3D Assembly Research Articles

Molecular mechanism of contactin 2 homophilic interaction

Contactin 2 (CNTN2) is a cell adhesion molecule involved in axon guidance, neuronal migration, and fasciculation. The ectodomains of CNTN1-CNTN6 are composed of six Ig domains (Ig1-Ig6) and four FN domains. Here, we show that CNTN2 forms transient homophilic interactions (KD ∼200nM). Cryo-EM structures of full-length CNTN2 and CNTN2_Ig1-Ig6 reveal a T-shaped homodimer formed by intertwined, parallel monomers. Unexpectedly, the horseshoe-shaped Ig1-Ig4 headpieces extend their Ig2-Ig3 tips outwards on either side of the homodimer, while Ig4, Ig5, Ig6, and the FN domains form a central stalk. Cross-linking mass spectrometry and cell-based binding assays confirm the 3D assembly of the CNTN2 homodimer. The interface mediating homodimer formation differs between CNTNs, as do the homophilic versus heterophilic interaction mechanisms. The CNTN family thus encodes a versatile molecular platform that supports a very diverse portfolio of protein interactions and that can be leveraged to strategically guide neural circuit development.

V-Doped CoSe2 Nanowire Catalysts in a 3D-Structured Electrode for Durable Li-S Pouch Cells.

Lithium-sulfur (Li-S) batteries have high theoretical energy density and are regarded as a promising candidate for next-generation energy storage systems. However, their practical applications are hindered by the slow kinetics of sulfur conversion and polysulfide shuttling. In particular, large-scale pouch cells show much poor cyclability. Here, we develop a high-efficiency catalyst of V-doped CoSe2 by studying the binary CoSe2-VSe2 system and confirming its effectiveness in accelerating polysulfide conversion. The coin cell tests reveal an initial capacity of 1414 mAh g-1 at 0.1 C and 1049 mAh g-1 at 1 C and demonstrate 1000 times cyclability with a decaying rate of 0.05% per cycle. Furthermore, the assembly and construction of pouch cells were optimized with monolithic three-dimensional (3D) electrodes and a multistacking strategy. Specifically, a 3D metallic scaffold (3MS) was developed to host V-doped CoSe2 nanowires and sulfur. In addition, Janus microspheres of C@TiO2 were synthesized to capture polar polysulfides with their polar part of TiO2 and adsorb nonpolar sulfur with their nonpolar part of carbon. By integrating with 3MS, C@TiO2 microspheres can block all ion channels of 3MS and only allow Li ions in and out. These integral designs and monolithic structures enable multistacking pouch cells with high cyclability. A high-loading pouch cell was demonstrated with a total capacity of 700 mAh. The cell can be cycled for 70 times with a capacity retention of 65.7%. In brief, this work provides an integral strategy of catalyst design and overall 3D assembly for practical Li-S batteries in a large pouch cell format.

3D Multispheroid Assembly Strategies towards Tissue Engineering and Disease Modeling.

Cell spheroids (esp. organoids) as 3D culture platforms are popular models for representing cell-cell and cell-extracellular matrix (ECM) interactions, bridging the gap between 2D cell cultures and natural tissues. 3D cell models with spatially organized multiple cell types are preferred for gaining comprehensive insights into tissue pathophysiology and constructing in vitro tissues and disease models because of the complexities of natural tissues. In recent years, an assembly strategy using cell spheroids (or organoids) as living building blocks has been developed to construct complex 3D tissue models with spatial organization. Here, a comprehensive overview of recent advances in multispheroid assembly studies is provided. The different mechanisms of the multispheroid assembly techniques, i.e., automated directed assembly, noncontact remote assembly, and programmed self-assembly, are introduced. The processing steps, advantages, and technical limitations of the existing methodologies are summarized. Applications of the multispheroid assembly strategies in disease modeling, drug screening, tissue engineering, and organogenesis are reviewed. Finally, this review concludes by emphasizing persistent issues and future perspectives, encouraging researchers to adopt multispheroid assembly techniques for generating advanced 3D cell models that better resemble real tissues.

