Structural Symmetry Research Articles

Hund’s three rules in actinide-containing superatoms with spin-orbit coupling calculations

The intriguing and challenge issue in magnetic superatoms is searching for the suitable candidates to validate the Hund’s rules. Here, early actinide elements (An: Ac, Th, Pa, U, Np, Pu, Am) whose 5f electrons may crossover the localization and delocalization characteristics have been chosen to alloy with Al atoms in designing magnetic An@Al12 superatoms. By doing the global minimum structure search and the spin-orbital coupling density functional theory calculations, we provide an original idea to give theoretical argument that Hund’s three rules are still applicable in superatoms, which can be related to the fillings of highly localized An-5f orbitals into large exchange-splitting 2 F superatom orbitals. Specifically, selective 5f sub-orbitals of several An dopants can exhibit a dual nature in superatomic bonding, i.e. partial 5f electrons of Pa, U and Pu are reactive whereas all 5f electrons of Np and Am are highly localized. The molecular orbital analyses, combined with the qualitative interpretation of the phenomenological superatom sub-shell model, address the intricate interplays between the structure symmetry, electronic structure, spin and orbital magnetic moments. These findings have important implications for understanding the bonding and magnetic behaviors of An-containing superatoms and pave the way for designing novel magnetic superatoms.

Analysis of pressure pulsation in a multi-stage double suction centrifugal pump

Abstract Pressure pulsation is a common phenomenon, which results from different causes. The intenser pressure pulsation occurs in the pump, the severer the damage to the pump. In the paper, with the assistance of detached eddy simulation method, the characteristic of pressure pulsation in the multi-stage double suction centrifugal pump is studied to understanding the internal flow circumstance. The results reveal that the pressure pulsation intensity reaches the maximum at blade trailing edge, which propagates to the tongue region of forward flow channel and double-volute under the low rates. Furthermore, it can be concluded that the pressure pulsation of region with obvious rotor–stator interaction between rotating impeller and stationary volute is generally larger at low flow rates. The pressure pulsation near the suction side of blade trailing edge shows the feature of broadband frequency and with increasing flow rate the bandwidth of broadband decreases drops rapidly except BP1. Due to the influence of the number of impeller blades, the dominant frequency of monitoring points in the inter-stage flow channel and the volute is basically located at a frequency that is twice the blade frequency. Meanwhile, because of the symmetry of the geometric structure of the reverse flow channel, the pressure pulsation curve changes of its internal monitoring points are similar under the same flow rate.

2D perovskite Ca2Nb3O10 nanosheet featuring Berry curvature dipole and canted persistent spin texture reversible with in-plane ferroelectricity

Two-dimensional materials can result in rich and unique electronic features through symmetry breaking. A wide band gap 2D perovskite Ca2Nb3O10 (CNO) nanosheet is investigated for exotic electronic or spin-related properties using state-of-the-art first-principles calculations. The CNO nanosheet exhibits spontaneous in-plane ferroelectric polarization confined in the y direction owing to the low symmetry of the crystal structure. A canted persistent spin texture (PST) can be observed in spin-split bands, which depict a unidirectional spin configuration tilted along the yz-plane. A correlation between the canted PST and ferroelectricity has been found, as in-plane ferroelectric switching can successfully reverse the typical PST. The nonvanishing Berry curvature dipole (BCD) resulting from the interplay of spin–orbit coupling (SOC) and inversion symmetry breaking is also reversible with in-plane ferroelectric polarization. Therefore, the possibility of fully electrically adjustable canted PST and BCD in a 2D perovskite CNO nanosheet provides a pathway toward creating affordable, non-volatile spintronic devices.

Трансцендентные измерения танцевальной античной культуры

The article presents a study of sacred dances in ancient culture. The origins of dance and their connection with the mysteries are considered. The approach to dance as a language born in the infancy of mankind and closely related to myth allows identifying the semantic units of dance which express the mythological foundations of the creation of the universe and the birth of order from chaos. The procedure of understanding mythological meanings is based on the identification of symmetry structures. The authors of the article analyse the forms of dance compositions as systems of non‐verbal semantic constructs and study the image of the Labyrinth in the choreographic ancient tradition as a symbol of mastering and accumulating experience with subsequent transformation and comprehension of a new development stage of the soul.

