Showing papers on "Energy conversion efficiency published in 2020"
TL;DR: A monolithic perovskite/silicon tandem with a certified power conversion efficiency of 29.15% is reported, made possible by a self-assembled, methyl-substituted carbazole monolayer as the hole-selective layer in the perovSKite cell.
Abstract: Tandem solar cells that pair silicon with a metal halide perovskite are a promising option for surpassing the single-cell efficiency limit. We report a monolithic perovskite/silicon tandem with a certified power conversion efficiency of 29.15%. The perovskite absorber, with a bandgap of 1.68 electron volts, remained phase-stable under illumination through a combination of fast hole extraction and minimized nonradiative recombination at the hole-selective interface. These features were made possible by a self-assembled, methyl-substituted carbazole monolayer as the hole-selective layer in the perovskite cell. The accelerated hole extraction was linked to a low ideality factor of 1.26 and single-junction fill factors of up to 84%, while enabling a tandem open-circuit voltage of as high as 1.92 volts. In air, without encapsulation, a tandem retained 95% of its initial efficiency after 300 hours of operation.
876 citations
689 citations
TL;DR: In this paper, the use of a small-molecule acceptor with torsion-free molecular conformation can achieve a very low degree of energetic disorder and mitigate energy loss in OSCs.
Abstract: Energy loss within organic solar cells (OSCs) is undesirable as it reduces cell efficiency1–4. In particular, non-radiative recombination loss3 and energetic disorder5, which are closely related to the tail states below the band edge and the overall photon energy loss, need to be minimized to improve cell performance. Here, we report how the use of a small-molecule acceptor with torsion-free molecular conformation can achieve a very low degree of energetic disorder and mitigate energy loss in OSCs. The resulting single-junction OSC has an energy loss due to non-radiative recombination of just 0.17 eV and a high power conversion efficiency of up to 16.54% (certified as 15.89% by the National Renewable Energy Laboratory). The findings take studies of organic photovoltaics deeper into a new regime, beyond the limits of energetic disorder and large energy offset for charge generation. An organic solar cell designed with minimal energetic disorder exhibits very low energy loss due to non-radiative recombination and highly efficient operation.
595 citations
450 citations
TL;DR: Xiao et al. as mentioned in this paper used strongly reductive surface-anchoring zwitterionic molecules to suppress Sn2+ oxidation and passivate defects at the grain surfaces in mixed lead-tin perovskite films, enabling an efficiency of 21.7% (certified 20.7%).
Abstract: Monolithic all-perovskite tandem solar cells offer an avenue to increase power conversion efficiency beyond the limits of single-junction cells. It is an important priority to unite efficiency, uniformity and stability, yet this has proven challenging because of high trap density and ready oxidation in narrow-bandgap mixed lead–tin perovskite subcells. Here we report simultaneous enhancements in the efficiency, uniformity and stability of narrow-bandgap subcells using strongly reductive surface-anchoring zwitterionic molecules. The zwitterionic antioxidant inhibits Sn2+ oxidation and passivates defects at the grain surfaces in mixed lead–tin perovskite films, enabling an efficiency of 21.7% (certified 20.7%) for single-junction solar cells. We further obtain a certified efficiency of 24.2% in 1-cm2-area all-perovskite tandem cells and in-lab power conversion efficiencies of 25.6% and 21.4% for 0.049 cm2 and 12 cm2 devices, respectively. The encapsulated tandem devices retain 88% of their initial performance following 500 hours of operation at a device temperature of 54–60 °C under one-sun illumination in ambient conditions. Ensuring both stability and efficiency in mixed lead–tin perovskite solar cells is crucial to the development of all-perovskite tandems. Xiao et al. use an antioxidant zwitterionic molecule to suppress tin oxidation thus enabling large-area tandem cells with 24.2% efficiency and operational stability over 500 hours.
406 citations
TL;DR: Indene-C 60 bisadduct with higher energy level is utilized as an electron transporting material for tin perovskite solar cells and a fullerene derivative is used to greatly suppress carrier interface recombination and obtain record high cell efficiency of 12%.