Origami of multi-layered spaced sheets

Two-dimensional (2D) origami tessellations such as the Miura-ori are often generalized to build three-dimensional (3D) architected materials with sandwich or cellular structures. However, such 3D blocks are densely packed with continuity of the internal material, while for many engineering structures with multi-physical functionality, it is necessary to have thin sheets that are separately spaced and sparsely connected. This work presents a framework for the design and analysis of multi-layered spaced origami, which provides an origami solution for 3D structures where multiple flat sheets are intentionally spaced apart. We connect Miura-ori sheets with sparsely installed thin-sheet parallelogram-like linkages. To explore how this connectivity approach affects the behavior of the origami system, we model the rigid-folding kinematics using analytic trigonometry and rigid-body transformations, and we characterize the elastic-folding mechanics by generalizing a reduced order bar and hinge model for these 3D assemblies. The orientation of the linkages in the multi-layered spaced origami determines which of three folding paths the system will follow including a flat foldable type, a self-locking type, and a double-branch type. When the origami is flat foldable, a maximized packing ratio and a uniform in-plane shear stiffness can be achieved by strategically choosing the link orientation. We show possible applications by demonstrating how the multi-layered spaced origami can be used to build deployable acoustic cloaks and heat shields.

3D Directional Assembly of Liquid Crystal Molecules.

The precise construction of hierarchically long-range ordered structures using molecules as fundamental building blocks can fully harness their anisotropy and potential. However, the 3D, high-precision, and single-step directional assembly of molecules is a long-pending challenge. Here, a 3D directional molecular assembly strategy via femtosecond laser direct writing (FsLDW) is proposed and the feasibility of this approach using liquid crystal (LC) molecules as an illustrative example is demonstrated. The physical mechanism for femtosecond (fs) laser-induced assembly of LC molecules is investigated, and precise 3D arbitrary assembly of LC molecules is achieved by defining the discretized laser scanning pathway. Additionally, an LC-based Fresnel zone plate array with polarization selection and colorization imaging functions is fabricated to further illustrate the potential of this method. This study not only introduces a 3D high-resolution alignment method for LC-based functional devices but also establishes a universal protocol for the precise 3D directional assembly of anisotropic molecules.

Demonstration of a 3D-Assembled Dual-Mode Photodetector Based on Tubular Graphene/III-V Semiconductors Heterostructure and Coplanar Three Electrodes.

3D assembly technology is a cutting-edge methodology for constructing high-performance and multifunctional photodetectors since some attractive photodetection features such as light trapping effect, omnidirectional ability, and high spatial resolution can be introduced. However, there has not been any report of 3D-assembled multimode photodetectors owing to the lack of design and fabrication guideline of electrodes serving for 3D heterostructures. In this study, a 3D-assembled dual-mode photodetector (3DdmPD) was realized successfully via the clever electrical contact between the rolled-up tubular graphene/GaAs/InGaAs heterostructure and planar metal electrode. Arbitrary switching of three coplanar electrodes makes the as-fabricated tubular 3D photodetector work at the unbiased photodiode mode, which is suitable for energy conservation high-speed photodetection, or the biased photoconductive mode, which favors extremely weak light photodetection, fully showing the advantages of multifunctional detection. In more detail, the Ilight/Idark ratio reached as high as 2 × 104, and a responsivity of 42.3 mA/W, a detectivity of 1.5 × 1010 Jones, as well as a rising/falling time (τr/τf) of 360/370 μs were achieved under the self-driven photodiode mode. Excitingly, 3DdmPD shows omnidirectional photodetection ability at the same time. When 3DdmPD works at the photoconductive mode with 5 V bias, its responsivity is extremely high as 7.9 × 104 A/W and corresponding detectivity is increased to 1.0 × 1011 Jones. Benefiting from the totally independent coplanar electrodes, 3DdmPD is much more easily integrated as arrays that are expected to offer the function of high-speed omnidirectional image-sensing with ultralow power consumption than the planar counterparts which share communal bottom electrodes. We believe that our work can contribute to the progress of 3D-assembled optoelectronic devices.

Programmed multimaterial assembly by synergized 3D printing and freeform laser induction

In nature, structural and functional materials often form programmed three-dimensional (3D) assembly to perform daily functions, inspiring researchers to engineer multifunctional 3D structures. Despite much progress, a general method to fabricate and assemble a broad range of materials into functional 3D objects remains limited. Herein, to bridge the gap, we demonstrate a freeform multimaterial assembly process (FMAP) by integrating 3D printing (fused filament fabrication (FFF), direct ink writing (DIW)) with freeform laser induction (FLI). 3D printing performs the 3D structural material assembly, while FLI fabricates the functional materials in predesigned 3D space by synergistic, programmed control. This paper showcases the versatility of FMAP in spatially fabricating various types of functional materials (metals, semiconductors) within 3D structures for applications in crossbar circuits for LED display, a strain sensor for multifunctional springs and haptic manipulators, a UV sensor, a 3D electromagnet as a magnetic encoder, capacitive sensors for human machine interface, and an integrated microfluidic reactor with a built-in Joule heater for nanomaterial synthesis. This success underscores the potential of FMAP to redefine 3D printing and FLI for programmed multimaterial assembly.

