Synthesis of ultra-narrow PbTe nanorods with extremely strong quantum confinement

Monodisperse, high-quality, ultra-narrow PbTe nanorods were synthesized for the first time in a one-pot, hot-injection reaction using trans-2-decenoic acid as the agents for lead precursors and tris(diethylamino)phosphine telluride together with free tris(diethylamino)phosphine as the telluride precursors. High monomer reactivity, rapid nucleation and fast growth rate derived from the new precursors led to the anisotropic growth of PbTe nanocrystals at low reaction temperatures

Ladder-like energy-relaying exciplex enables 100% internal quantum efficiency of white TADF-based diodes in a single emissive layer.

Development of white organic light-emitting diodes based on purely thermally activated delayed fluorescence with a single-emissive-layer configuration has been a formidable challenge. Here, we report the rational design of a donor-acceptor energy-relaying exciplex and its utility in fabricating single-emissive-layer, thermally activated delayed fluorescence-based white organic light-emitting diodes that exhibit 100% internal quantum efficiency, 108.2 lm W-1 power efficiency, and 32.7% external quantum efficiency. This strategy enables thin-film fabrication of an 8 cm × 8 cm thermally activated delayed fluorescence white organic light-emitting diodes (10 inch2) prototype with 82.7 lm W-1 power efficiency and 25.0% external quantum efficiency. Introduction of a phosphine oxide-based acceptor with a steric group to the exciplex limits donor-acceptor triplet coupling, providing dual levels of high-lying and low-lying triplet energy. Transient spectroscopic characterizations confirm that a ladder-like energy relaying occurs from the high-lying triplet level of the exciplex to a blue emitter, then to the low-lying triplet level of the phosphine oxide acceptor, and ultimately to the yellow emitter. Our results demonstrate the broad applicability of energy relaying in multicomponent systems for exciton harvesting, providing opportunities for the development of third-generation white organic light-emitting diode light sources

Effect of Substrates Performance on the Microstructure and Properties of Phosphate Chemical Conversion Coatings on Metal Surfaces

Phosphate chemical conversion (PCC) technology has attracted extensive attention for its ability to regulate the surface properties of biomedical metals. However, titanium (Ti)-based alloys exhibit inertia because of the native passive layer, whereas zinc (Zn)-based alloys show high activity in acidic PCC solutions. The substrate performance affects the chemical reaction in the phosphating solution, which further leads to diversity in coating properties. In this work, the zinc-phosphate (ZnP) coatings are prepared on Ti alloy (TA) and Zn alloy (ZA) substrates using the PCC method, respectively. The coatings prepared herein are detected by a scanning electron microscope (SEM), X-ray diffractometer (XRD), laser scanning confocal microscope (LSCM), universal testing machine, contact angle goniometer, and electrochemical workstation system. The results show that the substrate performance has little effect on the phase composition but can significantly affect the crystal microstructure, thickness, and bonding strength of the coatings. In addition, the ZnP coatings improve the surface roughness of the substrates and show good hydrophilicity and electrochemical corrosion resistance. The formation mechanism of the ZnP coating is revealed using potential-time curves, indicating that the metal–solution interfacial reaction plays a dominant role in the deposition process

Translocation, bioaccumulation, and distribution of perfluoroalkyl and polyfluoroalkyl substances (PFASs) in plants

Perfluoroalkyl and polyfluoroalkyl substances (PFASs) are persistent in the environment and have been detected in a variety of plants such as vegetables, cereals, and fruits. Increasing evidence shows that plants are at a risk of being adversely affected by PFASs. This review concludes that PFASs are predominantly absorbed by roots from sources in the soil; besides, the review also discusses several factors such as soil properties and the species of PFASs and plants. In addition, following uptake by root, long-chain PFASs (C ≥ 7 for PFCA and C ≥ 6 for PFSA) were preferentially retained within the root, whereas the short-chain PFASs were distributed across tissues above the ground — according to the studies. The bioaccumulation potential of PFASs within various plant structures are further expressed by calculating bioaccumulation factor (BAF) across various plant species. The results show that PFASs have a wide range of BAF values within root tissue, followed by straw, and then grain. Furthermore, owing to its high water solubility than other PFASs, PFOA is the predominant compound accumulated in both the soil itself and within the plant tissues. Among different plant groups, the potential BAF values rank from highest to lowest as follows: leaf vegetables > root vegetables > flower vegetables > shoot vegetables. Several PFAS groups such as PFOA, PFBA, and PFOS, may have an increased public health risk based on the daily intake rate (ID). Finally, future research is suggested on the possible PFASs degradation occurring in plant tissues and the explanations at genetic-level for the metabolite changes that occur under PFASs stress.publishedVersio

Overcoming power efficiency limitation of white fluorescence light‐emitting diodes via multilevel‐hydrogen‐bond matrix

Abstract High power efficiency and low efficiency roll‐off at practical luminance are two requirements for new‐generation energy‐saving lighting technologies, which are still bottlenecks of thermally activated delayed fluorescence (TADF) white organic light‐emitting diodes (WOLED), despite the advantages of TADF materials and devices in low cost and high sustainability. Herein, we developed a spiro phosphine oxide host named SSOXSPO, which can form multiple and multidirectional intermolecular hydrogen bonds (IHB). The resulted multilevel IHB network integrates long‐range ordered and short‐range disordered alignments for suppressing triplet‐polaron quenching (TPQ) and triplet‐triplet annihilation (TTA). Electronic characteristics of SSOXSPO matrix are further regulated, leading to the optimal exciton allocation through balancing energy and charge transfer. As consequence, using SSOXSPO as host, the single‐emissive‐layer TADF WOLEDs realized the record performance, including ultralow operation voltage as ∼4.0 V, power efficiency beyond fluorescent tube (70.1 lm W−1) and negligible external quantum efficiency roll‐off (3%) at 1000 nits for indoor lighting. This work demonstrates that multiple interplays supported by host matrixes in TADF WOLEDs can facilitate the synergistic effects of TADF emitters on 100% exciton utilization

Enhancing the Adsorption Performance of 2‑Methylisoborneol by Activated Carbon by Promoting Hydrophobic Effects

Powdered activated carbon (PAC) is the most widely used adsorbent for removing odorants like 2-methylisoborneol (MIB) for drinking water purification. The hydrophobicity exhibited by the moieties of the carbon structure is known to be important for the adsorption of activated carbon. Here we propose a novel approach for regulating the hydrophobicity of the carbon surface by rearranging carbon atoms without changing the pore structures markedly through thermal transformation using Fe(NO3)3 as the catalyst. Five different PACs were transformed into hydrophobic porous carbons (HPCs) with 2.47–3.00 times the adsorption capacity and faster adsorption rates, accompanied by the surface free energy being decreased by 26.67–36.40%, the IG2/IG1 representing the degree of order being increased by 17.31–53.68%, the C–C(sp2)/C–C(sp3) being increased by 31.9–49.8%, and the oxygen content being decreased by 4.71–8.63%. The increase in ordered planar crystals dominated by sp2 carbons as well as the decrease in the number of heteroatoms in HPCs might be the main reason for its enhanced adsorption of MIB. Simulation based on reactive force field molecular dynamics indicated that MIB molecules tended to be adsorbed in ordered structures. This study provides a novel angle for improving the surface hydrophobicity of activated carbon, which may lead to the development of high-performance adsorbents