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Attachment of Li+ ion on graphene surface to realize Li+‐ion conductor is a real challenge because of the weak interaction between the ions and the functional groups of graphene oxide; although, a large number of theoretical results are already available in the literature. To overcome this problem, graphene oxide is functionalized by 1‐aza‐15‐crown‐5, the cage‐like structure containing four oxygens that can bind Li+ ion through electrostatic interaction. Li+ migration on graphene surface has been investigated using ac relaxation mechanism. Perfect Debye‐type relaxation behavior with β (relaxation exponent) value ≈1 resulting from single ion is observed. The activation energy of Li+ migration arising due to cation‐π interaction is found to be 0.37 eV, which agrees well with recently reported theoretical value. It is believed that this study will help to design isolated ion conductors for Li+‐ion battery.  相似文献   

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Phase‐engineered type‐II metal–selenide heterostructures are demonstrated by directly selenizing indium‐tin oxide to form multimetal selenides in a single step. The utilization of a plasma system to assist the selenization facilitates a low‐temperature process, which results in large‐area films with high uniformity. Compared to single‐metal–selenide‐based photodetectors, the multimetal–selenide photodetectors exhibit obviously improved performance, which can be attributed to the Schottky contact at the interface for tuning the carrier transport, as well as the type‐II heterostructure that is beneficial for the separation of the electron–hole pairs. The multimetal–selenide photodetectors exhibit a response to light over a broad spectrum from UV to visible light with a high responsivity of 0.8 A W?1 and an on/off current ratio of up to 102. Interestingly, all‐transparent photodetectors are successfully produced in this work. Moreover, the possibility of fabricating devices on flexible substrates is also demonstrated with sustainable performance, high strain tolerance, and high durability during bending tests.  相似文献   

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We present the theory of novel time‐stepping algorithms for general nonlinear, non‐smooth, coupled, and thermomechanical problems. The proposed methods are thermodynamically consistent in the sense that their solutions rigorously comply with the two laws of thermodynamics: for isolated systems, they preserve the total energy and the entropy never decreases. Extending previous works on the subject, the newly proposed integrators are applicable to coupled mechanical systems with non‐smooth kinetics and can be formulated in arbitrary variables. The ideas are illustrated with a simple non‐smooth problem: a rheological model for a thermo‐elasto‐plastic material with hardening. Numerical simulations verify the qualitative features of the proposed methods and illustrate their excellent numerical stability, which stems precisely from their ability to preserve the structure of the evolution equations they discretize. Copyright © 2017 John Wiley & Sons, Ltd.  相似文献   

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