Angela B.
Seddon
*a,
Bruce
Napier
b,
Ian
Lindsay†
c,
Samir
Lamrini
d,
Peter M.
Moselund
e,
Nicholas
Stone
f,
Ole
Bang
g and
Mark
Farries
h
aMid-Infrared Photonics Group, George Green Institute for Electromagnetics’ Research, Faculty of Engineering, University of Nottingham, NG7 2RD, UK. E-mail: angela.seddon@nottingham.ac.uk
bVivid Components Ltd, German Office, Dr-Rörig-Damm 22, 33102 Paderborn, Germany
cGooch & Housego, UK
dLISA laser products OHG, Fuhrberg & Teichmann, Albert Einstein Straße, 1-9 37191 Katlenburg-Lindau, Germany
eNKT Photonics A/S, Blokken 84, DK-3460 Birkerød, Denmark
fPhysics and Astronomy, College of Engineering, Mathematics and Physical Sciences, University of Exeter, EX4 4QL, UK
gFibre Sensors and Supercontinuum Group, DTU Fotonik, Technical University of Denmark, DK-2800 Kongens Lyngby, Denmark
hGooch & Housego (Torquay), Broomhill Way, Torquay, TQ2 7QL, UK
First published on 20th April 2020
Correction for ‘Prospective on using fibre mid-infrared supercontinuum laser sources for in vivo spectral discrimination of disease’ by Angela B. Seddon et al., Analyst, 2018, 143, 5874–5887.
The correct version of the caption for Fig. 8 is as shown below.
Fig. 8 – Comparison of power spectral density (PSD) available in a diffraction-limited beam for various MIR sources. Compared are: blackbody thermal emitter at 1500 K e.g. common GloBar® sources; synchrotron bending magnet output, calculated for 0.5 A beam current,36 captured within a diffraction-limited solid angle; cartoon of typical quantum cascade laser array output (representative of data from ref. 35). Note that QCLs at wavelengths as low as 3 μm are now available); cartoon approximating the PSD of the most powerful wideband SIF MIR-SC to date;31 commercial fibre MWIR SC system34 and recently reported tapered chalcogenide photonic crystal fibre SC.32 Also shown are the non-diffraction-limited PSD for a 1500 K blackbody emitter imaged using a range of commercial reflective microscope objectives with magnifications of 15×, 25× and 74× (figure redrawn and amended from ref. 33).
Consequently, sections of the text in the manuscript should be adjusted according to this change, and these are detailed below.
The paragraph on page 5880 beginning “Taking the SIF (step-index-fibre) MIR-SC…” should be correctly given as “Taking the SIF (step-index-fibre) MIR-SC with best broadband power spectral density (PSD) from 2.2–12 μm now achieved31 (see Table 1), Fig. 8 (compiled in MINERVA) compares existing MIR sources33 emitting into a diffraction-limited beam. It can be seen from Fig. 8 that commercial fibre MWIR-SC covering ∼3–5 μm (ref. 34) are as spectrally bright as the longer wavelength quantum cascade lasers.35 Also compared are the calculated PSD of wideband blackbody thermal emitters (e.g. GloBar®) and representative synchrotron (SR) MIR output calculated for a 0.5 A beam current.36 Fig. 8 demonstrates that, when collecting radiation at the diffraction limit, fibre MIR-SC lasers have now been realised that yield several times the PSD of synchrotron-generated MIR beams over the broad ranges of spectroscopic significance represented here. It should be noted that typical synchrotron radiation extends far beyond the MWIR molecular fingerprint region of interest here. Fig. 8 also illustrates that while not having a PSD as high as an array of MIR-QCLs, MIR-SC sources cover several times the spectral range with a single device. Fig. 8, also shows the total PSD from a blackbody emitter imaged through typical reflective MIR microscope objectives of magnification: 15×, 25× and 74×. This optical configuration does not yield a diffraction-limited output, but emphasises that the clear advantage of high-radiance sources like a supercontinuum is maximised for point-scanned or stand-off spectral imaging.”
As a result of this change to both the caption of Fig. 8 and the text, the authors would like to replace ref. 36 with the reference listed below as ref. 1.
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
Footnote |
† Now at: H. H. Wills Physics Laboratory, Tyndall Ave., University of Bristol, BS8 1TL, UK. |
This journal is © The Royal Society of Chemistry 2020 |