OSCR

Topological acoustic synapse for high-dimensional neuromorphic computing.

Overview

Authors: Jinli Chen1,2, Akinsanmi S Ige1,2, Keith Runge1,2, Pierre A Deymier1,2, Xiaodong Yan1,2,3,4
  1. Department of Materials Science and Engineering, University of Arizona, Tucson, AZ 85721, USA
  2. New Frontiers of Sound Science and Technology Center, University of Arizona, Tucson, AZ 85721, USA
  3. Department of Electrical and Computer Engineering, University of Arizona, Tucson, AZ 85721, USA
  4. James C. Wyant College of Optical Sciences, University of Arizona, Tucson, AZ 85721, USA
Institutions: University of Arizona (United States)
Journal: Science advances, volume 12, issue 24, article eaec6633
Dates: received 28 September 2025; accepted 4 May 2026; published online 12 June 2026; in print June 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.1126/sciadv.aec6633 · PMID 42284405 · PMCID PMC13262634 · OpenAlex W7164542725
Open access: gold, a free copy (OpenAlex)
Status: data only
Categories: cellular / molecular (subfield)
Methods: Spectral & time-frequency, Machine learning
Topic: Ferroelectric and Negative Capacitance Devices (Electrical and Electronic Engineering, Engineering), according to OpenAlex
Funding: National Science Foundation (2441746, 2242925); Air Force Office of Scientific Research (FA9550-26-1-0326)
Citations: not cited yet (Europe PMC); 66 references in the paper

Abstract

The human brain performs complex, high-dimensional (HD) computations, such as causal reasoning, counterfactual thinking, and abstraction, with ~1011 neurons while consuming ~20 watts of power. Neuromorphic computing seeks similar efficiency, but current devices face bottlenecks in bandwidth, energy, wiring, footprint, and reliability that limit scalability. Here, we introduce the topological acoustic synapse (TAS), an acoustic-wave neuromorphic device that circumvents these limits by mapping information in multivariate state spaces. A single TAS generates and manipulates numerous computing channels that operate independently and in parallel. The TAS leverages nonlinear interactions to emulate biorealistic neuromorphic functionalities, including reconfigurable synaptic plasticity, neuromodulation, and hybrid analog-digital control. In classification tasks, a TAS handles multiple inputs simultaneously and generates various outputs, converging 20% faster while using 60% fewer parameters and at least an order of magnitude less power than state-of-the-art electrical devices. This work establishes the first acoustic synapse with parallel HD computing capabilities, presenting a scalable paradigm for neuromorphic hardware with high computational density.

Reproduced under the paper's license (CC BY), from the paper cited above.

Code

The paper links to its data, not to its authors' code: see the Data section.

The paper's code and data availability statement is in the Data section.

Tracing map

A tracing map links a paper to the code its authors published: this paper has none, so it has no map.

Data

Datasets cited

Data, code, and materials availability

Data and code are available at Harvard Dataverse (https://doi.org/10.7910/DVN/2CDQVI). All data and code needed to evaluate and reproduce the results in the paper are presented in the paper and online data and/or the Supplementary Materials. This study did not generate new materials.

Reproduced under the paper's license (CC BY), from the paper cited above.

Versions

The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.

Version 2, 28 September 2026

  • Funding: added National Science Foundation: 2441746, 2242925; Air Force Office of Scientific Research: FA9550-26-1-0326

Version 1, 27 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 5 authors, 40 references.

Cite

This paper

Chen, J., Ige, A. S., Runge, K., Deymier, P. A., & Yan, X. (2026). Topological acoustic synapse for high-dimensional neuromorphic computing. Science advances, 12(24), eaec6633. https://doi.org/10.1126/sciadv.aec6633

BibTeX

@article{chen2026topological,
author = {Chen, Jinli and Ige, Akinsanmi S and Runge, Keith and Deymier, Pierre A and Yan, Xiaodong},
title = {{Topological acoustic synapse for high-dimensional neuromorphic computing}},
journal = {Science advances},
year = {2026},
month = jun,
volume = {12},
number = {24},
pages = {eaec6633},
publisher = {American Association for the Advancement of Science},
issn = {2375-2548},
doi = {10.1126/sciadv.aec6633},
url = {https://doi.org/10.1126/sciadv.aec6633},
pmid = {42284405},
pmcid = {PMC13262634}
}

RIS

TY - JOUR
AU - Chen, Jinli
AU - Ige, Akinsanmi S
AU - Runge, Keith
AU - Deymier, Pierre A
AU - Yan, Xiaodong
TI - Topological acoustic synapse for high-dimensional neuromorphic computing
T2 - Science advances
J2 - Sci Adv
PY - 2026
DA - 2026/06/12
VL - 12
IS - 24
SP - eaec6633
SN - 2375-2548
PB - American Association for the Advancement of Science
DO - 10.1126/sciadv.aec6633
UR - https://doi.org/10.1126/sciadv.aec6633
LA - en
ER -

