High-performance Self-powered Photodetector Research Articles

Enhanced Performance of Self-Powered Ga2O3/ZnO:V Heterojunction Solar-Blind Ultraviolet Photodetectors by Coupling Ferroelectricity and Piezoelectricity.

Ferroelectric materials have aroused increasing interest in the field of self-powered ultraviolet (UV) photodetectors (PDs) for their switchable spontaneous polarization. However, the utilization of ferroelectric materials to modulate the built-in electric field and energy band at the junction interface has rarely been investigated. Herein, we design and fabricate self-powered solar-blind UV PDs based on a Ga2O3/ZnO:V heterojunction. The performance of the Ga2O3/ZnO:V PD is significantly enhanced through the reasonable coupling of ferroelectricity and piezoelectricity within the ZnO:V film. The device at 260 nm exhibits excellent photoelectric properties with high peak responsivity of 64.5 mA/W, a specific detectivity of 3.8 × 1010 Jones, and a rise/decay time of 1.9/45.2 μs, together with reproducibility and stability. Systematical energy band diagram analysis reveals that the excellent performance of Ga2O3/ZnO:V PD can be attributed to the driving forces arising from the addition of the depolarization field and piezoelectric field, which increases the intensity of built-in electric field and promotes the separation and transport of photogenerated carriers at the heterojunction interface. The findings of our research provide a novel avenue and valuable guidance for the design of high-performance self-powered photodetectors.

High performance Self-powered UV-visible photodetectors based on ZnO@CdS/PEDOS heterojunctions

In this study, we report the design and development of a high-performance self-powered UV-visible photodetector (UV-Vis PD) based on ZnO@CdS /poly(3,4- ethylenedioxyselenophene) nanoarrays (ZnO@CdS/PEDOS), in which ZnO nanorods (NRs) were modified with CdS to address the limitations of ZnO NRs-based photodetectors in detecting both UV and visible light. The findings of this study demonstrated that the modification of ZnO NRs with CdS led to the formation of a type II heterojunction. This modification not only enhanced the detection capability of the photodetectors under UV (365nm) light but also enabled efficient detection under visible light (450nm). The R and D* of the ZnO@CdS/PEDOS device were 7.68× 10-3A/W and 5.62×1011 Jones, respectively, with a τr of 0.19s using 0V and a UV light power (365nm) of 0.32mW/cm2. In addition, using a bias voltage of 0V and a visible light (450nm) at 0.32mW/cm2, the R was 2.53×10-3A/W and D* was 3.41×1010 Jones of the device were, the τr/τf were 0.23/0.29s, respectively. An excellent performance self-powered PD in the dual-wavelength range was constructed.

Enhanced Performance of Self-Powered Ga2O3/ZnO:V Heterojunction Solar-Blind Ultraviolet Photodetectors by Coupling Ferroelectricity and Piezoelectricity.

Ferroelectric materials have aroused increasing interest in the field of self-powered ultraviolet (UV) photodetectors (PDs) for their switchable spontaneous polarization. However, the utilization of ferroelectric materials to modulate the built-in electric field and energy band at the junction interface has rarely been investigated. Herein, we design and fabricate self-powered solar-blind UV PDs based on a Ga2O3/ZnO:V heterojunction. The performance of the Ga2O3/ZnO:V PD is significantly enhanced through the reasonable coupling of ferroelectricity and piezoelectricity within the ZnO:V film. The device at 260 nm exhibits excellent photoelectric properties with high peak responsivity of 64.5 mA/W, a specific detectivity of 3.8 × 1010 Jones, and a rise/decay time of 1.9/45.2 μs, together with reproducibility and stability. Systematical energy band diagram analysis reveals that the excellent performance of Ga2O3/ZnO:V PD can be attributed to the driving forces arising from the addition of the depolarization field and piezoelectric field, which increases the intensity of built-in electric field and promotes the separation and transport of photogenerated carriers at the heterojunction interface. The findings of our research provide a novel avenue and valuable guidance for the design of high-performance self-powered photodetectors.

