Chemical Vapor Deposition Method Research Articles

Effects of Plasma Ions/Radicals on Kinetic Interactions in Nanowall Deposition: A Review

Recent advances in the growth of carbon nanowalls (CNWs) and vertical graphene nanosheets using various plasma‐enhanced chemical vapor deposition (PECVD) methods are reviewed in this article. Growth methods are classified into hot‐ and cold‐wall reactors equipped with diverse plasma generation systems, and their respective characteristics are summarized, with particular attention to the behavior of reactive species, such as ions and radicals, generated within the plasma. Recent progress in this research domain is outlined for each method, and an organized account of the chemical kinetic phenomena occurring within the plasma is provided. Finally, future perspectives are discussed. Fundamental data are obtained through real‐time in situ measurements of ions and radicals, and the construction of a database from these data offers microscopic insights that significantly enhance processing outcomes for macroscopically controlling the mechanical shapes and chemical properties of CNWs.

Enhancing and broadening the photoresponse of CdS nanowire by constructing core–shell heterostructure

Limited by the severe surface recombination and large bandgap, it is still a challenge to achieve a high-performance broad-spectrum photodetector based on CdS nanowires (NWs). In this work, the CdS/GeS core–shell heterostructure is constructed to enhance and broaden the photoresponse of CdS NWs. The CdS/GeS core–shell heterostructure NWs are prepared by the chemical vapor deposition method, exhibiting smooth surfaces, controlled shell thicknesses, and compositions. From the UV-Vis-near-infrared (NIR) diffuse reflectance spectrum, PL, and time-resolved photoluminescence studies, it is found that the surface recombination is weakened and the light absorption range is widened after the constructing core–shell heterostructure. When configured into photodetectors, the responsivity of the CdS/GeS core–shell heterostructure NWs is up to 76.8 A W−1, which is 10 folds higher than that of pristine CdS NWs. Furthermore, the photoresponse wavelength of the CdS/GeS core–shell heterostructure NWs is extended from 405 to 850 nm. The improved photodetection performance is attributed to the effective separation of photogenerated carriers at the heterostructure interface, weakened surface recombination, and excellent light absorption of the GeS shell. All results imply that constructing core–shell heterostructures is an effective strategy for constructing high-performance photodetectors.

Enhancing and broadening the photoresponse of CdS nanowire by constructing core–shell heterostructure

Limited by the severe surface recombination and large bandgap, it is still a challenge to achieve a high-performance broad-spectrum photodetector based on CdS nanowires (NWs). In this work, the CdS/GeS core–shell heterostructure is constructed to enhance and broaden the photoresponse of CdS NWs. The CdS/GeS core–shell heterostructure NWs are prepared by the chemical vapor deposition method, exhibiting smooth surfaces, controlled shell thicknesses, and compositions. From the UV-Vis-near-infrared (NIR) diffuse reflectance spectrum, PL, and time-resolved photoluminescence studies, it is found that the surface recombination is weakened and the light absorption range is widened after the constructing core–shell heterostructure. When configured into photodetectors, the responsivity of the CdS/GeS core–shell heterostructure NWs is up to 76.8 A W−1, which is 10 folds higher than that of pristine CdS NWs. Furthermore, the photoresponse wavelength of the CdS/GeS core–shell heterostructure NWs is extended from 405 to 850 nm. The improved photodetection performance is attributed to the effective separation of photogenerated carriers at the heterostructure interface, weakened surface recombination, and excellent light absorption of the GeS shell. All results imply that constructing core–shell heterostructures is an effective strategy for constructing high-performance photodetectors.

