Visible Region Research Articles

Carbazole-Based Dual-Band Electrochromic Polymers: The Effect of Linkage Sites on Electrochromic Performance.

Dual-band electrochromic (EC) materials are expected to be utilized as building materials for energy saving, but their cycle stability is still an obstacle. Here, two D-A conjugated polymers, PDPPCz36 and PDPPCz27, based on diketopyrrolopyrrole and carbazole linked with different sites, are synthesized. Both of them exhibit dual-band EC behaviors with a dark blue color in the neutral state and high absorption in the near-infrared (NIR) region when oxidized. However, PDPPCz36 exhibits better cycle stability and a shorter response time than PDPPCz27. In the visible (VIS) region, the PDPPCz36 film exhibits an initial light modulation range (ΔT) of 43.0% and that of the PDPPCz27 film is 41.3%. After 100 cycles of redox, the ΔT of the PDPPCz36 film declines by 32%, while that of PDPPCz27 attenuates by more than 50%. A similar tendency is evident in the NIR region. Moreover, PDPPCz36 shows subsecond colored switch times both in the VIS (0.4 s) and NIR (0.7 s) regions, while those of PDPPCz27 are 2.1 and 1.6 s, respectively. Further research suggests that 3,6-linked carbazoles in PDPPCz36 simultaneously inhibit the side reaction and film aggregation, which leads to better redox stability and shorter response time in both EC tests and devices.

DFT study of electronic and nonlinear optical properties of alkaline earth metals and superalkalis doped all-cis-1, 2, 3, 4, 5, 6-hexafluorocyclohexane as an efficient excess electron system

Continual advancements are being pursued to discover innovative strategies for developing materials with remarkable nonlinear optical (NLO) response. Herein, electronic, geometric, thermodynamic and NLO properties of excess electron systems based on stacked Janus dimer, all-cis-1,2,3,4,5,6-hexafluorocyclohexane (C6H6F6)2 are thoroughly investigated. The excess electron systems are designed by doping alkaline earth metals (AEMs) on fluorine face and superalkalis on hydrogen face of Janus dimer. The higher values of vertical ionization energies (VIE) and interaction energies (Eint), confirm the electronic and thermodynamic stabilities of the designed complexes, respectively. Natural bond orbital (NBO) analysis is performed, and the excess electron character of the complexes is confirmed through frontier molecular orbital (FMO) analysis by highest occupied molecular orbital (HOMO) iso-densities. FMO shows a significant decrease in energy gaps (Egap) of the complexes (i.e., Eg = 1.80–3.12 eV), compared to the stacked Janus dimer (i.e., Eg = 9.41 eV). The transparency of the complexes to UV region is confirmed through UV–vis analyses, revealing their maximum absorption in visible and near-IR regions. The higher NLO response of the designed excess electron systems is further proved by the greater values of first hyperpolarizability (β o ) i.e., up to 1.70 × 106 au. Moreover, the time dependent-density functional theory (TD-DFT) computations and two-level model are employed to investigate the controlling factors of hyperpolarizability, illustrating the contribution of transition energy (∆E3), change in dipole moment (∆μ) and oscillator strength (f o ) in controlling the β o . Ab-initio molecular dynamics (AIMD) simulation further confirm that the designed superalkalide complexes are kinetically and thermally stable. The thorough investigation of these excess electron systems proves them an appropriate candidate for NLO applications.

Electronic and Optical Properties of 2D Heterostructure Bilayers of Graphene, Borophene and 2D Boron Carbides from First Principles.

In the present work the atomic, electronic and optical properties of two-dimensional graphene, borophene, and boron carbide heterojunction bilayer systems (Graphene-BC3, Graphene-Borophene and Graphene-B4C3) as well as their constituent monolayers are investigated on the basis of first-principles calculations using the HSE06 hybrid functional. Our calculations show that while borophene is metallic, both monolayer BC3 and B4C3 are indirect semiconductors, with band-gaps of 1.822 eV and 2.381 eV as obtained using HSE06. The Graphene-BC3 and Graphene-B4C3 bilayer heterojunction systems maintain the Dirac point-like character of graphene at the K-point with the opening of a very small gap (20-50 meV) and are essentially semi-metals, while Graphene-Borophene is metallic. All bilayer heterostructure systems possess absorbance in the visible region where the resonance frequency and resonance absorption peak intensity vary between structures. Remarkably, all heterojunctions support plasmons within the range 16.5-18.5 eV, while Graphene-B4C3 and Graphene-Borophene exhibit a π-type plasmon within the region 4-6 eV, with the latter possessing an additional plasmon at the lower energy of 1.5-3 eV. The dielectric tensor for Graphene-B4C3 exhibits complex off-diagonal elements due to the lower P3 space group symmetry indicating it has anisotropic dielectric properties and could exhibit optically active (chiral) effects. Our study shows that the two-dimensional heterostructures have desirable optical properties broadening the potential applications of the constituent monolayers.

