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Abstract Organic solar cells (OSCs) are considered as a crucial energy source for flexible and wearable electronics. Pseudo-planar heterojunction (PPHJ) OSCs simplify the solution preparation and morphology control. However, non-halogenated solvent-printed PPHJ often have an undesirable vertical component distribution and insufficient donor/acceptor interfaces. Additionally, the inherent brittleness of non-fullerene small molecule acceptors (NFSMAs) in PPHJ leads to poor flexibility, and the NFSMAs solution shows inadequate viscosity during the printing of acceptor layer. Herein, we propose a novel approach termed polymer-incorporated pseudo-planar heterojunction (PiPPHJ), wherein a small amount of polymer donor is introduced into the NFSMAs layer. Our findings demonstrate that the incorporation of polymer increases the viscosity of acceptor solution, thereby improving the blade-coating processability and overall film quality. Simultaneously, this strategy effectively modulates the vertical component distribution, resulting in more donor/acceptor interfaces and an improved power conversion efficiency of 17.26%. Furthermore, PiPPHJ-based films exhibit superior tensile properties, with a crack onset strain of 12.0%, surpassing PPHJ-based films (9.6%). Consequently, large-area (1 cm2) flexible devices achieve a considerable efficiency of 13.30% and maintain excellent mechanical flexibility with 82% of the initial efficiency after 1000 bending cycles. These findings underscore the significant potential of PiPPHJ-based OSCs in flexible and wearable electronics.

Abstract In this study, a novel wide‐bandgap small molecule guest material, ITOA, designed and synthesized for fabricating efficient ternary organic solar cells (OSCs) ITOA complements the absorbance of the PM6:Y6 binary system, exhibiting strong crystallinity and modest miscibility. ITOA optimizes the morphology by promoting intensive molecular packing, reducing domain size, and establishing a preferred vertical phase distribution. These features contribute to improved and well‐balanced charge transport, suppressed carrier recombination, and efficient exciton dissociation. Consequently, a significantly enhanced efficiency of 18.62% for the ternary device is achieved, accompanied by increased short‐circuit current density (JSC), fill factor (FF), and open‐circuit voltage (VOC). Building on this success, replacing Y6 with BTP‐eC9 leads to an outstanding PCE of 19.33% for the ternary OSCs. Notably, the introduction of ITOA expedites the formation of the optimized morphology, resulting in an impressive PCE of 18.04% for the ternary device without any postprocessing. Moreover, the ternary device exhibits enhanced operational stability under maximum power point (MPP) tracking. This comprehensive study demonstrates that a rationally designed guest molecule can optimize morphology, reduce energy loss, and streamline the fabrication process, essential for achieving high efficiency and stability in OSCs, paving the way for practical commercial applications.

The poly3,4-ethylenedioxythiophene) poly(styrene sulfonate) (PEDOT:PSS) hole transport layer (HTL) has always played a crucial role in achieving high-efficiency organic solar cells (OSCs) owing to its unique advantages of suitable energy levels and high optical transparency. However, the inherent insulation and easy aggregation property of PSS results in relatively low conductivity and high surface roughness of the PEDOT:PSS film, which is unfavorable for charge transport and the morphology of the top layer. To address these problems, we use PEDOT:PSS diluted in a series of alcoholic solvents and evaluate them on the PM6:Y6 system. Among these, the PM6:Y6 devices using PEDOT:PSS modified with ethanol as the HTL demonstrate the best vertical phase segregation and carrier extraction. In addition, the PEDOT:PSS film with added ethanol also has the smoothest surface compared to those diluted in the other alcoholic solvents. Finally, a high power conversion efficiency of 18.13% was obtained with the PM6:Y6 devices based on PEDOT:PSS modified by ethanol. This work provides a sufficient reference for the alcoholic modification of PEDOT:PSS and also proposes a feasible solution for high-efficiency OSCs.