Preparation and Electrical Performance Analysis of a GaAs‐Based Tritium Battery

A nuclear battery is a promising candidate for small power supply sources in the military and commercial fields, but its output power and energy conversion efficiency need to be improved. This paper mainly describes a design, preparation, and electrical performance analysis of a GaAs-based tritium battery. The design of the tritium battery uses a multistage process with Monte Carlo and Matlab simulations. A titanium tritide source was prepared by a high-temperature tritium absorption device, and a GaAs semiconductor transducer was developed using a metal-organic chemical vapor deposition method. The D/Ti ratio and T/Ti ratio of the deuterium/tritium titanium films were 1.9 and 1.7, respectively. Two kinds of GaAs-based PIN junction semiconductor transducers were proposed and irradiated with the prepared tritium source. Their electrical properties were measured in situ and analyzed qualitatively. Under the irradiation of a 0.61-Ci tritium source, the short-circuit current of the device was 0.3 to 0.38 μA, the open-circuit voltage was 35 to 63 mV, the peak power was 2.8 to 6.4 nW, and the energy conversion efficiency of the GaAs semiconductor transducer was about 1.86%. It was found that an air gap between the GaAs semiconductor transducer and the radioactive source caused serious loss of beta particle energy, resulting in low output power and low energy conversion efficiency of the nuclear battery. The open-circuit voltage of the devices with a SiO2 passivation layer on the surface decreased both in a dark environment and in light illumination, but SiO2 passivation did not reduce surface recombination as expected. The research work in this paper will provide some valuable reference for the preparation and performance optimization of nuclear batteries.

Preparation and Electrical Performance Analysis of a GaAs‐Based Tritium Battery

A nuclear battery is a promising candidate for small power supply sources in the military and commercial fields, but its output power and energy conversion efficiency need to be improved. This paper mainly describes a design, preparation, and electrical performance analysis of a GaAs-based tritium battery. The design of the tritium battery uses a multistage process with Monte Carlo and Matlab simulations. A titanium tritide source was prepared by a high-temperature tritium absorption device, and a GaAs semiconductor transducer was developed using a metal-organic chemical vapor deposition method. The D/Ti ratio and T/Ti ratio of the deuterium/tritium titanium films were 1.9 and 1.7, respectively. Two kinds of GaAs-based PIN junction semiconductor transducers were proposed and irradiated with the prepared tritium source. Their electrical properties were measured in situ and analyzed qualitatively. Under the irradiation of a 0.61-Ci tritium source, the short-circuit current of the device was 0.3 to 0.38 μA, the open-circuit voltage was 35 to 63 mV, the peak power was 2.8 to 6.4 nW, and the energy conversion efficiency of the GaAs semiconductor transducer was about 1.86%. It was found that an air gap between the GaAs semiconductor transducer and the radioactive source caused serious loss of beta particle energy, resulting in low output power and low energy conversion efficiency of the nuclear battery. The open-circuit voltage of the devices with a SiO2 passivation layer on the surface decreased both in a dark environment and in light illumination, but SiO2 passivation did not reduce surface recombination as expected. The research work in this paper will provide some valuable reference for the preparation and performance optimization of nuclear batteries.

The Effects of Some Factors on the Electrical Properties of Cu2O/ZnO Double Films Fabricated by Chemical Vapor Deposition Method

The Effects of Some Factors on the Electrical Properties of Cu2O/ZnO Double Films Fabricated by Chemical Vapor Deposition Method

Simultaneous purification and oxidation of the as-synthesized MWCNTs with KMnO4 using phase transfer catalyst at three different pH medium by the hydrothermal method

Improving and streamlining current oxidation techniques for experimental is the main goal of the research described in the present article. By applying the pressure created while on the hydrothermal process to an autoclave walled with Teflon, simplifying the procedure was accomplished. By comparing the degrees of functionalization attained with the dispersibility in the substantially pure and functionalized multi-walled carbon nanotubes (MWCNTs) final product, the beneficial effect of the procedure was evaluated. In order to achieve this, the study looked at and investigated how as-synthesized MWCNTs from Fe-Mo/MgO catalyst were simultaneously purified and oxidized using the chemical vapor deposition (CVD) method. Aliquot-336 was used as phase transfer catalyst (PTC) by hydrothermal method under three different pH conditions. Following functionalization, nanotubes of carbon might easily combine with various chemical reagents to generate homogeneous dispersions or even well-aligned structures because of the functional groups linked to their surfaces. In this case, a chemical called reagent potassium permanganate (KMnO4) is necessary in order to target particular π-bonds while entirely destroying the nanotubes' graphene structures. The techniques have been explained in terms of mechanism, and the Fourier transform-infrared (FT-IR) spectroscopy has confirmed the functionalizations of the CNTs. These approaches were further explored through FT-Raman spectrum analysis, thermal assessments, energy dispersive X-ray spectroscopy (EDX), TEM (transmission electron microscopy) along with the help of EDX, and visible-near IR absorption and UV–visible absorption spectroscopy (ABS) procedures.

Numerical Investigation on Thermal Conductivity of Graphene Foam Composite for Thermal Management Applications.