Cr2O3–NiO mixed oxides thin films for p-type transparent conductive electrodes

The Cr2O3–NiO mixed oxides’ thin films were formed by means of the layer-by-layer magnetron sputtering deposition of Cr2O3, NiO, and Cr2O3 layers on c-plane sapphire substrates. These thin-film structures, subjected to subsequent annealing, constituted a combination of the monocrystalline (0001) Cr2O3 and nonordered nickel oxide phase, which was a mixture of NiO and Ni2O3. The annealing at 900 and 1000 °С in air facilitated the diffusion of Ni and Cr atoms into the layers. Varying the annealing time allowed us to control the uniformity of the Ni and Cr distribution, the microrelief of the film surface, the transmittance in the visible region, and the sheet resistance of the Cr2O3–NiO thin-film structures. Thus, the films annealed at 900 °C during 30 min were characterized by a uniform distribution, a relatively weakly developed surface, a low sheet resistance, and the highest Haacke's Figure of Merit of 1.49 × 10–9 Ω–1. The formation of mixed Cr2O3–NiO oxides by the proposed approach was found to be an effective way to improve the performances of Cr2O3 based p-type transparent conductive electrodes.

Higly Luminescent Aceno[6]helicenones by Intramolecular Radical Cyclization.

Helicenes and helicenoid structures are promising candidates for future applications exploiting circularly polarized light. Ideal candidates should possess near-quantitative photoluminescence quantum yield, high a luminescence dissymmetry factor and an adjustable HOMO-LUMO gap. However, carbo[n]helicenes are poorly luminescent compounds and they absorb light mainly in the ultraviolet region. Here we show that the incorporation of a carbonyl group into helical scaffold significantly improves the fluorescence quantum yield and shifts the absorption to visible region. Although the carbonyl group is commonly considered as detrimental to efficient emission, fluorescence quantum yields up to Φ = 0.43 were recorded. A straightforward synthetic approach to a highly luminescent tetraceno[6]helicenone and an aza analogue has been developed. The key step is a radical cyclization which is achieving dehydrative π-extension. The aza-analogue was incorporated as an emitter in organic light emitting diodes (OLEDs) and showed good performance.

Novel Metal‐Free Porphyrin with Ionic Liquid and Sulphonic Acid Moieties for Visible Light Assisted Photocatalytic C‐N Coupling of Heterocyclic Compounds with Aryl Halides

Metal‐free Buchwald‐Hartwig type photocatalytic approach for N‐substitution of 1,2,4‐triazole at normal temperature was explored for the first‐time using novel imidazolium based Brønsted acid functionalized porphyrin (ImBAFPc). The energy band gap and Hammett acidity were determined by UV‐Vis spectrophotometer. The energy band gap, 1.06 eV supported absorption of radiation in the visible region. The N‐arylation of 1,2,4‐triazole with various Ar‐X was achieved in a home‐made photoreactor by heterogeneous, recyclable ImBAFPc photocatalyst under irradiation of 5W LED with good yields. The protocol tolerated electron donating and attracting Ar‐X, including inactivated chlorobenzene, affording the arylated triazole with admirable yields. under ambient photocatalytic conditions.

Synthesis and Photochemical Properties of Heterometallic Ti-Cu Ring Clusters Constructed from Myo-Inositol Ligand.

Incorporating heterometals into titanium-oxygen clusters represents an effective approach to adjusting the band gap and absorption properties. Herein, a family of heterometallic Ti-Cu clusters was synthesized under solvothermal conditions. The unique structural feature of these clusters is the formation of ring clusters with myo-inositol ligands serving as structure-directing ligands. The myo-inositol ligand, as a typical polyol ligand, demonstrates flexible and distinctive coordination modes capable of chelating up to eight transition metal ions simultaneously. Compounds 4 and 5 show significant absorption in the visible region, indicating that the incorporation of Cu ions can efficiently tune the band gap of titanium-oxygen clusters.

