Single Flakes Research Articles

High yield growth of centimeter-sized black phosphorus single crystal thin flakes through bidirectional vapor transport

High yield growth of centimeter-sized black phosphorus single crystal thin flakes through bidirectional vapor transport

Single Crystalline GeSe Van Der Waals Ribbons With Uniform Layer Stacking, High Carrier Mobility, and Adjustable Edge Morphology.

Performance of the group IV monochalcogenide GeSe in solar cells, electronic, and optoelectronic devices is expected to improve when high-quality single crystalline material is used rather than polycrystalline films. Crystalline flakes represent an attractive alternative to bulk single crystals as their synthesis may be developed to be scalable, faster, and with higher overall yield. However, large - and especially large and thin - single crystal flakes are notoriously hard to synthesize. Here it is demonstrated that vapor-liquid-solid growth combined with direct lateral vapor-solid incorporation produces high-quality single crystalline GeSe ribbons with tens of micrometers size and controllable thickness. Electron microscopy shows that the ribbons exhibit perfect equilibrium (AB) van der Waals stacking order without extended defects across the entire thickness, in contrast to the conventional case of substrate-supported flakes where material is added via layer-by-layer nucleation and growth on the basal plane. Electrical measurements show anisotropic transport and a high Hall mobility of 85 cm2V-1s-1, on par with the best single crystals to date. Growth from mixed GeSe and SnSe vapors, finally, yields ribbons with unchanged structure and composition but with jagged edges, promising for applications that rely on ample chemically active edge sites, such as catalysis or photocatalysis.

Tunable Magnetism in 2D Organic‐Ion‐Intercalated MnPS3 via Molecule‐Dependent Vacancy Generation

AbstractThe magnetic properties of van der Waals materials are profoundly influenced by structural defects. The layered antiferromagnet MnPS3 offers a unique opportunity to explore defect‐related magnetism, as Mn2+ vacancies can be generated by the intercalation of specific guest molecules. However, the effectiveness of this process in atomically thin flakes and the extent of the magnetic tunability remain unclear. Here, it is shown that the magnetic properties of MnPS3 can be tailored through the intercalation of different guest molecules. Notably, the insertion of four alkylammonium ions introduces different populations of Mn2+ vacancies, leading to a transition from the pristine antiferromagnetic state to more complex magnetic textures, including a ferrimagnetic state displaying a magnetic saturation of 1 µB per atom. Moreover, it is shown that the intercalation of few‐nm‐thick flakes also leads to the emergence of a ferrimagnetic response. This in‐flake intercalation, which can be monitored in real time using optical microscopy, can be interrupted before completion, generating lateral heterostructures between pristine and intercalated areas. This approach opens the way to the use of partial intercalation to define regions with distinct magnetic properties within a single flake.

Interplay of Phonon Directionality and Emission Polarization in Two-Dimensional Layered Metal Halide Perovskites.

ConspectusLayered metal halide perovskites represent a natural quantum well system for charge carriers that provides rich physics, and the organic encapsulation of the inorganic metal halide layers not only increases their stability in devices but also provides an immense freedom to design their functionality. Intriguingly, these organic moieties strongly impact the optical, electrical, and mechanical properties, not only through their dielectric, elastic, and chemical properties but also because of induced mechanical distortions in the inorganic lattice. This tunability makes two-dimensional layered perovskites (2DLPs) highly attractive as light emitters. Common consensus is that exciton-phonon coupling plays an important role in radiative recombination. For bulk and some two-dimensional (2D) materials, the band edge emission broadening can be described by the classic models for polar inorganic semiconductors, while for the temperature dependence of the self-trapped exciton emission, an analysis developed for color centers has been successfully applied. For many 2DLPs these approaches do not work because of the complexity of their vibrational spectra. However, their emission is still strongly determined by phonons, and therefore, an adequate understanding of the electron-phonon coupling needs to be developed.With polarized and angle-resolved Raman spectroscopy studies on single 2DLP flakes based on different ammonium molecules as organic cations, in 2020 we revealed very rich phonon spectra in the low-frequency regime. Although the phonon bands at low frequency can generally be attributed to the vibrations of the inorganic lattice, we found very different responses by only changing the type of organic cations. In addition, the intensity of the different phonon modes depended strongly on the angle of the linearly polarized excitation beam with respect to the in-plane axes of the octahedron lattice. In 2022, we mapped this angular dependence of the phonon modes, which allowed identification of the directionality of the different lattice vibrations. By correlating the phonon spectra with the temperature-dependent emission for a set of 2DLPs that featured very different self-trapped exciton (STE) emission, we demonstrated that the exciton relaxation cannot be related to coupling with a single (longitudinal-optical) phonon band and that several phonon bands should be involved in the emission process. To gain insights into the exciton-phonon coupling effects on the band edge emission, we performed both angle-resolved polarized emission and Raman spectroscopy on single 2D lead iodide perovskite microcrystals. These experiments revealed the impact of the organic cations on the linear polarization of the emission and corroborated that multiple phonon bands should be involved in the radiative recombination process. Analysis of the temperature-dependent line width broadening of the band edge emission showed that for many systems, the behavior cannot be described by assuming the involvement of only one phonon mode in the electron-phonon coupling process. Our studies revealed a wealth of highly directional low-frequency phonons in 2DLPs from which several bands are involved in the emission process, which leads to diverse optical and vibrational properties depending on the type of organic cation in the material.