Abstract: Tin perovskite is rising as a promising candidate to address the toxicity and theoretical efficiency limitation of lead perovskite. However, the voltage and efficiency of tin perovskite solar cells are much lower than lead counterparts. Herein, indene-C60 bisadduct with higher energy level is utilized as an electron transporting material for tin perovskite solar cells. It suppresses carrier concentration increase caused by remote doping, which significantly reduces interface carriers recombination. Moreover, indene-C60 bisadduct increases the maximum attainable photovoltage of the device. As a result, the use of indene-C60 bisadduct brings unprecedentedly high voltage of 0.94 V, which is over 50% higher than that of 0.6 V for device based on [6,6]-phenyl-C61-butyric acid methyl ester. The device shows a record power conversion efficiency of 12.4% reproduced in an accredited independent photovoltaic testing lab.
381 citations
TL;DR: In this article, a 2D Ruddlesden-Popper phase (2DRP) perovskite solar cells with improved photostability and environmental stability compared with their three-dimensional (3D) counterparts are presented.
Abstract: Two-dimensional Ruddlesden–Popper phase (2DRP) perovskites are known to exhibit improved photostability and environmental stability compared with their three-dimensional (3D) counterparts. However, fundamental questions remain over the interaction between the bulky alkylammoniums and the 2DRP perovskite framework. Here, we unambiguously demonstrate that a sulfur–sulfur interaction is present for a new bulky alkylammonium, 2-(methylthio)ethylamine hydrochloride (MTEACl). In addition to a weaker van der Waals interaction, the interaction between sulfur atoms in two MTEA molecules enables a (MTEA)2(MA)4Pb5I16 (n = 5) perovskite framework with enhanced charge transport and stabilization. The result is 2DRP perovskite solar cells with significantly improved efficiency and stability. Cells with a power conversion efficiency as high as 18.06% (17.8% certified) are achieved, along with moisture tolerance for up to 1,512 h (under 70% humidity conditions), thermal stability for 375 h (at 85 °C) and stability under continuous light stress (85% of the initial efficiency retained over 1,000 h of operation at the maximum power point). Two-dimensional perovskite solar cells have been engineered to be robust against moisture, high temperatures and light stress.
378 citations
TL;DR: The results indicate that PDINN is an effective cathode interfacial material and interlayer engineering via suitable intermolecular interactions is a feasible approach to improve device performance of OSCs.
Abstract: In organic solar cells (OSCs), cathode interfacial materials are generally designed with highly polar groups to increase the capability of lowering the work function of cathode. However, the strong polar group could result in a high surface energy and poor physical contact at the active layer surface, posing a challenge for interlayer engineering to address the trade-off between device stability and efficiency. Herein, we report a hydrogen-bonding interfacial material, aliphatic amine-functionalized perylene-diimide (PDINN), which simultaneously down-shifts the work function of the air stable cathodes (silver and copper), and maintains good interfacial contact with the active layer. The OSCs based on PDINN engineered silver-cathode demonstrate a high power conversion efficiency of 17.23% (certified value 16.77% by NREL) and high stability. Our results indicate that PDINN is an effective cathode interfacial material and interlayer engineering via suitable intermolecular interactions is a feasible approach to improve device performance of OSCs. It is desired to design cathode interfacial layers to simultaneously improve the efficiency and stability of organic solar cells and tune the cathode properties. Here, Yao et al. develop such interfacial layers for the best donor-acceptor system and achieve a high certified efficiency close to 17%.
366 citations
361 citations
TL;DR: Geisz et al. as discussed by the authors presented a series-connected, six-junction inverted metamorphic structure with a 1-Sun global efficiency of 39.2% when tuned to the global spectrum.
Abstract: Single-junction flat-plate terrestrial solar cells are fundamentally limited to about 30% solar-to-electricity conversion efficiency, but multiple junctions and concentrated light make much higher efficiencies practically achievable. Until now, four-junction III–V concentrator solar cells have demonstrated the highest solar conversion efficiencies. Here, we demonstrate 47.1% solar conversion efficiency using a monolithic, series-connected, six-junction inverted metamorphic structure operated under the direct spectrum at 143 Suns concentration. When tuned to the global spectrum, a variation of this structure achieves a 1-Sun global efficiency of 39.2%. Nearly optimal bandgaps for six junctions were fabricated using alloys of III–V semiconductors. To develop these junctions, it was necessary to minimize threading dislocations in lattice-mismatched III–V alloys, prevent phase segregation in metastable quaternary III–V alloys and understand dopant diffusion in complex structures. Further reduction of the series resistance within this structure could realistically enable efficiencies over 50%. Stacking multiple junctions with different bandgaps and operating under concentrated light allows solar cells to reach efficiencies beyond the limits of standard devices. Geisz et al. present a six-junction solar cell based on III–V materials with a 47.1% efficiency—the highest reported to date.
