The precise regulation of interfacial charge distribution highly determines the power conversion efficiency of perovskite solar cells (PSCs). Herein, inorganic (NiCo)1−yFeyOx nanoparticle decorated graphene oxide (GO) is successfully demonstrated as a hole booster for all‐inorganic CsPbIBr2 PSC free of precious metal electrode. Arising from the spontaneous electron transfer induced p‐type doping of GO from edged oxygen‐containing functional groups to (NiCo)1−yFeyOx, the best all‐inorganic CsPbIBr2 PSC achieves an efficiency of 10.95 % under one standard sun owing to the eliminated paradox between charge extraction and charge localization in GO surface. Furthermore, the champion device exhibits an excellent long‐term stability at 10 % relative humidity without encapsulation over 70 days because of the suppressed ions migration.
The trade-off between
selectivity and permeability as well as membrane
biofouling are major limitations of thin-film composite (TFC) membranes.
Graphene oxide quantum dot (GOQD) has aroused wide interest in membrane
preparation because of the hydrophilic groups and one-atom-thick structure
with lateral dimensions of 3–20 nm. GOQD could improve the
permeability by providing additional water channels in membranes without
compromising the selectivity. As an effective bactericidal material,
silver nanoparticles (Ag) were uniformly deposited on GOQD by a facile
method. The structure of the GOQD/Ag nanocomposite was verified by
high-resolution transmission electron microscopy, X-ray photoelectron
spectroscopy, attenuated total reflection Fourier transform infrared
spectroscopy, and Raman spectroscopy. Subsequently, GOQD/Ag was embedded
in the polyamide (PA) selective layer using an interfacial polymerization
method to obtain thin-film nanocomposite (TFN-GOQD/Ag) membranes.
The TFN membrane prepared at optimized conditions demonstrated a water
flux of 39.1 L·m–2·h–1 and a NaCl rejection rate of 98.9% at 16 bar, reflecting a remarkable
promotion in the flux (44.3%) compared with the pristine TFC membrane.
Furthermore, owing to the synergistic effect of GOQD and Ag, the TFN-GOQD/Ag200
membrane possessed prominent bactericidal capacity against both Gram-negative Escherichia coli (98.6%) and Gram-positive Staphylococcus aureus (96.5%). The bactericidal mechanism
was analyzed using a live/dead fluorescent imaging assay, scanning
electron microscopy, morphology analysis, and reactive oxygen species
detection. Furthermore, the bactericidal capacity of the TFN membrane
was also measured via silver ion leaching and during extended practical
application. This work demonstrates a new way to facilely prepare
reverse osmosis membranes with prominent separation performance and
excellent antibacterial and fouling resistance capacities.
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