School of Physics - Research Publications

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    Impact of Surface Functionalization on the Quantum Coherence of Nitrogen-Vacancy Centers in Nanodiamonds
    Ryan, RG ; Stacey, A ; O'Donnell, KM ; Ohshima, T ; Johnson, BC ; Hollenberg, LCL ; Mulvaney, P ; Simpson, DA (AMER CHEMICAL SOC, 2018-04-18)
    Nanoscale quantum probes such as the nitrogen-vacancy (NV) center in diamonds have demonstrated remarkable sensing capabilities over the past decade as control over fabrication and manipulation of these systems has evolved. The biocompatibility and rich surface chemistry of diamonds has added to the utility of these probes but, as the size of these nanoscale systems is reduced, the surface chemistry of diamond begins to impact the quantum properties of the NV center. In this work, we systematically study the effect of the diamond surface chemistry on the quantum coherence of the NV center in nanodiamonds (NDs) 50 nm in size. Our results show that a borane-reduced diamond surface can on average double the spin relaxation time of individual NV centers in nanodiamonds when compared to thermally oxidized surfaces. Using a combination of infrared and X-ray absorption spectroscopy techniques, we correlate the changes in quantum relaxation rates with the conversion of sp2 carbon to C-O and C-H bonds on the diamond surface. These findings implicate double-bonded carbon species as a dominant source of spin noise for near surface NV centers. The link between the surface chemistry and quantum coherence indicates that through tailored engineering of the surface, the quantum properties and magnetic sensitivity of these nanoscale systems may approach that observed in bulk diamond.
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    Room Temperature Bias-Selectable, Dual-Band Infrared Detectors Based on Lead Sulfide Colloidal Quantum Dots and Black Phosphorus
    Wang, S ; Ashokan, A ; Balendhran, S ; Yan, W ; Johnson, BC ; Peruzzo, A ; Crozier, KB ; Mulvaney, P ; Bullock, J (AMER CHEMICAL SOC, 2023-06-15)
    A single photodetector capable of switching its peak spectral photoresponse between two wavelength bands is highly useful, particularly for the infrared (IR) bands in applications such as remote sensing, object identification, and chemical sensing. Technologies exist for achieving dual-band IR detection with bulk III-V and II-VI materials, but the high cost and complexity as well as the necessity for active cooling associated with some of these technologies preclude their widespread adoption. In this study, we leverage the advantages of low-dimensional materials to demonstrate a bias-selectable dual-band IR detector that operates at room temperature by using lead sulfide colloidal quantum dots and black phosphorus nanosheets. By switching between zero and forward bias, these detectors switch peak photosensitive ranges between the mid- and short-wave IR bands with room temperature detectivities of 5 × 109 and 1.6 × 1011 cm Hz1/2 W-1, respectively. To the best of our knowledge, these are the highest reported room temperature values for low-dimensional material dual-band IR detectors to date. Unlike conventional bias-selectable detectors, which utilize a set of back-to-back photodiodes, we demonstrate that under zero/forward bias conditions the device's operation mode instead changes between a photodiode and a phototransistor, allowing additional functionalities that the conventional structure cannot provide.
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    Tuning the Photoluminescence Anisotropy of Semiconductor Nanocrystals
    Yuan, G ; Higginbotham, HF ; Han, J ; Yadav, A ; Kirkwood, N ; Mulvaney, P ; Bell, TDM ; Cole, JH ; Funston, AM (AMER CHEMICAL SOC, 2023-09-25)
    Semiconductor nanocrystals are promising optoelectronic materials. Understanding their anisotropic photoluminescence is fundamental for developing quantum-dot-based devices such as light-emitting diodes, solar cells, and polarized single-photon sources. In this study, we experimentally and theoretically investigate the photoluminescence anisotropy of CdSe semiconductor nanocrystals with various shapes, including plates, rods, and spheres, with either wurtzite or zincblende structures. We use defocused wide-field microscopy to visualize the emission dipole orientation and find that spheres, rods, and plates exhibit the optical properties of 2D, 1D, and 2D emission dipoles, respectively. We rationalize the seemingly counterintuitive observation that despite having similar aspect ratios (width/length), rods and long nanoplatelets exhibit different defocused emission patterns by considering valence band structures calculated using multiband effective mass theory and the dielectric effect. The principles are extended to provide general relationships that can be used to tune the emission dipole orientation for different materials, crystalline structures, and shapes.
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    Flexible Vanadium Dioxide Photodetectors for Visible to Longwave Infrared Detection at Room Temperature ((press release associated article should be online on 21.06.2023))
    Balendhran, S ; Taha, M ; Wang, S ; Yan, W ; Higashitarumizu, N ; Wen, D ; Azar, NS ; Bullock, J ; Mulvaney, P ; Javey, A ; Crozier, KB (WILEY-V C H VERLAG GMBH, 2023-10-13)
    Abstract Flexible optoelectronics is a rapidly growing field, with a wide range of potential applications. From wearable sensors to bendable solar cells, curved displays, and curved focal plane arrays, the possibilities are endless. The criticality of flexible photodetectors for many of these applications is acknowledged, however, devices that are demonstrated thus far are limited in their spectral range. In this study, flexible photodetectors are demonstrated using a VOx nanoparticle ink, with an extremely broad operating wavelength range of 0.4 to 20 µm. This ink is synthesized using a simple and scalable wet‐chemical process. These photodetectors operate at room temperature and exhibit minimal variance in performance even when bent at angles of up to 100 ° at a bend radius of 6.4 mm. In addition, rigorous strain testing of 100 bend and release cycles revealed a photoresponse with a standard deviation of only 0.55%. This combination of mechanical flexibility, wide spectral response, and ease of fabrication makes these devices highly desirable for a wide range of applications, including low‐cost wearable sensors and hyperspectral imaging systems.