360 citations
TL;DR: In this article, an effective oleic acid (OA) ligand-assisted cation exchange strategy was proposed for controllable synthesis of Cs1−xFAxPbI3 QDs across the whole composition range.
Abstract: The mixed caesium and formamidinium lead triiodide perovskite system (Cs1−xFAxPbI3) in the form of quantum dots (QDs) offers a pathway towards stable perovskite-based photovoltaics and optoelectronics. However, it remains challenging to synthesize such multinary QDs with desirable properties for high-performance QD solar cells (QDSCs). Here we report an effective oleic acid (OA) ligand-assisted cation-exchange strategy that allows controllable synthesis of Cs1−xFAxPbI3 QDs across the whole composition range (x = 0–1), which is inaccessible in large-grain polycrystalline thin films. In an OA-rich environment, the cross-exchange of cations is facilitated, enabling rapid formation of Cs1−xFAxPbI3 QDs with reduced defect density. The hero Cs0.5FA0.5PbI3 QDSC achieves a certified record power conversion efficiency (PCE) of 16.6% with negligible hysteresis. We further demonstrate that the QD devices exhibit substantially enhanced photostability compared with their thin-film counterparts because of suppressed phase segregation, and they retain 94% of the original PCE under continuous 1-sun illumination for 600 h.
TL;DR: In this article, the authors modified the end groups of BTP-4F from IC-2F to CPTCN-Cl to achieve near optimal energy level match, resulting in higher open-circuit voltage (VOC) and power conversion efficiency (PCE).
TL;DR: In this article, a new member of the Y-series acceptor family, Y18, was designed and synthesized, which adopts a fused benzotriazole segment with unique luminescence properties as its electron-deficient core.
Abstract: Finding effective molecular design strategies to enable efficient charge generation and small energy loss is among the long-standing challenges in developing high performance non-fullerene organic solar cells (OSCs). Recently, we reported Y-series non-fullerene acceptors with an electron-deficient-core-based fused structure (typically Y6), opening a new door to achieve high external quantum efficiency (∼80%) while maintaining low energy loss (∼0.57 eV). On this basis, further reducing the energy losses and ultimately improving the performance of OSCs has become a research hotspot. In this paper, we design and synthesize a new member of the Y-series acceptor family, Y18, which adopts a fused benzotriazole segment with unique luminescence properties as its electron-deficient core. Compared to Y6, the benzotriazole-based acceptor Y18 exhibits extended optical absorption and higher voltage. Consequently, the device delivers a promising power conversion efficiency of 16.52% with a very low energy loss of 0.53 eV. Further device optimization by exploiting a ternary blend strategy allowed us to achieve a high efficiency of 17.11% (certified as 16.76% by NREL). Y18 may become one of the most important candidate materials for its broader absorption spectra and higher voltage of Y18 (compared to Y6) in the OSCs field.
TL;DR: In this paper, a thermally-localized multistage solar still (TMSS) architecture was proposed to achieve a record-high solar-to-vapor conversion efficiency of 385% with a production rate of 5.78 L m−2 h−1 under one-sun illumination.
Abstract: Passive vapor generation systems with interfacial solar heat localization enable high-efficiency low-cost desalination. In particular, recent progress combining interfacial solar heating and vaporization enthalpy recycling through a capillary-fed multistage architecture, known as the thermally-localized multistage solar still (TMSS), significantly improves the performance of passive solar desalination. Yet, state-of-the-art experimental demonstrations of solar-to-vapor conversion efficiency are still limited since the dominant factors and the general design principle for TMSS were not well-understood. In this work, we show optimizing the overall heat and mass transport in a multistage configuration plays a key role for further improving the performance. This understanding also increases the flexibility of material choices for the TMSS design. Using a low-cost and free-of-salt accumulation TMSS architecture, we experimentally demonstrated a record-high solar-to-vapor conversion efficiency of 385% with a production rate of 5.78 L m−2 h−1 under one-sun illumination, where more than 75% of the total production was collected through condensation. This work not only significantly improves the performance of existing passive solar desalination technologies for portable and affordable drinking water, but also provides a comprehensive physical understanding and optimization principle for TMSS systems.
