Showing papers on "Energy conversion efficiency published in 2019"

Surface passivation of perovskite film for efficient solar cells

Abstract: In recent years, the power conversion efficiency of perovskite solar cells has increased to reach over 20%. Finding an effective means of defect passivation is thought to be a promising route for bringing further increases in the power conversion efficiency and the open-circuit voltage (VOC) of perovskite solar cells. Here, we report the use of an organic halide salt phenethylammonium iodide (PEAI) on HC(NH2)2–CH3NH3 mixed perovskite films for surface defect passivation. We find that PEAI can form on the perovskite surface and results in higher-efficiency cells by reducing the defects and suppressing non-radiative recombination. As a result, planar perovskite solar cells with a certificated efficiency of 23.32% (quasi-steady state) are obtained. In addition, a VOC as high as 1.18 V is achieved at the absorption threshold of 1.53 eV, which is 94.4% of the Shockley–Queisser limit VOC (1.25 V). Planar perovskite solar cells that have been passivated using the organic halide salt phenethylammonium iodide are shown to have suppressed non-radiative recombination and operate with a certified power conversion efficiency of 23.3%.

Efficient, stable and scalable perovskite solar cells using poly(3-hexylthiophene)

Abstract: Perovskite solar cells typically comprise electron- and hole-transport materials deposited on each side of a perovskite active layer. So far, only two organic hole-transport materials have led to state-of-the-art performance in these solar cells1: poly(triarylamine) (PTAA)2–5 and 2,2ʹ,7,7ʹ-tetrakis(N,N-di-p-methoxyphenylamine)-9,9ʹ-spirobifluorene (spiro-OMeTAD)6,7. However, these materials have several drawbacks in terms of commercialization, including high cost8, the need for hygroscopic dopants that trigger degradation of the perovskite layer9 and limitations in their deposition processes10. Poly(3-hexylthiophene) (P3HT) is an alternative hole-transport material with excellent optoelectronic properties11–13, low cost8,14 and ease of fabrication15–18, but so far the efficiencies of perovskite solar cells using P3HT have reached only around 16 per cent19. Here we propose a device architecture for highly efficient perovskite solar cells that use P3HT as a hole-transport material without any dopants. A thin layer of wide-bandgap halide perovskite is formed on top of the narrow-bandgap light-absorbing layer by an in situ reaction of n-hexyl trimethyl ammonium bromide on the perovskite surface. Our device has a certified power conversion efficiency of 22.7 per cent with hysteresis of ±0.51 per cent; exhibits good stability at 85 per cent relative humidity without encapsulation; and upon encapsulation demonstrates long-term operational stability for 1,370 hours under 1-Sun illumination at room temperature, maintaining 95 per cent of the initial efficiency. We extend our platform to large-area modules (24.97 square centimetres)—which are fabricated using a scalable bar-coating method for the deposition of P3HT—and achieve a power conversion efficiency of 16.0 per cent. Realizing the potential of P3HT as a hole-transport material by using a wide-bandgap halide could be a valuable direction for perovskite solar-cell research. A double-layered halide architecture for perovskite solar cells enables the use of dopant-free poly(3-hexylthiophene) as a hole-transport material, forming stable and scalable devices with a certified power conversion efficiency of 22.7 per cent.

Solar absorber material and system designs for photothermal water vaporization towards clean water and energy production

Abstract: Photothermal materials with broad solar absorption and high conversion efficiency have recently attracted significant interest. They are becoming a fast-growing research focus in the area of solar-driven vaporization for clean water production. The parallel development of thermal management strategies through both material and system designs has further improved the overall efficiency of solar vaporization. Collectively, this green solar-driven water vaporization technology has regained attention as a sustainable solution for water scarcity. In this review, we will report the recent progress in solar absorber material design based on various photothermal conversion mechanisms, evaluate the prerequisites in terms of optical, thermal and wetting properties for efficient solar-driven water vaporization, classify the systems based on different photothermal evaporation configurations and discuss other correlated applications in the areas of desalination, water purification and energy generation. This article aims to provide a comprehensive review on the current development in efficient photothermal evaporation, and suggest directions to further enhance its overall efficiency through the judicious choice of materials and system designs, while synchronously capitalizing waste energy to realize concurrent clean water and energy production.

