Publications by authors named "GuangYe Zhang"

The optimization of morphology in all-polymer solar cells (all-PSCs) often relies on the use of solvent additives. However, their tendency to remain trapped in the device due to high boiling points leads to performance degradation over time. In this study, we introduce a novel approach involving the design and synthesis of one dual-asymmetric solid additive featuring mono-brominated-asymmetric dithienothiophene (SL-1).

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The long exciton diffusion length (L) plays an important role in promoting exciton dissociation, suppressing charge recombination, and improving the charge transport process, thereby improving the performance of organic solar cells (OSCs), especially in thick-film OSCs. However, the limited L hinders further improvement in device performance as the film thickness increases. Here, an organic-metal platinum complex, namely TTz-Pt, is synthesized and served as a solid additive into the D18-Cl:L8-BO system.

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Morphology control of the photoactive layer is crucial for achieving high-performance organic solar cells (OSCs), yet it remains a significant challenge in this field. One effective approach is the additive strategy, which fine-tunes the morphology of the photoactive layer. However, the underlying mechanisms governing the impact of different types of additives from liquid, solid, to volatile solid, on the bulk heterojunction morphology and device performance are not fully understood.

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Carbazole-based self-assembled monolayer (SAM) materials as hole transport layers (HTL) have led organic solar cells (OSCs) to state-of-the-art photovoltaic performance. Nonetheless, the impact of the alkyl spacer length of SAMs remains inadequately understood. To improve the knowledge, four dichloride-substituted carbazole-based SAMs (from 2Cl-2PACz to 2Cl-5PACz) with spacer lengths of 2-5 carbon atoms is developed.

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Trap-assisted charge recombination is one of the primary limitations of restricting the performance of organic solar cells. However, effectively reducing the presence of traps in the photoactive layer remains challenging. Herein, wide bandgap polymer donor PTzBI-dF is demonstrated as an effective modulator for enhancing the crystallinity of the bulk heterojunction active layers composed of D18 derivatives blended with Y6, leading to dense and ordered molecular packings, and thus, improves photoluminescence quenching properties.

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A series of new small-molecule acceptors-NA9, NA10, and NA11-based on benzo[]phenazine are synthesized. The chlorinated NA10 and brominated NA11 exhibit improved molecular packing and enhanced charge transport, resulting in higher power conversion efficiencies (PCEs) of 15.65% and 16.

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Article Synopsis
  • All-polymer solar cells (all-PSCs) have advantages like mechanical durability and stability, but their polymer donors haven't kept pace with their polymer acceptors.
  • The study introduces a new electron-deficient compound, fluorinated bithiophene imide (F-BTI), and a polymer donor called SA1, which enhances energy levels and polymer aggregation.
  • With improved properties, SA1-based all-PSCs achieve an efficiency of 16.31%, reaching a record 19.33% with a ternary device, showcasing F-BTI's potential to advance high-performance polymer donors.
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Article Synopsis
  • - The development of non-fullerene acceptors with low voltage losses has improved the power conversion efficiency of organic solar cells (OSCs) to around 20%, aided by enhancements in material morphology through techniques like thermal annealing (TA).
  • - Researchers introduced a new method called reverse thermal annealing (RTA) that optimizes the dielectric constant of the active layer, leading to improved molecular structure and reduced voltage losses compared to traditional TA.
  • - The RTA technique demonstrated significant efficiency gains, with the PM6:L8-BO-X device achieving a power conversion efficiency of 19.91%, and it showed effectiveness across four other material systems, emphasizing its potential for widespread application in OSC technology.
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A sulphur-oxidizing bacterium, designated strain SCUT-2, was isolated from freshwater sediment collected from the Pearl River in Guangzhou, PR China. This strain was an obligate chemolithoautotroph, utilizing reduced sulphur compounds (elemental sulphur, thiosulphate, tetrathionate and sulphite) as the electron donor. Growth of strain SCUT-2 was observed at 20-40 ℃ (optimum at 30 °C), pH 5.

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The difluorobenzothiadizole (ffBT) unit is one of the most classic electron-accepting building blocks used to construct D-A copolymers for applications in organic solar cells (OSCs). Historically, ffBT-based polymers have achieved record power conversion efficiencies (PCEs) in fullerene-based OSCs owing to their strong temperature-dependent aggregation (TDA) characteristics. However, their excessive miscibility and rapid aggregation kinetics during film formation have hindered their performance with state-of-the-art non-fullerene acceptors (NFAs).

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The advancement of acceptors plays a pivotal role in determining photovoltaic performance. While previous efforts have focused on optimizing acceptor-donor-acceptor-donor-acceptor (A-DA-D-A)-typed acceptors by adjusting side chains, end groups, and conjugated extension of the electron-deficient central A unit, the systematic exploration of the impact of peripheral aryl substitutions, particularly with different electron groups, on the A unit and its influence on device performance is still lacking. In this study, three novel acceptors - QxTh, QxPh, and QxPy - with distinct substitutions on the quinoxaline (Qx) are designed and synthesized.

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Background: Previous 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.

Methods: Pooled 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.

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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.

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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.

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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.

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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.

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Objective: To analyze the clinical and genetic characteristics of three Chinese pedigrees affected with Citrullinemia type I (CTLN1).

Methods: Three children diagnosed at the Children's Hospital Affiliated to Shandong University from 2017 to 2020 were selected as the study subjects. Genomic DNA was extracted from peripheral blood samples of the probands and their parents.

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Article Synopsis
  • * BUCT_49532 was isolated from sewage, categorized as a Jedunavirus, and has a genome of 49,532 bp, suggesting it’s a novel species based on genomic analysis.
  • * With a favorable safety profile and potent lytic capabilities, BUCT_49532 could be used in combination with other phages to enhance its effectiveness in treating bacterial infections.
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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.

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Organic solar cells (OSCs) have attracted lots of attention owing to their low cost, lightweight, and flexibility properties. Nowadays, the performance of OSCs is continuously improving with the development of active layer materials. However, the traditional hole transport layer (HTL) material Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) presents insufficient conductivity and rapid degradation, which decreases the efficiency and stability of OSCs.

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Currently, nearly all high-efficiency organic photovoltaic devices use donor polymers based on the benzo-dithiophene (BDT) unit. To diversify the choices of building blocks for high-performance donor polymers, the use of benzo-difuran (BDF) units is explored, which can achieve reduced steric hindrance, stronger molecular packing, and tunable energy levels. In previous research, the performance of BDF-based devices lagged behind those of BDT-based devices.

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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). SnO 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 (MDACl) into the SnO precursor colloidal solution.

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In recent decades, terraces abandonment has been prevalent in the hilly areas of China. Soil fungi play an important role in clarifying soil ecosystematic feedback after ancient rice terraces abandonment, but how their community composition and function shift remains unclear. Soil profiles of 0-120 cm were excavated in ancient rice terraces, dry land, and forest land (formed from ancient rice terraces abandonment), respectively.

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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.

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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.

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