Diffraction Structure — Single-Atom Catalysts in Conductive Metal-Organic Frameworks: Enabling Reversible Gas Sensing at Room Temperature

2 measurement groups · 3 results

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

Pd1-cMOF powder · Powder

Pristine cMOF and Pd1-cMOF compared before and after NO2 exposure.

Property	Reported value	Normalised value	Uncertainty	Origin and quality	Source
Pristine cMOF (100) XRD peak relative intensity after NO2	reduced to 56%	—	—	Text Exact Reported	rendered page 23 / SI p.23 · Figure S20 · Figure S20
Pd1-cMOF (100) XRD peak relative intensity after NO2Marked as a best value within this paper	reduction alleviated to 73%	—	—	Text Exact Reported	rendered page 23 / SI p.23 · Figure S20 · Figure S20

Pd1-cMOF powder · Powder

XRD of pristine cMOF, Pd1-cMOF, Ir1-cMOF, Ag1-cMOF and Pd-NP@cMOF to assess structural retention.

Context: Target and composite samples compared with pristine Cu3(HITP)2.
Measurement source: rendered page 4 / article p.26069 · Characterization of SACs Stabilized in cMOF · Figure 3a; Figures S9, S10c and S20

Property	Reported value	Normalised value	Uncertainty	Origin and quality	Source
Pd1-cMOF XRD structural retention	primary Cu3(HITP)2 peaks retained with no significant intensity change	—	—	Text Qualitative	rendered page 4 / article p.26069 · Characterization of SACs Stabilized in cMOF · Figure 3a