Hole‐transporting layer (HTL) materials with sufficient hole collection ability, noncorrosive nature, and easy preparation are strongly desired for the field of organic solar cells (OSCs). The development of new materials and synthetic methods has been proved to be the essential approach to improve the HTL performances. Herein, a series of thiophene oligomers TO‐P1, TO‐P2, and TO‐P3 are designed and synthesized through coupling reaction by using the polyoxometalates as the oxidizing reagents. The thiophene oligomers can be readily synthesized under ambient condition with high yield. Among the as‐prepared thiophene oligomers, TO‐P2 exhibits neutral pH, sufficient work function, and high conductivity, endowing the HTL with excellent hole collection ability. Also, TO‐P2 possesses good chemical stability and satisfied solution processability, which is important for practical use. By using TO‐P2 as HTL, OSC shows a photovoltaic efficiency of 17.25%. Furthermore, TO‐P2 is a universal HTL that can be used to fabricate efficient OSCs with various active layers. More importantly, TO‐P2 shows good compatibility with large‐area processing technique. A 1 cm 2 OSC is fabricated by using a blade‐coated TO‐P2 HTL, exhibiting a power conversion efficiency of 15.0%. The easy preparation and noncorrosive nature endow TO‐P2 with great potential application in OSCs.

Although acceptor-donor-acceptor (A-D-A)-type molecules offer advantages in constructing NIR absorbing photothermal agents (PTAs) due to their strong intramolecular charge transfer and molecular planarity, their applications in photothermal therapy (PTT) of tumors remain insufficiently explored. In particular, the influence of ESP distribution on the optical properties of A-D-A photosensitizers has not been investigated. Herein, we analyze and compare the difference in ESP distribution between A-D-A-type small molecules and polymers to construct NIR absorbing PTAs with a high extinction coefficient (epsilon) and high photothermal conversion efficiency (PCE). The calculation results of density functional theory (DFT) indicate that the large ESP difference makes A-D-A-type small molecules superior to their polymer counterparts in realizing tight molecular packing and strong NIR absorbance. Among the as-prepared nanoparticles (NPs), Y6 NPs exhibited an obvious bathochromic shift of absorption peak from 711 nm to 822 nm, with the NIR-II emission extended to 1400 nm. Moreover, a high epsilon value of 5.69 L g-1 cm-1 and a PCE of 66.3% were attained, making Y6 NPs suitable for PTT. With a concentration of 100 mu g mL-1, Y6 NPs in aqueous dispersion yielded a death rate of 93.4% for 4T1 cells upon 808 nm laser irradiation (1 W cm-2) for 10 min, which is comparable with the best results of recently reported PTT agents. We explored a new way of utilizing the ESP difference to improve the molecular packing of (A-D-A) type molecules, and obtained a series of NIR PTAs with good PTT performance. The in vivo antitumor study demonstrates effective suppression of tumors.

Due to the inadequate photothermal conversion efficiency (PCE), most photothermal agents (PTAs) have to be used under high-power near-infrared (NIR) irradiation, which significantly exceeds medical safety standards, for achieving effective photothermal therapy (PTT) in antitumor treatment. This significantly hinders practical PTT application. Herein, three acceptor-donor-acceptor(A-D-A)-type molecules are synthesized based on cyclopentadithiophene unit to develop effective PTAs. By incorporating the large-size Si atom in the A-D-A molecules, the photosensitizer displays an increased packing distance in the aggregate state, leading to a blue-shifted absorption spectrum that better matches the medial laser wavelength. Also, the Si incorporation strategy elevates the nonradiative decay rate constants (knr) of the A-D-A photosensitizer, and thereby a further enhancement in PCE is achieved for the PTA. Consequently, the SiO-4F-based nanoparticles exhibited 64.23% PCE, with excellent biosafety and photothermal stability. Under NIR irradiation with medical safety (808 nm, 0.33 W cm-2), SiO-4F nanoparticles with 100 mu g mL-1 yield a death rate of over 91% for diverse tumor cells. Moreover, in vivo experiments, SiO-4F-based PTT effectively inhibited and eliminated tumors. These findings suggest that the Si-incorporated CDPT is promising for constructing effective A-D-A photosensitizers, enabling the PTT under NIR irradiation that meets medical safety standards.

Main observation and conclusionStyrene polymerization catalyzed by the half‐titanocenes CpTiCl2[1,3‐R2(CH2N)2C=N] (6b: R= 2,6‐Me2C6H3, T4: R = 2,4,6‐Me3C6H2; T5: R = 2,6‐iPr2C6H3) was carried out in the presence of methylaluminoxane (MAO). Compared to the styrene conversion (31%) and syndiospecific index (45%) using reported 6b as precatalyst, T5 bearing ligand with isopropyl substitutes on the N‐aryl‐rings exhibits much higher styrene conversion (61%) and syndiospecific index (99%), indicating that the catalytic behavior could be improved obviously by the introduction of electronic donating and steric bulky substituents. One N atom in imidazolin‐2‐iminato ligand was replaced by O atom, affording half‐titanocenes CpTiCl2[3‐C6H5(CH2N)(CH2O)C=N (T1) and CpTiCl2[2,6‐Me2(C6H3O)(NiPr2)C=N] (T2). Compared to 6b, both higher styrene conversion and syndiospecific index are afforded by using half‐titanocene T1 containing 2‐imino‐3‐phenyloxazolidine ligand. All the results illustrate that both the chemical structure and the nature of substituents of the ligand have obvious influence on the styrene conversion and syndiospecific index in the polymerization of styrene. All the resulting syndiotactic polystyrenes (sPSs) are highly syndiospecific (rrr > 99%). Correspondingly, the sPS prepared using T5/MAO catalytic system exhibits high melting point and narrow molecular weight distribution. The results might show new light on designing more efficient half‐titanocenes for styrene polymerization with both high styrene conversion and high syndiospecific selectivity.

Highly efficient terpolymerization of ethylene, propylene and 5-ethylidene-2-norbornene using a half-titanocene containing iminoimidazolidine with methylaluminoxane/Al(iBu) 3 /2,6-ditertbutyl-4-methyl-phenol was achieved.