Symmetry-Breaking of Nanoparticle Surface Function Via Conformal DNA Design.

Asymmetric surface functionalization of complex nanoparticles to control their directional self-assembly remains a considerable challenge. Here, we demonstrated a conformal DNA design strategy for flexible remodeling of the surface of complex nanoparticles, taking Au nanobipyramids (AuNBPs) as a model. We sheathed one or both tips of AuNBPs into conformal DNA origami with an exceptionally accurate orientation control. Such asymmetrically and symmetrically distributed surface patches possess regioselective, sequence, and site-specific DNA binding capabilities. As a result, we realized a series of prototypical multicomponent "colloidal molecules" made of AuNBPs and Au nanospheres (AuNSs) with defined directionality and number of "bonding valence" as well as 1D and 3D hierarchical assemblies, e.g., inverse core-satellites of AuNBPs and AuNSs, side-by-side and tip-to-tip linear assemblies of AuNBPs, and 3D helical superstructures of AuNBPs with tunable twists. These findings inspire new opportunities for nanoparticle surface engineering and the high-order self-assembly of nanoarchitectures with higher complexity and broadened functionalities.

Morphology engineering and electronic structure remodeling of manganese-incorporated VN for boosting urea-assisted energy-saving hydrogen production

Urea-assisted water electrolysis offers a promising route to reduce energy consumption for hydrogen production and meanwhile treat urea-rich wastewater. Herein, we devised a shear force-involved polyoxometalate-organic supramolecular self-assembly strategy to fabricate 3D hierarchical porous nanoribbon assembly Mn-VN cardoons. A bimetallic polyoxovanadate (POV) with the inherent structural feature of Mn surrounded by [VO6] octahedrons was introduced to trigger precise Mn incorporation in VN lattice, thereby achieving simultaneous morphology engineering and electronic structure modulation. The lattice contraction of VN caused by Mn incorporation drives electron redistribution. The unique hierarchical architecture with modulated electronic structure that provides more exposed active sites, facilitates mass and charge transfer, and optimizes the associated adsorption behavior. Mn-VN exhibits excellent activity with low overpotentials of 86 mV and 1.346 V at 10 mA/cm2 for hydrogen evolution reaction (HER) and urea oxidation reaction (UOR), respectively. Accordingly, in the two-electrode urea-assisted water electrolyzer utilizing Mn-VN as a bifunctional catalyst, hydrogen production can occur at low voltage (1.456 V@10 mA/cm2), which has the advantages of energy saving and competitive durability over traditional water electrolysis. This work provides a simple and mild route to construct nanostructures and modulate electronic structure for designing high-efficiency electrocatalysts.

Perylenediimide‐Derived Nonmacrocyclic Host–Guest Donor–Acceptor Assemblies for Long‐Wavelength Emissions and Low‐Threshold Microlasers

AbstractMacrocyclic hosts can bind appropriate guests in endo‐cavity or exo‐wall modes to yield Host–Guest cocrystals via weak intermolecular forces. Contrary, it remains challenging to achieve their nonmacrocyclic partners with high‐efficiency fluorescence even lasing due to profound adaptive behaviors during guest inclusion. Here, a variety of low dispersity 1D and 2D assemblies made of a sterically demanding perylenediimide derivative (PDI) host and diverse aromatic guests are realized. Depending on the types and the substituted groups of aromatic guests, these Host–Guest microcrystals show high‐efficiency solid‐state emissions ranging from orange to near‐infrared (NIR). Interestingly, either electron‐deficient or electron‐rich guests can adapt to the cavity of the nonmacrocyclic PDI host in diverse geometries and orientations. Theoretical analysis indicates that the long‐wavelength emissions stem from local or charge‐transfer excited states and the Host–Guest Donor–Acceptor cocrystals are stabilized largely by dispersion forces. The binding of appropriate π‐electron guests makes the PDI‐derived Host–Guest microcrystals function as microscale lasers with low lasing thresholds. The rational creation of these nonmacrocyclic Host–Guest Donor–Acceptor cocrystals offers new insights for developing new crystal structures and high‐efficiency optoelectronic devices.

