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Nature Communications logoLink to Nature Communications
. 2026 Jul 16;17:8708. doi: 10.1038/s41467-026-75638-w

Ultrafast non-volatile charge storage and mid-infrared photoluminescence in LuminoMem tellurium devices for in-memory computing

Delang Liang 1,2, Shiyu Wang 1, Yan Wang 3, Dong Li 2, Yuchun Chen 1, Bin Cheng 4, Mingyang Qin 1, Dehong Yang 1, Jie Sheng 1, Huawei Liu 5, Lin Li 4, Changgan Zeng 4, Dong Sun 1,6,7,8,9,✉, Anlian Pan 2,5,✉, Jing Liu 3,✉
PMCID: PMC13490502  PMID: 42463516

Abstract

Integrated optoelectronic systems strive to combine the logic and memory density of electronics with the bandwidth of photonics, but monolithic realization is impeded by the inefficient electronic-to-photonic interface. Current architectures rely on separate readout circuitry and modulators, creating bottlenecks in energy and latency, while existing direct transduction methods often compromise on switching speed or non-volatility. Here, we develop an ultrafast, non-volatile optoelectronic memory, named LuminoMem, that integrates electrical storage and mid-infrared light emission ( ~ 3.4 μm) in a single device. The device utilizes a floating-gate architecture, in which the semiconductor tellurium serves simultaneously as a charge-storage layer and an emissive medium. This design enables nanosecond-scale electrical programming of non-volatile photoluminescence, allowing direct optical access to stored states without external modulation. We demonstrate that LuminoMem achieves 4-bit optical storage capacity and enables highly accurate image-recognition neural network simulations, providing a hardware foundation that co-integrates optical emission, memory, and computing capabilities.

Subject terms: Information storage, Nanoscience and technology, Materials for optics, Optics and photonics, Electrical and electronic engineering


The monolithic integration of memory and photonic devices is normally limited by inefficient electronic-to-photonic interfaces. Here, the authors report optoelectronic floating-gate memory devices based on tellurium, integrating multi-bit electrical storage and mid-infrared light emission at 3.4 μm with nanosecond-scale electrical programming speed.

Introduction

The quest for next-generation intelligent platforms is accelerating the development of integrated optoelectronic systems that combine the strengths of electronics for dense, low-noise logic and memory with those of photonics for ultrafast, massively parallel data transport and processing1–4. By bringing these capabilities together on chip, such architectures could move beyond the performance and energy-efficiency ceilings of purely electronic hardware, and enable hardware-level co-integration of computing with communication and sensing5–7. However, monolithic realization remains elusive, limited by a central bottleneck: inefficient and power-hungry information transfer across the electronic-to-photonic interface4,8–10.

A primary source of inefficiency lies in converting electrically stored data in electronic memory into optical signals. In conventional architectures, data are first retrieved from memory by dedicated electronic readout circuitry and then routed to a separate optical modulator for electro-optic conversion (Fig. 1a), a two-step workflow that incurs substantial energy overheads and added latency8,11. This architectural discontinuity erodes the intrinsic advantages of photonics and frustrates truly dense integration, since the material stacks (e.g., LiNbO3, III–V, phase-change or plasmonic platforms) and the corresponding fabrication process flows that enable high-performance modulators are frequently incompatible with high-volume on-chip integrated manufacturing12–16.

Fig. 1. Concept and mechanism of LuminoMem.

Fig. 1

a Conventional hardware bottleneck and the redundant data chain. Schematic of the typical electronic-to-photonic interface where data must be fetched from memory, processed by a complementary metal-oxide-semiconductor (CMOS) application-specific integrated circuit (ASIC), and converted into the optical domain via an external electro-optic (E/O) modulator before entering the photonic integrated circuits for further processing. b Illustration of the proposed solution featuring a LuminoMem array where mid-infrared (MIR) photoluminescence (PL) is emitted directly upon electrical programming. cMonolithic architecture for in-memory computing.

Attempts to achieve direct electro-optic transduction on a single chip have introduced new tradeoffs. For example, doping-based approaches regulate optical emission or transmission by electrically tuning the carrier concentration, but such effects lack non-volatility17–21. Phase change materials (PCMs) offer an appealing route to non-volatile photonic modulation through electrically driven phase transitions, but their switching speeds are often too slow to match the throughput in high-bandwidth photonic systems14,22–26. Ferroelectric platforms can, in principle, enable non-volatile functionality through polarization switching, but they remain difficult to scale because their materials and integration flows are often incompatible with standard complementary metal-oxide- semiconductor (CMOS) manufacturing27–30.

