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Weijin Hu

Publications and source records attributed to Weijin Hu.

6 recordsLinked to original sources

2D ferroelectric narrow-bandgap semiconductor Wurtzite' type alpha-In2Se3 and its silicon-compatible growth

2D van der Waals ferroelectrics, particularly alpha-In2Se3, have emerged as an attractive building block for next-generation information storage technologies due to their moderate band gap and robust ferroelectricity stabilized by dipole locking. alpha-In2Se3 can adopt either the distorted zincblende or wurtzite structures; however, the wurtzite phase has yet to be experimental-ly validated, and its large-scale synthesis poses significant challenges. Here, we report an in-situ transport growth of centimeter-scale wurtzite type alpha-In2Se3 films directly on SiO2 substrates using a process combining pulsed laser deposition and chemical vapor deposition. We demonstrate that it is a narrow bandgap ferroelectric semiconductor, featuring a Curie tem-perature exceeding 620 K, a tunable bandgap (0.8-1.6 eV) modulated by charged domain walls, and a large optical absorption coefficient of 1.3 times 10 powers 6 per centemeter. Moreover, light absorption promotes the dynamic conductance range, linearity, and symmetry of the synapse devices, leading to a high recognition accuracy of 92.3 percent in a supervised pattern classification task for neuromorphic computing. Our findings demonstrate a ferroelectric polymorphism of In2Se3, highlighting its potential in ferroelectric synapses for neuromorphic computing.

cond-mat.mtrl-sci

Flash annealing-engineered wafer-scale relaxor antiferroelectrics for enhanced energy storage performance

Dielectric capacitors are essential for energy storage systems due to their high-power density and fast operation speed. However, optimizing energy storage density with concurrent thermal stability remains a substantial challenge. Here, we develop a flash annealing process with ultrafast heating and cooling rates of 1000 oC/s, which facilitates the rapid crystallization of PbZrO3 film within a mere second, while locking its high-temperature microstructure to room temperature. This produces compact films with sub-grain boundaries fraction of 36%, nanodomains of several nanometers, and negligible lead volatilization. These contribute to relaxor antiferroelectric film with a high breakdown strength (4800 kV/cm) and large polarization (70 uC/cm2). Consequently, we have achieved a high energy storage density of 63.5 J/cm3 and outstanding thermal stability with performance degradation less than 3% up to 250 oC. Our approach is extendable to ferroelectrics like Pb(Zr0.52Ti0.48)O3 and on wafer scale, providing on-chip nonlinear dielectric energy storage solutions with industrial scalability.

cond-mat.mtrl-sci

Ultralow-pressure mechanical-motion switching of ferroelectric polarization

Ferroelectric polarization switching, achieved by mechanical forces, enables the storage of stress information in ferroelectrics, and holds promise for human-interfacing applications. The prevailing mechanical approach is locally induced flexoelectricity with large strain gradients. However, this approach usually requires huge mechanical pressures, which greatly impedes device applications. Here, we report an approach of using triboelectric effect to mechanically, reversibly switch ferroelectric polarization across α-In2Se3 ferroelectric memristors. Through contact electrification and electrostatic induction effects, triboelectric units are used to sensitively detect mechanical forces and generate electrical voltage pulses to trigger α-In2Se3 resistance switching. We realize multilevel resistance states under different mechanical forces, by which a neuromorphic stress system is demonstrated. Strikingly, we achieve the reversal of α-In2Se3 ferroelectric polarization with a record-low mechanical pressure of ~ 10 kPa, and even with tactile touches. Our work provides a fundamental but pragmatic strategy for creating mechanical-tactile ferroelectric memory devices.

cond-mat.mtrl-sci

Proton-mediated reversible switching of metastable ferroelectric phases with low operation voltages

The exploration of ferroelectric phase transitions enables an in-depth understanding of ferroelectric switching and promising applications in information storage. However, controllably tuning the dynamics of ferroelectric phase transitions remains challenging owing to inaccessible hidden phases. Here, using protonic gating technology, we create a series of metastable ferroelectric phases and demonstrate their reversible transitions in van der Waals ferroelectric α-In2Se3 transistors. By varying the gate bias, protons can be incrementally injected or extracted, achieving controllable tuning of the ferroelectric α-In2Se3 protonic dynamics across the channel and obtaining numerous intermediate phases. Combining piezoelectric force microscopy and electrical hysteresis measurements, we surprisingly discover that the gate tuning of α-In2Se3 protonation is volatile, unlike the conventional gating effect, and the created new phases remain polar. Their origin, revealed by first-principles calculations, is related to the formation of metastable hydrogen-stabilized α-In2Se3 phases with switchable dipoles. Furthermore, our approach enables ultralow gate-voltage switching of different phases (below 0.4 V), and easy integration with transistor components. This work provides fundamental insights into the interactions between protons and ferroelectric phase transitions, providing a possible avenue for accessing hidden phases in ferroelectric switching and for developing energy-efficient, multilevel-switching memory devices.

cond-mat.mtrl-sci

Glassy crystals with colossal multi-baroresponsivities

As a nontrivial solid state of matter, the glassy-crystal state embraces physical features of both crystalline and amorphous solids, where a long-range ordered periodic structure formed by the mass centers of constituent molecules accommodates orientational glasses. Here, we discover and validate a glassy-crystal state in 2-amino-2-methyl-1,3-propanediol (AMP, C4H11NO2) by neutron scattering and complementary broadband dielectric spectroscopy (BDS) measurements. The freezing process of the dynamic orientational disorder is manifested at relaxation times well described by the Vogel-Fulcher-Tammann (VFT) law and the strongly frequency-dependent freezing temperature ranging from around 225 K at 0.1 Hz to above room temperature in the GHz region. At room temperature, the supercooled state is extremely sensitive to pressure such that a few MPa pressure can induce crystallization to the ordered crystal state, eventually leading to a temperature increase by 48 K within 20 s, a significant reduction of visible light transmittance from about 95% to a few percentages, and a remarkable decrease of electrical conductivity by three orders of magnitude. These ultrasensitive baroresponsivities might find their applications in low-grade waste heat recycling, pressure sensors and non-volatile memory devices. It is expected that glassy crystals serve as an emerging platform for exploiting exotic states of matter and the associated fantastic applications.

cond-mat.mtrl-sci

Ambipolar Solution-processed Hybrid Perovskite Phototransistors

Organolead halide perovskites have attracted substantial attention due to their excellent physical properties, which enable them to serve as the active material in emerging hybrid solid-state solar cells. Here we investigate the phototransistors based on hybrid perovskite films, and provide direct evidence for their superior carrier transport property with ambipolar characteristics. The field-effect mobilities for triiodide perovskites at room temperature are measured as 0.18 (0.17) cm2 V-1 s-1 for holes (electrons), which increase to 1.24 (1.01) cm2 V-1 s-1 for mixed halide perovskites. The photoresponsivity of our hybrid perovskite devices reaches 320 A W-1, which is among the largest values reported for phototransistors. Importantly, the phototransistors exhibit an ultrafast photoresponse speed of less than 10 μs. The solution-based process and excellent device performance strongly underscore hybrid perovskites as promising material candidates for photoelectronic applications.

cond-mat.mtrl-sci