Search

Organic solar cell (OSC) development continues to demonstrate impressive device efficiency improvements. However, the materials synthetic simplicity essential to industrialization remains seriously lacking attention, imparting inferior performance records in low‐cost devices. Hence, low bandgap and completely non‐fused electron acceptors (CNFEAs) having simple molecular structures are investigated herein. In contrast to typically explored fused‐ring acceptors with smaller backbone conformational variations, minimizing the interface recombination sites through a greater extent of localized domains is identified as more critical in CNFEAs, leading to remarkable fill factors (FFs) approaching 75%, among the highest currently realized for low‐cost systems. However, this comes with diminishing charge generation efficiency. The general ternary blend optimization strategy modifying the morphology of host components is limited in preserving such remarkably high FFs. To suppress the trade‐off while keeping notable FFs, a new perspective of constructing functionally bridged components based on optical, electronic, and thermodynamic properties is introduced here. Specifically, charge generation is unrestrained from the host acceptor localized domains through the introduction of a "bridge" component while also taking advantage of the configuration to channel polarons toward the efficient transport moieties of the host components. Accordingly, this work incubates understanding‐guided optimizations toward the advancement of more practical devices. [ABSTRACT FROM AUTHOR]

Moisture removal and water recovery from the air are vital for regulating indoor humidity and mitigating water scarcity. Most atmospheric water harvesters (AWH) focus primarily on increasing the moisture capture rate, but for it to be economical and sustainable, it is essential to consider the energy required to recover and harvest the captured water. Here, a mechanically flexible, biphilic sorption‐based AWH made of green, environmentally friendly material is presented. It consists of a hygroscopic chitosan polymer embedded within a flexible, hydrophobic silica xerogel that can harvest 86.3 g water/g chitosan at 97% relative humidity and 25°C reaching saturation after 30 days (i.e. 2.88 g water/g chitosan/day). Roughly 88% of the sorbed moisture was recovered by mechanical squeezing (ca. 0.020 MPa) within 150 s. Repeated water harvesting experiments and uniaxial compression tests demonstrate that chitosan‐silica xerogel is durable for long‐term operations, providing a fast, reliable, and sustainable moisture removal and water harvesting tool. [ABSTRACT FROM AUTHOR]

Polystyrene (PS)‐dioctyl phthalate (DOP) films were prepared by spin coating solutions of a mixture of PS and DOP on Si wafers and characterized by time‐of‐flight secondary ion mass spectrometry (ToF‐SIMS) and X‐ray photoelectron spectroscopy (XPS). ToF‐SIMS depth profile results showed that DOP mainly segregated to the top 10 nm of the surface of the PS‐DOP film as well as to the interface between the film and the substrate. The normalized intensities of the ions corresponding to DOP on the surface increased as the annealing temperature increased and reached a maximum at the annealing temperature of 60°C, and then decreased as the annealing temperature increased. XPS results indicate that the maximum amount of DOP segregated to the top surface of the PS‐DOP film can reach to 39 wt% at the annealing temperature of 60°C. In addition, DOP evaporated at 25°C under ultra‐high vacuum conditions; hence, ToF‐SIMS and XPS analyses need to be carried out at low temperatures (e.g., −40°C). [ABSTRACT FROM AUTHOR]

Defects were created on the surface of highly oriented pyrolytic graphite (HOPG) by sputtering with an Ar+ ion beam, then characterized using X‐ray photoelectron spectroscopy (XPS) and time‐of‐flight secondary ion mass spectrometry (ToF‐SIMS) at 500°C. In the XPS C1s spectrum of the sputtered HOPG, a sp3 carbon peak appeared at 285.3 eV, representing surface defects. In addition, 2 sets of peaks, the Cx− and CxH− ion series (where x = 1, 2, 3...), were identified in the ToF‐SIMS negative ion spectrum. In the positive ion spectrum, a series of CxH2+• ions indicating defects was observed. Annealing of the sputtered samples under Ar was conducted at different temperatures. The XPS and ToF‐SIMS spectra of the sputtered HOPG after 800°C annealing were observed to be similar to the spectra of the fresh HOPG. The sp3 carbon peak had disappeared from the C1s spectrum, and the normalized intensities of the CxH− and CxH2+• ions had decreased. These results indicate that defects created by sputtering on the surface of HOPG can be repaired by high‐temperature annealing. [ABSTRACT FROM AUTHOR]

We studied the time‐of‐flight secondary ion mass spectrometry fragmentation mechanisms of polystyrenes—phenyl‐fluorinated polystyrene (5FPS), phenyl‐deuterated polystyrene (5DPS), and hydrogenated polystyrene (PS). From the positive ion spectra of 5FPS, we identified some characteristic molecular ion structures with isomeric geometries such as benzylic, benzocyclobutene, benzocyclopentene, cyclopentane, and tropylium systems. These structures were evaluated by the B3LYP‐D/jun‐cc‐pVDZ computation method. The intensities of the C7H2F5+ (m/z = 181), CyPent‐C9H3F4+ (m/z = 187), CyPent‐C9H4F5+ (m/z = 207), and CyPent‐C9H2F5+ (m/z = 205) ions were enhanced by resonance stabilization. The positive fluorinated ions from 5FPS tended to rearrange and produce fewer fluorine‐containing molecular ions through the loss of F (m/z = 19), CF (m/z = 31), and CF2 (m/z = 50) ion fragments. Consequently, the fluorine‐containing polycyclic aromatic ions had much lower intensities than their hydrocarbon counterparts. We propose the fragmentation mechanisms for the formation of C5H5+, C6H5+, and C7H7+ ion fragments, substantiated with detailed analyses of the negative ion spectra. These ions were created through elimination of a pentafluoro‐phenyl anion (C6F5−) and H+, followed by a 1‐electron‐transfer process and then cyclization of the newly generated polyene with carbon‐carbon bond formation. The pendant groups with elements of different electronegativities exerted strong influences on the intensities and fragmentation processes of their corresponding ions. [ABSTRACT FROM AUTHOR]