Ti3C2Tz Supported Pulse‐Electrodeposited Pt Nanostructures for Enhanced Acidic Electrochemical Hydrogen Evolution

Platinum (Pt)‐based electrocatalysts are considered benchmark materials for the hydrogen evolution reaction (HER) in acidic solution. However, widespread use is limited by the high price of Pt. Tuning the Pt morphology to increase the catalytic surface area for the same mass loading is therefore essential to increase its utilization. Herein, single Ti3C2Tz flakes were deposited by electrophoresis onto a carbon‐fiber gas diffusion layer, after which Pt nanostructures were selectively deposited onto the Ti3C2Tz flakes by pulse electrodeposition. It was observed that the pulse on‐time (ton) and duration had a significant effect on the morphology and activity of the composite electrode towards HER. Flower‐like and spherical morphologies were produced at long and short values of ton, respectively. As‐synthesized electrocatalysts were studied for HER in 0.5 M sulfuric acid (H2SO4). The catalyst with the lowest Pt loading (10 mg/cm2), exhibited outstanding HER performance. It attained a current density of 10 mA/cm2 at an overpotential of 38 mV, close to that of commercial carbon supported platinum (Pt/C, Vulcan XC). This catalyst exhibited a high turnover frequency (23.9 H2 s‐1 @ 100 mV), small Tafel slope (41 mV/dec), and high mass‐specific activity (2.45 A/mgPt @ 100 mV).

EVALUATION OF THE GRAPHENE DISPERSIONS FOR KEVLAR FABRICS FUNCTIONALIZATION OBTAINED BY THE LIQUID-EXFOLIATION OF GRAPHITE

The process where pristine graphite is subjected to a solvent treatment seems simple and scalable and has attracted the attention of researchers over many years. However, for successful exfoliation, overcoming the van der Waals attractions between the adjacent layers of graphite is necessary. Over time, several methods have been created to overcome the attraction between layers. Graphene’s liquid phase exfoliation (LPE) occurs due to the strong interactions between the solvent molecules and the basal planes of graphite, overcoming the energetic resistance to exfoliation and subsequent dispersion. Ultra sonication used for exfoliation can produce single or few layered graphene flakes. During sonication the sound waves propagate through liquid medium in alternating high- and low-pressure cycles, strong mechanical and thermal energy released by acoustic cavitation results in splitting up large particles into fine ones and dispersing them. Simultaneous insertion of solvent and/or intercalation molecules in between the graphite layers takes place supporting graphite separation into graphene layers. ; The dispersion capacity of graphene flakes depends on how appropriate the solvent properties are to the corresponding properties of graphene, such as surface tension, Hildebrand, and Hansen solubility parameters. Only certain solvents can disperse graphene well and form a dispersion appropriate for specific future applications. In addition, after exfoliation by ultra sonication graphene flakes aggregation due to the van der Waals attractions must be overcome to prepare in long-term stable dispersions of nanometres-size graphene sheets. ; The research has focused on the preparation of stable dispersion ready for transfer without intermediate processes to the Kevlar fabrics. An experimental comparison of the potentials of the 4 solvents for the application resulted in three corresponding to the intended use, two of them examined in detail, supplementing the composition of the LPE liquid medium with triethanolamine to obtain sufficient performance graphene coverage on Kevlar textile fibres.