Self-Rolled-Up WSe2 One-Dimensional/Two-Dimensional Homojunctions: Enabling High-Performance Self-Powered Polarization-Sensitive Photodetectors.

Mixed-dimensional heterostructures integrate materials of diverse dimensions with unique electronic functionalities, providing a new platform for research in electron transport and optoelectronic detection. Here, we report a novel covalently bonded one-dimensional/two-dimensional (1D/2D) homojunction structure with robust junction contacts, which exhibits wide-spectrum (from the visible to near-infrared regions), self-driven photodetection, and polarization-sensitive photodetection capabilities. Benefiting from the ultralow dark current at zero bias voltage, the on/off ratio and detectivity of the device reach 1.5 × 103 and 3.24 × 109 Jones, respectively. Furthermore, the pronounced anisotropy of the WSe2 1D/2D homojunction is attributed to its low symmetry, enabling polarization-sensitive detection. In the absence of any external bias voltage, the device exhibits strong linear dichroism for wavelengths of 638 and 808 nm, with anisotropy ratios of 2.06 and 1.96, respectively. These results indicate that such mixed-dimensional structures can serve as attractive building blocks for novel optoelectronic detectors.

Self-powered poly(3-hexylthiophene)/ZnO heterojunction ultraviolet photodetectors decorated by silver nanoparticles

Self-powered poly (3-hexylthiophene)/zinc oxide (P3HT/ZnO) heterojunction ultraviolet photodetectors decorated by silver nanoparticles (Ag NPs) were fabricated by sol-gel and spin-coating techniques. The ultraviolet photoresponse performance of the P3HT/ZnO heterojunction photodetectors influenced by the position of plasmonic Ag NPs was investigated. The responsivity and detectivity of the P3HT/Ag/ZnO photodetector with placed Ag NPs at the interface of ZnO and P3HT layers enhanced to 1.92 and 1.15 times compared to the reference devices. When the Ag NPs embedded into ZnO layer, the responsivity, detectivity and external quantum efficiency were 16.42 mA/W, 5.97 × 1011 Jones, and 5.36 %, respectively, which were 5.77 times, 4.64 times and 5.77 times to that of the pristine P3HT/ZnO photodetector. The enhancement mechanism of plasmonic metallic nanoparticles to the performance of the photodetectors was discussed in details. This study presents a simple route to high performance self-powered photodetectors.

High-performance self-powered UV photodetectors using SnO2 thin film by reactive magnetron sputtering

Self-powered UV photodetector (UVPD) operates without the need for an external energy source and contributes to global energy conservation. With ongoing innovation, self-powered PDs are becoming increasingly appealing for industrial and innovation applications such as advanced environmental monitoring and communication devices. This study investigates the influence of varying working pressures (ranging from 3 to 15 mTorr) during reactive magnetron sputtering on the crystalline structure, surface morphology, and performance of SnO2 thin film photodetectors, aiming to fabricate self-powered UVPDs. The SnO2-based UVPD demonstrates exceptional self-powered UV photodetection capabilities, characterized by a sensitivity of 6.41×105%, responsivity of 0.09 mA/W, and detectivity of 2.99×1010 Jones. In addition, SnO2-based UVPD possesses a switching photo response and recovery time of 0.75 and 0.99 s. Henceforth, it was observed that 8 mTorr SnO2 thin film exhibits exceptional stability, superior photodetector performance, and remarkable repeatability, rendering them highly suitable for UVPD applications. Notably, these films demonstrate sustained functionality for approximately 100 days without necessitating encapsulation. These excellent results confirm that SnO2 thin films are suitable for fabricating future smart optoelectronics devices.

