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Verified CAS / Academic Author2 Decoded Studies

Prof. JIANG Cheng

SinoGreenTech Intelligence Archive (affiliated with Chinese Academy of Sciences research institutes)

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Showing 2 publications
SCIENCE CHINA Materials2026DOI: 10.1007/s40843-026-4447-3

Observation of Chargeable Photoconductivity in Bi0.85La0.15FeO3/Q2DEG-Based Multiferroic Heterostructure

Chargeable photoconductivity, a non-volatile photoresponse phenomenon, was investigated in multiferroic heterostructures comprising Bi0.85La0.15FeO3 (BLFO) and a quasi-two-dimensional electron gas (Q2DEG). Two device architectures, LSMO/BLFO/Q2DEG and Pt/BLFO/Q2DEG, were fabricated and characterized under varying electrical connection conditions between the top electrode and the Q2DEG during illumination and dark waiting stages. Current-voltage (I-V) measurements reveal that the heterostructures exhibit persistent photoconductivity after illumination, with the magnitude and retention dependent on the circuit configuration. Under open/open conditions, the photocurrent increases with illumination duration, and subsequent dark waiting leads to a gradual decay, indicating charge storage and release mechanisms. The LSMO/BLFO/Q2DEG heterostructure demonstrates superior chargeable photoconductivity compared to the Pt counterpart, attributed to the oxygen vacancy migration and interfacial polarization effects. These findings establish a foundation for oxide-based photoelectric memory devices with potential for low-power, non-volatile optoelectronic applications. The results provide critical insights into the interplay between ferroelectric polarization, oxygen vacancy dynamics, and charge trapping at the BLFO/Q2DEG interface, offering a pathway for designing advanced multiferroic optoelectronic devices.

SCIENCE CHINA Materials2025DOI: 10.1007/s40843-025-3453-y

Molecular engineering of buckybowl trichalcogenasumanene toward centimeter-sized organic single-crystal arrays and devices

Organic semiconductor single-crystal (OSSC) arrays are pivotal for high-performance integrated electronics, yet the fundamental principles governing molecular design for one-dimensional (1D) crystalline nanostructures and the role of intermolecular interactions in solution self-assembly remain unresolved. This study introduces a molecular engineering strategy employing hetero-buckybowl trichalcogenasumanenes to direct the self-assembly of OSSC arrays. The distinctive concave-convex architecture promotes 1D crystal formation via directional π-π interactions while suppressing intercolumnar coupling, thereby enhancing structural anisotropy and charge transport. Centimeter-sized OSSC arrays were fabricated on various substrates through solution self-assembly. Organic field-effect transistors (OFETs) based on these arrays exhibited hole mobility up to 0.89 cm² V⁻¹ s⁻¹ (average 0.65 cm² V⁻¹ s⁻¹), with minimal device-to-device variation, surpassing previous buckybowl-based devices. The six butoxy groups in molecule 4 improve solubility and stabilize molecular morphology against strain, yielding flexible OFETs with outstanding bendable durability. This strategy significantly enhances crystallinity and uniformity, offering a pathway for high-performance, large-area organic electronics.