Nanoscale Surface and Bulk Electronic Properties of Ti3C2Tx MXene Unraveled by Multimodal X-Ray Spectromicroscopy.

2D layered materials, such as transition metal carbides or nitrides, known as MXenes, offer an ideal platform to investigate charge transfer processes in confined environment, relevant for energy conversion and storage applications. Their rich surface chemistry plays an essential role in the pseudocapacitive behavior of MXenes. However, the local distribution of surface functional groups over single flakes and within few- or multilayered flakes remains unclear. In this work, scanning X-ray microscopy (SXM) is introduced with simultaneous transmission and electron yield detection, enabling multimodal nanoscale chemical imaging with bulk and surface sensitivity, respectively, of individual MXene flakes. The Ti chemical bonding environment is found to significantly vary between few-layered hydrofluoric acid-etched Ti3C2Tx MXenes and multilayered molten salt (MS)-etched Ti3C2Tx MXenes. Postmortem analysis of MS-etched Ti3C2Tx electrodes cycled in a Li-ion battery further illustrates that simultaneous bulk and surface chemical imaging using SXM offers a method well adapted to the characterization of the electrode-electrolyte interactions at the nanoscale.

Anisotropic sensing based on single ReS2 flake for VOCs discrimination

Selective and sensitive detection of volatile organic compounds (VOCs) holds paramount importance in real-world applications. This study proposes an innovative approach utilizing a single ReS2 field-effect transistor (FET) characterized by distinct in-plane anisotropy, specifically tailored for VOC recognition. The unique responses of ReS2, endowed with robust in-plane anisotropic properties, demonstrate significant difference along the a-axis and b-axis directions when exposed to four kinds of VOCs: acetone, methanol, ethanol, and IPA. Remarkably, the responses of ReS2 were significantly magnified under ultraviolet (UV) illumination, particularly in the case of acetone, where the response amplified by 10–15 times and the detection limit decreasing from 70 to 4 ppm compared to the dark conditions. Exploiting the discernible variances in responses along the a-axis and b-axis under both UV and dark conditions, the data points of acetone, ethanol, methanol and IPA gases were clearly separated in the principal component space without any overlap through principal component analysis, indicating that the single ReS2 FET has a high ability to distinguish various gas species. The exploration of anisotropic sensing materials and light excitation strategies can be applied to a broad range of sensing platforms based on two-dimensional materials for practical applications.

Downsizing nanoarchitectonics of multilayered MXenes electrocatalysts towards real time ion tracking via EQCM and electrocatalytic applications

Since their discovery, engineering two-dimensional (2D) MXene materials have attracted rapid interest in both energy storage and conversion applications. Among the several techniques being introduced for enhancing material properties, downsizing is one among the interesting approaches. Downsizing involves the deliberate scaling down of active 2D materials, such as MXenes, systematically. Although major studies are focused on the electrochemical applications of single layered MXene flakes, curiosity in evaluating the downsized multilayered MXenes for electrochemical applications motivates this project. Thus, in the current study, the multilayered bulk MXenes are sequentially stepped down to smaller multilayered fragments at definite time intervals, and subsequently the potential of this procured heterogeneous polydispersed solution are evaluated towards electrochemical applications without any further post-treatments. Real time monitoring of lithium-ion exchange in the downsized MXene materials at various time intervals was tracked using the electrochemical quartz crystal microbalance technique, where the downsized MXene system exhibited water-assisted lithium-ion transfer behavior. Increase in mass exchange was found to increase with increase in downsized MXene systems, thus making it very interesting towards ion storage applications. Further, downsized MXene electrocatalyst material delivered the lowest onset potential for hydrogen production among the set of catalysts studied. In short, this study outlines and pioneers some interesting observations regarding both energy storage and catalytic applications of multilayered downsized MXenes, thereby opening up new possibilities for facile, rapid and cost-effective material fabrication approaches.

Large area single crystal gold of single nanometer thickness for nanophotonics

Two-dimensional single crystal metals, in which the behavior of highly confined optical modes is intertwined with quantum phenomena, are highly sought after for next-generation technologies. Here, we report large area (>104 μm2), single crystal two-dimensional gold flakes (2DGFs) with thicknesses down to a single nanometer level, employing an atomic-level precision chemical etching approach. The decrease of the thickness down to such scales leads to the quantization of the electronic states, endowing 2DGFs with quantum-confinement-augmented optical nonlinearity, particularly leading to more than two orders of magnitude enhancement in harmonic generation compared with their thick polycrystalline counterparts. The nanometer-scale thickness and single crystal quality makes 2DGFs a promising platform for realizing plasmonic nanostructures with nanoscale optical confinement. This is demonstrated by patterning 2DGFs into nanoribbon arrays, exhibiting strongly confined near infrared plasmonic resonances with high quality factors. The developed 2DGFs provide an emerging platform for nanophotonic research and open up opportunities for applications in ultrathin plasmonic, optoelectronic and quantum devices.

