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We present a precise measurement of the asymptotic normalization coefficient (ANC) for the¹⁶O ground state (GS) through the¹²C(¹¹B,⁷Li)¹⁶O transfer reaction using the Quadrupole‐3‐Dipole (Q3D) magnetic spectrograph. The present work sheds light on the existing discrepancy of more than 2 orders of magnitude between the previously reported GS ANC values. This ANC is believed to have a strong effect on the¹²C(α,γ)¹⁶O reaction rate by constraining the external capture to the¹⁶O ground state, which can interfere with the high-energy tail of the 2⁺subthreshold state. Based on the new ANC, we determine the astrophysicalS-factor and the stellar rate of the¹²C(α,γ)¹⁶O reaction. An increase of up to 21% in the total reaction rate is found within the temperature range of astrophysical relevance compared with the previous recommendation of a recent review. Finally, we evaluate the impact of our new rate on the pair-instability mass gap for black holes (BH) by evolving massive helium core stars using the MESA stellar evolution code. The updated¹²C(α,γ)¹⁶O reaction rate decreases the lower and upper edges of the BH gap about 12% and 5%, respectively.

 

Polydimethylsiloxane (PDMS)—the simplest and most common silicone compound—exemplifies the central characteristics of its class and has attracted tremendous research attention. The development of PDMS‐based materials is a vivid reflection of the modern industry. In recent years, PDMS has stood out as the material of choice for various emerging technologies. The rapid improvement in bulk modification strategies and multifunctional surfaces has enabled a whole new generation of PDMS‐based materials and devices, facilitating, and even transforming enormous applications, including flexible electronics, superwetting surfaces, soft actuators, wearable and implantable sensors, biomedicals, and autonomous robotics. This paper reviews the latest advances in the field of PDMS‐based functional materials, with a focus on the added functionality and their use as programmable materials for smart devices. Recent breakthroughs regarding instant crosslinking and additive manufacturing are featured, and exciting opportunities for future research are highlighted. This review provides a quick entrance to this rapidly evolving field and will help guide the rational design of next‐generation soft materials and devices.

 

Many recent studies have highlighted the timescale for stress relaxation of biomaterials on the microscale as an important factor in regulating a number of cell-material interactions, including cell spreading, proliferation, and differentiation. Relevant timescales on the order of 0.1–100 s have been suggested by several studies. While such timescales are accessible through conventional mechanical rheology, several biomaterials have heterogeneous structures, and stress relaxation mechanisms of the bulk material may not correspond to that experienced in the cellular microenvironment. Here we employ X-ray photon correlation spectroscopy (XPCS) to explore the temperature-dependent dynamics, relaxation time, and microrheology of multicomponent hydrogels comprising of commercial poly(ethylene oxide)–poly(propylene oxide)–poly(ethylene oxide) (PEO–PPO–PEO) triblock copolymer F127 and alginate. Previous studies on this system have shown thermoreversible behavior in the bulk oscillatory shear rheology. At physiological temperatures, bulk rheology of these samples shows behavior characteristic of a soft solid, with G ′ > G ′′ and no crossover between G ′ and G ′′ over the measurable frequency range, indicating a relaxation time >125 s. By contrast, XPCS-based microrheology shows viscoelastic behavior at low frequencies, and XPCS-derived correlation functions show relaxation times ranging from 10–45 s on smaller length scales. Thus, we are able to use XPCS to effectively probe the viscoelasticity and relaxation behavior within the material microenvironments. 

Underground Nuclear Astrophysics Experiment in China (JUNA) has been commissioned by taking the advantage of the ultra-low background in Jinping underground lab. High current mA level 400 KV accelerator with an ECR source and BGO detectors were commissioned. JUNA studies directly a number of nuclear reactions important to hydrostatic stellar evolution at their relevant stellar energies. In the first quarter of 2021, JUNA performed the direct measurements of 25 Mg(p, γ ) 26 Al, 19 F(p, α ) 16 O, 13 C( α ,n) 16 O and 12 C( α , γ ) 16 O near the Gamow window. The experimental results reflect the potential of JUNA with higher statistics, precision and sensitivity of the data. The preliminary results of JUNA experiment and future plan are given.