Graphene foam prepared by the chemical vapor deposition method is a promising thermal interfacial material. However, the thermal properties of graphene foam highly depend on the experimental fabrication conditions during the chemical vapor deposition process. Aiming to reveal how to prepare the appropriate graphene foam for the various thermal management scenarios, the influence of experimental conditions on thermal properties of graphene foam was investigated. Furthermore, the contribution of thermal conductivity and thermal radiation to the effective thermal coefficient of graphene foam was carried out for comparison. The research results showed that the porosity and the cross-section shape of the struts of the growth template were two critical factors affecting the thermal transport of graphene foam, especially with the increase of temperature. In addition, the deposition time of graphene determined the wall thickness and affected the thermal conductivity directly. The thermal radiation contributed more than thermal conductivity when the temperature climbed continuously. Comparatively, the effective thermal coefficient of graphene foam composite with high porosity and circular-shape struts was much superior to that of others at high temperature. The research findings provide important guidance for graphene foam fabrication and its applications in the field of thermal management.

Electrochemical activity of self-supporting nitrogen-doped graphene for the degradation and in-situ determination of methylene blue

Environmentally friendly wastewater treatment and online pollution monitoring systems, important for water quality control, are yet to be developed. Electrochemical strategies combining the electrocatalytic degradation and electroanalysis of organic pollutants are expected to achieve this key technology. This study employed a chemical vapor deposition method using N₂ gas as the nitrogen source and applying an alternating electric field to prepare self-supporting nitrogen-doped graphene (NG) tubes with a wall thickness of up to 480 μm comprising few-layer NG nanosheets. The correlation between the properties of these materials and the electrocatalytic activity for methylene blue (MB) was investigated. The feasibility of the electrochemical strategy for online wastewater treatment and detection was validated using a combination of UV–visible spectroscopy and differential pulse voltammetry. The NG tube with the N-C bond distribution regulated by adjusting the methane flow rate and growth time exhibited high electrocatalytic activity, rapidly degrading 50 mg L⁻¹ of MB within 36 min and tracking changes in MB concentration. The NG tubes were assembled in an electrocatalytic meter pen for water treatment, achieving a degradation efficiency of 99.4 % and a detection limit of 0.3 mg L−1 for the MB solution, quite satisfactory for emerging simultaneous degradation and monitoring processes. The developed self-supporting NG tubes are promising materials for electrocatalytic degradation anodes and sensing electrodes in water treatment. Dual-functional electrocatalytic systems have potential applications in water quality monitoring and improvement.

MgO Modified by X2, HX, or Alkyl Halide (X = Cl, Br, or I) Catalytic Systems and Their Activity in Chemoselective Transfer Hydrogenation of Acrolein into Allyl Alcohol.

A new type of catalyst containing magnesium oxide modified with various modifiers ranging from bromine and iodine, to interhalogen compounds, hydrohalogenic acids, and alkyl halides have been prepared using chemical vapor deposition (CVD) and wet impregnation methods. The obtained systems were characterized using a number of methods: determination of the concentration of X- ions, surface area determination, powder X-ray diffraction (PXRD), surface acid-base strength measurements, TPD of probe molecules (acetonitrile, pivalonitrile, triethylamine, and n-butylamine), TPD-MS of reaction products of methyl iodide with MgO, and Fourier transform infrared spectroscopy (FTIR). The catalysts' activity and chemoselectivity during transfer hydrogenation from ethanol to acrolein to allyl alcohol was measured. A significant increase in the activity of modified MgO (up to 80% conversion) in the transfer hydrogenation of acrolein was found, while maintaining high chemoselectivity (>90%) to allyl alcohol. As a general conclusion, it was shown that the modification of MgO results in the suppression of strong basic sites of the oxide, with a simultaneous appearance of Brønsted acidic sites on its surface. Independently, extensive research on the reaction progress of thirty alkyl halides with MgO was also performed in order to determine its ability to neutralize chlorinated wastes.

