ArticleACS nano2026
Wrinkle-Assisted Nanofluidic Memristors for Geometry-Dependent Ionic Memory.
Article in ACS nano, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Activation of silent synapses driven by emerging technologies: mechanisms, disease associations, and prospects for clinical translation.Frontiers in synaptic neuroscience · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Electronic memristors have greatly advanced artificial synapse research, but their reliance on electron transport, which differs intrinsically from the ion-mediated signaling and spatiotemporal dynamics of biological synapses. Here, we present wrinkle-based, geometry-tunable nanochannels integrated within a hybrid polydimethylsiloxane (PDMS)-OSTEMER chip as a simple, low-cost, and reproducible platform for ionic memory. Exploiting the modulus mismatch between PDMS and OSTEMER, nanoscale wrinkles were selectively preserved only within the designated bridge region, forming a controllable array of nanochannels that govern ionic transport. By tailoring the number and length of these nanochannels, ionic conduction and memory characteristics could be precisely modulated. The resulting wrinkle-based nanochannel array device (WNAD) exhibited pronounced memristive hysteresis and effectively emulated key synaptic plasticity behaviors, including short-term plasticity (STP), paired-pulse facilitation (PPF), and reproducible potentiation-depression cycles. Moreover, the WNAD reproduced cumulative reinforcement under repeated stimulation, demonstrating geometry-dependent memory consolidation analogous to biological conditioning. Collectively, this study established wrinkle-based nanochannels as a bioinspired nanofluidic platform for ionic memory, bridging confined ionic transport and neuromorphic functionality.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.