Abstract Organic solar cells (OSCs) have demonstrated over 19% power conversion efficiency (PCE) with the help of material innovation and device optimization. Co‐working with newly designed materials, traditional solvent additives, 1‐chloronaphthalene (CN), and 1,8‐diodooctane (DIO) are still powerful in morphology modulation towards satisfying efficiencies. Here, we chose recently reported high‐performance polymer donors (PM6 & D18‐Fu) and small molecular acceptors (Y6 & L8‐BO) as active layer materials and processed them by different conditions (CN or DIO or none). Based on corresponding 12 groups of device results, and their film morphology characterizations (both ex‐situ and in‐situ ones), the property‐performance relationships are revealed case by case. It is thereby supposed to be taken as a successful attempt to demonstrate the importance and complexity of donor‐acceptor‐additive interaction, since the device performance and physics analyses are also tightly combined with morphology variation. Furthermore, ternary blend construction for PCE improvement provides an approaching 19% level and showcases the potential of understanding‐guided‐optimization (UGO) in the future of OSCs.

BackgroundPrevious studies have suggested that the gut microbiota (GM) is closely associated with the development of autoimmune cholestatic liver disease (ACLD), but limitations, such as the presence of confounding factors, have resulted in a causal relationship between the gut microbiota and autoimmune cholestatic liver disease that remains uncertain. Thus, we used two-sample Mendelian randomization as a research method to explore the causal relationship between the two.MethodsPooled statistics of gut microbiota from a meta-analysis of genome-wide association studies conducted by the MiBioGen consortium were used as an instrumental variable for exposure factors. The Pooled statistics for primary biliary cholangitis (PBC) and primary sclerosing cholangitis (PSC) were obtained from the R9 version of the FinnGen database (https://r9.finngen.fi/). Inverse-variance Weighted (IVW), cML-MA, MR-Egger regression, Weighted median (WME), Weighted mode (WM), and Simple mode (SM) were used to detect the association between intestinal flora and the causal relationship between intestinal flora and ACLD, in which IVW method was dominant, was assessed based on the effect indicator dominance ratio (odds ratio, OR) and 95% confidence interval (CI). Sensitivity analysis, heterogeneity test, gene pleiotropy test, MR pleiotropy residual sum and outlier test (MR-PRESSO) were combined to verify the stability and reliability of the results. Reverse Mendelian randomization analysis was performed on gut microbiota and found to be causally associated with ACLD.ResultsThe IVW results showed that the relative abundance of the genus Clostridium innocuum group, genus Butyricicoccus, and genus Erysipelatoclostridium was negatively correlated with the risk of PBC, that is, increased abundance reduced the risk of PBC and was a protective, and the relative abundance of the genus Eubacterium hallii was positively correlated with the risk of PSC, which is a risk factor for PSC. Family Clostridiaceae1 and family Lachnospiraceae were negatively correlated with the risk of PSC, which is a protective factor for PSC.ConclusionThis study found a causal relationship between gut microbiota and ACLD. This may provide valuable insights into gut microbiota-mediated pathogenesis of ACLD. It is necessary to conduct a large-sample randomized controlled trial (RCT) at a later stage to validate the associated role of the relevant gut microbiota in the risk of ACLD development and to explore the associated mechanisms.

Abstract Organic solar cells (OSCs) have emerged as a promising solution for sustainable energy production, offering advantages such as a low carbon footprint, short energy payback period, and compatibility with eco‐solvents. However, the use of hazardous solvents continues to dominate the best‐performing OSCs, mainly because of the challenges of controlling phase separation and domain crystallinity in eco‐solvents. In this study, we combined the solvent vapor treatment of CS2 and thermal annealing to precisely control the phase separation and domain crystallinity in PM6:M‐Cl and PM6:O‐Cl systems processed with the eco‐solvent o‐xylene. This method resulted in a maximum power conversion efficiency (PCE) of 18.4%, which is among the highest values reported for sustainable binary OSCs. Furthermore, the fabrication techniques were transferred from spin coating in a nitrogen environment to blade printing in ambient air, retaining a PCE of 16.0%, showing its potential for high‐throughput and scalable production. In addition, a comparative analysis of OSCs processed with hazardous and green solvents was conducted to reveal the differences in phase aggregation. This work not only underscores the significance of sustainability in OSCs but also lays the groundwork for unlocking the full potential of open‐air‐printable sustainable OSCs for commercialization.

