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. 2020 Dec 4;14(1):10–32. doi: 10.1002/cssc.202002002

Table 1.

Summary of major oxygen‐deficient Co‐based TMOs electrocatalysis for OER.

Synthesis method

Material

Method

Overpotential (b.t.) [mV]

Overpotential (a.t.) [mV]

Tafel slope (b.t.) [mV dec−1]

Tafel slope (a.t.) [mV dec−1]

KOH [m]

Ref.

thermal treatment

B‐CoO nanowires

CoO precursor was obtained by hydrothermal reaction of [Co (Ac)2 ⋅ 4H2O], (NH4HB4O7 ⋅ 3H2O) and water at 200 °C for 10 h, was annealed in Ar at 500 °C for 2 h

400 at 10 mA cm−2

280 at 10 mA cm−2

71

86

1

[24]

thermal treatment

Ni−Co/Co hydroxides

pristine Ni−Co/Co hydroxides were annealed in air at 300 °C

353 at 10 mA cm−2

320 at 10 mA cm−2

57

30

1

[25]

thermal treatment

PrBaCo2O5.75 PrBaCo2O5.5 perovskite

polycrystalline powders of PrBaCo2O6‐δ were annealed in N2 atmosphere at 250 and 600 °C for 30 min

360 (PrBaCo2O5.75) 420 (PrBaCo2O5.5) at 10 mA cm−2

70 (PrBaCo2O5.75) 80 (PrBaCo2O5.5)

1

[26]

hydrogen treatment

Fe2O3/CoOx

pristine Fe2O3/CoOx composite was annealed in 10 %H2/Ar at 150–300 °C for 30 min

316 at 10 mA cm−2

56

1

[27]

hydrogen treatment

Co3O4 quantum dots

pristine Co3O4 quantum dots were reduced 5 %H2/95 %Ar at 170 and 200 °C, 1 h

370 at 10 mA cm−2

315 (Co3O4‐200) 348 (Co3O4‐170) at 10 mA cm−2

72

49 (Co3O4‐200) 66 (Co3O4‐170)

1

[28]

hydrogen treatment

Ca2Mn2O5 perovskite

pristine CaMnO3 was annealed in 5 %H2 in Ar at 350 °C for 3 h

500 at 0.5 mA cm−2

380 at 1 mA cm−2

197

149

0.1

[23]

wet‐chemical reduction

Co3O4 mesoporous wires

pristine mesoporous Co3O4 NWs were reduced with NaBH4 solution at RT for 1 h

370 at 1.8 mA cm−2

370 at 13.1 mA cm−2

82

72

1

[16b]

wet‐chemical reduction

FexCoy‐ONS nanosheets

NaBH4 aqueous solution was added to a solution containing [Co(NO3)2, Fe(NO3)3, cetyltrimethylammonium bromide] at RT for 5 min

40 at 10 mA cm−2

308 at 10 mA cm−2

71.7

36.8

0.1

[29]

wet‐chemical reduction

Co2AlO4 nanosheets

pristine Co2AlO4 nanosheets were treated in a homogeneous solution of NaOH and ethylene glycol at 140 °C for 12 h

360 at 10 mA cm−2

280 at 10 mA cm−2

79.98

70.98

1

[30]

wet‐chemical reduction

CoFe2O4/graphene composite

pristine CoFe2O4/graphene was reduced with NaBH4 solution for 2 h

330 at 10 mA cm−2

300 at 10 mA cm−2

67

68

1

[31]

plasma treatment

Co3O4‐CoO nanosheets

Co3O4 nanosheets were treated by Ar–H2 plasma

330 at 10 mA cm−2

270 at 10 mA cm−2

49.3

49

1

[32]

plasma treatment

N‐doped Co3O4 nanosheets

pristine Co3O4 nanosheets were treated with N2 plasma at 300 W, 40 Pa for 60–80 s

560 at 10 mA cm−2

310 at 10 mA cm−2

234

59

0.1

[33]

plasma treatment

CoFe LDHs nanosheets

pristine CoFe LDHs were treated with H2O plasma with a dielectric barrier discharge (DBD) plasma reactor for 2–15 min

332 at 10 mA cm−2

290 at 10 mA cm−2

52

36

1

[34]

hydro‐thermal treatment

P‐doped Co3O4 nanosheet

Co3O4 and NaH2PO2⋅H2O with different weight ratios (2, 15, 30) were annealed in Ar atmosphere at low static pressure and at 250 °C for 1 h

395 at 20 mA cm−2

338 at 20 mA cm−2

62

52

1

[35]

laser irradiation

L–CoOOH

Co target was immersed in KOH solution was irradiated by nanosecond laser for 20 min at RT

410 at 10 mA cm−2

330 at 20 mA cm−2

75.4

63.2

1

[36]

laser irradiation

R‐FeCo2O4 nanoparticles

a water suspension of M‐FeCo2O4 microspheres was irradiated by laser for 30 min at RT

297 at 10 mA cm−2

276 at 10 mA cm−2

72.1

70.8

0.1

[37]

plasma treatment

La0.7Sr0.3CoO3‐δ

pristine La0.7Sr0.3CoO3‐δ was treated in Ar plasma for 10 min at 300 W and 70 Pa

433 at 10 mA cm−2

326 at 10 mA cm−2

92.1

61.6

1

[38]

thermal treatment

B‐doped CoO

a mixture of Co (Ac)2 and NH4HB4O7 (hydrothermally treated at 200 °C for 10 h) was annealed at 500 °C for 2 h in Ar

400 at 10 mA cm−2

280 at 10 mA cm−2

86

71

1

[24]

wet‐chemical reduction

CoFe2O4 nanosheets

pristine CoFe2O4 hollow nanospheres were reduced with NaBH4 solution for 1 h at RT

450 at 10 mA cm−2

320 at 10 mA cm−2

94

48

1

[39]

hydrogen treatment

reduced CaMn0.5Nb0.25O3‐δ

pristine CaMn0.5Nb0.25O3‐δ was annealed under 30 % H2/N2 at 350 °C for 2 h

300 at 0.5 mA cm−2

280 at 0.5 mA cm−2

140

98

0.1

[40]

ball milling

(Co0.2Mn0.2Ni0.2Fe0.2Zn0.2) Fe2O4

CoO, MnO, NiO, ZnO, and Fe3O4 powders were ball milled at a speed of 600 rpm for 65 h at a ball/powder ratio of 10 : 1

326 at 10 mA cm−2

53.6

1

[41]

b.t.=before treatment; a.t.=after treatment.