The Change in Winter Wheat Response to Deoxynivalenol and Fusarium Head Blight Through Technological and Agronomic Progress.

Fusarium head blight (FHB) in wheat causes yield loss, quality reduction, and mycotoxin contamination in temperate wheat production areas worldwide. The objective of this study was to quantify the progress of agronomic and FHB management strategies over the past two decades in FHB suppression and agronomic performance of winter wheat in environments favorable for FHB. Field experiments were conducted in environments typical of FHB epidemics to compare common agronomic and FHB management practices used in the 1996 era compared with those used in 2016. The experiments included a comparison of three different nitrogen (N) fertilizer application rates and six old (1996-era) and new (modern-era) winter wheat cultivars representing combinations of susceptibility and era to FHB, with and without a fungicide applied at flowering (pydiflumetofen + propiconazole). To mimic environments favorable for infection (similar to 1996 in Ontario, Canada), plots were challenged at 50% anthesis with F. graminearum macroconidia suspension followed by mist irrigation. The modern management strategy of using moderately resistant cultivars, a fungicide applied at flowering, and a high rate of N fertilizer reduced total deoxynivalenol by 67%, reduced Fusarium-damaged kernels by 49%, reduced FHB index by 86%, increased grain test weight by 11%, and increased grain yield by 31% compared with the standard management practice of seeding highly susceptible cultivars with no fungicide and a lower rate of N fertilizer recommended in the 1996 era. This study enabled a published economic assessment of the return on investment for the improvements in cultivars, fungicide, and N fertilizer applications since 1996.

Planar Heterojunction Organic Photodetectors Based on Fullerene and Non-fullerene Acceptor Bilayers for a Tunable Spectral Response.

Planar heterojunction (PHJ) organic photodetectors are potentially more stable than traditional bulk heterojunction counterparts because of the absence of uncontrolled phase separation in the donor and acceptor binary blend system. This work reports a new class of PHJ organic photodetectors based on the medium-band gap fullerene C60 and low-band gap fused-ring non-fullerene acceptor ID-MeIC bilayer structure, which allows a wide range of spectral response tuning across the UV-visible-near-infrared (UV-vis-NIR) region by tailoring individual layer thickness. The C60 layer not only increases the external quantum efficiency at 745 nm by 57% but also reduces dark currents by two orders of magnitude. More importantly, the p-type poly[N,N'-bis(4-butylphenyl)-N,N'-bis(phenyl)-benzi] is found to be the key compound to conduct the layer-by-layer fabrication as combined with n-type ID-MeIC for higher charge extraction efficiency. In light of the above information, PHJ organic photodetectors exhibited a specific detectivity of 6.5 × 1010 Jones to detect NIR light at 745 nm under -0.1 V. The linear dynamic range was estimated to be 80 dB. This work has demonstrated a feasible approach to develop a PHJ architecture with tunable spectral response in the UV-vis-NIR range toward long-term stable organic photodetectors for potential applications in flexible and wearable biomedical sensors.

Delocalization of exciton and electron wavefunction in non-fullerene acceptor molecules enables efficient organic solar cells.

A major challenge for organic solar cell (OSC) research is how to minimize the tradeoff between voltage loss and charge generation. In early 2019, we reported a non-fullerene acceptor (named Y6) that can simultaneously achieve high external quantum efficiency and low voltage loss for OSC. Here, we use a combination of experimental and theoretical modeling to reveal the structure-property-performance relationships of this state-of-the-art OSC system. We find that the distinctive π-π molecular packing of Y6 not only exists in molecular single crystals but also in thin films. Importantly, such molecular packing leads to (i) the formation of delocalized and emissive excitons that enable small non-radiative voltage loss, and (ii) delocalization of electron wavefunctions at donor/acceptor interfaces that significantly reduces the Coulomb attraction between interfacial electron-hole pairs. These properties are critical in enabling highly efficient charge generation in OSC systems with negligible donor-acceptor energy offset.

High-Performance Semitransparent Organic Solar Cells with Excellent Infrared Reflection and See-Through Functions.