Low-frequency broadband valley transport for acoustic topology based on extended resonance

This paper proposes an extended resonant structure to solve the problem that topological acoustic waveguides have a narrow bandwidth at low frequencies. This acoustic structure consists of a two-dimensional structure and a resonant cavity in the three-dimensional direction, and its essence is to extend the resonant cavity in the two-dimensional structure to the three-dimensional direction. The problem that the size of the resonant cavity is limited by the size of the two-dimensional structure can be solved by this special extension. At the same time, the resonant cavity can be maximized in the three-dimensional direction. The topological properties of the original structure are not affected as long as the radius of the resonant cavity is widened without changing the symmetry of the overall composite structure. The rotating scatterer remains a reliable method for realizing topological phase transitions. The effect of the resonant cavity length on the band position is obtained using the finite element method, and it is demonstrated that the topological acoustic waveguide has a wide operating band at low frequencies. Simulation results show that this structure still has a bandgap width of 100 Hz at a low frequency of 350 Hz. The topological acoustic waveguide structure proposed in this paper can provide a new idea for the study of low-frequency broadband acoustic topology, which promotes the control of low-frequency acoustic waves by the topological acoustic waveguide.

Executive Function and Spatial Skills in Children’s Block Play: A Cross-Cultural Comparison

ABSTRACT Research Findings: There are sparse data on children’s use of executive function (EF) and spatial skills in block play. However, there are important implications for studying EF and spatial skills with blocks across cultures, especially regarding best practices for supporting social-cognitive development in under-resourced populations and consideration of culturally unique customs and practices. Therefore, the current study compared EF-based skills and spatial block building behaviors in Canadian and Tzotzil Maya children. Participants included 82 preschoolers (55% Canadian) ages 48–59 months (M age = 54.37 months, SD = 3.37) observed and coded during a group block play session with peers. Controlling for demographic covariates, a composite EF-based variable including six behaviors (intentional selection of blocks, taking time, response inhibition, replacing/moving blocks, stabilizing, aligning) was significantly and positively associated with spatial configurations in block structures (symmetry, β = .34; tiered orientation, β = .37) The associations did not vary by culture. Practice or Policy: Results provide new knowledge about use of EF-based skills and spatial skills in an ecologically valid context and implications for cross-cultural measurement and practice.

<em>Spiderwoman/ mujer araña</em>: N-N compounds and structural symmetry. A view from bilingual heritage speakers.

This paper tests the hypothesis that N-N combinations (N-N word compounds and phrasal compounds) share a common underlying structural symmetry that needs to be dissolved through movement of one of the nouns. Certain types of N-N combinations are in complementary distribution in Spanish and English: N-N compounds are more productive in English, N-preposition-N compounds more productive in Spanish, and certain N-N compounds with the meaning of coordination of the nouns are possible in both languages. Bilingual heritage speakers of Spanish with English as the majority language have access to the English-type N-N compound, the Spanish-type NPN phrasal compound and the coordinated N-N type in both languages. Assuming that all three types start out as symmetric mergers of two nouns, we test whether bilinguals will prefer one of the symmetry-breaking strategies by using an acceptability judgement task. First, we found a certain degree of cross-linguistic influence in the higher acceptance of N-N compounds in Spanish vs. English. Second, participants preferred structures that have P (de), which we interpreted as the most salient strategy to break the N-N symmetry. We conclude that symmetry-breaking is a highly ranked preference for bilinguals as a result of having two active grammars.

Spectroscopic Investigations of Complex Electronic Interactions by Elemental Doping and Material Compositing of Cobalt Oxide for Enhanced Oxygen Evolution Reaction Activity

AbstractDoping and compositing are two universal design strategies used to engineer the electronic state of a material and mitigate its disadvantages. These two strategies are extensively applied to design efficient electrocatalysts for water splitting. Using cobalt oxide (CoO) as a model catalyst, it is proven that the oxygen evolution reaction (OER) performance can be progressively improved, first by Fe‐doping to form Fe‐CoO solid solution, and further by the addition of CeO2 to produce a Fe‐CoO/CeO2 composite. X‐ray absorption spectroscopy (XAS) reveals that distinct electronic interactions are induced by the processes of doping and compositing. Fe‐doping of CoO can break down the structural symmetry, changing the electronic structure of both Co and O species at the surface and decreasing the flat‐band potential (Vfb). In comparison, subsequent compositing of Fe‐CoO with CeO2 induces negligible electronic changes in the Fe‐CoO (as seen in ex situ characterizations), but significantly modifies the oxidative transformations of both Co and Fe under OER conditions. The spectroscopic investigations reveal that Fe‐doping and CeO2 compositing play different roles in modifying the electronic properties of CoO in its pristine state and during OER catalysis, in return, providing useful guidance for the design of more efficient electrocatalysts using these two strategies.