In this work, we introduce LuminoMem, an ultrafast and non-volatile optoelectronic memory that monolithically co-integrates memory and light-emitting functionality based on photoluminescence (PL) from a semiconductor. The LuminoMem demonstrated in this work uses a floating-gate architecture in which the semiconductor tellurium (Te) serves both as the charge-storage layer and as the light-emissive medium. This design enables ultrafast (nanosecond-scale) electrical programming that precisely and persistently tunes the PL intensity. By eliminating separate readout circuitry and external optical modulators, LuminoMem enables direct optical readout of non-volatile electrical states (Fig. 1b). In addition, Te-LuminoMem operates in the mid-infrared (MIR) region at ~3.4 μm, leveraging the narrow bandgap ( ~ 365 meV) of Te. This wavelength lies in a particularly important spectral region with strong molecular “fingerprints”31 and favorable atmospheric transmission windows32. Consequently, LuminoMem could potentially serve as a foundational building block for future integrated systems in free-space optical communication, gas sensing33, environmental monitoring34, industrial process control35, and security/homeland-defense applications when operation in the mid-infrared is preferable. These capabilities are far less accessible in the more commonly explored visible-to–near-infrared range where most prior devices operate27,30.

The LuminoMem demonstrated in this work exhibits robust multi-level memory characteristics, achieving 4-bit (16-level) precision in its optical readout. We further demonstrate its potential for in-memory computing by simulating an array of LuminoMem devices within an artificial neural network and successfully performing image classification on the Fashion Modified National Institute of Standards and Technology (MNIST) dataset. This work overcomes key bottlenecks by strategically leveraging the advantages of both electrons and photons, resulting in a high-speed non-volatile memory-light emitter. This performance breakthrough paves the way for greatly enhancing the efficiency of current computation hardware and the on-chip integration of memory, computing and sensing capabilities (Fig. 1c).

Results and Discussion

Monolithic device design and basic characterization

The LuminoMem device is built on a vertically stacked floating-gate architecture that combines two-dimensional (2D) materials with the recently rediscovered semiconductor Te. As shown in Fig. 2a, the device comprises a multilayer graphene/hexagonal boron nitride/Te (MLG/h-BN/Te) van der Waals (vdW) heterostructure fabricated on a SiO₂/Si substrate. In this configuration, the Te nanoflake simultaneously functions as the floating charge-storage layer and the light-emitting medium. Te has been identified as a semiconductor with a nearly direct bandgap of ~365 meV, corresponding to MIR emission centered at 3.4 μm (Supplementary Note 1). Our recent work shows that the PL of Te can be continuously tuned by its doping level36; consequently, changes in the charge-storage state directly modulate the emission intensity, enabling electrical programming with a direct MIR optical readout. In the device stack, an h-BN nanoflake acts as the tunneling barrier, electrically isolating the Te floating-gate layer from the MLG top electrode, which is held at ground potential. The p-doped Si substrate serves as the control gate (VCG), thereby modulating the channel potential and the stored charge state.

Fig. 2. Device characterization.

Fig. 2

a Schematic of the multilayer graphene (MLG)/hexagonal boron nitride (h-BN)/Te vdW heterostructure memory device on a SiO2/Si substrate. The doped Si serves as the control gate, and the top MLG electrode is grounded. b Optical micrograph of a typical floating-gate device. Dashed lines outline the Te nanoflake (red), MLG (yellow), and h-BN flake (blue). Scale bar, 20 μm. c Polarization-dependent Raman spectroscopy of Te nanoflakes using 633-nm laser excitation with polarization oriented either perpendicular or parallel to the c-axis. d MIR PL intensity versus control-gate voltage (VCG) measured with VCG dual-sweep ranging from ±20 V to ±50 V in 10 V steps. The prominent hysteresis demonstrates programmable charge storage within the floating-gate architecture. e Spatially mapped MIR PL intensity across the entire device after applying VCG = −40 V (top panel) and +40 V (bottom panel). Black dashed lines mark the junction area. Scale bar is 30 μm. f MIR PL spectra corresponding to the ‘ON’ and ‘OFF’ states at the positions marked by the red and blue points in (e), respectively.

