“…From above analysis, PEG fluorescent emission is well understood based on CTE mechanism, i.e., owing to aggregation of their chains, and the through-space electron conjugation arising therefrom. One of typical characteristic of CTE materials is that their emission is commonly dependent on their chain motion ability, which is adjustable by changing temperature of their solution and by adding poor or nonsolvent in the solution. ,,,,,, By lowering temperature, the conformation of the clusters and the mobility of the polymer chains will be surely affected, the emission is enhanced at lower temperature, because polymer chains are more rigidified, and their motion more limited, which would in general reduce the probability of the relaxation back to ground state through nonirradiative pathway for any excited electron, since it is well accepted that de-excitation of any exciton through nonirradiation is enhanced at higher temperature, attenuating therefore the emission intensity. , Fluorescence emission of PEG solutions of different M n was tested at temperatures from 5 to 70 °C under excitation λ ex = 280 nm, which showed a gradual decrease in emission intensity with increased temperature for all PEGs, regardless of their M n (Figure S13), in good agreement with the expectation. Similar to lowering the temperature, the chain mobility must be gradually restricted by adding poor or nonsolvent in P8k solution, the emission intensity was therefore enhanced by consequence (Figure S14).…”