Ultrasonication-assisted synthesis of transition metal carbide of MXene: an efficient and promising material for photocatalytic organic dyes degradation of rhodamine B and methylene blue in wastewater.

Water pollutants of non-biodegradable toxic aromatic dye including Methylene blue (MB) and Rhodamine (RhB) are extremely carcinogenic thiazines used in various industries such asleather industry, paper industry, and the dyeing industry. The presence of dyes in wastewater causes severe threats to human health that are responsible for various harmful chronic or acute diseases and also shows an adverse impact on the environment as it reduces transparency and is harmful to water microorganisms. To overcome severe issues, many traditional techniques have been used to remove toxic pollutants, but thesemethods are insufficient to remove chemically stable dyes that remain in the treated wastewater. However, the photocatalytic degradation process is an efficient approach to degrade the dye up to the maximum extent with improved efficiency. Therefore, in this work, a new class of two-dimensional (2D) transition metal carbide of Titanium Carbide (Ti3C2Tx) MXene material was used for the organic dyes degradation such as MB and RhB using a photocatalytic process. A layered structure of hexagonal lattice symmetry of Ti3C2Tx MXene was successfully synthesized from the Titanium Aluminum Carbide ofTi3AlC2 bulk phase using an exfoliation process. Further, the XRD spectrum confirms the transformation of bulk MAX phase having (002) plane at 9.2° to Ti3C2Tx MXene of (002) plane at 8.88° confirms the successful removal of Al layer from MAX phase. A smooth, transparent, thin sheet-like morphology of Ti3C2Txnanosheet sizewere found to be in the range of 70 to 150nm evaluated fromTEM images. Also,no holes or damages in the thin sheets were foundafter the treatment with strong hydrofluoric acid confirms the formationTi3C2Tx layered sheets. The synthesized Ti3C2Tx MXene possesses excellent photocatalytic activity for the degradation of dyes MB, RhB, and mixtures of MB and RhB dyes. MB dye degraded with a degradation percentage efficiency of 99.32% in 30min, while RhB dye was degraded upto98.9% in 30min. Also, experiments were conducted for degradation ofmixture of MB and RhB dyes by UV light, and the degradationpercentage efficiency were found to be 98.9% and 99.75% for mixture of MB and RhB dyein 45min, respectively. Moreover, reaction rate constant (k) was determined for each dye of MB, RhB, and mixtures of MB and RhB and was found to be 0.0215min-1 and 0.0058min-1, and for mixtures, it was 0.0020min-1 and 0.009min-1, respectively.

Enhancing Built-in Electric Fields via Molecular Symmetry Modulation in Supramolecular Photocatalysts for Highly Efficient Photocatalytic Hydrogen Evolution.

Nature-inspired supramolecular self-assemblies are attractive photocatalysts, but their quantum yields are limited by poor charge separation and transportation. A promising strategy for efficient charge transfer is to enhance the built-in electric field by symmetry breaking. Herein, an unsymmetric protonation, N-heterocyclic π-conjugated anthrazoline-based supramolecular photocatalyst SA-DADK-H+ was developed. The unsymmetric protonation breaks the initial structural symmetry of DADK, resulting in ca. 50-fold increase in the molecular dipole, and facilitates efficient charge separation and transfer within SA-DADK-H+. The protonation process also creates numerous active sites for H2O adsorption, and serves as crucial proton relays, significantly improving the photocatalytic efficiency. Remarkably, SA-DADK-H+ exhibits an outstanding hydrogen evolution rate of 278.2 mmol g-1 h-1 and a remarkable apparent quantum efficiency of 25.1 % at 450 nm, placing it among the state-of-the-art performances in organic semiconductor photocatalysts. Furthermore, the versatility of the unsymmetric protonation approach has been successfully applied to four other photocatalysts, enhancing their photocatalytic performance by 39 to 533 times. These findings highlight the considerable potential of unsymmetric protonation induced symmetry breaking strategy in tailoring supramolecular photocatalysts for efficient solar-to-fuel production.