Liquid Crystal Enables Extraordinarily Precise Tunability for a High‐Q Ultra‐Narrowband Filter Based on a Quasi‐BIC Metasurface

AbstractNotch filters usually involve high costs, great difficulties in processing, and very limited tunability. By coating a nematic liquid crystal (LC) layer onto a well‐designed quasi‐bound states in the continuum (quasi‐BICs) metasurface, this work designs and demonstrates a high‐Q tunable filtering system with precise tunability in the near‐infrared spectral range. Optimal structural parameters and the filtering performance are first determined by numerical simulations and then confirmed in experiments. The precise tunability is enabled by modifying the LC molecules’ principal axes with an applied voltage, where the least distinguishable central wavelength interval is smaller than 0.3 nm, and the largest Q factor extracted from experiments can be ≈256.1. Compared to most of the commercial notch filters that work in the visible region and have no tunability, this work achieves an ultra‐narrowband filtering system that features low manufacture difficulty and cost, and great control of light propagation. The proposed design also opens new avenues for developing BIC‐based high‐Q devices with enhanced signal‐to‐noise ratio and multifunctional properties.

Amorphous to Crystalline Transition in Nanoimprinted Sol-Gel Titanium Oxide Metasurfaces.

Crystalline titanium dioxide (TiO2) (anatase and rutile) possesses a higher refractive index than amorphous TiO2 and near-zero absorption in the visible region, making them an ideal material for visible metasurfaces. However, fabrication limitations hinder their implementation into flat optics. In this work, a wafer-scale manufacturing platform is proposed for crystalline TiO2 metasurfaces. Sol-gel TiO2 is developed as a printable material in which its material phase can be precisely controlled to produce amorphous, anatase, or rutile, depending on the crystallization temperature. Therefore, anatase or rutile metalenses can be fabricated on a wafer scale using thermal nanoimprint lithography and sintering process. The high refractive index of the crystalline TiO2 contributes to the enhanced conversion efficiency of the fabricated metalenses. The fabricated metalenses exhibit diffraction-limited focusing and imaging capabilities, comparable to the theoretically ideal lenses.

Exploring the impact of end-capped benzothiazine-based acceptors to lead the photovoltaic properties of solar cells: A DFT/TD-DFT approach

To improve the solar cells performance, usually end-capped acceptors are used in designing of new molecules. Therefore, in this study, the side-chain and end-capped moieties were modified in reference compound (BTZR) and proposed new compounds (BTZD1-BTZD6) to augment their photovoltaic and optoelectronic properties. The density functional method was employed at the M06/6-311G(d,p) level to optimize and interpret their frontier molecular orbitals (FMOs), density of states (DOS), transition density matrix (TDM), exciton binding energy (Eb), light absorption and open circuit voltage (Voc) characteristics. Their global reactivity parameters (GRPs) were calculated via the HOMO-LUMO energy band gap. Further, it was observed that all the investigated compounds showed lower band gaps (2.975–3.160 eV) and bathochromic shifts in the visible region (482.501–504.223 nm). Various plots such as the DOS, TDM and hole-electron further confirmed the efficiency of designed chromophores. Additionally, an interface of model donor–acceptor was constructed by considering the donor polymer (PBDB-T) and designed NFAs. Significant results were obtained for Voc (1.538–1.772 V). Among the selected candidates, BTZD3 and BTZD5 were obtained as high-performance non-fullerene acceptors (NFAs). They exhibited least band gaps (2.988 and 2.975 eV) and highest λmax (504.223 and 498.606, respectively). These compounds also demonstrated the least exciton binding energy values as 0.529 and 0.488 eV, respectively. Besides this, comparative study with the standard hole transport material (HTM) spiro-OMeTAD showed a reasonable agreement, suggesting that the entitled compounds could serve as effective HTMs. Overall, the findings suggested the crucial role of end-capped modification in elevating the charge mobility and photovoltaic characteristics of BTZD1-BTZD6. This study provides a valuable insight in the development of good photovoltaic materials.

Dressing AgNWs with MXenes Nanosheets: Transparent Printed Electrodes Combining High-Conductivity and Tunable Work Function for High-Performance Opto-Electronics.