TL;DR: Three-dimensional structured graphene metamaterial (SGM) is proposed and demonstrated that takes advantages of wavelength selectivity from metallic trench-like structures and broadband dispersionless nature and excellent thermal conductivity from the ultrathin graphene meetingamaterial film.
Abstract: An ideal solar-thermal absorber requires efficient selective absorption with a tunable bandwidth, excellent thermal conductivity and stability, and a simple structure for effective solar thermal energy conversion. Despite various solar absorbers having been demonstrated, these conditions are challenging to achieve simultaneously using conventional materials and structures. Here, we propose and demonstrate three-dimensional structured graphene metamaterial (SGM) that takes advantages of wavelength selectivity from metallic trench-like structures and broadband dispersionless nature and excellent thermal conductivity from the ultrathin graphene metamaterial film. The SGM absorbers exhibit superior solar selective and omnidirectional absorption, flexible tunability of wavelength selective absorption, excellent photothermal performance, and high thermal stability. Impressive solar-to-thermal conversion efficiency of 90.1% and solar-to-vapor efficiency of 96.2% have been achieved. These superior properties of the SGM absorber suggest it has a great potential for practical applications of solar thermal energy harvesting and manipulation. Here, the authors demonstrate a selective solar thermal absorber with wavelength selectivity, arising from metallic trench-like structures, using broadband dispersionless ultrathin graphene metamaterial film, with excellent thermal conductivity.
TL;DR: In this article, a novel polymer acceptor PJ1 that exhibits a narrow band gap around 1.4 eV and a high extinction coefficient about 1.39 × 105 cm−1.
TL;DR: Ammonia (NH3), one of the basic chemicals in most fertilizers and a promising carbon-free energy storage carrier, is typically synthesized via the Haber-Bosch process with high energy consumption as discussed by the authors.
Abstract: Ammonia (NH3), one of the basic chemicals in most fertilizers and a promising carbon-free energy storage carrier, is typically synthesized via the Haber–Bosch process with high energy consumption a...
TL;DR: This work provides an effective approach to simultaneously lower the energy loss and promote the charge separation of OPVs by molecular design strategy.
Abstract: Low energy loss and efficient charge separation under small driving forces are the prerequisites for realizing high power conversion efficiency (PCE) in organic photovoltaics (OPVs). Here, a new molecular design of nonfullerene acceptors (NFAs) is proposed to address above two issues simultaneously by introducing asymmetric terminals. Two NFAs, BTP-S1 and BTP-S2, are constructed by introducing halogenated indandione (A1 ) and 3-dicyanomethylene-1-indanone (A2 ) as two different conjugated terminals on the central fused core (D), wherein they share the same backbone as well-known NFA Y6, but at different terminals. Such asymmetric NFAs with A1 -D-A2 structure exhibit superior photovoltaic properties when blended with polymer donor PM6. Energy loss analysis reveals that asymmetric molecule BTP-S2 with six chlorine atoms attached at the terminals enables the corresponding devices to give an outstanding electroluminescence quantum efficiency of 2.3 × 10-2 %, one order of magnitude higher than devices based on symmetric Y6 (4.4 × 10-3 %), thus significantly lowering the nonradiative loss and energy loss of the corresponding devices. Besides, asymmetric BTP-S1 and BTP-S2 with multiple halogen atoms at the terminals exhibit fast hole transfer to the donor PM6. As a result, OPVs based on the PM6:BTP-S2 blend realize a PCE of 16.37%, higher than that (15.79%) of PM6:Y6-based OPVs. A further optimization of the ternary blend (PM6:Y6:BTP-S2) results in a best PCE of 17.43%, which is among the highest efficiencies for single-junction OPVs. This work provides an effective approach to simultaneously lower the energy loss and promote the charge separation of OPVs by molecular design strategy.
