ORCID Profile
0000-0002-9374-7423
Current Organisation
University of Cambridge
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Publisher: American Chemical Society (ACS)
Date: 11-12-2017
Abstract: We report on in idual-InAs nanowire optoelectronic devices which can be tailored to exhibit either negative or positive photoconductivity (NPC or PPC). The NPC photoresponse time and magnitude is found to be highly tunable by varying the nanowire diameter under controlled growth conditions. Using hysteresis characterization, we decouple the observed photoexcitation-induced hot electron trapping from conventional electric field-induced trapping to gain a fundamental insight into the interface trap states responsible for NPC. Furthermore, we demonstrate surface passivation without chemical etching which both enhances the field-effect mobility of the nanowires by approximately an order of magnitude and effectively eliminates the hot carrier trapping found to be responsible for NPC, thus restoring an "intrinsic" positive photoresponse. This opens pathways toward engineering semiconductor nanowires for novel optical-memory and photodetector applications.
Publisher: American Chemical Society (ACS)
Date: 26-10-2016
Publisher: Springer Science and Business Media LLC
Date: 16-11-2016
DOI: 10.1038/SREP37167
Abstract: Semiconducting single-walled carbon nanotubes are one-dimensional materials with great prospects for applications such as optoelectronic and quantum information devices. Yet, their optical performance is hindered by low fluorescent yield. Highly mobile excitons interacting with quenching sites are attributed to be one of the main non-radiative decay mechanisms that shortens the exciton lifetime. In this paper we report on time-integrated photoluminescence measurements on in idual polymer wrapped semiconducting carbon nanotubes. An ultra narrow linewidth we observed demonstrates intrinsic exciton dynamics. Furthermore, we identify a state filling effect in in idual carbon nanotubes at cryogenic temperatures as previously observed in quantum dots. We propose that each of the CNTs is segmented into a chain of zero-dimensional states confined by a varying local potential along the CNT, determined by local environmental factors such as the amount of polymer wrapping. Spectral diffusion is also observed, which is consistent with the tunneling of excitons between these confined states.
Publisher: Wiley
Date: 22-02-2013
Abstract: A scalable method to coat monochiral (7,5) semiconducting single-walled carbon nanotubes with a monolayer coating of a range of technologically useful polymers such as poly(3-hexylthiophene) (P3HT) and poly(9,9'-dioctylfluorene-co-benzothiadiazole) (F8BT) is presented. Optical spectroscopy and atomic force microscopy measurements show that the semiconducting tube purity (>99%) obtained from the selective wrapping of nanotubes by polymers such as poly(9,9-dioctylfluorenyl-2,7-diyl) (PFO) can be transferred to these other nanotube-polymer combinations by polymer exchange.
Publisher: American Chemical Society (ACS)
Date: 14-06-2021
Publisher: American Chemical Society (ACS)
Date: 29-08-2014
DOI: 10.1021/NL502016Q
Abstract: Semiconducting carbon nanotubes (CNTs) provide an exceptional platform for studying one-dimensional excitons (bound electron-hole pairs), but the role of defects and quenching centers in controlling emission remains controversial. Here we show that, by wrapping the CNT in a polymer sheath and cooling to 4.2 K, ultranarrow photoluminescence (PL) emission line widths below 80 μeV can be seen from in idual solution processed CNTs. Hyperspectral imaging of the tubes identifies local emission sites and shows that some previously dark quenching segments can be brightened by the application of high magnetic fields, and their effect on exciton transport and dynamics can be studied. Using focused high intensity laser irradiation, we introduce a single defect into an in idual nanotube which reduces its quantum efficiency by the creation of a shallow bound exciton state with enhanced electron-hole exchange interaction. The emission intensity of the nanotube is then reactivated by the application of the high magnetic field.
Publisher: Wiley
Date: 02-12-2015
Abstract: A general strategy for the in-plane structuring of organic-inorganic perovskite films is presented. The method is used to fabricate an industrially relevant distributed feedback (DFB) cavity, which is a critical step toward all-electrially pumped injection laser diodes. This approach opens the prospects of perovskite materials for much improved optical control in LEDs, solar cells, and also toward applications as optical devices.