Figure 2b presents an optical micrograph of the LuminoMem device, with dashed lines outlining the key components: MLG (yellow), h-BN (blue), and Te nanoflake (red). The MLG/h-BN heterostructure was assembled using a polymer-free dry transfer method and precisely aligned atop the Te nanoflake, as described in the Methods section. Atomic force microscopy (AFM) confirms that the thicknesses of Te, h-BN and MLG are ~68 nm, ~14 nm and ~3 nm, respectively (Supplementary Note 2). Polarization-dependent Raman spectroscopy confirmed the high crystalline quality and orientation of the Te nanoflake, with signature E1-TO (92 cm−1), A1 (121 cm−1), and E2 (143 cm−1) modes exhibiting maximum intensity for polarization parallel to the c-axis (Fig. 2c)37. Furthermore, additional characterizations (detailed in Supplementary Note 2) demonstrate the pristine and atomically flat interfaces of these layered materials, which are critical for efficient charge tunneling and reduced scattering38.

Non-volatile MIR PL modulation

Next, we study the non-volatile hysteresis character of the LuminoMem device. To read out the memory state, we optically excite the PL signal of the device, which reflects the charge storage level of Te according to our previous gate-dependent PL studies36. Owing to the narrow bandgap of Te, a low-energy telecommunication-band laser at 1550 nm is used as the optical read input, as its photon energy is insufficient to surmount the high internal energy barrier of h-BN, thereby enabling non-destructive optical readout. Figure 2d presents the MIR PL intensity variation of the device as a function of the control-gate voltage (VCG) obtained at 25 K. Under a constant excitation power of 170 μW, the VCG was swept bidirectionally, from negative to positive values and then back to negative values, with the maximum control-gate voltage (VCG, max) gradually expanding from ±20 V to ±50 V. All PL curves exhibit prominent hysteresis, in which the PL intensity at zero gate voltage depends strongly on the prior gate-voltage history, resembling the transfer characteristics of electrical floating-gate memories.

Specifically, applying a large positive gate voltage (e.g., VCG, max =+20 V) depletes holes in the Te nanoflake (program operation), driving the device into a low-PL-intensity (“OFF”) state. This low-PL state persists as the gate voltage is swept back to 0 V. When the gate voltage is subsequently swept from 0 V toward negative values, the Te nanoflake remains depleted until a threshold value is reached, at which point the gate field is strong enough to drive electrons back to the MLG electrode and restore the hole concentration in the Te nanoflake (erase operation), resulting in a high-PL-intensity (“ON”) state. As the gate voltage is then swept from this large negative voltage (e.g., VCG, max =−20 V) back to 0 V, the carriers are largely retained in the Te floating gate, so the device remains in the high-PL state. The memory window (ΔV), defined as the difference in threshold voltage between forward and backward sweeps, reflects the device's charge-storage capacity. A larger memory window indicates a greater number of charges stored in the Te floating gate, thereby enhancing memory reliability. As the gate-voltage sweep span expanded from 40 V ( ± 20 V) to 100 V ( ± 50 V), the memory window increased from 20 V to 80 V, comparable to that of conventional electrical memories.

To confirm that this hysteresis originates from charge storage in the floating Te layer rather than interface traps, we investigated the device performance in a different configuration, in which the Te nanoflake, instead of the MLG, is electrically grounded as shown in Supplementary Note 3. In this configuration, the PL intensity shows negligible hysteresis, which is obviously different from the performance when the Te layer is floated, confirming non-volatile charge storage in the Te floating gate. Furthermore, the reproducibility of this non-volatile LuminoMem was verified across seven additional devices with Te nanoflake thicknesses ranging from 45 nm to 295 nm. As illustrated in Supplementary Note 4, all devices consistently exhibit a clear and programmable memory window, demonstrating that the switching behavior is robust within the investigated thickness range. To confirm the room-temperature viability of the LuminoMem, temperature-dependent characteristics from 25 K up to 297 K were systematically investigated, demonstrating robust memory windows at room temperature (detailed in Supplementary Note 5). Nevertheless, to maintain optimal PL efficiency, all subsequent measurements were conducted at 25 K.

Figure 2e presents spatial PL mapping of the device to visualize the non-volatile switching behavior across the entire device. When a negative gate voltage (VCG = −40 V) is applied, the Te nanoflake is set to a high-emission “ON” state (see Fig. 2e top panel). The region beneath the MLG gate (outlined by the black dashed line) exhibits a slightly lower PL intensity than the exposed Te area, due to optical absorption by MLG. After applying a positive gate voltage (VCG = +40 V), the device switches to a uniform low-emission “OFF” state across the entire active region (see Fig. 2e bottom panel). This further confirms efficient charge carrier localization in the floating-gate region. Spectral measurements (Fig. 2f) reveal that switching between the “ON” and “OFF” states produces substantial PL intensity modulation while maintaining a constant peak wavelength. This wavelength stability is critical for maintaining signal purity and preventing chromatic dispersion, ensuring crosstalk-free operation in MIR integrated photonic systems.