Highly efficient self-powered CH3NH3Pbl3 perovskite photodiode with double-sided poly(methyl methacrylate) passivation layers

Hybrid organohalide perovskites have recently attracted significant attention due to their outstanding photovoltaic (PV) conversion capabilities in optoelectronic devices. Herein, to develop a highly sensitive and self-powered perovskite-based PV photodiode (PVPD), we implement the selective use of poly(methyl methacrylate) (PMMA) as noise-current-reducing passivation layers on both the front and rear sides of a CH3NH3PbI3 (MAPbI3) perovskite light-absorbing layer. It is found that the PMMA layers effectively suppress carrier recombinations at the interfaces, resulting in fairly high power conversion efficiency of 17.6%. Additionally, the double-sided PMMA-passivated MAPbI3 PVPD shows exceptional specific detectivity values (1.0 × 1014 Jones from the dark current and 1.3 × 1012 Jones from the noise current), significantly outperforming conventional MAPbI3 PVPDs without passivation layers. The device also exhibits a very wide linear dynamic response range of ∼139 dB, with rapid rise and decay response times of 57 and 18 μs, respectively. The double-sided PMMA-passivated MAPbI3 PVPD also is shown to be highly durable in terms of its dynamic responses even after a prolonged storage period of 1500 h. These results suggest that advanced interface engineering using double PMMA passivation layers holds great potential for developing high-performance self-powered perovskite photodetectors for a range of optoelectronic applications.

Self-powered deep ultraviolet photodetector based on p-CuI/n-ZnGa2O4 heterojunction with high sensitivity and fast speed.

Self-powered deep ultraviolet photodetectors (DUV PDs) are essential in environmental monitoring, flame detection, missile guidance, aerospace, and other fields. A heterojunction photodetector based on p-CuI/n-ZnGa2O4 has been fabricated by pulsed laser deposition combined with vacuum thermal evaporation. Under 260 nm DUV light irradiation, the photodetector exhibits apparent self-powered performance with a maximum responsivity and specific detectivity of 2.75 mA/W and 1.10 × 1011 Jones at 0 V. The photodetector exhibits high repeatability and stability under 260 nm periodic illumination. The response and recovery time are 205 ms and 133 ms, respectively. This work provides an effective strategy for fabricating high-performance self-powered DUV photodetectors.

Efficient and stable self-powered PbSe photodetectors via doping-induced asymmetric Cr electrodes modulation of surface work function

Conventional PbSe infrared photodetectors typically demands a substantial external electric field, posing challenges in energy-constrained environments. Self-powered photodetectors present a promising avenue for addressing such electricity-related challenges. Nevertheless, the inherent limitations of symmetric Schottky contacts in metal-semiconductor-metal (MSM) photodetectors constrain their self-powered performance, resulting in opposing photocurrents. Constructing asymmetric MSM structures usually requires intricate design or sustained external fields. In this study, we propose a novel contact engineering strategy based on iodine doping to modulate surface work functions of PbSe film. Utilizing Cr electrodes, we achieve Ohmic contact on the iodine-doped top surface of PbSe film and Schottky contact on the as-grown bottom surface. This approach establishes a self-powered PbSe infrared photodetector with an asymmetric top-bottom MSM structure. We comprehensively investigate contact engineering by investigating surface chemical states, elemental variations, and surface work functions variation. Remarkably, the photodetector demonstrates an exceptional zero-bias detectivity of 1.13 × 109 Jones, with an extremely low dark current of 3.67 pA, high Ilight/Idark ratio exceeding 104, and extremely short response times of less than 1 ms, respectively. Our work introduces a new strategy for modifying the band structure, contributing to the fabrication of high-performance self-powered photodetectors.

Dual-coupling effect enables a high-performance self-powered UV photodetector.