New Approaches to the Bipolar Flaking Technique: Qualitative, Quantitative, and Kinematic Perspectives

The bipolar technique is a flaking strategy that has been identified from 3.3 Ma until the twentieth century, with no geographical or chronological homogeneous distribution. It is represented by the intentional contact of an active percussive element against a core rested on an anvil. This tool composite has been described by some researchers as a sign of low-skill of hominins, unable to perform successfully free-hand flaking or for flaking low-quality raw materials. Based on this premise, our research focused on the following question: Are there any quantitative and qualitative differences in terms of both kinematic parameters and technical skills between knappers with different levels of expertise when flaking using the bipolar technique? To get an answer, we developed a systematic experimental program with 12 volunteer participants with different levels of expertise. Then, to assess potential quantifiable differences and to understand the mechanics of bipolar technology, we did a video motion analysis based on kinematic parameters (including position, velocity, acceleration, and kinetic energy of the hammerstone). In addition, we performed a technological analysis of the experimental lithic assemblages to assess the technological differences between knappers based on their levels of expertise. In kinematic parameters, both statistical analysis and observations from the experiment clearly show that there are differences between the levels of expertise in this technique. Intermediate knappers have been observed to apply more velocity and kinetic energy than experts and novices. Also, differences were observed in the flaking strategies. Expert knappers show a longer reduction sequence, while intermediates show shorter one. Moreover, some of the novice knappers did not even obtain a single flake. The results of our experiment stress the complexity of bipolar flaking and that previous assumptions about it might be reconsidered, especially in terms of reconsidering the negative connotations attributed to this flaking technique.

Writing and deleting skyrmions by electron beam in van der Waals ferromagnet Fe3GeTe2

Magnetic skyrmions are potential candidates for low-power spintronic devices. Recently, skyrmions have been observed in two-dimensional van der Waals ferromagnets, which extends the range of skyrmion hosting materials to atomically thin limit. However, creating and deleting skyrmions at precise locations is still a challenge for practical applications. In this study, we proposed a solution to this problem. Using in situ Lorentz transmission electron microscopy, we investigated magnetic domain structures in Fe3GeTe2 exfoliated single crystal flakes and found that the skyrmions in this sample are of the Néel type. Interestingly, we found that the skyrmions could be created and deleted at specific locations using a focused electron beam. Micromagnetic simulations results agree well with the experimental results, providing insights into the underlying mechanisms. The methods presented in this work can be extended to other skyrmion material systems, thereby advancing the field of skyrmion-based technologies.

Gold Recovery from E-Waste by Food-Waste Amyloid Aerogels.

Demand for gold recovery from e-waste grows steadily due to its pervasive use in the most diverse technical applications. Current methods of gold recovery are resource-intensive, necessitating the development of more efficient extraction materials. This study explores protein amyloid nanofibrils (AF) derived from whey, a dairy industry side-stream, as a novel adsorbent for gold recovery from e-waste. To do so, AF aerogels are prepared and assessed against gold adsorption capacity and selectivity over other metals present in waste electrical and electronic equipment (e-waste). The results demonstrate that AF aerogel has a remarkable gold adsorption capacity (166.7mg g-1) and selectivity, making it efficient and an adsorbent for gold recovery. Moreover, AF aerogels are efficient templates to convert gold ions into single crystalline flakes due to Au growth along the (111) plane. When used as templates to recover gold from e-waste solutions obtained by dissolving computer motherboards in suitable solvents, the process yields high-purity gold nuggets, constituted by ≈90.8wt% gold (21-22 carats), with trace amounts of other metals. Life cycle assessment and techno-economic analysis of the process finally consolidate the potential of protein nanofibril aerogels from food side-streams as an environmentally friendly and economically viable approach for gold recovery from e-waste.