Achieving over 16% efficiency for single-junction organic solar cells

Abstract: To achieve high photovoltaic performance of bulk hetero-junction organic solar cells (OSCs), a range of critical factors including absorption profiles, energy level alignment, charge carrier mobility and miscibility of donor and acceptor materials should be carefully considered. For electron-donating materials, the deep highest occupied molecular orbital (HOMO) energy level that is beneficial for high open-circuit voltage is much appreciated. However, a new issue in charge transfer emerges when matching such a donor with an acceptor that has a shallower HOMO energy level. More to this point, the chemical strategies used to enhance the absorption coefficient of acceptors may lead to increased molecular crystallinity, and thus result in less controllable phase-separation of photoactive layer. Therefore, to realize balanced photovoltaic parameters, the donor-acceptor combinations should simultaneously address the absorption spectra, energy levels, and film morphologies. Here, we selected two non-fullerene acceptors, namely BTPT-4F and BTPTT-4F, to match with a wide-bandgap polymer donor P2F-EHp consisting of an imide-functionalized benzotriazole moiety, as these materials presented complementary absorption and well-matched energy levels. By delicately optimizing the blend film morphology, we demonstrated an unprecedented power conversion efficiency of over 16% for the device based on P2F-EHp:BTPTT-4F, suggesting the great promise of materials matching toward high-performance OSCs.

Single-Crystal MAPbI3 Perovskite Solar Cells Exceeding 21% Power Conversion Efficiency

Abstract: Twenty-micrometer-thick single-crystal methylammonium lead triiodide (MAPbI3) perovskite (as an absorber layer) grown on a charge-selective contact using a solution space-limited inverse-temperatur...

Planar p–n homojunction perovskite solar cells with efficiency exceeding 21.3%

Abstract: Perovskite solar cells (PSCs) have emerged as an attractive photovoltaic technology thanks to their outstanding power conversion efficiency (PCE). Further improvement in the device efficiency is limited by the recombination of the charge carriers in the perovskite layer even when employing heterojunction-based architectures. Here, we propose and demonstrate a p-type perovskite/n-type perovskite homojunction whose built-in electric field promotes oriented transport of the photo-induced carriers, thus reducing carrier recombination losses. By controlling the stoichiometry of the perovskite precursors, we are able to induce n-type or p-type doping. We integrate the homojunction structure in a planar PSC combining a thermally evaporated p-type perovskite layer on a solution-processed n-type perovskite layer. The PSC with a MAPbI3 homojunction achieves a PCE of 20.80% (20.5% certified PCE), whereas the PSC based on a FA0.15MA0.85PbI3 homojunction delivers a PCE of 21.38%. We demonstrate that the homojunction structure is an effective approach, beyond existing planar heterojunction PSCs, to achieve highly efficient PSCs with reduced carrier recombination losses. Carrier recombination limits the power conversion efficiency of perovskite solar cells. Here the authors construct a planar p–n homojunction perovskite solar cell to promote the oriented transport of carriers and reduce recombination, thus enabling power conversion efficiency of 21.3%.

Wide-gap non-fullerene acceptor enabling high-performance organic photovoltaic cells for indoor applications

Abstract: Organic photovoltaic cells are potential candidates to drive low power consumption off-grid electronics for indoor applications. However, their power conversion efficiency is still limited by relat ...

Enabling low voltage losses and high photocurrent in fullerene-free organic photovoltaics

Abstract: 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%.

Multilayer Polypyrrole Nanosheets with Self-Organized Surface Structures for Flexible and Efficient Solar-Thermal Energy Conversion.

