Table 2 Modulated properties of photochromic carbon-based nanomaterials.

From: Coupling carbon nanomaterials with photochromic molecules for the generation of optically responsive materials

Function

Composition

Modulation range

References

Dipole moment

Azobenzene/CNTs

From 9 to 6 Debye

90

 

Spiropyran/CNTs

A change up to 24.1 Debye

91

 

Azobenzene/mechanical exfoliated graphene

From 9 to 6 Debye

92

 

Azobenzene—chemically rGO

A change up to 3 Debye

97

 

Spiropyran/chemically rGO

From 4 to 20 Debye

95

Current change

Dithienylethene-CNTs

Ion/Ioff ratio >105

82

 

Au/Azobenzene/mechanical exfoliated graphene

Ion/Ioff ratio of 100

87

 

Azobenzene-graphene

Ion/Ioff ratio of >100 (pH change)

84

 

Au/dihydroazulene/thermally rGO

Average Ion/Ioff ratio of 5–7

85

Charge transfer/separation

Dithienylethene-porphyrin-fullerene

Photoinduced electron transfer (25 ps) to singlet-singlet energy transfer (2.3 ps)

73

 

Azobenzene-fullerene-porphyrin

Photo-induced intramolecular charge separation much faster than photo-isomerization

75

 

Dihydroindolizine-porphyrin-fullerene

Quantum yield of electron transfer from 82 to 27%

76

 

Dithienylethene-fullerene- tetrathiafulvalene

Reduced charge-separated state lifetime (from open to closed form)

78

Charge transport

Spiropyran/chemically rGO

Hole mobility from 2.9 to 2.2 cm2 V−1 s−1, electron mobility remains almost constant at 2.6 cm2 V−1 s−1

95

 

Spiropyran/graphene grown by chemical vapour deposition

Hole and electron mobility from 508.8 to 392.4, and from 428.4 to 301.2 cm2 V−1s−1, respectively

94

 

Azobenzene/mechanical exfoliated graphene

Charge carrier concentration from 5 × 1013 to 4 × 1013 cm−2 (2.8 × 1012cm−2 for the other method)

93

 

Azobenzene/mechanical exfoliated graphene

Hole Concentrations from 4.3 × 1012 to 3.5 × 1012 cm−2

92

Magnetism

Azobenzene/graphene

0.8 μB (E)

0.0 μB (Z)

71

Photoconductivity

Hexabenzocoronene-

Dithienylethene

4.9 × 10−3 cm2V−1 s−1 (closed form)

9.6 × 10−4 cm2V−1 s−1 (open form)

72

Fluorescence

Carbon nanodots-spiropyran

5 times change in intensity between closed and open form

55

 

Carbon nanodots-spiropyran polymer

Reversible switching between blue-green and red

68

Dispersibility

Dendritic azobenzene/CNTs

Bundling–debundling

34

Morphology

Azobenzene-fullerene

Tunable 1D, 2D, 3D nanostructures

70

 

Azo-polymer/mechanical exfoliated multilayer graphene

Internal pressure exceeding 1 GPa

118

  1. CNT, carbon nanotube; rGO, reduced graphene oxide (the reduction can be done chemically, electrochemically or thermally and so on); 1D, one dimensional; 2D, two dimensional; 3D, three dimensional.