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Representation of THz spectroscopy of a metamaterial with a Nanowire THz sensor

Representation of THz spectroscopy of a metamaterial with a Nanowire THz sensor

Credit: Rendering by Dimitars Jevtics

Prof Michael Johnston

Professor of Physics

Research theme

  • Photovoltaics and nanoscience

Sub department

  • Condensed Matter Physics

Research groups

  • Terahertz photonics
  • Advanced Device Concepts for Next-Generation Photovoltaics
michael.johnston@physics.ox.ac.uk
Johnston Group Website
  • About
  • Publications

Single GaAs/AlGaAs nanowire photoconductive terahertz detectors

2014 Conference on Optoelectronic and Microelectronic Materials and Devices, COMMAD 2014 (2014) 221-222

Authors:

K Peng, P Parkinson, L Fu, Q Gao, N Jiang, YN Guo, F Wang, HJ Joyce, JL Boland, MB Johnston, HH Tan, C Jagadish

Abstract:

Photoconductive terahertz detectors based on single GaAs/AlGaAs core-shell nanowire have been designed and fabricated. The devices were characterised in a terahertz time-domain spectroscopy system, showing excellent sensitivity comparable to the standard bulk ion-implanted InP receiver, with a detection bandwidth of 0.1 ∼ 0.6 THz. Finite-difference time-domain simulations were performed to understand the origin of the narrow bandwidth of current detectors as well as optimize antenna designs to improve detector performance.
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Dependence of dye regeneration and charge collection on the pore-filling fraction in solid-state dye-sensitized solar cells

Advanced Functional Materials 24:5 (2014) 668-677

Authors:

CT Weisspfennig, DJ Hollman, C Menelaou, SD Stranks, HJ Joyce, MB Johnston, HJ Snaith, LM Herz

Abstract:

Solid-state dye-sensitized solar cells rely on effective infiltration of a solid-state hole-transporting material into the pores of a nanoporous TiO 2 network to allow for dye regeneration and hole extraction. Using microsecond transient absorption spectroscopy and femtosecond photoluminescence upconversion spectroscopy, the hole-transfer yield from the dye to the hole-transporting material 2,2′,7,7′-tetrakis(N,N-di-p- methoxyphenylamine)-9,9'-spirobifluorene (spiro-OMeTAD) is shown to rise rapidly with higher pore-filling fractions as the dye-coated pore surface is increasingly covered with hole-transporting material. Once a pore-filling fraction of ≈30% is reached, further increases do not significantly change the hole-transfer yield. Using simple models of infiltration of spiro-OMeTAD into the TiO2 porous network, it is shown that this pore-filling fraction is less than the amount required to cover the dye surface with at least a single layer of hole-transporting material, suggesting that charge diffusion through the dye monolayer network precedes transfer to the hole-transporting material. Comparison of these results with device parameters shows that improvements of the power-conversion efficiency beyond ≈30% pore filling are not caused by a higher hole-transfer yield, but by a higher charge-collection efficiency, which is found to occur in steps. The observed sharp onsets in photocurrent and power-conversion efficiencies with increasing pore-filling fraction correlate well with percolation theory, predicting the points of cohesive pathway formation in successive spiro-OMeTAD layers adhered to the pore walls. From percolation theory it is predicted that, for standard mesoporous TiO2 with 20 nm pore size, the photocurrent should show no further improvement beyond an ≈83% pore-filling fraction. Solid-state dye-sensitized solar cells capable of complete hole transfer with pore-filling fractions as low as ∼30% are demonstrated. Improvements of device efficiencies beyond ∼30% are explained by a stepwise increase in charge-collection efficiency in agreement with percolation theory. Furthermore, it is predicted that, for a 20 nm pore size, the photocurrent reaches a maximum at ∼83% pore-filling fraction. © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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An ultrafast carbon nanotube terahertz polarisation modulator

Journal of Applied Physics American Institute of Physics 115:20 (2014) 203108-203108

Authors:

Callum J Docherty, Sam Stranks, Severin N Habisreutinger, Hannah Joyce, Laura Herz, Robin Nicholas, Michael Johnston

Abstract:

We demonstrate ultrafast modulation of terahertz radiation by unaligned optically pumped single-walled carbon nanotubes. Photoexcitation by an ultrafast optical pump pulse induces transient terahertz absorption in nanowires aligned parallel to the optical pump. By controlling the polarisation of the optical pump, we show that terahertz polarisation and modulation can be tuned, allowing sub-picosecond modulation of terahertz radiation. Such speeds suggest potential for semiconductor nanowire devices in terahertz communication technologies.
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Chapter 10: Pump-probe spectroscopy at terahertz frequencies

Springer Series in Optical Sciences 171 (2013) 251-271

Authors:

MB Johnston, J Lloyd-Hughes

Abstract:

Optical-pump-terahertz-probe spectroscopy is a technique that can measure directly the conductivity of photoexcited carriers on a picosecond timescale. In this chapter, we introduce the technique and data analysis, and discuss suitable models of the interaction between terahertz radiation and quasiparticles in materials. We then review some recent studies of inorganic and organic semiconductors and nanomaterials. © Springer-Verlag Berlin Heidelberg 2013.
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Fast electron trapping in anodized TiO2 nanotubes

International Conference on Infrared, Millimeter, and Terahertz Waves, IRMMW-THz (2013)

Authors:

C Wehrenfennig, CM Palumbiny, L Schmidt-Mende, MB Johnston, HJ Snaith, LM Herz

Abstract:

We studied charge transport in anodized TiO2 nanotubes in the context of their application in dye-sensitized solar cells. Optical-pump-THz- probe spectroscopy revealed short free carrier lifetimes of about 15-30 ps, which we attribute to shallow trapping. © 2013 IEEE.
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