Measurement of C P asymmetries in B 0 → ϕ K s 0 decays with Belle II
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Astronomy & Astrophysics↗
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First Measurement of the B + → π + π 0 π 0 Branching Fraction and C P Asymmetry
We study B + → π + π 0 π 0 using 711 fb -1 of data collected at the Υ(4S) resonance with the Belle detector at the KEKB asymmetric-energy e + e - collider. Here we measure an inclusive branching fraction of (19.0 ±1.5 ±1.4)×10 -6 and an inclusive CP asymmetry of (9.2 ±6.8 ±0.7)%, where the first uncertainties are statistical and the second are systematic, and a B + → ρ(770) + π 0 branching fraction of (11.2 ± 1.1 ± 0.9 $^{+0.8}_{-1.6}$)× 10 -6 , where the third uncertainty is due to possible interference with B + → ρ(1450) + π 0 . We present the first observation of a structure around 1 GeV/c 2 in the π 0 π 0 mass spectrum, with a significance of 6.4σ, and measure a branching fraction to be (6.9 ±0.9 ±0.6) × 10 -6 . We also report a measurement of local CP asymmetry in this structure.
72 PHYSICS OF ELEMENTARY PARTICLES AND FIELDS↗
Modification of χ c 1 ( 3872 ) and ψ ( 2 S ) Production in p Pb Collisions at s NN = 8.16 TeV
The LHCb Collaboration measures production of the exotic hadron χ c 1 ( 3872 ) in proton-nucleus collisions for the first time. Comparison with the charmonium state ψ ( 2 S ) suggests that the exotic χ c 1 ( 3872 ) experiences different dynamics in the nuclear medium than conventional hadrons, and comparison with data from proton-proton collisions indicates that the presence of the nucleus may modify χ c 1 ( 3872 ) production rates. This is the first measurement of the nuclear modification factor of an exotic hadron. © 2024 CERN, for the LHCb Collaboration 2024 CERN
72 PHYSICS OF ELEMENTARY PARTICLES AND FIELDS↗
Neutron polarisation transfer, C x ′ , in π+ photoproduction off the proton, d ( γ ⊙ , n → π + ) n s p e c
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Astronomy & Astrophysics↗
Study of the h c ( 1 1 P 1 ) meson via ψ ( 2 S ) → π 0 h c decays at BESIII
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79 ASTRONOMY AND ASTROPHYSICS↗
Observation of Beam Spin Asymmetries in the Process e p → e ′ π + π − X with CLAS12
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73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
Observation of an Isoscalar Resonance with Exotic J P C = 1 − + Quantum Numbers in J / ψ → γ η η ′
Not Available
72 PHYSICS OF ELEMENTARY PARTICLES AND FIELDS↗
Observation of e + e – → ω χ b J ( 1 P ) and Search for X b → ω Υ ( 1 S ) at s near 10.75 GeV
We study the processes $e^{+}e^{–} → ωχ_{bJ}$(1P) (J=0, 1, or 2) using samples at center-of-mass energies $\sqrt{s}$ = 10.701, 10.745, and 10.805 GeV, corresponding to 1.6, 9.8, and 4.7 fb –1 of integrated luminosity, respectively. These data were collected with the Belle II detector during special operations of the SuperKEKB collider above the Υ(4S) resonance. We report the first observation of $ωχ_{bJ}$(1P) signals at $\sqrt{s}$ = 10.745 GeV. By combining Belle II data with Belle results at $\sqrt{s}$ = 10.867 GeV, we find energy dependencies of the Born cross sections for $e^{+}e^{–} → ωχ_{b1,b2}$(1P) to be consistent with the shape of the Υ(10753) state. These data indicate that the internal structures of the Υ(10753) and Υ(10860) states may differ. Including data at $\sqrt{s}$ = 10.653 GeV, we also search for the bottomonium equivalent of the X(3872) state decaying into ωΥ(1S). No significant signal is observed for masses between 10.45 and 10.65 GeV/c 2 .