Clean energy production and saving play vital impacts on the sustainability of the global community. Herein, high-performance semitransparent organic solar cells (ST-OSCs) with excellent features of power generation, being see-through, and infrared reflection of heat dissipation, with promising perspectives for building-integrated photovoltaics (BIPVs) are reported. To simultaneously improve average visible transmittance (AVT) and power conversion efficiency (PCE), formally in a trade-off relationship, of ST-OSCs, new ternary blends with alloy-like near-infrared (NIR) acceptors are employed, which are effective to improve device efficiency while maintaining visible absorption unchanged, resulting in PCEs of 16.8% for opaque devices and 13.1% for semitransparent OSCs (AVT of 22.4% and infrared photon radiation rejection (IRR) of 77%). Further, multifunctional ST-OSCs are realized via introducing simple, yet effective photonic reflectors, together with optical simulation, leading to not only perfect fitting of the visible transmittance peak (555 nm) to the photopic response of the human eye but also an excellent IRR of 90% (780-2500 nm), along with 23% AVT and over 12% PCE. This is thought to be the best-performing multifunctional ST-OSC with promising prospects as BIPVs in terms of power generation, heat dissipation, and being see-through.

Semitransparent Organic Solar Cells Enabled by a Sequentially Deposited Bilayer Structure.

Semitransparent organic solar cells (ST-OSCs) have been regarded as a promising candidate for building integrated photovoltaics. In general, most of the ST-OSCs are based on a bulk heterojunction (BHJ) structure in which the morphology of the BHJ film must be delicately optimized. In this work, we introduce a sequentially deposited bilayer structure into ST-OSCs by using a PTB7-Th/IEICO-4F combination. The adoption of the bilayer structure not only simplifies the device optimization, but it is also found that, as the donor and the acceptor are separately deposited, the power conversion efficiency (PCE) of bilayer ST-OSCs can be improved by simply increasing the thickness of IEICO-4F, which has strong near infrared absorption but weak visible light absorption, without significantly affecting the average visible light transmittance (AVT) of the device. However, in the BHJ structure, the increase in BHJ film thickness unavoidably enhances the donor absorption in the visible light region, leading to a tradeoff between the PCE and AVT in BHJ-structured ST-OSCs. Eventually, the bilayer-structured device exhibits a better overall performance than the BHJ-structured device, e.g., a PCE of 8.5% for the bilayer structure versus a PCE of 8.1% for the BHJ structure with an AVT around 21%. Our findings indicate that the sequentially deposited bilayer structure, aside from its easy processing characteristics, also has great potential for preparing high-performance ST-OSCs.

Performance optimization of tandem organic solar cells at varying incident angles based on optical analysis method.

Tandem organic solar cells (OSCs) show great potential due to advantages such as the utilization of wide-spectrum light and low thermalization loss. The current mismatch between sub-cells is one of the major issues reducing the final output efficiency of a tandem device. In this paper, we focus on the current mismatch of tandem OSCs at oblique incidence and aim to reduce its adverse effect on the performances of realistic devices working at varying incident angle. Firstly, we propose an optical analysis method based on the 4×4 matrix formalism to analyze and optimize the performance of tandem solar cells at arbitrary incident angles. Compared with those optimal designs via matching the currents of sub-cells only at normal incidence, the proposed method chooses the optimal structure of the tandem device by maximizing the generated energy density per day with considering the current match at different incident angles during daytime. With the proposed method, a typical tandem organic solar cell is optimized as an example, and the optimized tandem device has a balanced current match at all incident angles during a whole day. Experimental results demonstrate that the generated energy density per day of the optimized tandem device has increased by 4.9% compared to the conventional device optimized only at normal incidence. The proposed method and results are expected to provide some new insights for the performance analysis and optimization of tandem or multi-junction solar cells, especially those devices exhibiting serious current mismatch between sub-cells at varying incident angles in practical applications.

Surpassing the 10% efficiency milestone for 1-cm2 all-polymer solar cells.

Naphthalenediimide-based n-type polymeric semiconductors are extensively used for constructing high-performance all-polymer solar cells (all-PSCs). For such all-polymer systems, charge recombination can be reduced by using thinner active layers, yet suffering insufficient near-infrared light harvesting from the polymeric acceptor. Conversely, increasing the layer thickness overcomes the light harvesting issue, but at the cost of severe charge recombination effects. Here we demonstrate that to manage light propagation within all-PSCs, a thick bulk-heterojunction film of approximately 350 nm is needed to effectively enhance photo-harvesting in the near-infrared region. To overcome the severe charge recombination in such a thick film, a non-halogenic additive is used to induce a well-ordered micro-structure that inherently suppresses recombination loss. The combined strategies of light management and delicate morphology optimization lead to a promising efficiency over 10% for thick-film all-PSCs with active area of 1 cm2, showing great promise for future large-scale production and application of all-PSCs.