To evaluate the design efficacy of this architecture, we further compared our primary MLG/h-BN/Te structure with an alternative Te/h-BN/MLG configuration, in which the Te nanoflake serves as the grounded channel and graphite acts as the floating gate (Supplementary Note 6). The results show that the direct injection of carriers into the Te emitter in the MLG/h-BN/Te design facilitates more efficient control over radiative recombination than remote field-effect modulation in the alternative geometry, leading to a significantly enhanced optical on/off ratio.

Electro-optical conversion mechanism

Figure 3a illustrates the operating mechanism of the non-volatile LuminoMem. Device operation relies on the controlled modulation of the majority-carrier (hole) density in the Te nanoflake, which simultaneously serves as the charge-storage medium and the photon emitter. During the program operation (Fig. 3a, i), a positive control-gate voltage (VCG > 0) induces a steep band bending across the h-BN tunneling barrier, facilitating electrons to tunnel from the MLG into the Te floating gate via the Fowler-Nordheim mechanism. The injected electrons recombine with the majority of holes in the Te layer, leading to the reduction of carriers in the Te layer. This reduction in carrier doping density significantly decreases the radiative recombination rate, resulting in a low PL intensity, or the “OFF” state. After the voltage is removed, the injected electrons stay in the Te layer due to the h-BN barrier, and thus, the device remains in the “OFF” state (Fig. 3a, ii).

Fig. 3. Operating mechanism and performance benchmarks.

Fig. 3

a Schematic energy-band diagrams illustrating the device’s operating principles during program, read and erase operations. The filled blue circles and empty red circles represent injected electrons and accumulated holes, respectively. The dark curved arrows indicate the directions of carrier tunneling under gate pulses, while the wavy blue and red arrows denote the 1550-nm excitation laser and the generated MIR PL emission, respectively. The red glow intensity represents the corresponding PL signal strength. b Demonstration of 16 distinct, non-volatile memory states (4-bit storage) achieved by modulating the programming pulse amplitude from −20 to 23 V (pulse duration: 0.1 s). c Data retention tests for the binary memory states. The programmed and erased states were set using +25 V and −20 V 0.1 s pulses, respectively, and show negligible degradation in PL intensity over 104 s. d Endurance cycling test, showing robust switching between the programmed and erased states for over 1,000 cycles (pulse conditions: ± 25 V, 0.1 s duration).

Conversely, during the Erase operation (Fig. 3a, iii), a negative gate voltage pulse (VCG < 0) causes electrons to tunnel out of the Te layer back into the gate electrode, which is equivalent to hole accumulation in the Te layer. This high doping concentration of majority carriers boosts the radiative recombination efficiency, switching the device to a high PL intensity, or the “ON” state. When the negative gate voltage is removed (Fig. 3a, iv), the high hole-doping state remains in the Te layer since few electrons can tunnel into the Te layer through the h-BN barrier. Ultimately, this reversible charge tunneling enables precise and non-volatile modulation of the PL emission. The underlying electrostatic tuning of carrier density is further demonstrated by excitation power-dependent PL measurements (detailed in Supplementary Note 7). Specifically, the measured power-law slope shifts from ~1.1 in the “ON” state to ~1.4 in the “OFF” state, aligning with our recent work36.

Another key feature of this architecture is the non-destructive optical readout. The photon energy of the 1550 nm readout laser ( ~ 0.8 eV) is insufficient to excite the stored electrons in the Te layer over the high-energy barrier of h-BN back to the MLG, thus preserving the charge state during measurement. This mechanism is validated by contrasting the device’s response to short-wavelength visible light (520 nm, ~2.38 eV) presented in Supplementary Note 8. Unlike the non-perturbing NIR excitation, the higher energy at 520 nm photons enable stored carriers to surmount the h-BN barrier and return to the MLG. This pronounced wavelength selectivity, which is stable under NIR probing yet erasable under visible illumination, provides direct evidence that charge confinement is governed by the energy offsets of the vdW heterostructure, enabling optical erasure via photo-induced carrier de-trapping39–42.