High-work function transparent electrodes (HWFTEs) are key for establishing Schottky and Ohmic contacts with n-type and p-type semiconductors, respectively. However, the development of printable materials that combine high transmittance, low sheet resistance, and tunable work function remains an outstanding challenge. This work reports a high-performance HWFTE composed of Ag nanowires enveloped conformally by Ti3C2Tx nanosheets (TA), forming a shell-core network structure. The printed TA HWFTEs display an ultrahigh transmittance (>94%) from the deep-ultraviolet (DUV) to the entire visible spectral region, a low sheet resistance (<15 Ωsq-1), and a tunable work function ranging from 4.7 to 6.0eV. The introduction of additional oxygen terminations on the Ti3C2Tx surface generates positive dipoles, which not only increases the work function of the TA HWFTEs but also elevates the TA/Ga2O3 Schottky barrier, resulting in a high self-powered responsivity of 18mAW-1 in Ga2O3 diode DUV photodetectors, as demonstrated via experimental characterizations and theoretical calculations. Furthermore, the TA HWFTEs-based organic light-emitting transistors exhibit exceptional emission brightness of 5020cd m-2, being four-fold greater than that in Au electrodes-based devices. The innovative nano-structure design, work function tuning, and the revealed mechanisms of electrode-semiconductor contact physics constitute a substantial advancement in high-performance optoelectronic technology.

Enhanced broadband perfect absorption in visible and near-infrared regimes

ABSTRACT It is still a challenge to achieve perfect ((near-unity)) absorption across a wide wavelength range with a three-layer structure. This paper presents a metamaterial absorber (MA) based on MXene that can achieve broadband and perfect absorption in the near-infrared and visible regions. The MA with a simple three-layer structure consists of a top Ti3C2T x layer, an intermediate dielectric layer and a bottom gold layer. It can achieve perfect absorption (the absorptivity over 99%) in the wavelength range of 730–900 nm. The electric field distribution reveals that the localized surface plasmon resonance occurring at the interface of Ti3C2T x and SiO2 leads to strong absorption over the wide wavelength range. Furthermore, the MA exhibits excellent angular stability. This work provides a method to construct MAs with broadband perfect absorption in the near-infrared and visible band.

Nanosized Eu3+-Doped NaY9Si6O26 Oxyapatite Phosphor: A Comprehensive Insight into Its Hydrothermal Synthesis and Structural, Morphological, Electronic, and Optical Properties.

Detailed analysis covered the optical and structural properties of Eu3+-doped NaY9Si6O26 oxyapatite phosphors, which were obtained via hydrothermal synthesis. X-ray diffraction patterns of NaY9Si6O26:xEu3+ (x = 0, 1, 5, 7, 10 mol% Eu3+) samples proved a single-phase hexagonal structure (P63/m (176) space group). Differential thermal analysis showed an exothermic peak at 995 °C attributed to the amorphous to crystalline transformation of NaY9Si6O26. Electron microscopy showed agglomerates composed of round-shaped nanoparticles ~53 nm in size. Room temperature photoluminescent emission spectra consisted of emission bands in the visible spectral region corresponding to 5D0 → 7FJ (J = 0, 1, 2, 3, 4) f-f transitions of Eu3+. Lifetime measurements showed that the Eu3+ concentration had no substantial effect on the rather long 5D0-level lifetime. The Eu3+ energy levels in the structure were determined using room-temperature excitation/emission spectra. Using the 7F1 manifold, the Nv-crystal field strength parameter was calculated to be 1442.65 cm-1. Structural, electronic, and optical properties were calculated to determine the band gap value, density of states, and index of refraction. The calculated direct band gap value was 4.665 eV (local density approximation) and 3.765 eV (general gradient approximation). Finally, the complete Judd-Ofelt analysis performed on all samples confirmed the experimental findings.

