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The low degradability of common polymers composed of light elements, results in a serious impact on the environment, which has become an urgent problem to be solved. As the reverse process of monomer polymerization, what deviates degradation from the idealized sequential depolymerization process, thereby bringing strange degradation products or even hindering further degradation? This is a key issue at the atomic level that must be addressed. Herein, we reveal that hydrogen atom transfer (HAT) during degradation, which is usually attributed to the thermal effect, unexpectedly exhibits a strong high-temperature tunnelling effect. This gives a possible answer to the above question. High-precision first-principles calculations show that, in various possible HAT pathways, lower energy barrier and stronger tunnelling effect make the HAT reaction related to the active end of the polymer occur more easily. In particular, although the energy barrier of the HAT reaction is only of 0.01 magnitude different from depolymerization, the tunnelling probability of the former can be 14~32 orders of magnitude greater than that of the latter. Furthermore, chain scission following HAT will lead to a variety of products other than monomers. Our work highlights that quantum tunnelling may be an important source of uncertainty in degradation and will provide a direction for regulating the polymer degradation process.
Despite many advances towards improving the stability of organic photovoltaic devices, environmental degradation under ambient conditions remains a challenging obstacle for future application. Particularly conventional systems employing fullerene der
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Hybrid conjugated polymer/fullerene filaments based on MEH-PPV/PVP/PCBM are prepared by electrospinning, and their properties assessed by scanning electron, atomic and lateral force, tunnelling, and confocal microscopy, as well as by attenuated total
The paper presents the results of measurements of XPS valence band spectra of SiO2/MAPbI3 hybrid perovskites subjected to irradiation with visible light and annealing at an exposure of 0-1000 hours. It is found from XPS survey spectra that in both ca
We explore the degradation behaviour under continuous illumination and direct oxygen exposure of inverted unencapsulated formamidinium(FA)0.83Cs0.17Pb(I0.8Br0.2)3, CH3NH3PbI3, and CH3NH3PbI3-xClx perovskite solar cells. We continuously test the devic