The electric organs of electric eels are able to convert ionic gradients into high-efficiency electricity because their electrocytes contain numerous “subnanoscale” protein ion channels that can achieve highly selective and ultrafast ion transport. Despite increasing awareness of blue energy production through nanochannel membranes, achieving high-performance energy output remains considerably unexplored. Here, we report on a heterogeneous subnanochannel membrane, consisting of a continuous UiO-66-NH2 metal-organic framework (MOF) and a highly ordered alumina nanochannel membrane. In the positively charged membrane, the angstrom-scale windows function as ionic filters for screening anions with different hydrated sizes. Driven by osmosis, the subnanochannel membrane can produce an exceptionally high Br−/NO3− selectivity of ~1240, hence yielding an unprecedented power of up to 26.8 W/m2 under a 100-fold KBr gradient. Achieving ultrahigh selective and ultrafast osmotic transport in ion channel–mimetic MOF-based membranes opens previously unexplored avenues toward advanced separation technologies and energy-harvesting devices.

Nanofluidic osmotic power, which converts a difference in salinity between brine and fresh water into electricity with nanoscale channels, has received more and more attention in recent years. It is long believed that to gain high-performance osmotic power, highly charged channel materials should be exploited so as to enhance the ion selectivity. In this paper, we report counterintuitive surface-charge-density-dependent osmotic power in a single funnel-shaped nanochannel (FSN), violating the previous viewpoint. For the highly charged nanochannel, the performance of osmotic power decreases with a further increase in its surface charge density. With increasing pH (surface charge density), the FSN enables a local maximum power density as high as ∼3.5 kW/m2 in a 500 mM/1 mM KCl gradient. This observation is strongly supported by our rigorous model where the equilibrium chemical reaction between functional carboxylate ion groups on the channel wall and protons is taken into account. The modeling reveals that for a highly charged nanochannel, a significant increase in the surface charge density amplifies the ion concentration polarization effect, thus weakening the effective salinity ratio across the channel and undermining the osmotic power generated.

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