Research on the design and application of 3D scene animation game entertainment system based on user motion sensing participation

Developed a 3D indoor virtual scene assembly system based on dual touch screen. The system adopts a combination of 2D views and 3D views. The 2D and 3D views are displayed on the two touch screens. We have comprehensively designed various interactive operations of 2D view and 3D view from the perspectives of simplicity, easy learning and easy to use, and reduced the complex 3D interactive operations to 2D interactive operations. Users can conduct two-dimensional interactive operation and 3D interactive operation based on two display screens, which can realize the efficient assembly of 3D virtual scene. The results indicate significant differences in the number of modifications of mode A and B (t = 2.982, p = 0.006 < 0.01), effective design time (t = 4.990, p < 0.001), first design satisfaction (t = 5.074, p = <0.001) and final design satisfaction (t = 2.787, p = 0.010 < 0.05). Participants in mode A had fewer modifications and shorter effective design times compared to mode B. Study and design a new workbench supporting the collaborative design of 3D virtual scenes. The workbench can support a three-dimensional indoor virtual scene assembly system based on dual touch screen, and designers and users can assemble the virtual scene together. The workbench mainly consists of two touch displays and a holographic display device. The holographic display device displays the three-dimensional scene designed by the user in real time, and supports the designer and the user to operate the three-dimensional scene through the touch film attached to it. Touch display enables designers and users to assemble scenes on 2D views through simple touch operations such as drag and drop. The face-to-face collaborative design method provided by the workbench is more conducive to the communication between designers and users, so as to improve the design efficiency of 3D scenes.

La-doped CeO2/rGO hybrid with high oxygen vacancy to enhance phosphorus adsorption by capacitive deionization

Cerium oxide is one of the most attractive electrode materials in capacitive deionization (CDI) technology for selective phosphate adsorption due to the specific interaction. However, Ce3+/Ce4+ ratio and material conductivity of cerium oxide electrode determine the adsorption performance. Herein, a dual strategy was exploited with polyol-solvothermal reaction in the presence of graphite oxide and cerium salt followed by hydrothermal La-doping to obtain the three-dimensional (3D) assembly of La-doped CeO2 at the reduced graphene oxide (La-CeO2/rGO). The as-prepared La-CeO2/rGO hybrid exhibited interconnected structure with CeO2 uniformly distributed on the rGO support. La3+, by partially replacing Ce4+ in the lattice, was evenly fused into CeO2 nanosphere, enhancing the content of Ce3+ and oxygen vacancies and inhibiting lattice distortion. As a CDI positive electrode, the La0.15-CeO2/rGO with optimal La doping achieved the maximum theoretical adsorption capacity of 118.7 mg P/g with high separation factor (αSO42-P = 13.9), superior to the CeO2/rGO (67.8 mg P/g, αSO42-P = 10.1). In addition, the La-CeO2/rGO electrode is extremely robust, with excellent adsorption performance in wide pH range and good regeneration ability, compared to CeO2/rGO. This work proves that the synergy of trace La doping and 3D rGO support effectively improves the adsorption performance of La-CeO2/rGO electrodes and enhances the cycling stability of CDI devices. The corresponding adsorption mechanism was demonstrated.

Functional Requirements and Design Features for the Implementation of 3D CAD-Based Graphical Interactive Configurators

Configuring complex computer-aided design (CAD) assemblies just by modifying parameters requires the attention and abstraction of the users. This interaction cost can be lowered significantly by graphical interactive control elements that allow for drag and drop modifications directly in the 3D assembly. Contributing techniques, such as working with skeletons and advanced or external knowledge-based parameter control, are available. This contribution examines their integration and implementation into a given CAD system through a case study on creating a pipe routing configuration system which uses drag points to adjust the position of instrumentation and routing segments. The results are then generalized to functional requirements and basic design features of such graphical interactive configurators.

