As T+ oscillates, θ0 changes in the expression for UB,
¯UB=μo2{qv4πr2.r2ea2e}2(|1cos2(θ)e−2resin(ϕ/2)aecos(θ)2cos2(ϕ/2)sin(ϕ/2)|θ00+|2aerecos(θ)e−2resin(ϕ/2)aecos(θ)cos(ϕ/2)|θ00−|a2er2ecot(ϕ/2)e−2resin(ϕ/2)aecos(θ)|θ00)2
and
x=2resin(ϕ/2)
rT+x=tan(θ0)
where rT+ is the T+ particle orbit.
¯UB=μo2{qv4πr2.r2ea2e}2{(√22cos2(θ0)+√2aerecos(θ0)−a2er2e)e−re√2aecos(θ0)+(−√22−√2aer+a2er2e)e−re√2ae}2
at ϕ=π2.
The change of UB at ϕ=π2 with θ0 due to the electrons is obtained illustratively from a plot of
(((2)^(1/2)/(2*cos(x)*cos(x))+(2)^(1/2)*a/(cos(x))-a^2)*e^(-(2^(1/2))/(a*cos(x)))+(-(2^(1/2)/2)-2^(1/2)*a+a^2)*e^(-(2^(1/2)/a)))^2,
where 1.5≥a≥0.7
At θ0=π2, the T+ particle is in an orbit just over the electron. At θ0=0, the T+ particle is far from the electron. theta0 can attain zero only if re is sufficiently large. Otherwise, θ0 is limited by,
tan(θ0min)=rT+√2.re
as re→∞, θ0min→0
It is possible that a>1, the electron is then spinning about an axis passing through it. In this case, the orbit that captures T+ particles has only one electron.
Since cos(π2)=cos(−π2, to account for UB in the presence of another electron, we simply add two graphs and obtain 2UB. The same plot scaled by two along UB is obtained.
As T+ oscillates about ϕ=0, θ varies from θ0max to θ0min. As the amplitude of the oscillation increases θ0max increases. The energy states available for the T+ particles in oscillation are between θ0max and θ0min.
Energy at specific θ0 within this range can be absorbed by the T+ particles and free itself from the orbit.
If UB is directly proportional to the number of T+ particles captured in orbit,
UB∝nT+,
nT+ being the number of T+
If intensity is the number of T+ emitting through an unit area per unit time and the distribution of θ0 among that T+ particles is uniform, then the zoomed graph above also presents the emission spectrum of T+ over the range of permissible θ0.
When broad spectrum illumination is passed through a material with T+ particles, this is the emission spectrum recorded after parts of the illumination has been absorbed by the material.
As re increases with increasing temperature, so a increases with increasing temperature. At a specific value of UB across the graphs of varying a,
θ0 can decrease as temperature increases. This means for that range of temperature, the amplitude of oscillation decreases with increasing temperature.
This type of oscillation is characteristic of Brownian motion where the amplitude of oscillation can decrease with higher temperature. Oscillating T+ particles can be the reason for Brownian motion.