Abstract High-efficiency organic solar cells are often achieved using toxic halogenated solvents and additives that are constrained in organic solar cells industry. Therefore, it is important to develop materials or processing methods that enabled highly efficient organic solar cells processed by halogen free solvents. In this paper, we report an innovative processing method named auxiliary sequential deposition that enables 19%-efficiency organic solar cells processed by halogen free solvents. Our auxiliary sequential deposition method is different from the conventional blend casting or sequential deposition methods in that it involves an additional casting of dithieno[3,2-b:2’,3’-d]thiophene between the sequential depositions of the donor (D18-Cl) and acceptor (L8-BO) layers. The auxiliary sequential deposition method enables dramatic performance enhancement from 15% to over 18% compared to the blend casting and sequential deposition methods. Furthermore, by incorporating a branched-chain-engineered acceptor called L8-BO-X, device performance can be boosted to over 19% due to increased intermolecular packing, representing top-tier values for green-solvent processed organic solar cells. Comprehensive morphological and time-resolved characterizations reveal that the superior blend morphology achieved through the auxiliary sequential deposition method promotes charge generation while simultaneously suppressing charge recombination. This research underscores the potential of the auxiliary sequential deposition method for fabricating highly efficient organic solar cells using environmentally friendly solvents.

The two-step layer-by-layer (LBL) deposition of donor and acceptor films enables desired vertical phase separation and high performance in organic solar cells (OSCs), which becomes a promising technology for large-scale printing devices. However, limitations including the use of toxic solvents and unpredictable infiltration between donor and acceptor still hinder the commercial production of LBL OSCs. Herein, we developed a water-based nanoparticle (NP) ink containing donor polymer to construct a mesoscale structure that could be infiltrated with an acceptor solution. Using non-halogen o-xylene for acceptor deposition, the LBL strategy with a mesoscale structure delivered outstanding efficiencies of 18.5% for binary PM6:L8-BObased LBL OSCs. Enhanced charge carrier mobility and restricted trap states were observed in the meso-LBL devices with optimized vertical morphology. It is believed that the findings in this work will bring about more research interest and effort on eco-friendly processing in preparation for the industrial production of OSCs.

IntroductionGlobally, terraces, and rice terrace systems face problems that affect their sustainability, such as terrace degradation, abandonment, de-agriculturalization, labor migration, etc. The implementation of development projects such as reforestation, poverty alleviation, and tourism development have changed traditional smallholder livelihood patterns. It is not clear whether farmers' livelihoods have become more resilient or vulnerable as a result.MethodsUsing survey data on households' livelihoods in a rice terrace system in Southern China, we evaluated the livelihood impacts of multiple changes.ResultsThe results show that development projects are not entirely beneficial. The attributes and intensity of the disturbance of projects (e.g., tourism) on land functions, and differentiated farmer strategies jointly drive the hierarchical evolution of livelihood vulnerability. In detail, underdeveloped tourism increased rather than reduced livelihood vulnerability; the role of agriculture in livelihood directly exacerbated the variation in vulnerability levels; this resulted in the most vulnerable livelihood for households that are exogenously dependent or located in the core tourism area.DiscussionSubsequently, an evolutionary model of livelihood vulnerability is proposed in this study. Based on this, we judged that the livelihood vulnerability of rice terrace systems has entered a chaotic stage of adaptation. Reducing livelihood vulnerability will require the support of a tangible and circular pathway of benefits between farmers and the land. Policies should focus on the heterogeneity of farmers and the “negative effects” of development projects on livelihood. This household-level farmer livelihood vulnerability dynamics study goes beyond anti-poverty to provide science-based practical guidance to promote the sustainable development of rice terrace systems.

