cMOF Evidence Base
Spectroscopy — Heteroatom-doped 3D porous carbon architectures for highly stable aqueous zinc metal batteries and non-aqueous lithium metal batteries

Measurement evidence

Spectroscopy

Heteroatom-doped 3D porous carbon architectures for highly stable aqueous zinc metal batteries and non-aqueous lithium metal batteries · An Y., Tian Y., Li Y. et al. · Chemical Engineering Journal · 2020 · 125843

2 measurement groups · 29 results

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

Raman spectroscopy

Raman spectroscopy

NOCA@CF · Electrode

D and G bands of carbon-based NOCA@CF.

Context
Derived carbon target sample
Measurement source
7 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2d
PropertyReported valueNormalised valueUncertaintyOrigin and qualitySource
Electronic conductivity assessmenthigh electronic conductivity inferred from graphitization——Qualitative
Qualitative		7 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2d
Raman ID/IG ratio1.138——Text
Exact Reported		7 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2d
Raman D band1340 cm-1——Text
Exact Reported		7 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2d
Raman G band1573 cm-1——Text
Exact Reported		7 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2d

X-ray photoelectron spectroscopy

X-ray photoelectron spectroscopy

NOCA@CF · Electrode

High-resolution C 1s, N 1s, and O 1s spectra of NOCA@CF.

Context
Derived carbon target sample
Measurement source
7 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2g-i
PropertyReported valueNormalised valueUncertaintyOrigin and qualitySource
C 1s C-C binding energy284.4 eV——Text
Exact Reported		7-8 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2g-i
C 1s C=N binding energy285.2 eV——Text
Exact Reported		7-8 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2g-i
C 1s C=O atomic content6.5%——Text
Approximate		7 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2g-i; Fig. S5
C 1s C=O binding energy286.9 eV——Text
Exact Reported		7-8 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2g-i
C 1s C-OH atomic content12.1%——Text
Approximate		7 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2g-i; Fig. S5
C 1s C-OH binding energy285.9 eV——Text
Exact Reported		7-8 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2g-i
NOCA@CF total carbon atomic content~76.5%——Calculated From Reported
Approximate		7 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2g-i; Fig. S5
C 1s COOH atomic content4.9%——Text
Approximate		7 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2g-i; Fig. S5
C 1s COOH binding energy289 eV——Text
Exact Reported		7-8 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2g-i
N 1s N-5 binding energy400.1 eV——Text
Exact Reported		7-8 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2g-i
N 1s N-6 binding energy398.4 eV——Text
Exact Reported		7-8 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2g-i
NOCA@CF total nitrogen atomic content~18.7%——Calculated From Reported
Approximate		7 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2g-i; Fig. S5
N 1s N-Q binding energy401.1 eV——Text
Exact Reported		7-8 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2g-i
O 1s O-I atomic content3.1%——Text
Approximate		7 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2g-i; Fig. S5
O 1s O-I binding energy531.2 eV——Text
Exact Reported		7-8 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2g-i
O 1s O-II atomic content1.2%——Text
Approximate		7 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2g-i; Fig. S5
O 1s O-II binding energy532.4 eV——Text
Exact Reported		7-8 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2g-i
O 1s O-III atomic content0.4%——Text
Approximate		7 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2g-i; Fig. S5
O 1s O-III binding energy533.4 eV——Text
Exact Reported		7-8 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2g-i
NOCA@CF total oxygen atomic content~4.7%——Calculated From Reported
Approximate		7 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2g-i; Fig. S5
C 1s C-C atomic content33.3%—aboutText
Rounded Reported		7 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2g
C 1s C=N atomic content19.7%—aboutText
Rounded Reported		7 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2g
N 1s pyrrolic nitrogen (N-5) atomic content3.1%—aroundText
Rounded Reported		8 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2h
N 1s pyridinic nitrogen (N-6) atomic content12.3%—aroundText
Rounded Reported		8 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2h
N 1s quaternary nitrogen (N-Q) atomic content3.3%—aroundText
Rounded Reported		8 · 3.1. Synthesis and characterization of NOCA@CF · Fig. 2h