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Three kinds of fluorinated PI/CEs composite films prepared by a thermal imidization process have a low dielectric constant and low dielectric loss at a high frequency (10 GHz).

The effect of Mg addition on the microstructure and sacrificial anode protection performance of a hot-dip Al-5Zn-4Si-xMg coating was studied by scanning electron microscopy (SEM-EDS), an X-ray diffractometer, and an electrochemical workstation. The results showed that Al-Zn-Si alloy was composed of an Al-rich phase and a Zn-rich phase. The MgZn2 phase appears after Mg addition. When the addition of Mg increased to 0.15 wt.%, the Mg2Si phase began to appear in the alloy. The hot-dip Al-5Zn-4Si-xMg coating consisted of Si particles, an Al-rich phase and a Zn-rich phase. When the Mg content increased to 0.15 wt.%, the Mg2Si phase and Al + Zn + MgZn2 eutectoid phase began to appear in the coating. In the full immersion corrosion test of the hot-dip Al-5Zn-4Si-xMg coating, the order of corrosion resistance was 0.15% Mg coating > 0.2% Mg coating > 0.05% Mg coating > 0 Mg coating. In the corrosion process of the hot-dip Al-5Zn-4Si-0.15Mg coating, with the increase in immersion, the self-corrosion current of the coating decreased, and the sacrificial protection performance was the best.

To evaluate the role of the charge transfer (CT) state in the singlet fission (SF) process, we prepared three 3,6-bis(thiophen-2-yl)diketopyrrolopyrrole (TDPP) derivatives with zero (Ph

To harvest two triplet excitons of singlet fission (SF) via a two-electron transfer efficiently, the revelation of the key factors that influence the two-electron-transfer process is necessary. Here, by using steady-state and transient absorption/fluorescence spectroscopy, we investigated the two-electron-transfer process from the two triplet excitons of intramolecular SF (iSF) in a series of tetracene oligomers (dimer, trimer, and tetramer) with 7,7,8,8-tetracyanoquinodimethane (TCNQ) as an electron acceptor in solution. Quantitative two-electron transfer could be conducted for the trimer and tetramer, and the rate for the tetramer is faster than that for the trimer. However, the maximum efficiency of the two-electron transfer in the dimer is relatively low (∼47%). The calculation result of the free energy change (Δ

An efficient SF material (ΦT = 164%) based on an anthracene dimer with high triplet energy (1.51 eV) and good stability simultaneously was achieved for the first time.

Accelerated hole extraction efficiency through effective BSBF–NH2 molecule surface passivation.

Fast symmetry breaking charge separation (SB-CS) rate and slow CS recombination rate were achieved simultaneously via tuning the molecular geometry.

An efficient SF material with broadband light harvesting ability was prepared by means of ultrafast intramolecular Förster resonance energy transfer.