TL;DR: In this article, a device simulation of FASnI3-based solar cells is performed by using SCAPS to inspect their impact on device performance, including the effect of changing conduction band offset and valence band offset, doping concentration and thickness of electron transport layer and hole transport layer (HTL).
TL;DR: This Perspective analyzes the key design strategies of high-performance n-type molecular photovoltaic materials and highlights instructive examples of their various applications, including in ternary and tandem solar cells towards high efficiency, semitransparentSolar cells towards power generating building facades and windows, and indoor photvoltaics for driving low power consumption devices.
Abstract: The use of photovoltaic technologies has been regarded as a promising approach for converting solar energy to electricity and mitigating the energy crisis, and among these, organic photovoltaics (O...
TL;DR: In this article, a non-fullerene acceptor DTY6 is designed to apply in organic solar cell (OSC) module devices, and when blended with donor PM6, they exhibit excellent performance with power conversion efficiency over 16% when using non-halogen solvent o-xylene.
TL;DR: It is shown that the photocatalytic activities and energy conversion efficiency can be well tuned by ferroelectric-paraelectric phase transition of AgBiP2Se6 monolayer, and the importance of ferro electric polarization on water splitting is revealed.
Abstract: Photocatalytic water splitting is a promising technology to solve the energy crisis and provide renewable and clean energies. Recently, although numerous 2D materials have been proposed as the photocatalytic candidates, the strategies to effectively modulate photocatalytic reactions and conversion efficiency are still lacking. Herein, based on first-principles calculations, we show that the photocatalytic activities and energy conversion efficiency can be well tuned by ferroelectric-paraelectric phase transition of a AgBiP2Se6 monolayer. It is found that the AgBiP2Se6 monolayer has a higher potential and driving forces of photogenerated holes for water oxidation in the ferroelectric phase, but higher corresponding values of photogenerated electrons for the hydrogen reduction reaction in the paraelectric phase. Besides, the solar-to-hydrogen energy conversion efficiency is also tunable with the phase transition; it is up to 10.04% at the ferroelectric phase due to the better carrier utilization, but only 6.66% at the paraelectric phase. Moreover, the exciton binding energy is always smaller in the paraelectric state than that in the ferroelectric state, indicating that the ferroelectric switch could also make a directional adjustment to the photoexcited carrier separation. Our theoretical investigation not only reveals the importance of ferroelectric polarization on water splitting, but also opens an avenue to modify the photocatalytic properties of 2D ferroelectric materials via a ferroelectric switch.
TL;DR: Here, the efficiency and stability of planar PSCs are enhanced by improving the interface contact between the SnO2 electron-transport layer (ETL) and the perovskite layer, which results in high operational stability and promising potential for application in flexible and large-area devices.
Abstract: Perovskite solar cells (PSCs) have rapidly developed and achieved power conversion efficiencies of over 20% with diverse technical routes. Particularly, planar-structured PSCs can be fabricated with low-temperature (≤150 °C) solution-based processes, which is energy efficient and compatible with flexible substrates. Here, the efficiency and stability of planar PSCs are enhanced by improving the interface contact between the SnO2 electron-transport layer (ETL) and the perovskite layer. A biological polymer (heparin potassium, HP) is introduced to regulate the arrangement of SnO2 nanocrystals, and induce vertically aligned crystal growth of perovskites on top. Correspondingly, SnO2 -HP-based devices can demonstrate an average efficiency of 23.03% on rigid substrates with enhanced open-circuit voltage (VOC ) of 1.162 V and high reproducibility. Attributed to the strengthened interface binding, the devices obtain high operational stability, retaining 97% of their initial performance (power conversion efficiency, PCE > 22%) after 1000 h operation at their maximum power point under 1 sun illumination. Besides, the HP-modified SnO2 ETL exhibits promising potential for application in flexible and large-area devices.
01 Nov 2020
TL;DR: In this article, a gradient Mg doping strategy is introduced to engineer tantalum nitride's band structure and control its defects, leading to an applied bias photon-to-current efficiency of 3.25%.