Microbial communities and functions play an important role in soil carbon and nitrogen transformations, and, in recent decades, the abandonment of terraces is prevalant in the hilly areas of China. However, it is unclear how soil carbon and nitrogen contents and prokaryotic communities changed as a result of the abandonment of ancient rice terraces. Soil profiles ranging from 0 to 120 cm were excavated on drylands, forestlands (both converted due to the abandonment of ancient rice terraces), and ancient rice terraces. The FAPROTAX database was used to predict soil prokaryotic functional groups. The results showed that soil organic carbon (SOC) and total nitrogen (TN) contents of abandoned ancient rice terraces in drylands (51.09 and 33.20%) and forestlands (31.76 and 16.59%) were significantly reduced. Soil prokaryotic diversity and community composition changed dramatically after the abandonment of terraces and were mainly affected by soil pH and ammoniacal nitrogen (NH4+-N). Community composition was more similar in drylands and forestlands. Moreover, the abundance of transformation functional genes of carbon (57.01 and 50.80%) and nitrogen (15.25 and 22.36%) in bacterial communities was significantly reduced, and of carbon in the archaeal communities decreased sharply (28.10 and 46.50%), in drylands and forestlands. These findings indicate that short-term abandonment of ancient rice terraces reduces soil carbon and nitrogen contents, which may be closely related to the decline of prokaryotic functional groups. The prevalence of short-term abandonment of rice terraces in the hilly areas of China may pose adverse ecological risks.

Organic solar cells (OSCs) have gained increasing attention. Among the various directions in OSCs, all-polymer solar cells (all-PSCs) have emerged as a highly promising and currently active research area due to their excellent film formation properties, mechanical properties, and thermal stabilities. However, most of the high-efficiency all-PSCs are processed from chloroform with an active layer thickness of ~100 nm. In order to meet the requirements for industrialization, a thicker active layer processed from low-vapor pressure solvents (preferentially a hydrocarbon solvent) is strongly desired. Herein, we employ toluene (a hydrocarbon solvent with a much higher boiling point than chloroform) and a method known as sequential processing (SqP) to mitigate the rapid decline in efficiency with increasing film thickness. We show that SqP enables a more favorable vertical phase segregation that leads to less trap-assisted recombination and enhanced charge extraction and lifetime than blend-cast devices at higher film thicknesses.

For thousands of years, terracing has been one of the most important systems for preventing soil erosion, conserving water, and increasing agricultural production. Despite having a long history, the wide-ranging effects and mechanisms of terracing are poorly understood owing to large-scale spatial and temporal distribution patterns and the challenges related to assessing the ecosystem services of terraced landscapes. Thus, our study aims to review comprehensively the effect of terraces by describing the mechanisms behind terraced systems. Terraces provide many ecosystem services, including the reduction of runoff and sediment by over 41.9% and 52%, respectively, and the improvement of grain yields and soil moisture content by 44.8% and 12.9%, respectively. In addition, terracing can also contribute toward the conservation of plant biodiversity on a local scale. However, as terraces age, a number of disadvantages gradually emerge, including interference with water circulation and the development of serious environmental problems caused by poorly designed or mismanaged terraces, where the average runoff and soil loss can be 1–5 times that of well-managed terraces. Although understanding the complexity and multifaceted effects of terracing is vital for terrace construction and management, the negative effects of terracing are often not considered, and existing studies have several shortcomings. Within this context, this paper aims to describe both the benefits and disadvantages of terracing, investigate the gaps in current research, as well as discuss preventive and remedial measures so as to negate the possible bad impacts of terracing.