Self-powered ultraviolet photodetectors generally operate by utilizing the built-in electric field within heterojunctions or Schottky junctions. However, the effectiveness of self-powered detection is severely limited by the weak built-in electric field. Hence, advances in modulating the built-in electric field within heterojunctions are crucial for performance breakthroughs. Here, we suggest a method to enhance the built-in electric field by taking advantage of the dual-coupling effect between heterojunction and the self-polarization field of ferroelectrics. Under zero bias, the fabricated AgNWs/TiO2/PZT/GaN device achieves a responsivity of 184.31 mA/W and a specific detectivity of 1.7 × 1013 Jones, with an on/off ratio of 8.2 × 106 and rise/decay times reaching 0.16 ms/0.98 ms, respectively. The outstanding properties are primarily attributed to the substantial self-polarization of PZT induced by the p-GaN and the subsequent enhancement of the built-in electric field of the TiO2/PZT heterojunction. Under UV illumination, the dual coupling of the enhanced heterojunction and the self-polarizing field synergistically boost the photo-generated carrier separation and transport, leading to breakthroughs in ferroelectric-based self-powered photodetectors.

A Self-Powered Broadband Photodetector with High Photocurrent Based on Ferroelectric Thin Film Using Energy Band Structure Design

Self-powered photodetectors have the advantages of high sensitivity, sustainability, and small size and have become a research hotspot in advanced optoelectronic systems. However, the low output photocurrent density seriously hinders the practical application of ferroelectric self-powered photodetectors. Herein, the high-efficiency photoelectric detection performance of the Bi1-xHoxFeO3 ferroelectric self-powered photodetector is realized by doping Ho. The responsivity (R) and detectivity (D*) can reach 0.0159 A/W and 1.94 × 1011 Jones under monochromatic light with a wavelength of 900 nm. Meanwhile, the R and D* can reach 0.022 A/W and 2.65 × 1011 Jones under sunlight. These excellent photodetection performances are attributed to the high short-circuit current density (Jsc). When the Ho content is 6%, the output photocurrent reaches up to 0.81 mA/cm2. The systematic structure and photo-electric characteristic analysis suggest that the decrease in the band gap leads to the generation of a larger photocurrent while the ferroelectric polarization is reduced slightly. This work provides a new way to obtain high-performance self-powered photodetectors.

High performance self-powered solar-blind photodetector based on amorphous MgGa2O4/p-Si heterojunction

Self-powered solar-blind photodetectors are extensively implemented in military and industrial applications. Spinel ternary oxide MgGa2O4 with a wide bandgap of 4.92 eV is suitable for solar-blind photodetectors. Optoelectronic integration is a challenging research area, in terms of growing foreign semiconductors on Si substrates. Herein, a solar-blind photodetector based on amorphous MgGa2O4/p-Si heterojunction was fabricated by using RF magnetron sputtering. Under self-powered operation, the device exhibited good performance characteristics, including a high response sensitivity of 11.7 mA/W, a specific detectivity of 7.29 × 1011 Jones, and a fast photoresponse time (τr/τd = 0.200/0.021 s). This work demonstrates that the amorphous MgGa2O4/p-Si heterojunction is a promising approach to realize high-performance self-powered solar-blind photodetectors.

Element Diffusion Induced Carrier Transport Enhancement in High-Performance CZTSSe Self-Powered Photodetector.

Cu2ZnSn(S,Se)4 (CZTSSe) has attracted great interest in thin-film solar cells due to its excellent photoelectric performance in past decades, and recently is gradually expanding to the field of photodetectors. Here, the CZTSSe self-powered photodetector is prepared by using traditional photovoltaic device structure. Under zero bias, it exhibits the excellent performance with a maximum responsivity of 0.77 A W-1, a high detectivity of 8.78 × 1012 Jones, and a wide linear dynamic range of 103dB. Very fast response speed with the rise/decay times of 0.576/1.792 µs, and ultra-high switching ratio of 3.54 × 105 are obtained. Comprehensive electrical and microstructure characterizations confirm that element diffusion among ITO, CdS, and CZTSSe layers not only optimizes band alignment of CdS/CZTSSe, but also suppresses the formation of interface defects. Such a suppression of interface defects and spike-like band alignment significantly inhibit carrier nonradiative recombination at interface and promote carrier transport capability. The low trap density in CZTSSe and low back contact barrier of CZTSSe/Mo could be responsible for the very fast response time of photodetector. This work definitely provides guidance for designing a high performance self-powered photodetector with high photoresponse, high switching ratio, fast response speed, and broad linear dynamic range.