Enhancing Built‐in Electric Fields via Molecular Symmetry Modulation in Supramolecular Photocatalysts for Highly Efficient Photocatalytic Hydrogen Evolution

AbstractNature‐inspired supramolecular self‐assemblies are attractive photocatalysts, but their quantum yields are limited by poor charge separation and transportation. A promising strategy for efficient charge transfer is to enhance the built‐in electric field by symmetry breaking. Herein, an unsymmetric protonation, N‐heterocyclic π‐conjugated anthrazoline‐based supramolecular photocatalyst SA‐DADK‐H+ was developed. The unsymmetric protonation breaks the initial structural symmetry of DADK, resulting in ca. 50‐fold increase in the molecular dipole, and facilitates efficient charge separation and transfer within SA‐DADK‐H+. The protonation process also creates numerous active sites for H2O adsorption, and serves as crucial proton relays, significantly improving the photocatalytic efficiency. Remarkably, SA‐DADK‐H+ exhibits an outstanding hydrogen evolution rate of 278.2 mmol g−1 h−1 and a remarkable apparent quantum efficiency of 25.1 % at 450 nm, placing it among the state‐of‐the‐art performances in organic semiconductor photocatalysts. Furthermore, the versatility of the unsymmetric protonation approach has been successfully applied to four other photocatalysts, enhancing their photocatalytic performance by 39 to 533 times. These findings highlight the considerable potential of unsymmetric protonation induced symmetry breaking strategy in tailoring supramolecular photocatalysts for efficient solar‐to‐fuel production.

Tuning the electronic and magnetic properties of MoS2 bilayers by transition-metal intercalation

Two dimensional (2D) transition-metal dichalcogenides and their heterostructures are important materials for future electronic device applications. By using the first-principles calculations we investigate how the electronic and magnetic properties of MoS2 bilayer is modified by intercalating transition-metals (Fe, Co, and Ni). The Fe-intercalated MoS2 bilayer is found to be a non-magnetic gapless semimetal. Without spin–orbit coupling it has the Dirac state on the Γ-M line in k space at the Fermi level. The spin degeneracy of the Dirac state is removed by spin–orbit coupling. However, the bottom of the conduction band and the top of the valence band are in contact with the Fermi level making the system a non-magnetic gapless semimetal. The Dirac state is also observed in both Co-intercalated and Ni-intercalated MoS2 bilayers because they have the same symmetry in crystal structure as the Fe-intercalated MoS2 bilayer. The difference in the number of valence electrons in the intercalated atoms drastically change the electronic and magnetic properties. The Co-intercalated MoS2 bilayer is a ferromagnetic metal, where the Dirac state is below the Fermi level. The Ni-intercalated MoS2 bilayer is a non-magnetic narrow gap semiconductor, where the Dirac state is far below the Fermi level. The results revealed the electronic and magnetic properties of the transition-metal-intercalated MoS2 bilayers and will be useful for designing a variety of 2D materials.

Symmetrical structure design of PLGA Biodegradable sinus stents and structure optimization based on surrogate models.

This study aims to enhance the degradation uniformity of PLGA sinus stents to minimize fracture risk caused by stress corrosion. Symmetric stent structures were introduced and compared to sinusoidal structure in terms of stress and degradation uniformity during implantation and degradation processes. Three surrogate models were employed to optimize the honeycomb-like structure. Results showed honeycomb-like structures exhibited the superior stress distribution and highest degradation uniformity. The kriging model achieved the smallest error and degradation uniformity of 83.24%. In conclusion, enhancing the symmetry of stent structures improves degradation uniformity, and the kriging model has potential for the optimization of stent structures.