Multi-level storage and reliability characterization

Beyond binary operation, the analog nature of charge accumulation in the floating-gate structure enables multilevel data storage, a critical feature for high-density memory and neuromorphic computing applications. By fine-tuning the amplitude of the programming voltage pulses, we can precisely control the quantity of charges injected into the Te floating gate, thereby achieving fine-grained modulation of the PL readout intensity. Figure 3b demonstrates the realization of 4-bit (16 distinct levels) memory capacity. This was achieved by applying programming pulses with amplitudes ranging from -20 to +23 V (pulse duration: 0.1 s), which produced clearly separated and stable PL intensity levels. The well-defined separation between adjacent levels confirms the deterministic and highly controllable nature of the electro-optical modulation.

The device’s reliability was rigorously evaluated through data retention and endurance tests. As shown in Fig. 3c, the programmed ( + 25 V, “OFF”) and erased (-20 V, “ON”) states exhibit high stability, with negligible degradation in PL intensity over 104 s. This stable data retention underscores the efficient charge confinement provided by the h-BN/Te/SiO2 heterostructure43,44. Furthermore, endurance cycling tests as shown in Fig. 3d reveal the robust switching endurance of the device. Under repeated program/erase cycling ( ± 25 V, 0.1 s pulses), the memory window maintained a stable on/off ratio for over 1,000 cycles without signs of fatigue. Meanwhile, these optical retention and endurance characteristics are highly reproducible with two additional devices, as shown in Supplementary Note 9. The combination of multi-level programmability, long-term retention and robust cycling endurance establishes this Te-based floating-gate device as a highly promising platform for reliable non-volatile optoelectronic memory and in-memory computing systems.

Ultrafast operation capability

To assess the device's suitability for high-speed photonic computing, we examined its transient response to nanosecond-scale electrical pulses. Although static measurements confirm reliable switching, practical memories, particularly those targeted for electro-optical hybrid systems, require write speeds compatible with the bandwidth of modern logic and computing circuits. As shown in Fig.4, ultrafast switching is achieved using voltage pulses with a full width at half maximum (FWHM) of 70 ns. This programming speed significantly surpasses that of other LuminoMem devices demonstrated previously in the visible-near infrared range27, and is comparable to state-of-the-art ultrafast non-volatile memories, such as those based on phase-change25, ferroelectric45 and resistance-change46 mechanisms. The nanosecond operation is consistent with intrinsic charge-tunneling dynamics in high-performance van der Waals floating-gate devices38,47, efficiently utilizing high-speed electronic switching to set a non-volatile, optically readable state.

Fig. 4. Ultrafast switching dynamics and synaptic plasticity.

Fig. 4

a Stepwise decrease of PL intensity in response to a sequence of ultrafast pulses (amplitude: +27 V, full width at half maximum (FWHM): 70 ns), corresponding to the incremental depletion of holes and a gradual weakening of the synaptic weight. b Stepwise increase of PL intensity under a sequence of ultrafast pulses (amplitude: −18 V, FWHM: 70 ns), reflecting controlled hole injection and strengthening of the synaptic connection. These results demonstrate reproducible 4-bit storage per cell and high-speed, linear synaptic weight updates, which are essential for optical neuromorphic computing.

Specifically, the device shows precise, analog control over the stored charge density at a 70 ns programming speed. Applying a sequence of positive pulses ( + 27 V, 70 ns) resulted in a stepwise decrease in the MIR PL intensity (Fig. 4a), corresponding to the incremental depletion of holes. Conversely, a sequence of negative pulses (−18 V, 70 ns) produced a stepwise increase in the PL intensity (Fig. 4b), corresponding to the controlled injection of holes. During these stepwise updates, each intermediate PL state was continuously monitored for ~10 s before applying the subsequent pulse, exhibiting no obvious degradation. The stability of the synaptic weight is due to the high barrier provided by the h-BN layer, which offers high insulating properties and prevents carrier leakage or back-tunneling. Critically, the memory states can be deterministically tuned by modulating the pulse amplitude and duration, as the carrier injection density is highly sensitive to the applied electric field and temporal width (Supplementary Note 10). Remarkably, the device resolves over 16 distinct PL levels in both the programming and erasing directions, confirming a storage capacity of 4 bits per cell. The switching speed is primarily constrained by the temporal resolution of the stimulus electrical pulse and the resolving capability of the PL levels, both of which are determined by the stimulation and detection equipment used in the measurement. While all the data presented in Fig. 4 are stimulated with a 70-ns electrical pulse, a 50-ns pulse still stimulates an effective switch of the PL signal, as demonstrated in Fig. 5c and Supplementary Note 10. We note that the actual switching speed of LuminoMem could be even faster. This quasi-continuous modulation overcomes the density limitations of binary optical switches while preserving non-volatility.