Chemical preparation methods of MXenes materials and exploration and application of their chemical mechanisms

As a new generation of 2D materials, MXenes have demonstrated various application prospects in fields such as energy storage, electromagnetic interference shielding, sensing devices, medicine, seawater desalination, and environmental restoration due to their rich functional groups, adjustable interlayer spacing structure, and high electrical conductivity. In recent years, this has led to widespread exploration and research from the outside world. This article mainly focuses on the latest developments in the production of MXenes by Chemical Vapor Deposition (CVD) method, and briefly discusses the pseudocapacitive effects and photovoltaic effects of MXenes materials within the energy storage domain, highlighting their outstanding performance in potassium-ion supercapacitors and perovskite solar cells in the photovoltaic field.

Superwetting PVA/cellulose aerogel with asymmetric structure for oil/water separation and solar-driven seawater desalination

Extracting clean water from oily wastewater and seawater is one of the effective strategies to alleviate the freshwater crisis. However, achieving both high separation efficiency and excellent salt resistance remain challenges for materials. Herein, a novel methyltrichlorosilane-modified polyvinyl alcohol/cellulose aerogel (MPCA) was prepared by freeze drying, chemical cross-linking, and chemical vapor deposition (CVD) methods. The superwetting MPCA presented an asymmetric structure, in which the small dense pores at the top surface facilitated the efficient separation of water-in-oil (W/O) emulsions and the large pores on the bottom surface were beneficial for brine exchange. The as-prepared superwetting aerogel was suitable for the separation of various W/O emulsions with excellent separation flux (631.9-2368.7L·m-2·h-1) and outstanding separation efficiency (99.5%). In addition, MPCA achieved a high evaporation efficiency of 1.39kg·m-2·h-1 and a satisfactory energy conversion efficiency of 89.7%. Moreover, the unique asymmetric structure endowed the evaporator excellent salt resistance and could self-dissolve the accumulated salt in 20minutes. The as-prepared MPCA could achieve efficient W/O emulsion separation as well as produce freshwater in seawater, providing a new strategy for oily waste seawater purification. Environmental ImplicationsThe discharge of oily wastewater not only damages the ecosystem but also threatens human health. Superwetting separation materials can efficiently treat various oily wastewaters, but they cannot remove water-soluble pollutants in the water. A novel superwetting Janus cellulose/PVA aerogel (MPCA) was prepared, with dense pores on the top surface to facilitate the separation of water-in-oil emulsion, and large honeycomb pores on the bottom to facilitate the continuous supply of water and ion exchange. The as-prepared MPCA could not only efficiently separate water-in-oil emulsions, but also produce clean water under light irradiation, providing a new strategy for alleviating the freshwater crisis.

High Mobility Transistors and Flexible Optical Synapses Enabled by Wafer-Scale Chemical Transformation of Pt-Based 2D Layers.

Electronic devices employing two-dimensional (2D) van der Waals (vdW) transition-metal dichalcogenide (TMD) layers as semiconducting channels often exhibit limited performance (e.g., low carrier mobility), in part, due to their high contact resistances caused by interfacing non-vdW three-dimensional (3D) metal electrodes. Herein, we report that this intrinsic contact issue can be efficiently mitigated by forming the 2D/2D in-plane junctions of 2D semiconductor channels seamlessly interfaced with 2D metal electrodes. For this, we demonstrated the selectively patterned conversion of semiconducting 2D PtSe2 (channels) to metallic 2D PtTe2 (electrodes) layers by employing a wafer-scale low-temperature chemical vapor deposition (CVD) process. We investigated a variety of field-effect transistors (FETs) employing wafer-scale CVD-2D PtSe2/2D PtTe2 heterolayers and identified that silicon dioxide (SiO2) top-gated FETs exhibited an extremely high hole mobility of ∼120 cm2 V-1 s-1 at room temperature, significantly surpassing performances with previous wafer-scale 2D PtSe2-based FETs. The low-temperature nature of the CVD method further allowed for the direct fabrication of wafer-scale arrays of 2D PtSe2/2D PtTe2 heterolayers on polyamide (PI) substrates, which intrinsically displayed optical pulse-induced artificial synaptic behaviors. This study is believed to vastly broaden the applicability of 2D TMD layers for next-generation, high-performance electronic devices with unconventional functionalities.