Prediction of 2D XC2N4 (X= Ti, Mo, and W) monolayers with high mobility as an encouraging candidate for photovoltaic devices

In this study, the impacts of strain and an electric field on the electronic and optical characteristics of monolayer XC2N4 (X=Ti, Mo, and W) were systematically examined using the density functional theory. The results corroborated that the dynamically, mechanically, and thermodynamically stable XC2N4 monolayers displayed semiconductor properties when the Heyd-Scuseria-Ernzerhof (HSE06) method was used. The TiC2N4 monolayer is shown to be a direct-gap semiconductor of 1.179 eV whereas the MoC2N4 and WC2N4 monolayers are indicated to have indirect bandgaps of 2.819 eV and 2.661 eV, respectively. Notably, the TiC2N4, WC2N4, and MoC2N4 monolayers possess comparatively high electron mobilities of 2776.85 cm2/V s, 1576.79 cm2/V s, and 1316.41 cm2/V s, respectively. The influence of strain on the bandgap of the MoC2N4 and WC2N4 monolayers led to a decrease in their gap, whereas in the TiC2N4 monolayer, the applied tensile strain caused an increase in the bandgap. Moreover, the compressive strain significantly caused a transition from semiconducting to metallic characteristics (zero band gap). The optical absorption spectra indicated the existence of three separate maxima for the XC2N4 (X=Ti, Mo, and W) monolayers with an extreme intensity of up to 2.0 × 105 cm−1. Interestingly, compared with pure monolayers, strained monolayers enhance the beginning of coefficient absorption in the visible range, with widespread range absorption in the ultraviolet and visible regions. Our results suggest that these monolayers can be promising options for nanoelectronic, optical and photovoltaic applications.

A Prediction of All-Inorganic Lead-Free Halide Perovskites for Photovoltaic Application: Rb3Mo2Br9 and Rb3Mo2Cl9.

Lead-based organic-inorganic hybrid perovskites show promise as photovoltaic materials due to their high energy conversion efficiencies. However, concerns regarding lead toxicity and the poor environmental and operational stability of the organic cationic group have limited their widespread application. To address these challenges, the design of all-inorganic lead-free halide perovskites offers potential solutions for photovoltaic applications. Here, two layered perovskite derivatives, Rb3Mo2Cl9 and Rb3Mo2Br9, are explored, and their electronic, structural, and photovoltaic properties are analyzed using advanced theoretical calculations. Rb3Mo2Br9 exhibits a suitable direct bandgap of 1.60eV, making it a promising candidate for use as a light absorber in low-cost, high-efficiency solar cells. On the other hand, Rb3Mo2Cl9 demonstrates a wide direct bandgap exceeding 1.70eV, positioning it as a viable option for use as a top cell in tandem photovoltaic systems alongside silicon. Both materials display ideal optical properties in the visible light region and hold promise as excellent inorganic lead-free perovskite alternatives.

Photothermal performance of carbon nanotubes in the visible and near-infrared regions: applications in water evaporation and destroying cancer cells

Photothermal performance of carbon nanotubes in the visible and near-infrared regions: applications in water evaporation and destroying cancer cells

Synthesis of multifunctional NiFe2O4-Zns-Ag nanocomposite for sunlight driven photocatalytic dye degradation and solar cells applications: Structural, magnetic and optical properties

This article focuses on the fabrication and investigation of the novel multifunctional NiFe2O4-Zns-Ag core-bi-shell nanocomposite and their magnetic optical properties. The nanocomposite was prepared by a simple co-precipitation method and characterized using various techniques such as XRD, SEM, TEM, UV–Vis spectroscopy, Fourier transform infrared spectroscopy (FTIR) and VSM. The results showed that the nanocomposite had a spinel cubic structure with an average crystallite size of 29 nm. The SEM and TEM images revealed that the nanocomposite had a spherical shape with an average particle size of 61 nm. The optical study demonstrated that the nanocomposite had high absorption in the visible region, indicating its potential for photocatalytic applications. The magnetic study showed that the nanocomposite was superparamagnetic in nature, which could be useful in magnetic separation processes. Furthermore, the potential application of the nanocomposite in solar cells was explored by studying its optical absorption properties. Finally, the photocatalytic activity of the nanocomposite was evaluated using two different azoic dyes under sunlight irradiation. The results showed that the nanocomposite exhibited excellent photocatalytic activity, with a degradation efficiency of 96.22 % within 90 min. Overall, this study provides insights into the potential use of NiFe2O4-Zns-Ag nanocomposite as an efficient photocatalyst for environmental remediation.

Optical investigation of degradation of graphene oxide in alkaline environment: Evidence of two distinct photon-emitting phases in visible region.