Fig. 5. Neuromorphic computing demonstration for fashion image recognition.

Fig. 5

a Schematic diagram of the human nervous system. b Schematic architecture of the simulated three-layer backpropagation artificial neural network (BP-ANN). c Seventeen potentiation and depression cycles of the device with 20 stable weight updates, emulating synaptic plasticity. d Classification accuracy of the ANN benchmarked on the Fashion Modified National Institute of Standards and Technology (MNIST) dataset51 (distributed under the MIT License) under ideal software, original device-mapped, and noisy input (10% and 20%) conditions, highlighting the impact of device non-idealities and the overall fault tolerance. e Evolution of the confusion matrix (multicolor display) over training, where the strengthening diagonal (from initial 5 to 100 epochs) validates the network’s successful learning and discriminative capability.

The nanosecond switching speed, which is rare even in state‑of‑the‑art electronic flash memories, stems from the atomically sharp, defect‑free van der Waals interfaces and strong electrical field across the h-BN layer38,47. These features collectively enable near‑ballistic Fowler–Nordheim tunneling. In conventional silicon floating‑gate devices, dangling bonds and deep-level interface states at the semiconductor/dielectric boundary act as detrimental trapping centers. These defects lead to trap-assisted tunneling or charge-scattering, causing a significant lag in injection kinetics. By contrast, the pristine MLG/h‑BN/Te heterostructure suppresses such parasitic pathways, achieving minimal electronic latency48. Furthermore, the high dielectric strength of few-layer h‑BN further sustains large local electric fields without breakdown47, and the microscale device footprint reduces parasitic RC delays. Consequently, the inherent properties of the heterostructure minimize the dominant non-ideal factors that plague conventional devices, thereby enabling an ultrafast switching speed. Accompanying this ultrafast switching capability, the intrinsic operating energy is estimated to be ~4.29 pJ/state for programming and ~1.91 pJ/state for erasing, rivaling state-of-the-art 2D vdW floating-gate memories38,47 (Supplementary Note 11).

Neural network inference based on LuminoMem device characteristics

The linear, analog modulation of LuminoMem PL, as shown in Fig. 4, naturally emulates synaptic plasticity. In neuromorphic terms, stepwise increases in PL intensity correspond to long-term potentiation (LTP), whereas stepwise decreases emulate long-term depression (LTD). The ability to finely tune optical synaptic weight using ultrafast electrical pulses, achieving adjustable weight-update granularity through various pulse configurations (Supplementary Note 12), underscores LuminoMem’s promise as a high-speed, linear synapse for infrared optical neural networks49,50.

The highly parallel and interconnected architecture of the human brain fundamentally relies on a vast network of biological neurons and synapses (Fig. 5a). Inspired by this biological framework, we simulated a three-layer backpropagation artificial neural network (BP-ANN) utilizing the LuminoMem array as synapses (Fig. 5b)46,49. We benchmarked the network’s capability on the Fashion-MNIST dataset51 using the CrossSim simulator, mapping the measured potentiation-depression characteristics into the network model (see Methods for details). The essential synaptic programmability of the device was meticulously optimized by modulating programming parameters, including pulse voltage, duration, and readout power (Supplementary Note 13). Under these optimized conditions (specifically +30 V with 300 ns for potentiation and −26 V with 50 ns for depression), the device exhibits reproducible weight-update characteristics, as confirmed by 17 potentiation-depression cycles (Fig. 5c). These cycles demonstrate 20 stable and repeatable switching weights. Within this network framework, while the weights are updated by ultrafast electrical pulses, the network inputs are mapped to the intensity of the incident 1550 nm excitation laser. Consequently, the multiply-accumulate operations are performed optically, and the results are output as MIR PL signals, enabling direct optical processing in the MIR regime.

To evaluate system-level pattern recognition performance, we simulated network inference on the Fashion-MNIST dataset. As shown in Fig. 5d, the recognition accuracy reaches 86.9% when experimentally measured analog weights and practical hardware non-idealities are incorporated, representing only a modest decrease compared to the ideal software baseline (92.47%). To further evaluate the fault tolerance of this neural network, we introduced 10% and 20% random noise into the “ankle boot” category images. After 100 training epochs, the recognition accuracies for the 10%-noise, and 20%-noise datasets reached approximately 82.5%, and 76.6%, respectively. The sustained accuracy under substantial input perturbation highlights the network’s robust learning capability. Consistently, the evolution of the confusion matrix during the training process (Fig.5e) shows progressively enhanced diagonal dominance, indicating improved class separability and reliable classification across all categories.

