Electrochemistry Application — Nanopore-induced host-guest charge transfer phenomena in a metal-organic framework

Measurement evidence

Electrochemistry Application

Nanopore-induced host-guest charge transfer phenomena in a metal-organic framework · Yamamoto S., Pirillo J., Hijikata Y. et al. · Chemical Science · 2018 · 3282-3289

2 measurement groups · 4 results

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

Solid-state cyclic voltammetry

As-prepared Mn-MOF crystals · Single Crystal

Mn-MOF and 2,7-AQDC measured under conditions from prior paper; potentials versus Li+/Li.

Geometry
solid-state electrochemical configuration
Context
pristine framework control
Measurement source
SI p.4 · S3. Cyclic voltammetry · Fig. S3
PropertyReported valueNormalised valueUncertaintyOrigin and qualitySource
Solid-state anthraquinone E1/2 range in Mn-MOF and AQDCaround 2.4-2.5 V vs Li+/LiCaption
Range
SI p.4 · S3. Cyclic voltammetry · Fig. S3

Cyclic voltammetry

Free 2,7-AQDC, TTF and TMPDA in DMF electrolyte · Unknown

Saturated DMF solution with 1.0 mol/L [Bu4N]PF6 electrolyte; potentials versus Ag/AgCl.

Geometry
solution electrochemical cell
Context
free donor/acceptor model molecules
Measurement source
SI p.4 · S3. Cyclic voltammetry · Fig. S2
PropertyReported valueNormalised valueUncertaintyOrigin and qualitySource
2,7-AQDC first reduction potential-0.67 V vs Ag/AgClCaption
Exact Reported
SI p.4 · S3. Cyclic voltammetry · Fig. S2
TMPDA first oxidation potential0.37 V vs Ag/AgClCaption
Exact Reported
SI p.4 · S3. Cyclic voltammetry · Fig. S2
TTF first oxidation potential0.45 V vs Ag/AgClCaption
Exact Reported
SI p.4 · S3. Cyclic voltammetry · Fig. S2