Evidence map›Paper›PMID 41102202›Full record

ArticleNature communications2025

Photonic neuromorphic computing using symmetry-protected zero modes in coupled nanolaser arrays.

Kaiwen Ji, Giulio Tirabassi, Cristina Masoller, Li Ge, Alejandro M Yacomotti

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Kaiwen JiLaboratoire Photonique Numérique et Nanosciences, Institut d'Optique d'Aquitaine, Université Bordeaux, CNRS, Talence, France.ORCID http://orcid.org/0000-0002-5644-8395
Giulio TirabassiDepartament de Física, Universitat Politécnica de Catalunya, Terrassa, Barcelona, Spain.ORCID http://orcid.org/0000-0002-8028-9005
Cristina MasollerDepartament de Física, Universitat Politécnica de Catalunya, Terrassa, Barcelona, Spain.ORCID http://orcid.org/0000-0003-0768-2019
Li GeDepartment of Engineering Science and Physics, College of Staten Island, CUNY, New York City, NY, USA.ORCID http://orcid.org/0000-0002-1922-4464
Alejandro M YacomottiLaboratoire Photonique Numérique et Nanosciences, Institut d'Optique d'Aquitaine, Université Bordeaux, CNRS, Talence, France. alejandro.giacomotti@institutoptique.fr.ORCID http://orcid.org/0000-0002-0570-0749

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-22- CE24-0012-01National Science Foundation (NSF) DMR-2326698National Science Foundation (NSF) PHY-1847240
6 · The paper itself

Abstract

Photonic neuromorphic computing has emerged as a promising approach toward energy-efficient artificial neural networks (ANN). Nanolasers, in particular, have become attractive candidates due to their ultra-low power consumption and intrinsic nonlinear characteristics. In this work, we propose a photonic neuromorphic computing architecture based on symmetry-protected robust zero modes at the center of the optical spectrum in coupled semiconductor nanolaser arrays. We experimentally demonstrate that even a small set of coupled nanolasers inherently provides non-convex classification capabilities, enabling it to solve non-trivial classification tasks. As a benchmark, we show that a 2 × 2 nanolaser array, acting as a hidden nonlinear layer with recurrent coupling is able to solve the XNOR logical gate. Our results further highlight the computation capabilities of such nanolaser array by showing robust classification performance even under challenging conditions, such as the classification of highly compressed handwritten digits with significantly overlapping feature boundaries. These findings suggest that symmetry or topologically protected modes in nanolaser arrays can leverage robust optical connections to tackle complex problems without the need of scaling up the number of neurons.

Identifiers

PMID41102202
PMCPMC12533018

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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.