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Verified CAS / Academic Author2 Decoded Studies

Prof. Shiyi Li

Not explicitly stated in the provided text; likely a Chinese university or research institute.

Co-Affiliations:Chinese Academy of Sciences

Research Publications & English Decoded Briefs

Showing 2 publications
SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-3757-2

Full-space built-in electric field inside gradient Sn-doped β-Ga2O3 photoanodes for enhanced photoelectrochemical solar-blind UV photodetection

β-Ga2O3 is a promising candidate for solar-blind ultraviolet photodetection owing to its suitable bandgap of approximately 4.9 eV, excellent photoresponse characteristics, and high stability. However, the lack of a sufficient driving force within the material leads to extensive bulk charge recombination, limiting its photocurrent and thus posing significant challenges in designing high-performance Ga2O3-based photodetection. In this study, we propose a gradient doping strategy to achieve a Sn-doping concentration gradient along the β-Ga2O3 film thickness. By combining sol–gel synthesis with rapid thermal annealing, a spatially graded band structure with a full-space built-in electric field is constructed, which increases the width of band bending over a large region and is crucial for significantly enhancing carrier separation and transport in the bulk. The resulting gradient Sn-doped β-Ga2O3 enables exceptional photoelectric performance without an external bias under 254 nm irradiation, including a superior responsivity of 66.88 mA W−1, a high detectivity of 8.12 × 10^11 Jones, and a fast rise/decay time of 79/65 ms, outstanding most existing similar reported photoelectrochemical (PEC) type optoelectronic devices. Additionally, the device exhibits excellent long-term stability and enables high-resolution underwater ultraviolet imaging. This study demonstrates that the gradient doping strategy provides a feasible approach for enhancing the PEC performance of β-Ga2O3 photoelectrodes.

SCIENCE CHINA Materials2026DOI: 10.1007/s40843-026-4148-3

Bioinspired voltage-gated multi-state ion channels in MXene nanoconfinement for emulating synaptic plasticity

Biological ion channels exhibit multistate transport behavior beyond simple binary open-closed conformations, enabling dynamic control of neural signaling and transmembrane substance transport. Inspired by this, we synthesized a triphenylamine-ketone donor-acceptor (D-A) type poly(aryl amine-ketone) with multiple redox sites, allowing continuously tunable electrochemical states via hierarchical electron transfer. Combining this polymer with two-dimensional conductive MXene, we constructed a biomimetic nanofluidic transistor. Through side-group tuning to optimize redox matching, the polymer undergoes reversible conformation switching via intramolecular charge transfer at voltages below 1 V. The field-driven conformational changes induce electrostatic attraction, promoting reversible contraction of MXene interlayers. Synergistic coupling of interlayer spacing variation and dynamic interfacial charge rearrangement enables precise hierarchical control of ion flux. The device achieves three switchable ion transport states—closed, partially open, and fully open—with an ion switching ratio of 10 and outstanding cycling stability. Furthermore, synaptic plasticity features emulate fundamental attributes of biological signaling, providing a foundation for bioinspired neuromorphic devices.