CSL-JSON

{
"id": "10.1126/sciadv.aec6633",
"type": "article-journal",
"title": "Topological acoustic synapse for high-dimensional neuromorphic computing",
"container-title": "Science advances",
"author": [
{
"family": "Chen",
"given": "Jinli"
},
{
"family": "Ige",
"given": "Akinsanmi S"
},
{
"family": "Runge",
"given": "Keith"
},
{
"family": "Deymier",
"given": "Pierre A"
},
{
"family": "Yan",
"given": "Xiaodong"
}
],
"container-title-short": "Sci Adv",
"volume": "12",
"issue": "24",
"page": "eaec6633",
"DOI": "10.1126/sciadv.aec6633",
"PMID": "42284405",
"PMCID": "PMC13262634",
"ISSN": "2375-2548",
"publisher": "American Association for the Advancement of Science",
"URL": "https://doi.org/10.1126/sciadv.aec6633",
"language": "en",
"issued": {
"date-parts": [
[
2026,
6,
12
]
]
}
}

Similar papers

The papers with a page that share the most with this one: the tools found in their code, their categories, datasets, cited references and authors, the rarest counting most.

[1] doi:10.1371/journal.pcbi.1013487 [code]
Flexible navigation with neuromodulated cognitive maps.
Journal: PLoS computational biology
In common: 3 references
[2] doi:10.1038/s41467-026-75488-6
Realization of the Bienenstock-Cooper-Munro rule in a single memristor.
Journal: Nature communications
In common: cellular / molecular, 2 references
[3] doi:10.3389/fnbeh.2026.1878769 [code]
<i>ADAMTS18</i> as a candidate gene linking social stress and depression: a cross-species study in African wild dogs (<i>Lycaon pictus</i>) and humans.
Journal: Frontiers in behavioral neuroscience
In common: cellular / molecular, 1 reference
[4] doi:10.1038/s41598-026-55218-0
Amorphous metal-oxide semiconductor thin-film neuron, synapse, and neuromorphic system.
Journal: Scientific reports
In common: cellular / molecular, 1 reference
[5] doi:10.1073/pnas.2537017123
Distinct cell type-specific mechanisms underlie cognitive dysfunction during persistent integrated stress response activation.
Journal: Proceedings of the National Academy of Sciences of the United States of America
In common: cellular / molecular, 1 reference
[6] doi:10.1016/j.isci.2026.115766 [code]
RNA-binding protein family diversification correlates with neural complexity across metazoan evolution.
Journal: iScience
In common: cellular / molecular, 1 reference
[7] doi:10.1038/s41467-026-71112-9 [code]
Modelling synaptic dysfunction in childhood dementia using human iPSC-derived cortical networks.
Journal: Nature communications
In common: cellular / molecular, 1 reference
[8] doi:10.1523/jneurosci.1506-25.2026 [code]
Controlling Spatio-Temporal Sequences of Neural Activity by Local Synaptic Changes.
Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience
In common: cellular / molecular, 1 reference
[9] doi:10.1038/s42003-025-09444-3 [code]
Decoupling of neurophysiological activity from structure mirrors global microarchitectural and neuromodulatory trends.
Journal: Communications biology
In common: cellular / molecular, 1 reference
[10] doi:10.1016/j.isci.2026.117309 [code]
Intracellular regulation of a serotonin-gated ion channel links receptor trafficking to memory.
Journal: iScience
In common: cellular / molecular, 1 reference

Contribute

The authors of this paper can claim it, correct its record and validate its tracing map, and the maintainers of its code (its owner, or a public member of its organization) correct what it says of their repository; anyone signed in can ask for its removal. Every request goes to OSCR's own machine, which answers it; your account page follows them.

Sign in with ORCID to claim this paper as one of its authors, correct its record or validate its tracing map: when the paper's metadata lists your ORCID iD, you are recognized at once. Maintainers of its code: sign in with GitHub, then claim the repository on your account page.

Request its removal

To ask OSCR to remove this record, the copies of its authors' scripts or its tracing map, use the removal request page: signed in, you say who you are, what to remove and why, then review and confirm the request. Published rules decide every request (how).

Discussion, reproductions, activity

Discussion: questions and error reports about this paper and its code, from signed-in readers and its authors. It opens with sign-in.

Reproductions: reports from readers who ran the authors' code: what they reproduced, with which environment, commit and data. It opens with sign-in.

Activity: what happens around this paper: new versions of its record, its map's validation, discussions and reproductions. It opens with sign-in.