Organic photodetectors (OPDs) are promising candidates for next-generation digital imaging and wearable sensors due to their low cost, tuneable optoelectrical properties combined with high-level performance, and solution-processed fabrication techniques. However, OPD detection is often limited to shorter wavelengths, whereas photodetection in the near-infrared (NIR) region is increasingly being required for wearable electronics and medical device applications. NIR sensing suffers from low responsivity and high dark currents. A common approach to enhance NIR photon detection is lowering the optical band gap via donor−acceptor (D−A) molecular engineering. Herein, we present the synthesis of two novel indacenodithiophene (IDT)based D−A conjugated polymers, namely, PDPPy-IT and PSNT-IT via palladium-catalyzed Stille coupling reactions. These novel polymers exhibit optical band gaps of 1.81 and 1.27 eV for PDPPy-IT and PSNT-IT, respectively, with highly desirable visible and NIR light detection through energy-level manipulation. Moreover, excellent materials' solubility and thin-film processability allow easy incorporation of these polymers as an active layer into OPDs for light detection. In the case of PSNT-IT devices, a photodetection up to 1000 nm is demonstrated with a peak sensitivity centered at 875 nm, whereas PDPPy-IT devices are efficient in detecting the visible spectrum with the highest sensitivity at 660 nm. Overall, both OPDs exhibit spectral responsivities up to 0.11 A W −1 and dark currents in the nA cm −2 range. With linear dynamic ranges exceeding 140 dB and fast response times recorded below 100 μs, the use of novel IDT-based polymers in OPDs shows great potential for wearable optoelectronics.

Microscopic dynamical features in the relaxation of glass structures are one of the most important unsolved problems in condensed matter physics. Although the structural relaxation processes in the vicinity of glass transition temperature are phenomenologically expressed by the Kohlrausch–Williams–Watts function and the relaxation time can be successfully interpreted by Adam–Gibbs theory and/or Narayanaswamy’s model, the atomic rearrangement, which is the origin of the volume change, and its driving force have not been elucidated. Using the microsecond time-scale molecular dynamics simulations, this study provides insights to quantitatively determine the origin of the thermal shrinkage below Tg in a soda-lime silicate glass. We found that during annealing below Tg, Na ions penetrate into the six-membered silicate rings, which remedies the acute O–O–O angles of the energetically unstable rings. The ring structure change makes the space to possess the cation inside the rings, but the ring volume is eventually reduced, which results in thermal shrinkage of the soda-lime silica glass. In conclusion, the dynamical structural relaxation due to the cation displacement evokes the overall volume relaxation at low temperature in the glassy material.

Demand of large size flat panel displays are emerging. For upcoming displays, extra features are demanded in addition to the visual performance. One of the attracting features is the combination with an acoustic function. To utilize the display panel as a speaker, glass substrate plays important role to improve its acoustic quality. In this study, the effect of elastic property on display panel performance was investigated.

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The impact of the characteristics of carrier glass substrate on flexible OLED display production was studied. Non-negligible thermal shrinkage was observed even though heating temperature is relatively low. In addition, deformation of the substrate was found to be caused by dividing into two or more sheets.