Abstract Considering the robust and stable nature of the active layers, advancing the power conversion efficiency (PCE) has long been the priority for all‐polymer solar cells (all‐PSCs). Despite the recent surge of PCE, the photovoltaic parameters of the state‐of‐the‐art all‐PSC still lag those of the polymer:small molecule‐based devices. To compete with the counterparts, judicious modulation of the morphology and thus the device electrical properties are needed. It is difficult to improve all the parameters concurrently for the all‐PSCs with advanced efficiency, and one increase is typically accompanied by the drop of the other(s). In this work, with the aids of the solvent additive (1‐chloronaphthalene) and the n‐type polymer additive (N2200), we can fine‐tune the morphology of the active layer and demonstrate a 16.04% efficient all‐PSC based on the PM6:PY‐IT active layer. The grazing incidence wide‐angle X‐ray scattering measurements show that the shape of the crystallites can be altered, and the reshaped crystallites lead to enhanced and more balanced charge transport, reduced recombination, and suppressed energy loss, which lead to concurrently improved and device efficiency and stability.

The electron transport layer (ETL) with excellent charge extraction and transport ability is one of the key components of high-performance perovskite solar cells (PSCs). SnO2 has been considered as a more promising ETL for the future commercialization of PSCs due to its excellent photoelectric properties and easy processing. Herein, we propose a facile and effective ETL modification strategy based on the incorporation of methylenediammonium dichloride (MDACl2) into the SnO2 precursor colloidal solution. The effects of MDACl2 incorporation on charge transport, defect passivation, perovskite crystallization, and PSC performance are systematically investigated. First, the surface defects of the SnO2 film are effectively passivated, resulting in the increased conductivity of the SnO2 film, which is conducive to electron extraction and transport. Second, the MDACl2 modification contributes to the formation of high-quality perovskite films with improved crystallinity and reduced defect density. Furthermore, a more suitable energy level alignment is achieved at the ETL/perovskite interface, which facilitates the charge transport due to the lower energy barrier. Consequently, the MDACl2-modified PSCs exhibit a champion efficiency of 22.30% compared with 19.62% of the control device, and the device stability is also significantly improved.

The batch reproducibility of polymer donor materials limits the performance of polymer solar cells. Here Wu et al. develop a polymer donor PM1 by random terpolymerization strategy with a high efficiency of 17.6% in the device and excellent batch-to-batch reproducibility.

Water processing is an ideal strategy for the ecofriendly fabrication of organic photovoltaics (OPVs) and exhibits a strong market−driven demand. Here, we report a state−of−the−art active material, namely PM6:BTP−eC9, for the synthesis of water−borne nanoparticle (NP) dispersion towards ecofriendly OPV fabrication. The surfactant−stripping technique, combined with a poloxamer, facilitates purification and eliminates excess surfactant in water−dispersed organic semiconducting NPs. The introduction of 1,8−diiodooctane (DIO) for the synthesis of surfactant−stripped NP (ssNP) further promotes a percolated microstructure of the polymer and NFA in each ssNP, yielding water−processed OPVs with a record efficiency of over 11%. The use of an additive during water−borne ssNP synthesis is a promising strategy for morphology optimization in NP OPVs. It is believed that the findings in this work will engender more research interest and effort relating to water−processing in preparation of the industrial production of OPVs.

Multicomponent organic solar cells (OSCs), such as the ternary and quaternary OSCs, not only inherit the simplicity of binary OSCs but further promote light harvesting and power conversion efficiency (PCE). Here, we propose a new type of multicomponent solar cells with non-fullerene acceptor isomers. Specifically, we fabricate OSCs with the polymer donor J71 and a mixture of isomers, ITCF, as the acceptors. In comparison, the ternary OSC devices with J71 and two structurally similar (not isomeric) NFAs (IT-DM and IT-4F) are made as control. The morphology experiments reveal that the isomers-containing blend film demonstrates increased crystallinity, more ideal domain size, and a more favorable packing orientation compared with the IT-DM/IT-4F ternary blend. The favorable orientation is correlated with the balanced charge transport, increased exciton dissociation and decreased bimolecular recombination in the ITCF-isomer-based blend film, which contributes to the high fill factor (FF), and thus the high PCE. Additionally, to evaluate the generality of this method, we examine other acceptor isomers including IT-M, IXIC-2Cl and SY1, which show same trend as the ITCF isomers. These results demonstrate that using isomeric blends as the acceptor can be a promising approach to promote the performance of multicomponent non-fullerene OSCs.