A concrete answer for circular construction: three prototypes reusing saw-cut elements

Existing concrete buildings should be retained for as long as possible to reduce the environmental burden of demolition and new construction. However, when urban pressure makes demolition unavoidable, salvaging and reusing concrete elements elsewhere in new structures, rather than reducing them to rubble, efficiently prolongs the use of existing resources at their highest structural value. Concrete reuse is not a new approach: pioneer cases have demonstrated its potential, but broader adoption has still not been seen across the wider industry. Three prototypes recently built by Ecole Polytechnique Fédérale de Lausanne researchers and students in Switzerland demonstrate the feasibility and potential of reusing elements saw-cut from cast in situ concrete structures. The prototypes deal with different scales of elements, from small blocks to large slab elements and 3D assemblies. Lifecycle assessments confirm that reusing concrete elements drastically reduces the upfront global warming potential of new construction, providing a new lower-bound benchmark for sustainable, circular construction.

3D and 4D assembly of functional structures using shape-morphing materials for biological applications.

3D structures are crucial to biological function in the human body, driving interest in their in vitro fabrication. Advances in shape-morphing materials allow the assembly of 3D functional materials with the ability to modulate the architecture, flexibility, functionality, and other properties of the final product that suit the desired application. The principles of these techniques correspond to the principles of origami and kirigami, which enable the transformation of planar materials into 3D structures by folding, cutting, and twisting the 2D structure. In these approaches, materials responding to a certain stimulus will be used to manufacture a preliminary structure. Upon applying the stimuli, the architecture changes, which could be considered the fourth dimension in the manufacturing process. Here, we briefly summarize manufacturing techniques, such as lithography and 3D printing, that can be used in fabricating complex structures based on the aforementioned principles. We then discuss the common architectures that have been developed using these methods, which include but are not limited to gripping, rolling, and folding structures. Then, we describe the biomedical applications of these structures, such as sensors, scaffolds, and minimally invasive medical devices. Finally, we discuss challenges and future directions in using shape-morphing materials to develop biomimetic and bioinspired designs.

3D hierarchic interfacial assembly of Au nanocage@Au along with IS-AgMNPs for simultaneous, ultrasensitive, reliable, and quantitative SERS detection of colorectal cancer related miRNAs

Simultaneous, reliable, and ultra-sensitive analysis of promising miRNA biomarkers of colorectal cancer (CRC) in serum is critical for early diagnosis and prognosis of CRC. In this work, we proposed a novel 3D hierarchic assembly clusters-based SERS strategy with dual enrichment and enhancement designed for the ultrasensitive and quantitative analysis of two upregulated CRC-related miRNAs (miR-21 and miR-31). The biosensor contains the following: (1) SERS probe, Au nanocage@Au nanoparticles (AuNC@Au NPs) labeled with Raman reporters (RaRs). (2) magnetic capture unit, Ag-coated Fe3O4 magnetic nanoparticles (AgMNPs) modified with internal standard (IS). (3) signal amplify probes (SA probes) for the formation of hierarchic assembly clusters. Based on this sensing strategy, the intensity ratio IRaRs/IIS with Lg miRNAs presents a wide linear range (10 aM–100 pM) with a limit of detection of 3.46 aM for miR-21, 6.49 aM for miR-31, respectively. Moreover, the biosensor shows good specificity and anti-interference ability, and the reliability and repeatability of the strategy were then verified by practical detection of clinical serum. Finally, the biosensor can distinguish CRC cancer subjects from normal ones and guide the distinct tumor, lymph node, and metastasis (TNM) stages. Overall, benefiting from the face-to-face coupling of hierarchic assembly clusters, rapid magnetic enrichment and IS signal calibration of AgMNPs, the established biosensor achieves ultra-sensitive and simultaneous detection of dual miRNAs and opens potential avenues for prediction and staging of CRC.

INTEGRATION OF 3D SPATIAL INFORMATION FOR MULTI-MODAL EXPERIENCE OF THE URBAN ARCHIVE

Abstract. This paper focused on the case of Semal Village, the region that will be demolished due to undergoing recent redevelopment in Paju. We experimented utilizing 3D spatial information to capture precise urban morphology of present status before redevelopment and to transform such data into multi-modal experience of the urban archive. We investigated feasible techniques of photogrammetry and hybrid 3D modelling that could render the situated reality of the village communicatively with various medium such as 3D-printed scale model, and augmented reality (AR) contents. Through drone photography, the entire Semal village was captured, and three-dimensional data were obtained using photogrammetry. Along with information from on-site surveys, the mesh model was segmented into buildings, terrain, and vegetation for focused work. Each models reconstructed and retextured using images from the on-site surveys. All data were compiled for full-colour 3D printing and assembly. The 3D-printed scale model replicating Semal is on display at the Paju Central Library. Additionally, an AR content was created using the 3D-printed scale model and ethnographic data, aiming to archive and share people's memories, thereby continuously building a sustainable archive of the village.

