optimal outcomes, set the acceptor and donor concentrations in the absorber and buffer layers to 10 17 and 10 18 cm –3 , respectively. Furthermore, keep the thicknesses of the absorber layer at 2000 nm, the window and buffer layers at 50 nm, and the ER-HTL at 10 nm. The optimized model demonstrates PV performance characteristics of 1.0642 V for V OC , 36.10 mA/cm 2 for J SC , 81.06% for FF, and 31.15% for PCE under the AM1.5G spectrum. Furthermore, it exhibits a quantum efficiency of around 95.23% at visible wavelengths.