Discussion

The non-volatile LuminoMem helps close the long-standing gap between fast optical processing and comparatively slow, conversion-heavy electronic storage. By exploiting a vdW floating-gate architecture in which semiconductor Te simultaneously serves as charge storage and light-emitting medium, LuminoMem achieves 70-ns electrical programming with zero static power consumption. Data are accessed through direct optical readout in MIR, avoiding repeated electro–optic conversions and their associated latency and energy overheads. The device supports 4-bit multilevel storage with endurance exceeding 1000 cycles, enabling analog weight representation. These device characteristics are further exploited for fashion image classification by constructing an artificial photonic synaptic array in a three-layer BP-ANN, thereby preliminarily demonstrating its potential for neural network applications.

Although the current proof-of-concept demonstration relies on isolated devices operating at cryogenic temperatures, further work will be necessary to improve the scalability and room-temperature performance of the LuminoMem devices. Nevertheless, the capability to electrically program and update synaptic weights while enabling high-speed optical readout positions LuminoMem as a promising building block for large-scale, hardware-level photonic neural networks. Looking ahead, advances in large-area growth of low-defect Te and the integration of plasmonic nanostructures18 or nanophotonic cavities52 to enhance emission efficiency are expected to significantly boost its room-temperature performance. These material optimizations will ultimately enable large-scale heterogeneous integration, facilitating the dense assembly of memory units into arrays on standard CMOS platforms. Combined with wavelength-division multiplexing, photonic interconnect, and CMOS-compatible control circuitry, such systems could support massively parallel, in-memory computing architectures that surpass the bandwidth and energy efficiency limits of purely electronic systems, as discussed in Supplementary Note 14.

Beyond the performance demonstrated here, Te offers substantial additional opportunities. As a Weyl material, Te exhibits topologically enhanced nonlinear optical responses53,54 and polarization-tunable emission55, which could be exploited to improve device functionality and increase information transmission capacity in photonic neural networks. Furthermore, the present optoelectronic operating scheme is not fundamentally limiting: PL-based optical readout may be replaced by electrically driven electroluminescence, while electrical programming and erasing could be extended to fully optical operation through modest modifications of the device architecture. Together, these multifaceted advances, spanning novel physical operating schemes, array-level integration and on-chip learning, may pave the way toward scalable photonic processors for neuromorphic computing, reconfigurable MIR optical communications and intelligent sensing.

Methods

Synthesis of Te nanoflakes and fabrication of LuminoMem devices

Te nanoflakes were grown through a hydrothermal method37,56. First, 3 g of polyvinylpyrrolidone (PVP, molecular weight = 58,000) was dissolved in 32 mL of deionized (DI) water. Subsequently, 92 mg of Na2TeO3 was put into the PVP solution with continuous stirring. After that, 3.32 mL of ammonium hydroxide solution (25–28%, wt/wt%) and 1.68 mL of hydrazine hydrate (80%, wt/wt%) were added into the solution. Following 5 min of magnetic stirring, the solution was transferred into a 50 mL Teflon-lined stainless-steel autoclave and maintained at 180 °C for 10 h. The resulting product was washed with deionized water to remove any residual ions.

To fabricate the memory devices, the synthesized Te nanoflakes were dispersed in ethanol and drop-cast onto a p++-Si/SiO2 (285 nm) substrate. Separately, a MLG/h-BN heterostructure was pre-assembled using a polycarbonate/polydimethylsiloxane (PC/PDMS) sequential pick-up technique at 80 °C. This heterostructure was then precisely aligned and laminated onto a selected Te nanoflake at 170 °C. Following the lamination, the sacrificial PC layer was dissolved in chloroform, and the sample was thoroughly rinsed with acetone and isopropanol to eliminate organic residues. This PC-assisted dry transfer process was employed to ensure the formation of atomically clean vdW interfaces between the MLG, h-BN and Te layers57. Electrical contacts and electrode geometries were defined using electron beam lithography (EBL). Finally, Ti/Pd/Au (0.5/20/70 nm) metal layers were deposited via electron-beam evaporation to form the source, drain, and gate contacts.