Synthesis of multilayered h-BN film on the molten Ni–B and the influence of underneath W substrate

High-quality two-dimensional hexagonal boron nitride (h-BN) film with tens of layers has been used as a universal substrate and capping layer for the van der Waals devices. Various approaches have been carried out for the synthesis of multilayered h-BN. Among them, the metal flux method is reliable in yielding h-BN crystals with high crystalline quality. However, this time- and energy-demanding method hinders its scale application. Herein, inspired by the metal flux method, we reported the time-effective growth of high-quality multilayered h-BN film (ca. 20 nm) on a molten Ni–B layer wetting on W substrate with chemical vapor deposition method. The film exhibits an excellent stacking sequence and a full-width at half maximum of the Raman E2g peak narrow to 9.5 cm−1. Cross-sectional high-resolution transmission electron microscopy and in-situ x-ray diffraction spectroscopy were carried out to investigate the crystal structure evolution of Ni–B layer wetting on W substrate. It is found that the low surface tension caused by the spreading of Ni–B alloy on the W substrate and the presence of the Ni subsurface may be responsible for the formation of multilayered h-BN with excellent crystalline quality. Meanwhile, the W diffusion in Ni–B-based melt can hinder the formation of h-BN under certain growth conditions. The approach demonstrates the feasibility of large-scale growth of multilayered h-BN, paving the way to future applications in van der Waals electronic and optoelectronic devices.

Polyvinyl alcohol nanofibrous mat impregnated with ClCNTs/Fe2O3 nanocomposite for absorption of diesel oil in water

Abstract Oil contamination is one of the main sources of water pollution in the world. In this study, a sorption material that showed great promise as an absorbent for diesel oil in aqueous solution was developed. Chlorinated carbon nanotubes (CNTs) previously synthesized using a chemical vapor deposition (CVD) method were loaded with iron oxide nanoparticles via a co-precipitation method. The sorption materials were prepared by embedding ClCNTs/Fe2O3 nanocomposite into a polyvinyl alcohol (PVA) polymer matrix via electrospinning. The PVA mat containing only ClCNTs was also prepared for comparison and the maximum sorption capacity of 9.7 g/g was obtained. The optimum concentration of ClCNTs/Fe2O3 nanocomposite that gave uniform, and well-distributed nanofibers was 0.5 wt.%. Crosslinking the PVA/ClCNTs/Fe2O3 nanofiber mat with glutaraldehyde (GA) resulted in increased absorption capacity for oil of ~ 9.4 g/g in comparison with an absorption capacity of ~ 7.6 g/g attained with a pure nanofiber mat. The crosslinked nanofiber mat remained stable even after 60 min of oil absorption which proves that crosslinking assisted in increasing the affinity of PVA for oil by reducing the amount of OH groups through acetal formation making PVA less soluble to water. The oil sorption capacity of the prepared materials was not maintained even after two cycles indicating poor reusability. 

Ytterbium-Doped Double-Clad Fiber with High Uniformity of Concentration Distribution and Suppressed Photodarkening

Photodarkening (PD) effect in ytterbium-doped fiber (YDF) has a significant impact on the high-power operational stability of fiber lasers, which seriously hinders the power scaling. In this paper, the relationship between ytterbium ions uniformity and the photodarkening effect in the YDF was investigated, and the fabrication process allowing improving the ytterbium ions uniformity in the core of preforms for suppressing the photodarkening effect was developed. The Modified Chemical Vapor Deposition (MCVD) method combined with Chelate Vapor Deposition (CVD) technology was adopted for multi-layer fiber core deposition, and an all-gas-phase technical process was proposed to improve the ytterbium ions uniformity in the Al/P co-doped glass matrix. The 25/400 μm YDFs obtained by this technology achieved stable 3.5 kW laser output power for 8 h with suppressed PD and nonlinear effects.

Comparison of GeSn alloy films prepared by ion implantation and remote plasma-enhanced chemical vapor deposition methods

Thin films of germanium-tin (GeSn) alloy with Sn content well above its equilibrium solubility limit in Ge are produced using both remote plasma-enhanced chemical vapor deposition (RPECVD) directly on silicon substrates and ion implantation of Sn into Ge. For RPECVD, the growth temperature of 302 °C resulted in fully relaxed GeSn alloys with high defect density, principally threading dislocations related to the large lattice mismatch between Si and GeSn. For the implantation case, pulsed laser melting was used to melt and crystallize the GeSn layer on a time scale of a few tens of nanoseconds. The resulting GeSn layers were also relaxed and defective, presumably again as a result of lattice mismatch with the underlying Ge lattice. However, the nature of the defects was quite different to the RPECVD method, whereby the line defects were not threading dislocations but stackinglike defects, which developed into arrays of these defects in the high Sn content region close to the surface. For the purpose of comparing RPECVD and ion-implantation methods, alloy films of similar thickness (400–450 nm) and Sn content (4.5–6.5 at. %) were examined. Film parameters (thickness, Sn content, Sn solubility, and segregation), as well as film quality and defect structures, were examined for both fabrication methods using several analytical techniques. This comparison provided us with a better physical understanding of our GeSn films and will help inform future growth/fabrication strategies targeted at minimizing defects formed in the GeSn films for the realization of optoelectronic devices.