A Tandem Organic Solar Cell with PCE of 14.52% Employing Subcells with the Same Polymer Donor and Two Absorption Complementary Acceptors.

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 Voc 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 Voc of their series-connected tandem device. Although there is much absorption overlap for the subcells, a decent Jsc 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 Voc of 1.82 V, a notable FF of 74.7%, and a decent Jsc 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 Voc and Jsc of the tandem cells.

Near-Infrared Electron Acceptors with Fluorinated Regioisomeric Backbone for Highly Efficient Polymer Solar Cells.

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.

Organic and solution-processed tandem solar cells with 17.3% efficiency.

Although organic photovoltaic (OPV) cells have many advantages, their performance still lags far behind that of other photovoltaic platforms. A fundamental reason for their low performance is the low charge mobility of organic materials, leading to a limit on the active-layer thickness and efficient light absorption. In this work, guided by a semi-empirical model analysis and using the tandem cell strategy to overcome such issues, and taking advantage of the high diversity and easily tunable band structure of organic materials, a record and certified 17.29% power conversion efficiency for a two-terminal monolithic solution-processed tandem OPV is achieved.

11.2% All-Polymer Tandem Solar Cells with Simultaneously Improved Efficiency and Stability.

All-polymer solar cells (all-PSCs) that contain both p-type and n-type polymeric materials blended together as light-absorption layers have attracted much attention, since the blend of a polymeric donor and acceptor should present superior photochemical, thermal, and mechanical stability to those of small molecular-based organic solar cells. In this work, the interfacial stability is studied by using highly stable all-polymer solar cell as a platform. It is found that the thermally deposited metal electrode atoms can diffuse into the active layer during device storage, which consequently greatly decreases the power conversion efficiency. Fortunately, the diffusion of metal atoms can be slowed down and even blocked by using thicker interlayer materials, high-glass-transition-temperature interlayer materials, or a tandem device structure. Learning from this, homojunction tandem all-PSCs are successfully developed that simultaneously exhibit a record power conversion efficiency over 11% and remarkable stability with efficiency retaining 93% of the initial value after thermally aging at 80 °C for 1000 h.

Nonfullerene Tandem Organic Solar Cells with High Performance of 14.11.

Fabricating solar cells with tandem structure is an efficient way to broaden the photon response range without further increasing the thermalization loss in the system. In this work, a tandem organic solar cell (TOSC) based on highly efficient nonfullerene acceptors (NFAs) with series connection type is demonstrated. To meet the different demands of front and rear sub-cells, two NFAs named F-M and NOBDT with a whole absorption range from 300 to 900 nm are designed, when blended with wide bandgap polymer 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 narrow bandgap polymer PTB7-Th, respectively, the PBDB-T: F-M system exhibits a high Voc of 0.98 V and the PTB7-Th: NOBDT system shows a remarkable Jsc of 19.16 mA cm-2 , which demonstrate their potential in the TOSCs. With the guidance of optical simulation, by systematically optimizing the thickness of each layer in the TOSC, an outstanding power conversion efficiency of 14.11%, with a Voc of 1.71 V, a Jsc of 11.72 mA cm-2 , and a satisfactory fill factor of 0.70 is achieved; this result is one of the top efficiencies reported to date in the field of organic solar cells.

High-Performance Color-Tunable Perovskite Light Emitting Devices through Structural Modulation from Bulk to Layered Film.

Adding 2-phenoxyethylamine (POEA) into a CH3 NH3 PbBr3 precursor solution can modulate the organic-inorganic hybrid perovskite structure from bulk to layered, with a photoluminescence and electroluminescence shift from green to blue. Meanwhile, POEA can passivate the CH3 NH3 PbBr3 surface and help to obtain a pure CH3 NH3 PbBr3 phase, leading to an improvement of the external quantum efficiency to nearly 3% in CH3 NH3 PbBr3 LED.

High-Performance Polymer Tandem Solar Cells Employing a New n-Type Conjugated Polymer as an Interconnecting Layer.

A new n-type polymer, PF3N-2TNDI, with high electron mobility, is developed as efficient cathode interfacial material and interconnecting layer (ICL) for constructing high-performance tandem organic solar cells. Tandem cells employing the ICL with structure of PF3N-2TNDI/Ag/ PEDOT: PSS achieve a high power conversion efficiency (PCE) of 11.35%. Moreover, flexible tandem cells with PCE over 10% are also demonstrated.