Abstract: Converting solar energy into concentrated heat is very appealing for various applications. Polypyrrole (PPy) is known to possess excellent photothermal property with low thermal conductivity, and thus is an ideal candidate for solar-thermal energy conversion. However, solar-thermal materials based on PPy or other conducting polymers still exhibit limited energy conversion efficiency due to the lack of effective light-trapping schemes. Here, it is demonstrated that multilayer PPy nanosheets with spontaneously formed surface structures such as wrinkles and ridges via sequential polymerization on paper substrates can dramatically enhance broadband and wide-angle light absorption across the full solar spectrum, leading to an impressive solar-thermal conversion efficiency of 95.33%. The intriguing solar-thermal properties and structural features of multilayer PPy nanosheets can be used for solar heating and photoactuators. Meanwhile, when used for solar steam generation, the measured efficiency could achieve ≈92% under one sun irradiation. The hierarchically multilayer structure is mechanically flexible and robust, holding great potential for practical solar energy utilization. This study provides a simple and straightforward approach toward engineering light-weight and thermally insulating polymers into efficient solar-thermal materials for emerging solar energy-related applications.

13.6% Efficient Organic Dye-Sensitized Solar Cells by Minimizing Energy Losses of the Excited State

Abstract: The electron-injection energy losses of dye-sensitized solar cells (DSSCs) are among the fundamental problems hindering their successful breakthrough application. Two triazatruxene (TAT)-based sensitizers, with one containing a flexible Z-type double bond and another a rigid single bond, coded as ZL001 and ZL003, respectively, have been synthesized and applied in DSSCs to probe the energy losses in the process of electron injection. Using time-resolved laser spectroscopic techniques in the kinetic study, ZL003 with the rigid single bond promotes much faster electron injection into the conductive band of TiO2 especially in the locally excited state (hot injection), which leads to higher electron density in TiO2 and a higher Voc. The devices based on ZL003 exhibited a champion power conversion efficiency (PCE) of 13.6% with Voc = 956 mV, Jsc = 20.73 mA cm–2, and FF = 68.5%, which are among the highest recorded results to date on single dye-sensitized DSSCs. An independent certified PCE of 12.4% has been obt...

Vertically Aligned Janus MXene-Based Aerogels for Solar Desalination with High Efficiency and Salt Resistance

Abstract: Solar desalination is an effective way of converting solar energy to heat for seawater purification. The structure of absorbers and salt resistance are two crucial parameters for water transport and desalination stability. Here, we designed a vertically aligned Janus MXene aerogel (VA-MXA) with hydrophobic upper layer and hydrophilic bottom layer. Compared with irregular porous channels, such regulatable and well-ordered vertical array structure gives competitive advantage in the capillary water transport, light absorption, and vapor escape. MXene, which possesses a theoretical light-to-heat conversion efficiency of 100%, combined with the Janus structure, can efficiently convert light to heat and prevent the photothermal layer from "direct bulk water contact" with the hydrophobic upper layer, thus decreasing heat loss, while the hydrophilic bottom layer submerged in water can quickly pump water upward through the vertically aligned channels with low transport resistance and, meanwhile, enable effective inhibition of salt crystallization due to rapid dissolution with continuously pumping water. With a vertically aligned and Janus structure by flexible design, the Janus VA-MXA exhibited a high conversion efficiency (87%) and stable water yield for 15 days (∼1.46 kg·m-2·h-1) under 1 sun. About 6 L·m-2 of freshwater was output daily from seawater.

Infrared Light Management Using a Nanocrystalline Silicon Oxide Interlayer in Monolithic Perovskite/Silicon Heterojunction Tandem Solar Cells with Efficiency above 25%

Abstract: Perovskite/silicon tandem solar cells are attractive for their potential for boosting cell efficiency beyond the crystalline silicon (Si) single-junction limit. However, the relatively large optical refractive index of Si, in comparison to that of transparent conducting oxides and perovskite absorber layers, results in significant reflection losses at the internal junction between the cells in monolithic (two-terminal) devices. Therefore, light management is crucial to improve photocurrent absorption in the Si bottom cell. Here it is shown that the infrared reflection losses in tandem cells processed on a flat silicon substrate can be significantly reduced by using an optical interlayer consisting of nanocrystalline silicon oxide. It is demonstrated that 110 nm thick interlayers with a refractive index of 2.6 (at 800 nm) result in 1.4 mA cm − ² current gain in the silicon bottom cell. Under AM1.5G irradiation, the champion 1 cm 2 perovskite/silicon monolithic tandem cell exhibits a top cell + bottom cell total current density of 38.7 mA cm −2 and a certified stabilized power conversion efficiency of 25.2%.

