Spectroscopy — Conductive Metal-Organic Frameworks Bearing M−O4 Active Sites as Highly Active Biomass Valorization Electrocatalysts

Measurement evidence

Spectroscopy

Conductive Metal-Organic Frameworks Bearing M−O4 Active Sites as Highly Active Biomass Valorization Electrocatalysts · Zhang Y., Kornienko N. · ChemSusChem · 2022 · e202101587

4 measurement groups · 14 results

Reported values remain attached to the sample, method, conditions, extraction quality and source location that produced them.

ATR-IR adsorption spectroscopy

Co-CAT on flexible carbon cloth · Electrode

10 mM HMF in 1 M KOH; M-CAT electrode immersed and hydrated MOF spectrum subtracted.

Geometry
M-CAT electrode in ATR configuration
Context
Composite electrode sample
Measurement source
5 · Results and Discussion · Figure 4a,b
PropertyReported valueNormalised valueUncertaintyOrigin and qualitySource
C=O band shift on Co-CAT adsorption82.4 cm-1Text
Exact Reported
5 · Results and Discussion · Figure 4a
HMF alcohol-group IR band1027 cm-1Text
Rounded Reported
5 · Results and Discussion · Figure 4b
HMF C=C band in alkaline solution1515.8 cm-1Text
Exact Reported
5 · Results and Discussion · Figure 4a
HMF C=O band in alkaline solution1654.7 cm-1Text
Exact Reported
5 · Results and Discussion · Figure 4a
C=O band shift on Ni-CAT adsorption88.2 cm-1Text
Exact Reported
5 · Results and Discussion · Figure 4a
Ni-CAT adsorbed-HMF alcohol band 11023.4 cm-1Text
Exact Reported
5 · Results and Discussion · Figure 4b
Ni-CAT adsorbed-HMF alcohol band 21011.2 cm-1Text
Exact Reported
5 · Results and Discussion · Figure 4b

Potential-dependent operando ATR-IR difference spectroscopy

Co-CAT on flexible carbon cloth · Electrode

Custom spectroelectrochemical cell; carbon cloth counter, Ag/AgCl reference; potentials stepped from most negative, approximately 4 min at each potential.

Geometry
Co-CAT on carbon cloth working electrode
Context
Composite electrode sample
Measurement source
4 · 1.4 Operando spectroscopy · Figure 4c,e
PropertyReported valueNormalised valueUncertaintyOrigin and qualitySource
Operando IR HMFCA band on Co-CAT1560 cm-1Text
Rounded Reported
5 · Results and Discussion · Figure 4c
Co-CAT operando band-growth thresholdbands begin to rise just past the CoII/III redox potentialFigure Axis
Approximate
6 · Figure 4 caption · Figure 4e
Operando IR FDCA carboxylate band1357.7 cm-1Text
Exact Reported
5 · Results and Discussion · Figure 4c,d

Potential-dependent operando ATR-IR difference spectroscopy

Ni-CAT on flexible carbon cloth · Electrode

Custom spectroelectrochemical cell; carbon cloth counter, Ag/AgCl reference; potentials stepped from most negative, approximately 4 min at each potential.

Geometry
Ni-CAT on carbon cloth working electrode
Context
Composite electrode sample
Measurement source
4 · 1.4 Operando spectroscopy · Figure 4d,f
PropertyReported valueNormalised valueUncertaintyOrigin and qualitySource
Operando IR HMFCA band on Ni-CAT1569.8 cm-1Text
Exact Reported
5 · Results and Discussion · Figure 4d
Ni-CAT rapid spectral-change thresholdrapid increase once the NiII/III redox potential is reachedFigure Axis
Approximate
6 · Figure 4 caption · Figure 4f

X-ray photoelectron spectroscopy

Co-CAT-Carbon Paper · Electrode

XPS before and after 6 h electrolysis at 1.42 V vs RHE; Mg X-ray source; calibrated to C 1s at 284.8 eV.

Geometry
M-CAT electrode after electrolysis
Context
Composite electrode sample
Measurement source
3 · 1.2 Synthesis and characterization of M-CAT · Figure S7
PropertyReported valueNormalised valueUncertaintyOrigin and qualitySource
SEM structure retention after electrolysisSEM after electrolysis showed retention of MOF structures on the surfaceQualitative
Qualitative
5 · Results and Discussion · Figure S8
Transition-metal species retained after electrolysisretained Co 2p and Ni 2p peaks suggest retention of transition metal speciesQualitative
Qualitative
5 · Results and Discussion · Figure S7