All-polymer solar cells (all-PSCs) are organic solar cells in which both the electron donor and the acceptor are polymers and are considered more promising in large-scale production. Thanks to the polymerizing small molecule acceptor strategy, the power conversion efficiency of all-PSCs has ushered in a leap in recent years. However, due to the electrical properties of polymerized small-molecule acceptors (PSMAs), the FF of the devices is generally not high. The typical electron transport material widely used in these devices is PNDIT-F3N, and it is a common strategy to improve the device fill factor (FF) through interface engineering. This work improves the efficiency of all-polymer solar cells through interfacial layer engineering. Using PDINN as the electron transport layer, we boost the FF of the devices from 69.21% to 72.05% and the power conversion efficiency (PCE) from 15.47% to 16.41%. This is the highest efficiency for a PY-IT-based binary all-polymer solar cell. This improvement is demonstrated in different all-polymer material systems.

In this work, we performed a systematic comparison of different duration of solvent vapor annealing (SVA) treatment upon state-of-the-art PM6:SY1 blend film, which is to say for the first time, the insufficient, appropriate, and over-treatment’s effect on the active layer is investigated. The power conversion efficiency (PCE) of corresponding organic solar cell (OSC) devices is up to 17.57% for the optimized system, surpassing the two counterparts. The properly tuned phase separation and formed interpenetrating network plays an important role in achieving high efficiency, which is also well-discussed by the morphological characterizations and understanding of device physics. Specifically, these improvements result in enhanced charge generation, transport, and collection. This work is of importance due to correlating post-treatment delicacy, thin-film morphology, and device performance in a decent way.

All-polymer solar cells (All-PSCs), whose electron donor and acceptors are both polymeric materials, have attracted great research attention in the past few years. However, most all-PSC devices with top-of-the-line efficiencies are processed from chloroform. In this work, we apply the sequential processing (SqP) method to fabricate All-PSCs from an aromatic hydrocarbon solvent, toluene, and obtain efficiencies up to 17.0%. By conducting a series of characterizations on our films and devices, we demonstrate that the preparation of SqP devices using toluene can effectively reduce carrier recombination, enhance carrier mobility and promote the fill factor of the device.

The spread of multidrug-resistant Klebsiella pneumoniae (MDR-KP) has become an emerging threat as a result of the overuse of antibiotics. Bacteriophage (phage) therapy is considered to be a promising alternative treatment for MDR-KP infection compared with antibiotic therapy. In this research, a lytic phage BUCT610 was isolated from hospital sewage. The assembled genome of BUCT610 was 46,774 bp in length, with a GC content of 48%. A total of 83 open reading frames (ORFs) and no virulence or antimicrobial resistance genes were annotated in the BUCT610 genome. Comparative genomics and phylogenetic analyses showed that BUCT610 was most closely linked with the Vibrio phage pYD38-A and shared 69% homology. In addition, bacteriophage BUCT610 exhibited excellent thermal stability (4–75 °C) and broad pH tolerance (pH 3–12) in the stability test. In vivo investigation results showed that BUCT610 significantly increased the survival rate of Klebsiella pneumonia-infected Galleria mellonella larvae from 13.33% to 83.33% within 72 h. In conclusion, these findings indicate that phage BUCT610 holds great promise as an alternative agent with excellent stability for the treatment of MDR-KP infection.

The trade-offs between ecological construction and urbanization changes in land-use, which can affect ecosystem services. This study aimed to analyze the trade-offs between urbanization and ecological construction through land-use change, and then to explore its impact on ecosystem services. We developed a coefficient for analyzing LUCC caused by ecological construction and urbanization. The spatio-temporal patterns of three ecosystem services (Water yield, Net primary production, Soil conservation) in the Xiangjiang River Basin (XRB) of China were identified and the trade-offs and synergies between ecosystem services explored at different spatial scales. The average trade-off coefficients between ecological construction and urbanization of upstream, midstream, downstream, and the whole basin were 0.20, −0.27, −0.46 and −0.37 respectively show that the LUCC was dominated by urbanization in the XRB from 2000 to 2015. However, ecological construction improved ecosystem services. The growth rates in NPP, soil conservation, and water yield were 10.88%, 2.23%, and 19.82%, respectively, between 2000 and 2015. We also confirmed three ecosystem services were spatially dominated by synergies (0