Two-Dimensional Ti3C2Tx MXene Membranes as Nanofluidic Osmotic Power Generators.

Abstract: Salinity-gradient is emerging as one of the promising renewable energy sources but its energy conversion is severely limited by unsatisfactory performance of available semipermeable membranes. Recently, nanoconfined channels, as osmotic conduits, have shown superior energy conversion performance to conventional technologies. Here, ion selective nanochannels in lamellar Ti3C2Tx MXene membranes are reported for efficient osmotic power harvesting. These subnanometer channels in the Ti3C2Tx membranes enable cation-selective passage, assisted with tailored surface terminal groups, under salinity gradient. A record-high output power density of 21 W·m-2 at room temperature with an energy conversion efficiency of up to 40.6% is achieved by controlled surface charges at a 1000-fold salinity gradient. In addition, due to thermal regulation of surface charges and ionic mobility, the MXene membrane produces a large thermal enhancement at 331 K, yielding a power density of up to 54 W·m-2. The MXene lamellar structure, coupled with its scalability and chemical tunability, may be an important platform for high-performance osmotic power generators.

Periodically poled thin-film lithium niobate microring resonators with a second-harmonic generation efficiency of 250,000%/W

Abstract: Lithium niobate (LN), dubbed by many as the silicon of photonics, has recently risen to the forefront of chip-scale nonlinear optics research since its demonstration as an ultralow-loss integrated photonics platform. Due to its significant quadratic nonlinearity (χ(2)), LN inspires many important applications such as second-harmonic generation (SHG), spontaneous parametric downconversion, and optical parametric oscillation. Here, we demonstrate high-efficiency SHG in dual-resonant, periodically poled z-cut LN microrings, where quasi-phase matching is realized by field-assisted domain engineering. Meanwhile, dual-band operation is accessed by optimizing the coupling conditions in fundamental and second-harmonic bands via a single pulley waveguide. As a result, when pumping a periodically poled LN microring in the low power regime at around 1617 nm, an on-chip SHG efficiency of 250,000%/W is achieved, a state-of-the-art value reported among current integrated photonics platforms. An absolute conversion efficiency of 15% is recorded with a low pump power of 115 μW in the waveguide. Such periodically poled LN microrings also present a versatile platform for other cavity-enhanced quasi-phase-matched χ(2) nonlinear optical processes.

Selective light absorber-assisted single nickel atom catalysts for ambient sunlight-driven CO2 methanation.

Abstract: Ambient sunlight-driven CO2 methanation cannot be realized due to the temperature being less than 80 °C upon irradiation with dispersed solar energy. In this work, a selective light absorber was used to construct a photothermal system to generate a high temperature (up to 288 °C) under weak solar irradiation (1 kW m−2), and this temperature is three times higher than that in traditional photothermal catalysis systems. Moreover, ultrathin amorphous Y2O3 nanosheets with confined single nickel atoms (SA Ni/Y2O3) were synthesized, and they exhibited superior CO2 methanation activity. As a result, 80% CO2 conversion efficiency and a CH4 production rate of 7.5 L m−2 h−1 were achieved through SA Ni/Y2O3 under solar irradiation (from 0.52 to 0.7 kW m−2) when assisted by a selective light absorber, demonstrating that this system can serve as a platform for directly harnessing dispersed solar energy to convert CO2 to valuable chemicals. While light-driven CO2 methanation provides a renewable means to upgrade waste emissions, the sunlight is insufficient to drive high temperature CO2 methanation. Here, authors prepare single-atom Ni on Y2O3 with a selective light absorber for ambient-sunlight-driven photothermal CO2 methanation.