A high-performance self-powered broadband photodetector based on vertical MAPbBr3/ZnO heterojunction

A high-performance self-powered broadband photodetector based on vertical MAPbBr3/ZnO heterojunction

High performance self-powered photodetectors based on graphene nanoribbons/Al2O3/InGaZnO heterojunctions

High performance self-powered photodetectors based on graphene nanoribbons/Al₂O₃/InGaZnO heterojunctions

High-performance visible-near-infrared photodetector based on the N2200/Sb2Se3 nanorod arrays organic-inorganic hybrid heterostructure.

Antimony selenide (Sb2Se3) is a suitable candidate for a broadband photodetector owing to its remarkable optoelectronic properties. Achieving a high-performance self-powered photodetector through a desirable heterojunction still needs more efforts to explore. In this work, we demonstrate a broadband photodetector based on the hybrid heterostructure of Sb2Se3 nanorod arrays (NRAs) absorber and polymer acceptor (P(NDI2OD-T2), N2200). Owing to the well-matched energy levels between N2200 and Sb2Se3, the recombination of photogenerated electrons and holes in N2200/Sb2Se3 hybrid heterostructure is greatly inhibited. The photodetector can detect the wavelength from 405 to 980 nm, and exhibit high responsivity of 0.39 A/W and specific detectivity of 1.84 × 1011 Jones at 780 nm without bias voltage. Meanwhile, ultrafast response rise time (0.25 ms) and fall time (0.35 ms) are obtained. Moreover, the time-dependent photocurrent of this heterostructure-based photodetector keeps almost the same value after the storge for 40 days, indicating the excellent stability and reproducibility. These results demonstrate the potential application of a N2200/Sb2Se3 NRAs heterojunction in visible-near-infrared photodetectors.

Passivation-free high performance self-powered photodetector based on Si nanostructure-PEDOT:PSS hybrid heterojunction

Hybrid heterojunction between organic PEDOT:PSS and inorganic Silicon (Si) nanostructures is promising for high-performance self-powered photodetectors due to their favourable band energetics and ease of processing. Traditionally, Si nanostructures require additional passivation layers to reduce surface defect states, which adds complexity and involves the use of harmful organic solvents. Here in, we demonstrate a simple chemical polishing process to reduce defects and fabricate a conformable heterojunction between Si nanostructures and PEDOT:PSS. Si nanostructures fabricated by metal-assisted chemical etching (MACE) technique and subsequently treated by the chemical polishing process are spin-coated with PEDOT:PSS to form heterojunction and employed as self-powered broadband photodetector. The optimized device shows superior performance, such as high responsivity of 555.34 mA/W, quick rise/fall times of 79 ms/81 ms, high External Quantum Efficiency (EQE) of 0.8 at zero bias (0 V) and high photostability up to 500 illumination cycles. Dark I-V characteristics and carrier lifetime measurements reveal that the enhanced performance of chemically polished devices is attributed to the formation of a conformable heterojunction and reduction in defects in the Si nanostructures. Given the scalability and simplicity of the demonstrated passivation-free approach, this work may aid the fabrication of high-performance hybrid Si nanostructured photodetectors.