Variation of maternal gut microbiota may increase the risk of autism spectrum disorders (ASDs) in offspring. Animal studies have indicated that maternal gut microbiota is related to neurodevelopmental abnormalities in mouse offspring, while it is unclear whether there is a correlation between gut microbiota of ASD children and their mothers. We examined the relationships between gut microbiome profiles of ASD children and those of their mothers, and evaluated the clinical discriminatory power of discovered bacterial biomarkers. Gut microbiome was profiled and evaluated by 16S ribosomal RNA gene sequencing in stool samples of 59 mother–child pairs of ASD children and 30 matched mother–child pairs of healthy children. Significant differences were observed in the gut microbiome composition between ASD and healthy children in our Chinese cohort. Several unique bacterial biomarkers, such as Alcaligenaceae and Acinetobacter, were identified. Mothers of ASD children had more Proteobacteria, Alphaproteobacteria, Moraxellaceae, and Acinetobacter than mothers of healthy children. There was a clear correlation between gut microbiome profiles of children and their mothers; however, children with ASD still had unique bacterial biomarkers, such as Alcaligenaceae, Enterobacteriaceae, and Clostridium. Candidate biomarkers discovered in this study had remarkable discriminatory power. The identified patterns of mother–child gut microbiome profiles may be important for assessing risks during the early stage and planning of personalized treatment and prevention of ASD via microbiota modulation. Keywords: Autism spectrum disorders, Gut microbiome, Biomarker, Mother–child pair, Microbiota-gut-immune-brain axis

In this work, we apply the sequential processing (SqP) method to address the relatively low electron mobility in recent all-polymer solar cells (all-PSCs) based on the polymerized small-molecule acceptor (PSMA). Compared to the blend-casting (BC) method, all-PSCs composed of PM6/PY-IT via the SqP method show boosted electron mobility and a more balanced charge carrier transport, which increases the FF of the SqP device and compensates for the short-circuit current loss, rendering comparable overall performance with the BC device. Through film-depth-dependent light absorption spectroscopy, we analyze the sub-layer absorption and exciton generation rate in the vertical direction of the device, and discuss the effect of the increased electron mobility on device performance, accordingly.

Abstract Energy loss (Eloss) consisting of radiative recombination loss (ΔE1 and ΔE2) and nonradiative recombination loss (ΔE3) is considered as an important factor for organic solar cells (OSCs). Herein, two N‐functionalized asymmetrical small molecule acceptors (SMAs), namely N7IT and N8IT are designed and synthesized, to explore the effect of N on reducing Eloss with sulfur (S) as a comparison. N7IT‐based OSCs achieve not only a higher PCE (13.8%), but also a much lower Eloss (0.57 eV) than those of the analogue (a‐IT)‐based OSCs (PCE of 11.5% and Eloss of 0.72 eV), which are mainly attributed to N7IT's significantly enhanced charge carrier density (promoting JSC) and largely suppressed nonradiative Eloss by over 0.1 eV (enhancing VOC). In comparison, N8IT, with an extended π‐conjugated length, shows relatively lower photovoltaic performance than N7IT (but higher than a‐IT) due to the less favorable morphology caused by the excessively large dipole moment of the asymmetrical molecule. Finally, this work sheds light on the structure–property relationship of the N‐functionalization, particularly on its effects on reducing the Eloss, which could inspire the community to design and synthesize more N‐functionalized SMAs.