Nanoimprint Lithography for Next-Generation Carbon Nanotube-Based Devices.

This research reports the development of 3D carbon nanostructures that can provide unique capabilities for manufacturing carbon nanotube (CNT) electronic components, electrochemical probes, biosensors, and tissue scaffolds. The shaped CNT arrays were grown on patterned catalytic substrate by chemical vapor deposition (CVD) method. The new fabrication process for catalyst patterning based on combination of nanoimprint lithography (NIL), magnetron sputtering, and reactive etching techniques was studied. The optimal process parameters for each technique were evaluated. The catalyst was made by deposition of Fe and Co nanoparticles over an alumina support layer on a Si/SiO2 substrate. The metal particles were deposited using direct current (DC) magnetron sputtering technique, with a particle ranging from 6 nm to 12 nm and density from 70 to 1000 particles/micron. The Alumina layer was deposited by radio frequency (RF) and reactive pulsed DC sputtering, and the effect of sputtering parameters on surface roughness was studied. The pattern was developed by thermal NIL using Si master-molds with PMMA and NRX1025 polymers as thermal resists. Catalyst patterns of lines, dots, and holes ranging from 70 nm to 500 nm were produced and characterized by scanning electron microscopy (SEM) and atomic force microscopy (AFM). Vertically aligned CNTs were successfully grown on patterned catalyst and their quality was evaluated by SEM and micro-Raman. The results confirm that the new fabrication process has the ability to control the size and shape of CNT arrays with superior quality.

Two-Dimensional Ultrathin Fe3Sn2 Kagome Metal with Defect-Dependent Magnetic Property.

Two-dimensional (2D) Fe3Sn2, which is a room-temperature ferromagnetic kagome metal, has potential applications in spintronic devices. However, the systematic synthesis and magnetic study of 2D Fe3Sn2 single crystals have rarely been reported. Here we have synthesized 2D hexagonal and triangular Fe3Sn2 nanosheets by controlling the amount of FeCl2 precursors in the chemical vapor deposition (CVD) method. It is found that the hexagonal Fe3Sn2 nanosheets exist with Fe vacancy defects and show no obvious coercivity. While the triangular Fe3Sn2 nanosheet has obvious hysteresis loops at room temperature, its coercivity first increases and then remains stable with an increase in temperature, which should result from the competition of the thermal activation mechanism and spin direction rotation mechanism. A first-principles calculation study shows that the Fe vacancy defects in Fe3Sn2 can increase the distances between Fe atoms and weaken the ferromagnetism of Fe3Sn2. The resulting 2D Fe3Sn2 nanosheets provide a new choice for spintronic devices.

Intrinsic Grain Boundary Structure and Enhanced Defect States in Air-Sensitive Polycrystalline 1T'-WTe2 Monolayer.

Monolayer WTe2 has attracted significant attention for its unconventional superconductivity and topological edge states. However, its air sensitivity poses challenges for studying intrinsic defect structures. This study addresses this issue using a custom-built inert gas interconnected system, and investigate the intrinsic grain boundary (GB) structures of monolayer polycrystalline 1T' WTe2 grown by nucleation-controlled chemical vapor deposition (CVD) method. These findings reveal that GBs in this system are predominantly governed by W-Te rhombi with saturated coordination, resulting in three specific GB prototypes without dislocation cores. The GBs exhibit anisotropic orientations influenced by kinks formed from these fundamental units, which in turn affect the distribution of grains in various shapes within polycrystalline flakes. Scanning tunneling microscopy/spectroscopy (STM/S) analysis further reveals metallic states along the intrinsic 120° twin grain boundary (TGB), consistent with computed band structures. This systematic exploration of GBs in air-sensitive 1T' WTe2 monolayers provides valuable insights into emerging GB-related phenomena.