Long‐persistent circularly polarized phosphorescence (LPCPP) is achieved for the first time in chiral organic ionic crystals at room temperature. The co‐crystal composed of terephtalic acid (TPA) and chiral α‐phenylethyamines (PEAs) gave rise to LPCPP with lifetimes up to 862 ms and large dissymmetric factor (glum). The hybridization of TPA with chiral PEAs allows circular polarization of the generated long‐persistent phosphorescence. The observed mirror‐image twisted molecular structures in the rigid lattices were responsible for the chiroptical activation of the generated long‐persistent phosphorescence.

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A photoelectrochemical device was achieved by interfacial self-assembly of macrocyclic π-conjugated copper phthalocyanine (CuPc) on surface of TiO 2 nanorod arrays (NRs). The photocurrent density of the elegant TiO 2 @CuPc NRs photoanode reaches 2.40 mA/cm 2 at 1.23 V vs. RHE under the illumination of 100 mW/cm 2 from AM 1.5G sun simulator, which is 2.4 times higher than that of the pure TiO 2 . At the same time, the photoelectrochemical device constructed through this strategy has good stability and the photocurrent density remain almost no decline after 8 h of continuous operation. The Mott-Schottky and LSV curves demonstrate that CuPc act as a co-catalyst for water oxidation and a possible mechanism is proposed for water oxidation based on careful analysis of the detailed results. The holes from VB of TiO 2 photogenerated by electrons exciting are consumed by a process in which Cu 2+ is oxidized to Cu 3+ and Cu 4+ , and then oxidize water to produce oxygen. CuPc species is considered to be a fast redox mediator to reduce the activation energy of water oxidation in and effectively promote charge separation.