Seed‐Induced Living Two‐Dimensional (2D) Supramolecular Polymerization in Water: Implications on Protein Adsorption and Enzyme Inhibition

AbstractIn biological systems, programmable supramolecular frameworks characterized by coordinated directional non‐covalent interactions are widespread. However, only a small number of reports involve pure water‐based dynamic supramolecular assembly of artificial π‐amphiphiles, primarily due to the formidable challenge of counteracting the strong hydrophobic dominance of the π‐surface in water, leading to undesired kinetic traps. This study reveals the pathway complexity in hydrogen‐bonding‐mediated supramolecular polymerization of an amide‐functionalized naphthalene monoimide (NMI) building block with a hydrophilic oligo‐oxyethylene (OE) wedge. O‐NMI‐2 initially produced entropically driven, collapsed spherical particles in water (Agg‐1); however, over a span of 72 h, these metastable Agg‐1 gradually transformed into two‐dimensional (2D) nanosheets (Agg‐2), favoured by both entropy and enthalpy contributions. The intricate self‐assembly pathways in O‐NMI‐2 enable us to explore seed‐induced living supramolecular polymerization (LSP) in water for controlled synthesis of monolayered 2D assemblies. Furthermore, we demonstrated the nonspecific surface adsorption of a model enzyme, serine protease α‐Chymotrypsin (α‐ChT), and consequently the enzyme activity, which could be regulated by controlling the morphological transformation of O‐NMI‐2 from Agg‐1 to Agg‐2. We delve into the thermodynamic aspects of such shape‐dependent protein‐surface interactions and unravel the impact of seed‐induced LSP on temporally controlling the catalytic activity of α‐ChT.

Seed-Induced Living Two-Dimensional (2D) Supramolecular Polymerization in Water: Implications on Protein Adsorption and Enzyme Inhibition.

In biological systems, programmable supramolecular frameworks characterized by coordinated directional non-covalent interactions are widespread. However, only a small number of reports involve pure water-based dynamic supramolecular assembly of artificial π-amphiphiles, primarily due to the formidable challenge of counteracting the strong hydrophobic dominance of the π-surface in water, leading to undesired kinetic traps. This study reveals the pathway complexity in hydrogen-bonding-mediated supramolecular polymerization of an amide-functionalized naphthalene monoimide (NMI) building block with a hydrophilic oligo-oxyethylene (OE) wedge. O-NMI-2 initially produced entropically driven, collapsed spherical particles in water (Agg-1); however, over a span of 72 h, these metastable Agg-1 gradually transformed into two-dimensional (2D) nanosheets (Agg-2), favoured by both entropy and enthalpy contributions. The intricate self-assembly pathways in O-NMI-2 enable us to explore seed-induced living supramolecular polymerization (LSP) in water for controlled synthesis of monolayered 2D assemblies. Furthermore, we demonstrated the nonspecific surface adsorption of a model enzyme, serine protease α-Chymotrypsin (α-ChT), and consequently the enzyme activity, which could be regulated by controlling the morphological transformation of O-NMI-2 from Agg-1 to Agg-2. We delve into the thermodynamic aspects of such shape-dependent protein-surface interactions and unravel the impact of seed-induced LSP on temporally controlling the catalytic activity of α-ChT.

Single-Gate MoS2 Tunnel FET with a Thickness-Modulated Homojunction.

Two-dimensional (2D) materials stand as a promising platform for tunnel field-effect transistors (TFETs) in the pursuit of low-power electronics for the Internet of Things era. This promise arises from their dangling bond-free van der Waals heterointerface. Nevertheless, the attainment of high device performance is markedly impeded by the requirement of precise control over the 2D assembly with multiple stacks of different layers. In this study, we addressed a thickness-modulated n/p+-homojunction prepared from Nb-doped p+-MoS2 crystal, where the issue on interface traps can be neglected without any external interface control due to the homojunction. Notably, our observations reveal the existence of a negative differential resistance, even at room temperature (RT). This signifies the successful realization of TFET operation under type III band alignment conditions by a single gate at RT, suggesting that the dominant current mechanism is band-to-band tunneling due to the ideal interface.