Detailed information Magnitude inspIRe Quint 27. October 2025

inspIRe™

Nanosecond MIR TA spectrometer

Introducing the first broadband nanosecond
mid-IR TA spectrometer – the compact inspIRe™ achieves a breakthrough detection limit of 100 ΔnanoO.D. thanks to its patented noise suppression technology and enables the complete acquisition of transient absorption data over time and wavelength – a true revolution in mid-IR TA spectroscopy.

InspIRe_Metrology_Spectrometers_TA_TOPAG
Developed and manufactured by:
Features
  • Integrated scanning light source
  • Integrated excitation laser
  • Large, modular sample compartment
  • Integrated detection system
  • Integrated high-performance computer
  • Analysis and automation software
Special features
  • Compact tabletop device
  • Versatile compatibility: suitable for samples in cuvettes, flow cells, thin films, powders and cryostats
  • Unique detection limit of 100 ΔnanoOD
  • Supports transmission and reflection geometries of sample illumination
  • Complete time axis is captured with a single laser shot
  • Time resolution of ≥5 ns and delay times down to the ms range
  • Stationary absorption spectroscopy
    (e.g. acquisition of vibration spectra analogous to FTIR spectroscopy)
  • Time-resolved emission spectroscopy
Applications
  • Charge traps and recombination processes
  • Dynamics of biological systems and materials
  • Investigation of chemical reaction mechanisms

Personal consultation or product inquiry

CUSTOMERS ABOUT THE FEMTOLUX SERIES
What users like about the FemtoLux
Applications
Ultrabroadband
Ultra-wideband MIR TA spectroscopy in photovoltaics

Recent advances in Magnitude Instruments’ noise suppression technology have fundamentally changed nanosecond mid-IR transient absorption (TA) spectroscopy. They enable the use of low-intensity, ultra-broadband mid-IR probe sources…

Applications
Scientific publications

Yilei Wu, Yue Yuan, Diego Sorbelli, Christina Cheng, Lukas Michalek, Hao-Wen Cheng, Vishal Jindal, Song Zhang, Garret LeCroy, Enrique D. Gomez, Scott T. Miller, Alberto Salleo, Giulia Galli, John B. Asbury, Michael F. Toney, and Zhenana Bao. Nat. commun . 2024, 15, 2170.

All-polymer solar cells (all-PSCs) offer improved morphological and mechanical stability compared with those containing small-molecule-acceptors (SMAs). They can be processed with a broader range of conditions, making them desirable for printing techniques. In this study, we report a high-performance polymer acceptor design based on bithiazole linker (PY-BTz) that are on par with SMAs. We demonstrate that bithiazole induces a more coplanar and ordered conformation compared to bithiophene due to the synergistic effect of non-covalent backbone planarization and reduced steric encumbrances. As a result, PY-BTz shows a significantly higher efficiency of 16.4% in comparison to the polymer acceptors based on commonly used thiophene-based linkers (i.e., PY-2T, 9.8%). Detailed analyses reveal that this improvement is associated with enhanced conjugation along the backbone and closer interchain π-stacking, resulting in higher charge mobilities, suppressed charge recombination, and reduced energetic disorder. Remarkably, an efficiency of 14.7% is realized for all-PSCs that are solution-sheared in ambient conditions, which is among the highest for devices prepared under conditions relevant to scalable printing techniques. This work uncovers a strategy for promoting backbone conjugation and planarization in emerging polymer acceptors that can lead to superior all-PSCs.

Kyle T. Munson, Eric R. Kennehan, Grayson S. Doucette, John B. Asbury
Chem 2018, 4, 2826-2843

The remarkable efficiency of halide perovskite photovoltaic devices can be traced to their curiously long charge-carrier lifetimes and high mobilities, but the underlying origins of these properties and their ability to tolerate defects from solution processing remain unclear. Elucidating these origins is particularly important for efforts to develop new perovskite materials that are more stable and that avoid toxic components such as lead.
We reveal that localization of charge carriers into electronic states known as large polarons slows their recombination through a combination of reduced wavefunction overlap and the formation of energetic barriers to electron-hole recombination. Importantly, this localization is mediated by thermally induced dynamic disorder of the anharmonic perovskite lattice. These findings reveal pathways to vary the composition of halide perovskites to tune the interplay between charge transport and recombination to optimize their optoelectronic properties.
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