Orientation of Cobalt-Phthalocyanines on Molybdenum Disulfide: Distinguishing between Single Crystals and Small Flakes

Orientation of Cobalt-Phthalocyanines on Molybdenum Disulfide: Distinguishing between Single Crystals and Small Flakes

Loading Mode-Induced Enhancement in Friction for Microscale Graphite/Hexagonal Boron Nitride Heterojunction.

Classical friction laws traditionally assume that the friction between solid pairs remains constant with a given normal load. However, our study has unveiled a remarkable deviation from conventional wisdom. In this paper, we discovered that altering the loading mode of micro graphite flakes led to significant changes in the lateral friction under identical normal loads. By adding a cap onto a single graphite flake to disperse the normal load applied by an atomic force microscope (AFM) tip, we were able to distribute the concentrated force. Astonishingly, our results demonstrated a notable 4-7 times increase in friction as a consequence of load dispersion. Finite element analysis (FEA) further confirmed that the increase in compressive stress at the edges of the graphite flake, resulting from load dispersion, led to a significant increase in friction. This study underscores the critical role of the loading mode in microscale friction dynamics, challenging the prevailing notion that friction remains static with a given normal force. Importantly, our research sheds light on the potential for achieving macroscale structural superlubricity (SSL) by assembling microscale SSL graphite flakes by using a larger cap.

Synthesis of Nb-MXenes for Electrocatalysis Applications

MXene is the newest class of 2D materials composed of carbides, nitrides and carbonitrides of transition metals. They are promising materials for electrochemical energy storage and in the field of electrocatalysis1. This work proposes the synthesis of Nb-MXene from MAX phase precursor and its characterization regarding morphology, structure and electrochemical activity.First, the precursor MAX phase of niobium was produced by mixing Nb, Al and NbC in powder and the reaction process in a tubular furnace, argon atmosphere, at 1640°C, for 3 h. Subsequently, the chemical synthesis was performed at 60 °C, 96 h, by LiF+HCl (1:10 w/w) + 1g of MAX phase, centrifuged and washed with DI water until pH~6 and dried in a vacuum oven.SEM images (Fig. 1 left) confirmed the morphology2,3 typical of the MAX phase and the effective process of chemical synthesis. The etching process occurred indicating success in the exfoliation, separating the layers forming multilayer MXenes (Fig. 1, right side)2. A mixture of Nb4AlC3 and Nb2AlC was obtained in the MAX phase.Successful synthesis of MXene is confirmed by shift of the diffraction peaks corresponding to the reflection from (002) plane from 7.36° and 12.75° in case of MAX phase to 5.28°, indicating the removal of Al from the structure2 (Fig. 2).MXene in a form of a thin film on a conductive substrate was tested for oxygen reduction reaction (ORR) in 3 M KOH electrolyte. Fig. 3 shows a clear increase of current density in O2-saturated solution corresponding to O2 reduction. The peak was visible at 0.7 V with peak current density reaching 0.53 mAcm-2. This supports further exploration of MXene as an electrocatalyst for ORR, including tolerance and stability tests.References1- C. Zhan, M. Naguib, M. Lukatskaya, P. R. C. Kent, Y. Gogotsi, D. Jiang. Understanding the MXene Pseudocapacitance, J. Phys. Chem. Lett, 9 (2018) 1223−1228. DOI: 10.1021/acs.jpclett.8b002002- Y. Tan, Z. Zhu, X. Zhang, J. Zhang, Y. Zhou, H. Li, H. Qin, Y. Bo, Z. Pan, Nb4C3Tx (MXene) as a new stable catalyst for the hydrogen evolution reaction, International Journal of Hydrogen Energy, 46 (2021) 1955-1966. DOI: 10.1016/j.ijhydene.2020.10.046.3- M. Shekhirev, C. E. Shuck, A. Sarycheva, Y. Gogotsi, Characterization of MXenes at every step, from their precursors to single flakes and assembled films, Progress in Materials Science, 120 (2021) 100757https://doi.org/10.1016/j.pmatsci.2020.100757. Figure 1

Analysis on bimodal complex permeability spectrum of a noise suppression sheet and single constituent flakes

