Table 1.
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.