High efficiency and fast van der Waals hetero-photodiodes with a unilateral depletion region.

Abstract: Van der Waals (vdW) heterodiodes based on two-dimensional (2D) materials have shown tremendous potential in photovoltaic detectors and solar cells. However, such 2D photovoltaic devices are limited by low quantum efficiencies due to the severe interface recombination and the inefficient contacts. Here, we report an efficient MoS2/AsP vdW hetero-photodiode utilizing a unilateral depletion region band design and a narrow bandgap AsP as an effective carrier selective contact. The unilateral depletion region is verified via both the Fermi level and the infrared response measurements. The device demonstrates a pronounced photovoltaic behavior with a short-circuit current of 1.3 μA and a large open-circuit voltage of 0.61 V under visible light illumination. Especially, a high external quantum efficiency of 71%, a record high power conversion efficiency of 9% and a fast response time of 9 μs are achieved. Our work suggests an effective scheme to design high-performance photovoltaic devices assembled by 2D materials. Photovoltaic devices based on 2D materials still suffer from low quantum efficiencies due to interfacial charge recombination and inefficient contacts. Here, the authors design photovoltaic detectors and photodiodes based on MoS2 and doped AsP heterojunction with unilateral depletion region reporting high external quantum efficiency of 71% under zero applied bias.

Reconfiguration of interfacial energy band structure for high-performance inverted structure perovskite solar cells.

Abstract: Charged defects at the surface of the organic-inorganic perovskite active layer are detrimental to solar cells due to exacerbated charge carrier recombination. Here we show that charged surface defects can be benign after passivation and further exploited for reconfiguration of interfacial energy band structure. Based on the electrostatic interaction between oppositely charged ions, Lewis-acid-featured fullerene skeleton after iodide ionization (PCBB-3N-3I) not only efficiently passivates positively charged surface defects but also assembles on top of the perovskite active layer with preferred orientation. Consequently, PCBB-3N-3I with a strong molecular electric dipole forms a dipole interlayer to reconfigure interfacial energy band structure, leading to enhanced built-in potential and charge collection. As a result, inverted structure planar heterojunction perovskite solar cells exhibit the promising power conversion efficiency of 21.1% and robust ambient stability. This work opens up a new window to boost perovskite solar cells via rational exploitation of charged defects beyond passivation.

Efficient All-Polymer Solar Cells based on a New Polymer Acceptor Achieving 10.3% Power Conversion Efficiency

Abstract: Here we demonstrate efficient all-polymer solar cells (all-PSCs) based on a polymer acceptor named PFBDT-IDTIC. By combining PFBDT-IDTIC with a fluorinated donor polymer (PM6), a high power conversion efficiency of 10.3% can be achieved, which is the highest value reported to date for single-junction all-PSCs. This performance can be attributed to its good absorption property (absorption coefficient: 2.74 × 105 cm–1) and high electron mobility of PFBDT-IDTIC. It is also found that the choice of donor polymer has major impacts on the performance of the cell. By replacing PBDB-T with its fluorinated counterpart, PM6, the VOC, JSC, and FF of the devices were all improved, which can be attributed to the deeper HOMO level of PM6 and more crystalline and pure domains of the active layer blends. Our study provides a promising polymer acceptor for all-PSCs and also shows that selecting a matching donor polymer is important in achieving the optimal all-PSC performance.

Fluorinated Low-Dimensional Ruddlesden-Popper Perovskite Solar Cells with over 17% Power Conversion Efficiency and Improved Stability.

