Recently, biological materials such as DNA molecules, proteins, and albumen have been extensively investigated for various applications, as they are environmentally friendly and exhibit novel optical and electronic properties. Especially, over the last decades, DNA–lipid complex have been frequently reported as components of optical electronic devices. In this mini-review, the physicochemical performance of DNA–lipid complex is introduced, and then the related research progress in electronic devices such as organic thin film transistors and other optical-electrical devices are discussed. Finally, the challenges and prospects of other possible applications are also presented.

2,2′,7,7′-Tetrakis(N,N-di-p-methoxyphenyl-amine)-9,9′-spirobifluorene (spiro-OMeTAD) film currently prevails as hole transport layer (HTL) employed in perovskite solar cells (PSCs). However, the standard preparation method for spin-coated, Lithium bis(trifluoromethylsulfony) imide (LiTFSI)-doped, spiro-OMeTAD HTL depends on a time-consuming and uncontrolled oxidation process to gain desirable electrical conductivity to favor device operation. Our previous work demonstrated that ~10 s oxygen or oxygen containing gas discharge plasma exposure can oxidize spiro-OMeTAD HTL effectively and make PSCs work well. In this communication, hole-only devices are fabricated and in-situ current density-voltage measurements are performed to investigate the change in hole mobility of LiTFSI-doped spiro-OMeTAD films under plasma exposure. The results reveal that hole mobility values can be increased averagely from ~5.0 × 10⁻⁵ cm²V⁻¹s⁻¹ to 7.89 × 10⁻⁴ cm²V⁻¹s⁻¹ with 7 s O₂ plasma exposure, and 9.33 × 10⁻⁴ cm²V⁻¹s⁻¹ with 9 s O₂/Ar plasma exposure. The effects on the photovoltaic performance of complete PSC devices are examined, and optical emission spectroscopy (OES) is used for a diagnostic to explain the different exposure effects of O₂ and O₂/Ar plasma. High efficiency, fine controllability and good compatibility with current plasma surface cleaning techniques may make this method an important step towards the future commercialization of photovoltaic technologies employing spiro-OMeTAD hole transport material.

Organic nonvolatile transistor memory with synthetic polypeptide derivatives as dielectric was fabricated by a solution process. When only poly (γ-benzyl-l-glutamate) (PBLG) was used as dielectric, the device did not show obvious hysteresis in transfer curves. However, PBLG blended with PMMA led to a remarkable increase in memory window up to 20 V. The device performance was observed to remarkably depend on the blend ratio. This study suggests the crystal structure and the molecular alignment significantly affect the electrical performance in transistor-type memory devices, thereby provides an alternative to prepare nonvolatile memory with polymer dielectrics.

In recent years, biopolymers have been widely used in optoelectronic devices because of their unique structure, novel optical and physical properties. In this paper, novel RNA-based photofunctional materials were fabricated by associating an RNA–OTMA (octadecyltrimethylammonium chloride) lipid complex with a luminescent Eu (III) complex. The fluorescence emission intensity, fluorescence quantum yield and fluorescence lifetime were characterized in both solution and thin film states, and the interaction between the RNA–OTMA lipid complex and Eu (III) complexes was analyzed. This study suggests that the luminescence performance of the Eu (III) complexes doped with RNA–OTMARNA–OTMA was significantly enhanced compared with those of the complex in a conventional poly (methyl methacrylate) matrix, thereby providing an important basis for the application of biomaterials in optoelectronic devices.