Using the Bernstein theorem we prove the complete monotonicity of the three
parameter Mittag?Leffler function E??,? (?w) for w ? 0 and suitably constrained parameters ?, ? and ?.
The photoluminescence (PL) of thermally evaporated Alq3 thin films has been studied in a few samples annealed and non-annealed and afterwards exposed to the laboratory atmosphere for over six years. It was found that the measured emission intensity decays with a long lifespan and with four different time-spectral behaviors, which imply the existence of four molecular aggregations, or components. In particular, the time behavior of each component follows the trend of a Kohlrausch−Williams−Watt (KWW) function, which is well known in mathematics but without any physical meaning. Here, by introducing the concept of the material clock, the system has been described by a damped harmonic oscillator, which in certain conditions, fulfilled in the present case, allows the expansion of the KWW function in the so-called Prony series. The terms of this series can be attributed to chemical and physical processes that really contribute to the decay, i.e. the degradation, of the Alq3 thin films when interacting with internal and environmental agents. These insights unveiled the usefulness of proper mathematical procedures and properties, such as the monotonicity and the complete monotonicity, for investigating the PL of this ubiquitous organometallic molecule, which possesses one among the highest emission yield. Moreover, this method is also promising for describing the photoluminescent processes of similar organic molecules important both for basic research and optoelectronic applications.
Physically natural assumption says that the any relaxation process taking place in the time interval [t0, t2], t2 > t0 ≥ 0 may be represented as a composition of processes taking place during time intervals [t0, t1] and [t1, t2] where t1 is an arbitrary instant of time such that t0 ≤ t1 ≤ t2. For the Debye relaxation such a composition is realized by usual multiplication which claim is not valid any longer for more advanced models of relaxation processes. We investigate the composition law required to be satisfied by the Cole-Cole relaxation and find its explicit form given by an integrodifferential relation playing the role of the time evolution equation. The latter leads to differential equations involving fractional derivatives, either of the Caputo or the Riemann-Liouville senses, which are equivalent to the special case of the fractional Fokker-Planck equation satisfied by the Mittag-Leffler function known to describe the Cole-Cole relaxation in the time domain.
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