In recent years, highly integrated active components inside small mobile communication devices have led to serious electromagnetic interference problems. The countermeasure to this problem is covering a noise source with a noise suppression sheet (NSS) which is composed of ferromagnetic flakes and polymers. The NSS absorbs effectively electromagnetic waves due to a large imaginary part of relative permeability μr″ at the specific frequency region. This function is attributed to the bimodal μr″ spectrum of NSS, but its physical origin has not been revealed so far. In this study, the bimodal μr″ spectrum of NSS has been analyzed and its physical mechanism has been discussed. The μr″ spectrum of a constituent single magnetic flake was measured by using a newly developed high-sensitivity permeability measurement system, which showed a bimodal spectrum quite similar to that of NSS. This fact indicates that the physical origin of the bimodal μr″ spectrum is attributed to the magnetization dynamics of each single constituent flake. After measuring the μr″ spectra of single flakes with various materials, such as Fe, Fe-Al, Fe-Co-V, and Fe-Si-Al alloys, these bimodal μr″ spectra were quantitatively explained by the magnetization dynamics of the flux closure states inside the flake. The magnetic domain structure of a single flake was observed by a micro-beam X-ray magnetic circular dichroism microscopy. The result confirmed that the segmented magnetic domains form the local flux closure states inside the flake.

Reentrant Proximity-Induced Superconductivity for GeTe Semimetal

We experimentally investigate charge transport in In–GeTe and In–GeTe–In proximity devices, which are formed as junctions between superconducting indium leads and thick single crystal flakes of α-GeTe topological semimetal. We observe nonmonotonic effects of the applied external magnetic field, including reentrant superconductivity in In–GeTe–In Josephson junctions: supercurrent reappears at some finite magnetic field. For a single In–GeTe Andreev junction, the superconducting gap is partially suppressed in zero magnetic field, while the gap is increased nearly to the bulk value for some finite field before its full suppression. We discuss possible reasons for the results obtained, taking into account spin polarization of Fermi arc surface states in topological semimetal \\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\alpha $$\\end{document}-GeTe with a strong spin–orbit coupling. In particular, the zero-field surface state spin polarization partially suppresses the superconductivity, while it is recovered due to the modified spin-split surface state configuration in finite fields. As an alternative possible scenario, the transition into the Fulde–Ferrell–Larkin–Ovchinnikov state is discussed. However, the role of strong spin–orbit coupling in forming the nonmonotonic behavior has not been analyzed for heterostructures in the Fulde–Ferrell–Larkin–Ovchinnikov state, which is crucial for junctions involving GeTe topological semimetal.

Growth and Local Structures of Single Crystalline Flakes of Three-Dimensional Covalent Organic Frameworks in Water.

Due to the enormous chemical and structural diversities and designable properties and functionalities, covalent organic frameworks (COFs) hold great promise as tailored materials for industrial applications in electronics, biology, and energy technologies. They were typically obtained as partially crystalline materials, although a few single-crystal three-dimensional (3D) COFs have been obtained recently with structures probed by diffraction techniques. However, it remains challenging to grow single-crystal COFs with controlled morphology and to elucidate the local structures of 3D COFs, imposing severe limitations on the applications and understanding of the local structure-property correlations. Herein, we develop a method for designed growth of five types of single crystalline flakes of 3D COFs with controlled morphology, front crystal facets, and defined edge structures as well as surface chemistry using surfactants that can be self-assembled into layered structures to confine crystal growth in water. The flakes enable direct observation of local structures including monomer units, pore structure, edge structure, grain boundary, and lattice distortion of 3D COFs as well as gradually curved surfaces in kinked but single crystalline 3D COFs with a resolution of up to ∼1.7 Å. In comparison with flakes of two-dimensional crystals, the synthesized flakes show much higher chemical, mechanical, and thermal stability.

Germanane and (3‐Hydroxypropyl)germanane as Single Crystal Photodetectors

Abstract2D materials are being widely investigated for their potential application in light‐detecting devices. Very recently, a spin‐coated flexible 2D germanium‐based photodetector with great photocurrent density and responsivity as well as short rise and decay time is presented by Liu et. al. In this paper, the solid‐state single flake photodetector base on either pure germanane or (3‐hydroxypropyl)germanane is reported. Both prepared photodetectors while irradiated with different wavelengths of light exhibit outstanding responsivity of 1157 mA W−1 for GeH and 362 mA W−1 for (3‐hydroxypropyl)germanane, which exceeds Liu's flexible reported GeH photodetector (22 µA W−1) by more than five orders of magnitude. These constructed photodetectors also exhibit rise and fall times lower than 20 ms, which is also significantly faster than the GeH photodetector reported by Liu with rise and decay times 240 and 740 ms, respectively.