Abstract Significant progress has been made in nonfullerene small molecule acceptors (NF‐SMAs) that leads to a consistent increase of power conversion efficiency (PCE) of nonfullerene organic solar cells (NF‐OSCs). To achieve better compatibility with high‐performance NF‐SMAs, the direction of molecular design for donor polymers is toward wide bandgap (WBG), tailored properties, and preferentially ecofriendly processability for device fabrication. Here, a weak acceptor unit, methyl 2,5‐dibromo‐4‐fluorothiophene‐3‐carboxylate (FE‐T), is synthesized and copolymerized with benzo[1,2‐b:4,5‐b′]dithiophene (BDT) to afford a series of nonhalogenated solvent processable WBG polymers P1‐P3 with a distinct side chain on FE‐T. The incorporation of FE‐T leads to polymers with a deep highest occupied molecular orbital (HOMO) level of −5.60−5.70 eV, a complementary absorption to NF‐SMAs, and a planar molecular conformation. When combined with the narrow bandgap acceptor ITIC‐Th, the solar cell based on P1 with the shortest methyl chain on FE‐T achieves a PCE of 11.39% with a large Voc of 1.01 V and a Jsc of 17.89 mA cm−2. Moreover, a PCE of 12.11% is attained for ternary cells based on WBG P1, narrow bandgap PTB7‐Th, and acceptor IEICO‐4F. These results demonstrate that the new FE‐T is a highly promising acceptor unit to construct WBG polymers for efficient NF‐OSCs.

Palladium diselenide as a thus-far rarely studied group-10 transition metal dichalcogenide, has exhibited great potential in the field of optoelectronics due to their superior conductivity, high carrier mobility, and excellent stability. However, few works are reported on the application of low-dimensional PdSe2 in organic solar cells (OSCs). Herein, PdSe2 quantum dots (QDs) are introduced into the high-efficient nonfullerene OSCs for the first time by incorporating the solution-processable QDs in the hole transport layer (HTL) of the OSCs, leading to a dramatic efficiency enhancement of the devices. Upon PdSe2 QD addition, the maximum efficiency of the devices based on different active layer blends, including D18:Y6 and PM6:L8-BO, is improved to 18.12%, and 18.29%, with efficiency enhancement of 8.96% and 6.90%, respectively, compared with that of the reference devices. The effects of PdSe2 QDs on the optical absorption, photoluminescence spectrum of the hybrid HTL as well as the carrier mobility, electrochemical impedance spectroscopy, and transient photocurrent/transient photovoltage of the devices are deeply investigated, revealing the efficiency enhancement of the OSCs with PdSe2 QDs addition results from the improved conductivity, light scattering, and hole transport properties of the hybrid HTL embedded with PdSe2 QDs. [ABSTRACT FROM AUTHOR]

2D conjugated side-chain engineering is an effective strategy that is widely utilized to construct benzodithiophene-based polymers. Herein, an unconjugated side-chain strategy to design fused-benzodithiophene-based non-fullerene small molecule acceptors (SMAs) via vertical aromatic side-chain engineering on the ladder-type core is employed. Three SMAs named BTTIC-Th, BTTIC-TT, and BTTIC-Ph with thiophene, thieno[3,2-b]thiophene, and benzene, respectively, as side chains, are designed and synthesized. Three SMAs exhibit similar absorption ranges but different lowest unoccupied molecular orbital (LUMO) energy levels due to the different strength of the δ-inductive effect between vertical aromatic side chains and their electron-rich core. Organic solar cells based on PBDB-T:BTTIC-TT achieve a power conversion efficiency (PCE) of 13.44%, which is higher than the PCE of devices based on PBDB-T:BTTIC-Th (12.91%) and PBDB-T:BTTIC-Ph (9.14%). The difference in device performance is investigated by electrical and morphological characterizations. A large domain size and different types of π- π stacking are found in the bulk heterojunction layer of PBDB-T:BTTIC-Ph blend film, which are detrimental to exciton dissociation and charge transport. Overall, it is demonstrated that when designing unconjugated side chains, thieno[3,2-b]thiophene is superior to thiophene and benzene through its dual roles of promoting the LUMO energy level and optimizing the morphology. These results shed light on the side-chain engineering of high-performance non-fullerene SMAs. [ABSTRACT FROM AUTHOR]