Publisher: Springer Science and Business Media LLC
Date: 30-01-2015
DOI: 10.1038/NCOMMS7142
Abstract: To date, there have been a plethora of reports on different means to fabricate organic-inorganic metal halide perovskite thin films however, the inorganic starting materials have been limited to halide-based anions. Here we study the role of the anions in the perovskite solution and their influence upon perovskite crystal growth, film formation and device performance. We find that by using a non-halide lead source (lead acetate) instead of lead chloride or iodide, the perovskite crystal growth is much faster, which allows us to obtain ultrasmooth and almost pinhole-free perovskite films by a simple one-step solution coating with only a few minutes annealing. This synthesis leads to improved device performance in planar heterojunction architectures and answers a critical question as to the role of the anion and excess organic component during crystallization. Our work paves the way to tune the crystal growth kinetics by simple chemistry.
Publisher: American Chemical Society (ACS)
Date: 05-12-2014
DOI: 10.1021/NN505860A
Abstract: Organic and hybrid organic-inorganic systems are promising candidates for low cost photovoltaics. Recently, perovskite-based systems have been attracting a large amount of research attention, where the highest performing devices employ a small molecule (2,2',7,7'-tetrakis(N,N-di-p-methoxyphenyl-amine)-9,9'-spirobifluorene) (Spiro-OMeTAD) hole transporter. Here, we demonstrate the production of single-walled carbon nanotube (SWNT)/single molecule nanostructures using a simple solution processing technique for effective and strong binding of Spiro-OMeTAD to in idual polymer-wrapped SWNTs. These small molecules bind very strongly, which causes both large mechanical strain of the nanotubes and also improves the separation of in idual SWNTs, thus improving the nanotube photoluminescence quantum efficiency by 1 order of magnitude compared to simple polymer-nanotube nanohybrids. Using absorption and photoluminescence measurements, we show that there is a dramatic variation in the electronic properties of the polymer-NT nanocomposites due to the band alignment formed with Spiro-OMeTAD. These self-assembled nanocomposites offer the potential for integration into high performance optoelectronic such as photovoltaic cells and light emission devices.
Publisher: American Chemical Society (ACS)
Date: 13-05-2021
Publisher: American Association for the Advancement of Science (AAAS)
Date: 06-09-2019
Abstract: Spectrometers with ever-smaller footprints are sought after for a wide range of applications in which minimized size and weight are paramount, including emerging in situ characterization techniques. We report on an ultracompact microspectrometer design based on a single compositionally engineered nanowire. This platform is independent of the complex optical components or cavities that tend to constrain further miniaturization of current systems. We show that incident spectra can be computationally reconstructed from the different spectral response functions and measured photocurrents along the length of the nanowire. Our devices are capable of accurate, visible-range monochromatic and broadband light reconstruction, as well as spectral imaging from centimeter-scale focal planes down to lensless, single-cell-scale in situ mapping.
Publisher: American Chemical Society (ACS)
Date: 16-08-1970
Publisher: American Chemical Society (ACS)
Date: 20-06-2012
DOI: 10.1021/NN301133V
Abstract: We describe studies of new nanostructured materials consisting of carbon nanotubes wrapped in sequential coatings of two different semiconducting polymers, namely, poly(3-hexylthiophene) (P3HT) and poly(9,9'-dioctylfluorene-co-benzothiadiazole) (F8BT). Using absorption spectroscopy and steady-state and ultrafast photoluminescence measurements, we demonstrate the role of the different layer structures in controlling energy levels and charge transfer in both solution and film s les. By varying the simple solution processing steps, we can control the ordering and proportions of the wrapping polymers in the solid state. The resulting novel coaxial structures open up a variety of new applications for nanotube blends and are particularly promising for implementation into organic photovoltaic devices. The carbon nanotube template can also be used to optimize both the electronic properties and morphology of polymer composites in a much more controlled fashion than achieved previously, offering a route to producing a new generation of polymer nanostructures.
Location: United Kingdom of Great Britain and Northern Ireland
Location: United Kingdom of Great Britain and Northern Ireland
Location: United Kingdom of Great Britain and Northern Ireland
Location: United Kingdom of Great Britain and Northern Ireland
No related grants have been discovered for Jack Alexander-Webber.