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    A General Method for Direct Assembly of Single Nanocrystals
    Zhang, H ; Liu, Y ; Ashokan, A ; Gao, C ; Dong, Y ; Kinnear, C ; Kirkwood, N ; Zaman, S ; Maasoumi, F ; James, TD ; Widmer-Cooper, A ; Roberts, A ; Mulvaney, P (WILEY-V C H VERLAG GMBH, 2022-07)
    Abstract Controlled nanocrystal assembly is a pre‐requisite for incorporation of these materials into solid state devices. Many assembly methods have been investigated which target precise nanocrystal positioning, high process controllability, scalability, and universality. However, most methods are unable to achieve all of these goals. Here, surface templated electrophoretic deposition (STED) is presented as a potential assembly method for a wide variety of nanocrystals. Controlled positioning and deposition of a wide range of nanocrystals into arbitrary spatial arrangements − including gold nanocrystals of different shapes and sizes, magnetic nanocrystals, fluorescent organic nanoparticles, and semiconductor quantum dots − is demonstrated. Nanoparticles with diameters <10 nm are unable to be deposited due to their low surface charge and strong Brownian motion (low Péclet number). It is shown that this limit can be circumvented by forming clusters of nanocrystals or by silica coating nanocrystals to increase their effective size.
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    Direct Assembly of Large Area Nanoparticle Arrays
    Zhang, H ; Cadusch, J ; Kinnear, C ; James, T ; Roberts, A ; Mulvaney, P (AMER CHEMICAL SOC, 2018-08)
    A major goal of nanotechnology is the assembly of nanoscale building blocks into functional optical, electrical, or chemical devices. Many of these applications depend on an ability to optically or electrically address single nanoparticles. However, positioning large numbers of single nanocrystals with nanometer precision on a substrate for integration into solid-state devices remains a fundamental roadblock. Here, we report fast, scalable assembly of thousands of single nanoparticles using electrophoretic deposition. We demonstrate that gold nanospheres down to 30 nm in size and gold nanorods <100 nm in length can be assembled into predefined patterns on transparent conductive substrates within a few seconds. We find that rod orientation can be preserved during deposition. As proof of high fidelity scale-up, we have created centimeter scale patterns comprising more than 1 million gold nanorods.
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    A Tunable Polymer-Metal Based Anti-Reflective Metasurface
    Brasse, Y ; Ng, C ; Magnozzi, M ; Zhang, H ; Mulvaney, P ; Fery, A ; Gomez, DE (WILEY-V C H VERLAG GMBH, 2020-01)
    Anti-reflective surfaces are of great interest for optical devices, sensing, photovoltaics, and photocatalysis. However, most of the anti-reflective surfaces lack in situ tunability of the extinction with respect to wavelength. This communication demonstrates a tunable anti-reflective surface based on colloidal particles comprising a metal core with an electrochromic polymer shell. Random deposition of these particles on a reflective surface results in a decrease in the reflectance of up to 99.8% at the localized surface plasmon resonance frequency. This narrow band feature can be tuned by varying the pH or by application of an electric potential, resulting in wavelength shifts of up to 30 nm. Electrophoretic particle deposition is shown to be an efficient method for controlling the interparticle distance and thereby further optimizing the overall efficiency of the anti-reflective metasurface.
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    Directed Chemical Assembly of Single and Clustered Nanoparticles with Silanized Templates
    Kinnear, C ; Cadusch, J ; Zhang, H ; Lu, J ; James, TD ; Roberts, A ; Mulvaney, P (AMER CHEMICAL SOC, 2018-06-26)
    The assembly of nanoscale materials into arbitrary, organized structures remains a major challenge in nanotechnology. Herein, we report a general method for creating 2D structures by combining top-down lithography with bottom-up chemical assembly. Under optimal conditions, the assembly of gold nanoparticles was achieved in less than 30 min. Single gold nanoparticles, from 10 to 100 nm, can be placed in predetermined patterns with high fidelity, and higher-order structures can be generated consisting of dimers or trimers. It is shown that the nanoparticle arrays can be transferred to, and embedded within, polymer films. This provides a new method for the large-scale fabrication of nanoparticle arrays onto diverse substrates using wet chemistry.
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    Concealed Structural Colors Uncovered by Light Scattering
    Akinoglu, EM ; Song, J ; Kinnear, C ; Xue, Y ; Zhang, H ; Roberts, A ; Koehler, J ; Mulvaney, P (WILEY-V C H VERLAG GMBH, 2020-11)
    Abstract Unusual structural colors are demonstrated in thin‐film coatings due to a combination of optical interference and light scattering effects. These vivid colors are concealed under ambient illumination but can be observed when light is reflected from the film surface. The origin of the effect is explored computationally and it is shown that, in thin‐films of lossless dielectrics coated on near‐perfect conductors, incident electromagnetic waves form standing waves. Electric field intensities at the thin film interfaces are maximized for wavelengths that fulfil destructive interference conditions, while nanoscale roughness can enhance scattering at these boundaries. The interplay of these two factors yields vivid, thickness‐dependent colors. This approach increases the repertoire of optical effects and perceived colors in thin coatings. When combined with traditional thin‐film interference colours, dichromatic images with distinctly changing colors can be generated, which can function as a covert, optical security feature.
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    Direct Assembly of Large Area Nanoparticle Arrays
    Mulvaney, P ; ZHANG, H ; KINNEAR, C ; Cadusch, J ; JAMES, T ; ROBERTS, ANN ( 2018-07-13)
    We describe the fabrication of large area arrays of single nanoparticles using electrophoretic deposition.