In this work we show a procedure of treating of the graphene oxide in alkaline environment as a function of the treatment time in order to obtain novel structures with strong luminescence properties, water-stable, useful as potential replacement for critical raw materials employed as example in optical and optoelectronic devices or for diagnostic and therapeutic technology. These structures have distinct blue and green-luminescence properties which derived most likely from different structural conformations, one associable with that of carbon quantum dots (or as an alternative to that of the Oxidative Debris), the other, lighter and more similar to organic compounds, reported in literature as fulvic-like molecules, but whose nature has to be further investigated. We show that the lighter fraction has a dual mechanism of photoemission: the excitation-independent PL for excitation wavelength within 350 nm and the excitation-dependent component for excitation wavelength ranging in the visible spectrum. The PL dual behaviour could depend on fluorescent nanoclusters composed by specific organic fluorophores with a carbonaceous core. FTIR analysis shows reasonably the same functional groups unless of some difference discussed in the text, meanwhile UV–Vis and PL analysis clearly highlight two distinct emissions (450 nm and 530 nm) in the visible region of the electromagnetic spectrum. Excitation-dependent photoluminescence, water stability and organic fluorescent nanostructures are issues particularly required for application in the biological field but also in materials science.

Optical properties of crystals and two-phase ceramics of the AgCl0.25Br0.75 – AgI system

Research of materials’ optical properties is critical for further development and manufacturing of optical products. While recently, single crystals and two-phase ceramics of the AgCl0.25Br0.75 – AgI system have been developed by the authors. This work is focused on studying the transmission ranges, refractive index dispersion, optical losses, and photoresistance of materials in the AgCl0.25Br0.75 – AgI system, as well as comparing the properties of single-crystals and ceramics. The materials are transparent in the visible and IR regions from 0.49 to 54 um, as well as in the terahertz (far IR and millimeter regions) of 300–1500 um (0.3–1.0 THz). For all compositions, the refractive index in the IR varied from 2.107 to 2.436. The materials’ absorption coefficients were (0.06–6.67) ∙ 10-4 in the middle IR, which is lower compared to other halide materials known and indicates low optical loss. Finally, both single-crystals and two-phase ceramics showed a trend towards an increase in photoresistance with a rise of the AgI content in the AgCl0.25Br0.75 solid solution. After UV irradiation, the materials showed a decrease in transmission in the visible and middle IR (to 10 µm) with negligible loss at a wavelength of 10 µm or more. For a single crystal and two samples of ceramics with a composition of 20 mol. % AgI in AgCl0.25Br0.75, a comparison of properties was conducted in this study. Based on the comparison results, close but not identical values of the refractive indices, an increase in the absorption coefficient for ceramic materials, and a low photoresistance of the sample obtained from the mechanical mixture were revealed. The last two characteristics are associated with the high heterogeneity of two-phase ceramics based on a mechanical mixture, which leads to a deterioration in functional properties. These results prove high prospects for the use of these materials in fiber optics and photonics for medical technologies, thermography, and optoelectronics.

Surface-Reconstructed InAs Colloidal Nanorod Quantum Dots for Efficient Deep-Shortwave Infrared Emission and Photodetection.

Shortwave infrared (SWIR) light emitters and detectors are crucial in numerous applications. Conventionally, SWIR devices rely on epitaxially grown narrow bandgap semiconductors, such as InGaAs, which are expensive to fabricate and difficult to integrate with silicon complementary metal-oxide-semiconductors (CMOS). Colloidal quantum dots (CQDs) have emerged as low-cost alternatives to epitaxially grown semiconductors, offering integration with CMOS through solution-processing methods. However, the predominant SWIR-active CQD systems rely on heavy-metal-containing compositions (PbS and HgTe), hindering the adoption of CQD SWIR technology. InAs CQDs are promising substitutes in SWIR applications. However, synthesizing SWIR-active InAs CQDs is challenging, often constraining them to the visible or near-infrared regions. To achieve SWIR bandgaps, large InAs CQDs are typically required; such CQDs are prone to having surface traps that quench photogenerated charge carriers, adversely affecting device performance. Here, we report a two-step synthesis of surface-passivated SWIR-active InAs/ZnSe core/shell colloidal nanorod quantum dots (CNQDs). These surface-passivated CNQDs are highly emissive and tunable over the entire technologically important region (1200-1800 nm) of the SWIR window with photoluminescence quantum yields as high as 60%. Using these SWIR-active InAs/ZnSe CNQDs, we demonstrated an SWIR-active InAs CQD photodetector, achieving a record high external quantum efficiency of ∼15% at ∼1450 nm and a low dark current of ∼10-2 mA/cm2.