Enhanced Electron Delocalization Induced by Ferromagnetic Sulfur doped C 3 N 4 Triggers Selective H 2 O 2 Production

For the 2D metal‐free carbon catalysts, the atomic coplanar architecture enables a large number of pz orbitals to overlap laterally, thus forming π‐electron delocalization, and the delocalization degree of the central atom dominates the catalytic activity. Herein, designing sulfur‐doped defect‐rich graphitic carbon nitride (S‐Nv‐C3N4) materials as a model, we propose a strategy to promote localized electron polarization by enhancing the ferromagnetism of ultra‐thin 2D carbon nitride nanosheets. The introduction of sulfur (S) further promotes localized ferromagnetic coupling, thereby inducing long‐range ferromagnetic ordering and accelerating the electron interface transport. Meanwhile, the hybridization of sulfur atoms breaks the symmetry and integrity of the unit structure, promotes electron enrichment and stimulating electron delocalization at the active site. This optimization enhances the *OOH desorption, providing a favorable kinetic pathway for the production of hydrogen peroxide (H2O2). Consequently, S‐Nv‐C3N4 exhibits high selectivity (>95%) and achieves a superb H2O2 production rate, approaching 4374.8 ppm during continuous electrolysis over 300‐hour. According to theoretical calculation and in‐situ spectroscopy, the ortho‐S configuration can provide ferromagnetic perturbation in carbon active centers, leading to the electron delocalization, which optimizes the OOH* adsorption during the catalytic process.

Structural Regulations of Layered Borates: From Centric Layers to Chiral Porous Layers.

Three pentaborates were made by precise structural regulations under hydrothermal conditions, namely, K2Cs[B5O8(OH)]·0.5CO3 (1), KNa4Cs[B5O8(OH)]2·2OH (2), and NaBa[B5O8.5(OH)] (3). Compound 1 features the typical 2D layers constructed from the four-connected B5O10(OH) clusters. By adjustment of the reactants and pH values of the systems to remove interlayered CO3 2- groups, the centric layers in 1 were transformed to the chiral layers of 2. By further adjusting cationic templates based on host-guest charge matching, the B5O10(OH) cluster unit was transformed to B5O11(OH), which built the chiral porous layers of 3. The chiral compounds 2 and 3 exhibit moderate second harmonic generation (SHG) responses of 1.1 and 1.7 times that of KDP (KH2PO4). The structural regulations actualize the evolutions on both structural symmetries and dimensions.

Oxidation behavior and atomic structural transition of size-selected coalescence-resistant tantalum nanoclusters

Herein a series of size-selected Ta N (N = 147, 309, 561, 923, 1415, 2057, 6525, 10 000, 20 000) clusters are generated using a gas-phase condensation cluster beam source equipped with a lateral time-of-flight mass-selector. Aberration-corrected scanning transmission electron microscopy (AC-STEM) imaging reveals good thermal stability of Ta N clusters in this study. The oxidation-induced amorphization is observed from AC-STEM imaging and further demonstrated through x-ray photoelectron spectroscopy and energy-dispersive spectroscopy. The oxidized Ta predominantly exists in the +5 oxidation state and the maximum spontaneous oxidation depth of the Ta cluster is observed to be 5 nm under prolonged atmosphere exposure. Furthermore, the size-dependent sintering and crystallization processes of oxidized Ta N clusters are observed with an in situ heating technique, and eventually, ordered structures are restored. As the temperature reaches 1300 °C, a fraction of oxidized Ta309 clusters exhibit decahedral and icosahedral structures. However, the five-fold symmetry structures are absent in larger clusters, instead, these clusters exhibit ordered structures resembling those of the crystalline Ta2O5 films. Notably, the sintering and crystallization process occurs at temperatures significantly lower than the melting point of Ta and Ta2O5, and the ordered structures resulting from annealing remain well-preserved after six months of exposure to ambient conditions.

Ultra-high Q-factor quasi-BIC BaTiO3 metasurface for electro-optic modulation

Metasurfaces play a crucial role in trapping electromagnetic waves with specific wavelengths, serving as a significant platform for enhancing light–matter interactions. In all kinds of dynamic modulation metasurfaces, electro-optic modulation metasurfaces have attracted much attention due to its advantages of fast, stable and high efficiency. In order to respond to the extremely weak refractive index change of the electro-optical effect of the materials, the metasurfaces are required to support optical signals with high Q values. The quasi-bound state in the continuum (Q-BIC) is often used to enhance the light-field modulation capability of metasurfaces and to improve the modulation sensitivity of electro-optic modulators due to its ability to generate high Q-factor resonances. However, the design of an electro-optic modulation metasurface that facilitates the application of voltage and achieves modulation efficiency of nearly 100% is still in urgent need of development. In this study, single-crystal BTO metasurfaces are modeled using finite-difference time-domain method, and the structural symmetry is broken to introduce a Q-BIC resonance to generate a high Q-factor optical signal of 2.45 × 104 for high-depth electro-optic modulation. By simulating an applied electric field of 143 V/mm on the metasurface, a slight refractive index change of BTO of 8 × 10−4 was produced, leading to an electro-optical intensity modulation depth of 100%. Furthermore, the nanostructure of the metasurface was carefully designed to facilitate nano-fabrication and voltage application, and it is ideal for the development of low-power, CMOS-compatible, and miniaturized electro-optic modulation devices. Although the results of this study are based on simulations, they provide a crucial theoretical basis and guidance for the realization of efficient and realistic design of dynamic metasurfaces.

