We report for the
first time that alkali carbonates (Li
2
CO
3
, K
2
CO
3
, and Rb
2
CO
3
) based on
a low-temperature solution process can be used
as interfacial modifiers for SnO
2
as robust electron-transport
layers (ETL) for inverted organic solar cells (iOSCs). The room-temperature
photoluminescence, the electron-only devices, and the impedance studies
altogether suggested the interfacial properties of the alkali carbonates–modified
SnO
2
ETLs, which were much better than those based on the
SnO
2
only, provided efficient charge transport, and reduced
the charge recombination rates for iOSCs. The iOSCs using the polymer
donor poly[4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-
b
;4,5-
b
′]dithiophene-2,6-diyl-
alt
-(4-(2-ethylhexyl)-3-fluorothieno[3,4-
b
]thiophene-)-2-carboxylate-2-6-diyl] and the fullerene acceptor phenyl-C
70
-butyric acid methyl ester as the active layer showed the
average power-conversion efficiencies (PCEs) based on ten devices
of 6.70, 6.85, and 7.35% with Li
2
CO
3
-, K
2
CO
3
-, and Rb
2
CO
3
-modified
SnO
2
as ETLs, respectively; these are more than 22, 24,
and 33% higher than those based on the SnO
2
only (5.49%).
Moreover, these iOSC devices exhibited long-term stabilities, with
over 90% PCEs remaining after the devices were stored in ambient air
for 6 weeks without encapsulations. We believe that alkali carbonates–modified
SnO
2
approaches are an effective way to achieve stable
and highly efficient iOSCs and might also be suitable for other optoelectronic
devices where an ETL is needed, such as perovskite solar cells or
organic light-emitting diodes.