High performance self-powered photodetector based on van der Waals heterojunction

Self-powered photodetectors that do not require external power support are expected to play a key role in future photodetectors due to their low power characteristics, but achieving high responsivity remains a challenge. 2D van der Waals heterojunctions are a promising technology for high-performance self-powered photodetectors due to their excellent optical and electrical properties. Here, we fabricate a self-powered photodetector based on In2Se3/WSe2/ReS2 van der Waals heterojunction self-powered photodetector. Due to the presence of ReS2 layer, photocurrent is enhanced as a result of the increase in light absorption efficiency and the effective region for generating photogenerated carriers. The built-in electric field is enhanced by a negative ‘back-gate voltage’ along the p–n junction vertical direction generated by the electrons in the photo-generated electrons accumulation layer. Accordingly, the optical responsivity and the photoresponse speed of this heterojunction self-powered photodetector are greatly boosted. The proposed self-powered photodetector based on the In2Se3/WSe2/ReS2 heterojunction exhibits a high responsivity of 438 mA W−1, which is 17 times higher compared to the In2Se3/WSe2 photodetector, a self-powered current (1.1 nA) that is an order of magnitude higher than that of the In2Se3/WSe2 photodetector, and a fast response time that is 250% faster. Thus the self-powered photodetector with a stronger built-in electric field and a wider depletion zone can provide a new technological support for the fabrication of high responsivity, low power consumption and high speed self-powered photodetectors based on van der Waals heterojunctions.

High performance self-powered photodetector based on CuBi2O4/MAPbI3 heterostructure

Methylammonium lead halide perovskites have garnered significant consideration for application in numerous optoelectronic devices due to their remarkable physical properties. However, the photoconductivity performance of these organolead halide perovskites is still lower than the conventional Si optoelectronic devices such as photodetectors, which is one of the major barriers to their practical applications. Combining suitable inorganic semiconductors with organolead halide perovskite may provide an alternative route for fabricating photodetectors that are expected to have improved photosensitivity. Here, a high performance self-power photodetector based on CuBi2O4/CH3NH3PbI3 (MAPbI3) heterojunction was synthesized under ambient conditions using the spin-coating technique. The severely reduced peak intensity in PL spectra and short decay time of CuBi2O4/MAPbI3 compared to MAPbI3 indicate efficient charge separation at the interface. The self-powered CuBi2O4/MAPbI3 showed photovoltaic-like effect with a maximum open circuit voltage Vo of ∼0.34 ± 0.02 V under the illumination of 365 nm light with 8.63 μW/cm2 power density. Moreover, CuBi2O4/MAPbI3 heterojunction base photodetector exhibits a high responsivity of ∼0.39 ± 0.04 W/A, a detectivity of ∼1.79 ± 0.17 × 1011 Jones, a fast response speed (rise time ∼ 36 ± 0.14 ms, fall time 81 ± 0.21 ms) and self-powering ability compared to that of MAPbI3 only device. This work offers an effective and feasible way to improve the performance of MAPbI3-based devices for photoelectronic applications.

Asymmetric Schottky contacts induced via localized ultrafast laser irradiation for ultrasensitive, self-powered, 2D photodetectors

Self-powered photodetectors hold great promise for addressing power-related challenges in the “Internet of Things (IoT)” era. However, the self-powered performances of a metal-semiconductor-metal (MSM) structure photodetector are inherently limited due to the presence of the symmetric Schottky contacts, leading to canceling photocurrents in opposite directions, while constructing an asymmetric MSM structure demands complicated design or sustained external fields. Herein, we propose a novel contact engineering strategy based on localized femtosecond (fs) laser irradiation, achieving an asymmetric band structure in an MSM-structure photodetector with pristine symmetric Schottky contacts. As a result, a MoS2 photodetector that exhibits exceptional photoresponse and self-powered performances is successfully fabricated. The device type transitions from a photoconductor to a photodiode, exhibiting a significant improvement in the rectification ratio from 1 to > 104. A comprehensive study on fs laser-based contact engineering is conducted by investigating atom diffusion, element variation, and Schottky barrier height variation. Notably, the photodetector demonstrates an exceptional zero-bias responsivity of 1.72 A/W, with a short circuit current of 37.2 nA and maximum output electric power of 1.67 nW. Our work provides a new strategy for modifying the energy band structure and facilitates the fabrication of high-performance self-powered photodetectors.