PL readout with electrical gating

PL readout was conducted using a self-built micro-PL measurement system. A steady 1550-nm CW laser was employed to excite the Te nanoflake. To ensure precise collinear optical alignment in the invisible mid-infrared regime, a 532-nm visible laser was utilized as a strictly co-aligned guide beam. A ×40 reflective objective with a numerical aperture of 0.5 was used to focus the excitation laser onto the sample and collect the PL signal. The focused laser spot diameter was measured to be ~6 μm via the standard knife-edge method. All measurements were performed under vacuum in a liquid-helium-flow cryostat with electrical contact, enabling temperature control from 25 K. The cryostat was mounted on a high-precision XY scanner stage for spatial scanning. The collected PL signal was delivered to a spectrometer (Princeton SP2500i) equipped with a 150 g mm−1 grating and detected by a liquid nitrogen-cooled single-channel InSb photodetector with a preamplifier. The detector output was processed with a lock-in amplifier referenced to an optical chopper that modulated the excitation laser at 521 Hz. For memory measurements, control-gate voltages were applied using Keithley 2612B source meters for 0.1 s pulses and a Keithley 4200 semiconductor characterization system (4200-SCS) for shorter pulses.

Hardware-aware neural network simulations

A hardware-aware three-layer fully connected BP-ANN was implemented on the CrossSim platform for neuromorphic pattern recognition. The network adopted an input-hidden-output architecture with 784 × 300 × 10 neurons for the Fashion-MNIST dataset (28 × 28 grayscale images, ten classes)51. For the input mapping scheme, raw grayscale pixel values were normalized to have approximately zero mean and unit variance, which were then linearly mapped and clipped to an operational analog range of [-1, 1]. Synaptic weights were mapped to the PL intensity, where weight potentiation and depression corresponded to the experimentally observed LTP and LTD characteristics. Input noise of 0–20% amplitude was added to assess robustness, and classification performance was evaluated via accuracy and confusion matrices after training.

To capture hardware non-idealities, a lookup table (LUT) describing the measured PL-based weight-update behavior was embedded into both the forward computation and weight update within CrossSim, forming a hardware-aware training loop. Quantization and range constraints were included to emulate the limited precision and dynamic range of peripheral circuits. Specifically, the mapped input values and intermediate activations were quantized to a 7-bit signed representation. Network parameters were trained using standard backpropagation with gradient descent and cross-entropy loss, and accuracy was tested on an independent validation set.

Supplementary information

Author contributions

J.L. and D.S. conceived the idea and supervised the project. B.C. synthesized the Te nanoflakes under the supervision of C.G.Z. and L.L.; D.L.L. performed the measurements and basic characterizations with the help of S.Y.W., D.L., Y.C.C., H.W.L., M.Y.Q., D.H.Y., and J.S. under the supervision of A.L.P. and D.S.; Y.W. performed the ANN simulation under the supervision of J.L.; D.L.L., J.L., and D.S. wrote the manuscript with input and feedback from all of the authors.

Peer review

Peer review information

Nature Communications thanks Carlo Grazianetti, Jiajia Zha, and the other, anonymous, reviewer for their contribution to the peer review of this work. A peer review file is available.

Funding

D.S. discloses support for the research of this work from the National Key Research and Development Program of China [grant number 2021YFA1400100] and the National Natural Science Foundation of China [grant numbers 62325401, 62227822]. J.L. discloses support for the research of this work from the National Natural Science Foundation of China [grant number 62431018] and the National Key Research and Development Program of China [grant number 2024YFA1208400]. A.L.P. discloses support for the research of this work from the National Key Research and Development Program of China [grant number 2022YFA1204300] and the National Natural Science Foundation of China [grant number 52221001]. C.G.Z. discloses support for the research of this work from the National Key Research and Development Program of China [grant number 2023YFA1406300]. All other authors declare no relevant funding.

Data availability

The Source Data underlying the figures of this study are available at 10.6084/m9.figshare.32414655. All raw data generated during the current study are available from the corresponding authors upon request.

Competing interests

The authors declare no competing interests.

Footnotes

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Contributor Information

Dong Sun, Email: sundong@pku.edu.cn.

Anlian Pan, Email: anlian.pan@hnu.edu.cn.

Jing Liu, Email: Jingliu_1112@tju.edu.cn.

Supplementary information

The online version contains supplementary material available at 10.1038/s41467-026-75638-w.

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Data Availability Statement

The Source Data underlying the figures of this study are available at 10.6084/m9.figshare.32414655. All raw data generated during the current study are available from the corresponding authors upon request.


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