72 PHYSICS OF ELEMENTARY PARTICLES AND FIELDS↗
Flight Measurements of the Rudder Control and Sideslip Characteristics of Four Vertical Tail Arrangements on the P-40 Series Airplanes
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RUDDER CONTROLS- CURTISS P-40E & F TAIL SURFACES, ↗
From p- to n-Type Mixed Conduction in Isoindigo-Based Polymers through Molecular Design
Organic mixed ionic and electronic conductors are of significant interest for bioelectronic applications. Here, we use three different isoindigoid building blocks to obtain polymeric mixed conductors with vastly different structural and electronic properties which can be further fine-tuned through the choice of comonomer unit. We show how careful design of the isoindigoid scaffold can afford highly planar polymer structures with high degrees of electronic delocalization, while subtle structural modifications can control the dominant charge carrier (hole or electron) when probed in organic electrochemical transistors. We employ a combination of experimental and computational techniques to probe electrochemical, structural and mixed ionic and electronic properties of the polymer series which in turn allows us to derive important structure-property relations for this promising class of materials in the context of organic bioelectronics. Ultimately, we use these findings to outline robust molecular design strategies for isoindigo-based mixed conductors that can support efficient p-type, n-type and ambipolar transistor operation in an aqueous environment.
36 MATERIALS SCIENCE↗
Local p‐ and n‐Type Doping of an Oxide Semiconductor via Electric‐Field‐Driven Defect Migration
Layered oxides exhibit high ionic mobility and chemical flexibility, attracting interest as cathode materials for lithium-ion batteries and the pairing of hydrogen production and carbon capture. Recently, layered oxides emerged as highly tunable semiconductors. For example, by introducing anti-Frenkel defects, the electronic hopping conductance in hexagonal manganites is increased locally by orders of magnitude. Here, local acceptor and donor doping in Er(Mn,Ti)O3 is demonstrated, facilitated by the controlled splitting of anti-Frenkel defects under applied d.c. voltage. By combining density functional theory calculations, scanning probe microscopy, atom probe tomography, and scanning transmission electron microscopy, it is shown that the oxygen defects can readily be moved through the layered crystal structure, leading to nano-sized interstitial-rich (p-type) and vacancy-rich (n-type) regions. The resulting pattern is comparable to dipolar npn-junctions and stable on the timescale of days. These findings reveal the possibility of temporarily functionalizing oxide semiconductors at the nanoscale, giving additional opportunities for the field of oxide electronics and the development of transient electronics in general.
He, Jiali↗
Semiconducting Small Molecules as Active Materials for p-Type Accumulation Mode Organic Electrochemical Transistors
A series of semiconducting small molecules with bithiophene or bis-3,4-ethylenedioxythiophene cores are designed and synthesized. The molecules display stable reversible oxidation in solution and can be reversibly oxidized in the solid state with aqueous electrolyte when functionalized with polar triethylene glycol side chains. Evidence of promising ion injection properties observed with cyclic voltammetry is complemented by strong electrochromism probed by spectroelectrochemistry. Blending these molecules with high molecular weight polyethylene oxide (PEO) is found to improve both ion injection and thin film stability. The molecules and their corresponding PEO blends are investigated as active layers in organic electrochemical transistors (OECTs). For the most promising molecule:polymer blend (P4E4:PEO), p-type accumulation mode OECTs with µA drain currents, μS peak transconductances, and a µC* figure-of-merit value of 0.81 F V -1 cm -1 s -1 are obtained.
36 MATERIALS SCIENCE↗
Correlating Macro and Atomic Structure with Elastic Properties and Ionic Transport of Glassy Li 2 S‐P 2 S 5 (LPS) Solid Electrolyte for Solid‐State Li Metal Batteries
Abstract A combination of high ionic conductivity and facile processing suggest that sulfide‐based materials are promising solid electrolytes that have the potential to enable Li metal batteries. Although the Li 2 S‐P 2 S 5 (LPS) family of compounds exhibit desirable characteristics, it is known that Li metal preferentially propagates through microstructural defects, such as particle boundaries and/or pores. Herein, it is demonstrated that a near theoretical density (98% relative density) LPS 75‐25 glassy electrolyte exhibiting high ionic conductivity can be achieved by optimizing the molding pressure and temperature. The optimal molding pressure reduces porosity and particle boundaries while preserving the preferred amorphous structure. Moreover, molecular rearrangements and favorable Li coordination environments for conduction are attained. Consequently, the Young's Modulus approximately doubles (30 GPa) and the ionic conductivity increases by a factor of five (1.1 mS cm −1 ) compared to conventional room temperature molding conditions. It is believed that this study can provide mechanistic insight into processing‐structure‐property relationships that can be used as a guide to tune microstructural defects/properties that have been identified to have an effect on the maximum charging current that a solid electrolyte can withstand during cycling without short‐circuiting.