Abstract: Low-dimensional Ruddlesden-Popper perovskites (RPPs) exhibit excellent stability in comparison with 3D perovskites; however, the relatively low power conversion efficiency (PCE) limits their future application. In this work, a new fluorine-substituted phenylethlammonium (PEA) cation is developed as a spacer to fabricate quasi-2D (4FPEA)2 (MA)4 Pb5 I16 (n = 5) perovskite solar cells. The champion device exhibits a remarkable PCE of 17.3% with a Jsc of 19.00 mA cm-2 , a Voc of 1.16 V, and a fill factor (FF) of 79%, which are among the best results for low-dimensional RPP solar cells (n ≤ 5). The enhanced device performance can be attributed as follows: first, the strong dipole field induced by the 4-fluoro-phenethylammonium (4FPEA) organic spacer facilitates charge dissociation. Second, fluorinated RPP crystals preferentially grow along the vertical direction, and form a phase distribution with the increasing n number from bottom to the top surface, resulting in efficient charge transport. Third, 4FPEA-based RPP films exhibit higher film crystallinity, enlarged grain size, and reduced trap-state density. Lastly, the unsealed fluorinated RPP devices demonstrate superior humidity and thermal stability. Therefore, the fluorination of the long-chain organic cations provides a feasible approach for simultaneously improving the efficiency and stability of low-dimensional RPP solar cells.

Compositional Engineering for Thermally Stable, Highly Efficient Perovskite Solar Cells Exceeding 20% Power Conversion Efficiency with 85 °C/85% 1000 h Stability.

Abstract: Perovskite solar cells have received great attention because of their rapid progress in efficiency, with a present certified highest efficiency of 23.3%. Achieving both high efficiency and high thermal stability is one of the biggest challenges currently limiting perovskite solar cells because devices displaying stability at high temperature frequently suffer from a marked decrease of efficiency. In this report, the relationship between perovskite composition and device thermal stability is examined. It is revealed that Rb can suppress the growth of PbI2 even under PbI2 -rich conditions and decreasing the Br ratio in the perovskite absorber layer can prevent the generation of unwanted RbBr-based aggregations. The optimized device achieved by engineering perovskite composition exhibits 92% power conversion efficiency retention in a stress test conducted at 85 °C/85% relative humidity (RH) according to an international standard (IEC 61215) while exceeding 20% power conversion efficiency (certified efficiency of 20.8% at 1 cm2 ). These results reveal the great potential for the practical use of perovskite solar cells in the near future.

Efficiency vs. stability: dopant-free hole transporting materials towards stabilized perovskite solar cells

Abstract: In the last decade, perovskite solar cells have been considered a promising and burgeoning technology for solar energy conversion with a power conversion efficiency currently exceeding 24%. However, although perovskite solar cells have achieved high power conversion efficiency, there are still several challenges limiting their industrial realization. The actual bottleneck for real uptake in the market still remains the cost-ineffective components and instability, to which doping-induced degradation of charge selective layers may contribute significantly. This article overviews the highest performance molecular and polymeric doped and dopant-free HTMs, showing how small changes in the molecular structure such as different atoms and different functional groups and changes in substitution positions or the length of the π-conjugated systems can affect photovoltaic performance and long-term stability of perovskite solar cells.

Highly Efficient and Stable Perovskite Solar Cells via Modification of Energy Levels at the Perovskite/Carbon Electrode Interface.

Abstract: Perovskite solar cells (PSCs) have attracted great attention in the past few years due to their rapid increase in efficiency and low-cost fabrication. However, instability against thermal stress and humidity is a big issue hindering their commercialization and practical applications. Here, by combining thermally stable formamidinium-cesium-based perovskite and a moisture-resistant carbon electrode, successful fabrication of stable PSCs is reported, which maintain on average 77% of the initial value after being aged for 192 h under conditions of 85 °C and 85% relative humidity (the "double 85" aging condition) without encapsulation. However, the mismatch of energy levels at the interface between the perovskite and the carbon electrode limits charge collection and leads to poor device performance. To address this issue, a thin-layer of poly(ethylene oxide) (PEO) is introduced to achieve improved interfacial energy level alignment, which is verified by ultraviolet photoemission spectroscopy measurements. Indeed as a result, power conversion efficiency increases from 12.2% to 14.9% after suitable energy level modification by intentionally introducing a thin layer of PEO at the perovskite/carbon interface.