Improved detection of magnetic interactions in proteins based on long-lived coherences

Living systems rely on molecular building blocks with low structural symmetry. Therefore, constituent amino acids and nucleotides yield short-lived nuclear magnetic responses to electromagnetic radiation. Magnetic signals are at the basis of molecular imaging, structure determination and interaction studies. In solution state, as the molecular weight of analytes increases, coherences with long lifetimes are needed to yield advantageous through-space magnetisation transfers. Interactions between magnetic nuclei can only be detected provided the lifetimes of spin order are sufficient. In J-coupled pairs of nuclei, long-lived coherences (LLC’s) connect states with different spin-permutation symmetry. Here in, we show sustained LLC’s in protein Lysozyme, weighing 14.3 kDa, with lifetimes twice as long as those of classical magnetisation for the aliphatic protons of glycine residues. We found for the first time that, in a protein of significant molecular weight, LLC’s yield substantial through-space magnetisation transfers: spin-order transfer stemming from LLC’s overcame transfers from classical coherences by factors > 2. Furthermore, in agreement with theory, the permutation symmetry of LLC-based transfers allows mapping interacting atoms in the protein structure with respect to the molecular plane of glycine residues in a stereospecific manner. These findings can extend the scope of liquid-state high-resolution biomolecular spectroscopy.

Structural, dielectric, electrical, and energy storage properties of Mn‐doped Ba0.55Sr0.45TiO3 ceramics

AbstractA conventional solid‐state reaction route was utilized for the fabrication of Ba0.55Sr0.45Ti1−xMnxO3 (x = .004, .006, .008, .01, and .015) ceramics. X‐ray diffraction (XRD) diffractograms revealed pseudo‐cubic structural symmetry with a single phase. The scanning electron microscope (SEM) images revealed fine grain morphology for x = .006, while an obvious increase in grain size was detected at x > .006. A high‐energy storage density (Ws) of 2.47 J cm−3 and a recoverable energy density (Wrec) of 1.36 J cm−3 at an applied electric field of 220 kV cm−1 were achieved for x = .006. An impedance spectroscopic study showed the electrical response relationship with microstructure. The observed two semicircles in Nyquist plots are an indication of the contribution of grains (bulk) and grain boundaries as a resistive medium for conduction of charge carriers, which led to enhanced the capability in capacitor applications.

Reconfiguring the Optical Selection Rule in Ultramicrotome‐Crafted Vertically Aligned InSe Ribbons

AbstractDue to the high carrier mobility and direct bandgap character, indium selenide (InSe) exhibits great advantages for advanced optoelectronic applications. However, the unique optical section rule in InSe weakens the light‐matter interaction when the electric field of illuminated light is perpendicular to the c‐axis of planar InSe flake. To overcome this constraint, ultramicrotome technique is introduced to achieve vertically aligned InSe ribbons, aiming to reconfigure the optical paths for improved optical absorption and device performance. The well‐designed InSe ribbons are acquired with uniform morphology, showing an integrated structure free of cracks or fragments. First, the structural symmetry, crystal orientation, and optical anisotropy of InSe ribbon are carefully revealed by polarization‐dependent Raman spectrum, second harmonic generation (SHG), and photoluminescence measurements. Then, the back focal plane (BFP) imaging of photoluminescence distinguishes the in‐plane and out‐of‐plane dipole emission of InSe ribbons and planar InSe flakes, respectively. Notably, the ribbon exhibits new PL peaks with energy lower than the exciton peak of InSe at low temperature, which is attributed to Se vacancies. The work by introducing vertically aligned InSe nanoribbons provides a new strategy to manipulate the light‐matter interactions and defect engineering for novel optoelectronics, which can be also extended to other 2D semiconductors.