Garcia‐Mendez, Regina↗
Anomalous Charge Transfer from Organic Ligands to Metal Halides in Zero‐Dimensional [(C 6 H 5 ) 4 P] 2 SbCl 5 Enabled by Pressure‐Induced Lone Pair‐π Interaction
Abstract Low‐dimensional (low‐D) organic metal halide hybrids (OMHHs) have emerged as fascinating candidates for optoelectronics due to their integrated properties from both organic and inorganic components. However, for most of low‐D OMHHs, especially the zero‐D (0D) compounds, the inferior electronic coupling between organic ligands and inorganic metal halides prevents efficient charge transfer at the hybrid interfaces and thus limits their further tunability of optical and electronic properties. Here, using pressure to regulate the interfacial interactions, efficient charge transfer from organic ligands to metal halides is achieved, which leads to a near‐unity photoluminescence quantum yield (PLQY) at around 6.0 GPa in a 0D OMHH, [(C 6 H 5 ) 4 P] 2 SbCl 5 . In situ experimental characterizations and theoretical simulations reveal that the pressure‐induced electronic coupling between the lone‐pair electrons of Sb 3+ and the π electrons of benzene ring (lp‐π interaction) serves as an unexpected “bridge” for the charge transfer. Our work opens a versatile strategy for the new materials design by manipulating the lp‐π interactions in organic–inorganic hybrid systems.
Luo, Hui↗
Anomalous Charge Transfer from Organic Ligands to Metal Halides in Zero-Dimensional [(C 6 H 5 ) 4 P] 2 SbCl 5 Enabled by Pressure-Induced Lone Pair-π Interaction
Low-dimensional (low-D) organic metal halide hybrids (OMHHs) have emerged as fascinating candidates for optoelectronics due to their integrated properties from both organic and inorganic components. However, for most of low-D OMHHs, especially the zero-D (0D) compounds, the inferior electronic coupling between organic ligands and inorganic metal halides prevents efficient charge transfer at the hybrid interfaces and thus limits their further tunability of optical and electronic properties. Here, using pressure to regulate the interfacial interactions, efficient charge transfer from organic ligands to metal halides is achieved, which leads to a near-unity photoluminescence quantum yield (PLQY) at around 6.0 GPa in a 0D OMHH, [(C 6 H 5 ) 4 P] 2 SbCl 5 . In situ experimental characterizations and theoretical simulations reveal that the pressure-induced electronic coupling between the lone-pair electrons of Sb 3+ and the π electrons of benzene ring (lp-π interaction) serves as an unexpected “bridge” for the charge transfer. Further, our work opens a versatile strategy for the new materials design by manipulating the lp-π interactions in organic–inorganic hybrid systems.
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
Trifluoromethylation of 2D Transition Metal Dichalcogenides: A Mild Functionalization and Tunable p‐Type Doping Method
Chemical modification is a powerful strategy for tuning the electronic properties of 2D semiconductors. Here, in this study, we report the electrophilic trifluoromethylation of 2D WSe2 and MoS 2 under mild conditions using the reagent trifluoromethyl thianthrenium triflate (TTT). Chemical characterization and density functional theory calculations reveal that the trifluoromethyl groups bind covalently to surface chalcogen atoms as well as oxygen substitution sites. Trifluoromethylation induces p-type doping in the underlying 2D material, enabling the modulation of charge transport and optical emission properties in WSe 2 . This work introduces a versatile and efficient method for tailoring the optical and electronic properties of 2D transition metal dichalcogenides.
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
Energetic Tug-of-War between Pt and Leaky TiO 2 : Positive and Negative Effects on the Function of Molecularly-Modified p -Si(111)|TiO 2 |Pt Photocathodes
Photoelectrochemical solar energy conversion to chemical products is a promising avenue towards renewable fuels, and TiO 2 deposition on semiconductor photocathodes is a widespread surface protection strategy. However, the electronic, thermodynamic, and kinetic effects of protection layers on interfacial energetics remains poorly understood. Here, electrochemical data (photocurrent onset and flatband potentials) of p-Si(111)|TiO 2 |Pt is collected in contact with an outer-sphere redox couple. We find that onset potentials shift negatively as a function of increasing oxide thickness, but this effect is not reflected in the flatband potentials. This reveals the mechanism of these shifts is kinetic rather than thermodynamic,and suggests that hole leakage through the TiO 2 is responsible. When Pt nanoparticles are deposited onto the TiO 2 , positive shifts in both the onset and flatband potentials are observed, revealing Pt catalysts are beneficial for more than just increased catalytic rates. These results highlight the importance of understanding the effects of surface modifications on the energetics at the interface in both catalytic and simple electron transfer systems.
14 SOLAR ENERGY↗