Abstract: Ta3N5 is a promising photoanode material with a theoretical maximum solar conversion efficiency of 15.9% for photoelectrochemical water splitting. However, the highest applied bias photon-to-current efficiency achieved so far is only 2.72%. To bridge the efficiency gap, effective carrier management strategies for Ta3N5 photoanodes should be developed. Here, we propose to use gradient Mg doping for band structure engineering and defect control of Ta3N5. The gradient Mg doping profile in Ta3N5 induces a gradient of the band edge energetics, which greatly enhances the charge separation efficiency. Furthermore, defect-related recombination is significantly suppressed due to the passivation effect of Mg dopants on deep-level defects and, more importantly, the matching of the gradient Mg doping profile with the distribution of defects within Ta3N5. As a result, a photoanode based on the gradient Mg-doped Ta3N5 delivers a low onset potential of 0.4 V versus that of a reversible hydrogen electrode and a high applied bias photon-to-current efficiency of 3.25 ± 0.05%. Despite the efforts to tune their properties, the efficiency of tantalum nitride photoanodes falls short of the theoretical value. Here, a gradient Mg doping strategy is introduced to engineer tantalum nitride’s band structure and control its defects, leading to an applied bias photon-to-current efficiency of 3.25%.
TL;DR: Stabilization of the desired α-FAPbI3 perovskite phase by protecting it with a two-dimensional (2D) IBA2F APb2I7 (IBA = iso-butylammonium overlayer, formed via stepwise annealing) is reported on.
Abstract: As a result of their attractive optoelectronic properties, metal halide APbI3 perovskites employing formamidinium (FA+ ) as the A cation are the focus of research. The superior chemical and thermal stability of FA+ cations makes α-FAPbI3 more suitable for solar-cell applications than methylammonium lead iodide (MAPbI3 ). However, its spontaneous conversion into the yellow non-perovskite phase (δ-FAPbI3 ) under ambient conditions poses a serious challenge for practical applications. Herein, we report on the stabilization of the desired α-FAPbI3 perovskite phase by protecting it with a two-dimensional (2D) IBA2 FAPb2 I7 (IBA=iso-butylammonium overlayer, formed via stepwise annealing. The α-FAPbI3 /IBA2 FAPb2 I7 based perovskite solar cell (PSC) reached a high power conversion efficiency (PCE) of close to 23 %. In addition, it showed excellent operational stability, retaining around 85 % of its initial efficiency under severe combined heat and light stress, that is, simultaneous exposure with maximum power tracking to full simulated sunlight at 80 °C over 500 h.
TL;DR: A simple low-temperature-processed In2 O3 /SnO2 bilayer ETL is developed and used for fabricating a new PSC device that maintains 97.5% initial efficiency after 80 d in N2 without encapsulation and retains 91% of itsInitial efficiency after 180 h under 1 sun continuous illumination.
Abstract: An electron-transport layer (ETL) with appropriate energy alignment and enhanced charge transfer is critical for perovskite solar cells (PSCs). However, interfacial energy level mismatch limits the electrical performance of PSCs, particularly the open-circuit voltage (VOC ). Herein, a simple low-temperature-processed In2 O3 /SnO2 bilayer ETL is developed and used for fabricating a new PSC device. The presence of In2 O3 results in uniform, compact, and low-trap-density perovskite films. Moreover, the conduction band of In2 O3 is shallower than that of Sn-doped In2 O3 (ITO), enhancing the charge transfer from perovskite to ETL, thus minimizing VOC loss at the perovskite and ETL interface. A planar PSC with a power conversion efficiency of 23.24% (certified efficiency of 22.54%) is obtained. A high VOC of 1.17 V is achieved with the potential loss at only 0.36 V. In contrast, devices based on single SnO2 layers achieve 21.42% efficiency with a VOC of 1.13 V. In addition, the new device maintains 97.5% initial efficiency after 80 d in N2 without encapsulation and retains 91% of its initial efficiency after 180 h under 1 sun continuous illumination. The results demonstrate and pave the way for the development of efficient photovoltaic devices.
TL;DR: In this article, a trifluoromethylation was used for non-fullerene acceptors, resulting in an ultra-narrow band-gap molecule named BTIC-CF3-γ.
TL;DR: A fractal-designed switched-capacitor-convertor is reported as a high efficiency power management strategy for triboelectric nanogenerators with characteristics including high conversion efficiency, minimum output impedance, and electrostatic voltage applicability.
Abstract: Owing to the advantages of integration and being magnet-free and light-weight, the switched-capacitor-convertor plays an increasing role compared to traditional transformer in some specific power supply systems. However, the high output impedance and switching loss largely reduces its power efficiency, due to imperfect topology and transistors. Herein, we propose a fractal-design based switched-capacitor-convertors with characteristics including high conversion efficiency, minimum output impedance, and electrostatic voltage applicability. As a double-function output power management system for triboelectric nanogenerators, it delivers over 67 times charge boosting and 954 W m−2 power density in pulse mode, and achieves over 94% total energy transfer efficiency in constant mode. The establishment of the fractal-design switched-capacitor-convertors provides significant guidance for the development of power management toward multi-functional output for numerous applications. The successful demonstration in triboelectric nanogenerators also declares its great potential in electric vehicles, DC micro-grids etc. Power management systems are urgently needed for maximally utilizing the energy generated from triboelectric energy devices. Here, the authors report a fractal-designed switched-capacitor-convertor as a high efficiency power management strategy for triboelectric nanogenerators.
TL;DR: A polymer acceptor-doping general strategy is shown and a thermally stable bulk heterojunction photovoltaic system is reported, which exhibits an improved power conversion efficiency and shows a longer lifetime.
Abstract: The thermal stability of organic solar cells is critical for practical applications of this emerging technology. Thus, effective approaches and strategies need to be found to alleviate their inherent thermal instability. Here, we show a polymer acceptor-doping general strategy and report a thermally stable bulk heterojunction photovoltaic system, which exhibits an improved power conversion efficiency of 15.10%. Supported by statistical analyses of device degradation data, and morphological characteristics and physical mechanisms study, this polymer-doping blend shows a longer lifetime, nearly keeping its efficiency (t = 800 h) under accelerated aging tests at 150 oC. Further analysis of the degradation behaviors indicates a bright future of this system in outer space applications. Notably, the use of polymer acceptor as a dual function additive in the other four photovoltaic systems was also confirmed, demonstrating the good generality of this polymer-doping strategy. Thermal instability is a critical bottleneck for bulk heterojunction organic solar cells. Here Yang et al. use barely 1 wt% of a polymer acceptor as an additive to simultaneously improve the device efficiency and thermal stability of several state-of-the-art organic photovoltaic systems at high temperatures.
University of Electronic Science and Technology of China1, Fuzhou University2, Huazhong University of Science and Technology3, China University of Science and Technology4, Queensland University of Technology5, University of Newcastle6, National University of Singapore7, Hazara University8, University of New South Wales9
TL;DR: In this paper, a successful synthesis of CdSe quantum dots (QDs) modified phosphorus doped g-C3N4 (P-CN) for advanced photocatalytic applications is reported.
Abstract: Solar energy harvesting and conversion into useful chemical energy with the aid of semiconductor photocatalysts is a promising technique to solve both energy and environmental issues. This work reports a successful synthesis of CdSe quantum dots (QDs) modified phosphorus doped g-C3N4 (P-CN) for advanced photocatalytic applications. Phosphorus doping and structural coupling with CdSe QDs are shown to significantly extend visible-light response of g-C3N4 up to 700 nm. The optimized sample 4CdSe/P-CN demonstrates enhanced visible-light driven overall water splitting activities for H2 and O2 evolution i.e. 113 and 55.5 μmol.h−1. g−1, respectively, as well as very high photocatalytic CO2 to CH4 conversion efficiency (47 μmol.h−1. g−1). It also exhibit higher activity (78 %) for 2,4-dichlorophenol degradation as compared to pristine CN-sample. Combined photoluminescence, transient/single wavelength photocurrent, photoelectrochemical, and coumarin fluorescence spectroscopy demonstrate that 4CdSe/P-CN nanocomposite exhibit enhanced charge separation efficiency which is responsible for improved visible light catalytic activities. Our work thus provide a new strategy to design low-cost and sustainable photocatalysis with wide visible-light activity for practical overall water splitting and CO2 reduction applications.