MAX phase metal carbide-enabled triboelectric nanogenerator for integrated ammonia generation

dc.contributor.authorMappoli, Shidhincs
dc.contributor.authorSonigara, Kevalkumar Kishorbhaics
dc.contributor.authorNittoor Veedu, Radhikacs
dc.contributor.authorPumera, Martincs
dc.coverage.issue12cs
dc.coverage.volume47cs
dc.date.accessioned2026-01-22T07:54:03Z
dc.date.issued2025-12-01cs
dc.description.abstractElectrochemical ammonia synthesis at ambient conditions offers a promising and eco-friendly alternative to conventional methods, which are highly energy-intensive and major contributors to global greenhouse gas emissions. To make this approach sustainable, it must be integrated with a renewable, clean, and affordable energy source. Here, we developed an eco-friendly approach to produce electrocatalytic ammonia powered by electricity generated from a triboelectric nanogenerator (TENG) device through mechanical energy. The TENG device performance is improved by ternary MAX phase carbide Ti2AlC and polydimethylsiloxane (PDMS) polymer composite electrodes, and it can be operated with low-frequency mechanical energy. Ti2AlC was found suitable to modulate the triboelectric properties of PDMS with improved charge transfer, dielectric behavior, and surface roughness. We employed an optimized Ti2AlC/PDMS TENG to power electrocatalytic ammonia synthesis by electrochemical nitrate reduction using a V2C MXene catalyst, which efficiently triggers the reaction from the TENG output. Further, continuous ammonia generation during long-term mechanically operated TENG experiments validates the feasibility of developing such a clean energy loop. While TENG-driven electrochemical systems have been demonstrated for hydrogen evolution, pollutant degradation, and ammonia synthesis using non-MAX-based TENG devices. Here, we integrate a MAX (Ti2AlC)/PDMS-based TENG with a V2C MXene electrocatalyst for nitrate reduction to ammonia, establishing a previously unexplored triboelectric-catalyst pairing for self-powered ammonia synthesis. This integration presents a novel direction for the utilization of MAX phase compounds for triboelectric application and TENG-based ammonia production systems.en
dc.description.abstractElectrochemical ammonia synthesis at ambient conditions offers a promising and eco-friendly alternative to conventional methods, which are highly energy-intensive and major contributors to global greenhouse gas emissions. To make this approach sustainable, it must be integrated with a renewable, clean, and affordable energy source. Here, we developed an eco-friendly approach to produce electrocatalytic ammonia powered by electricity generated from a triboelectric nanogenerator (TENG) device through mechanical energy. The TENG device performance is improved by ternary MAX phase carbide Ti2AlC and polydimethylsiloxane (PDMS) polymer composite electrodes, and it can be operated with low-frequency mechanical energy. Ti2AlC was found suitable to modulate the triboelectric properties of PDMS with improved charge transfer, dielectric behavior, and surface roughness. We employed an optimized Ti2AlC/PDMS TENG to power electrocatalytic ammonia synthesis by electrochemical nitrate reduction using a V2C MXene catalyst, which efficiently triggers the reaction from the TENG output. Further, continuous ammonia generation during long-term mechanically operated TENG experiments validates the feasibility of developing such a clean energy loop. While TENG-driven electrochemical systems have been demonstrated for hydrogen evolution, pollutant degradation, and ammonia synthesis using non-MAX-based TENG devices. Here, we integrate a MAX (Ti2AlC)/PDMS-based TENG with a V2C MXene electrocatalyst for nitrate reduction to ammonia, establishing a previously unexplored triboelectric-catalyst pairing for self-powered ammonia synthesis. This integration presents a novel direction for the utilization of MAX phase compounds for triboelectric application and TENG-based ammonia production systems.en
dc.formattextcs
dc.format.extent1-11cs
dc.format.mimetypeapplication/pdfcs
dc.identifier.citationApplied Materials Today. 2025, vol. 47, issue 12, p. 1-11.en
dc.identifier.doi10.1016/j.apmt.2025.102919cs
dc.identifier.issn2352-9407cs
dc.identifier.orcid0000-0001-8073-3949cs
dc.identifier.orcid0000-0002-3385-0226cs
dc.identifier.orcid0000-0002-2779-2373cs
dc.identifier.orcid0000-0001-5846-2951cs
dc.identifier.other199451cs
dc.identifier.researcheridGVS-6569-2022cs
dc.identifier.researcheridGXG-1794-2022cs
dc.identifier.researcheridF-2724-2010cs
dc.identifier.scopus58913929100cs
dc.identifier.urihttps://hdl.handle.net/11012/255864
dc.language.isoencs
dc.relation.ispartofApplied Materials Todaycs
dc.relation.urihttps://www.sciencedirect.com/science/article/pii/S2352940725003373cs
dc.rightsCreative Commons Attribution 4.0 Internationalcs
dc.rights.accessopenAccesscs
dc.rights.sherpahttp://www.sherpa.ac.uk/romeo/issn/2352-9407/cs
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/cs
dc.subjectAmmoniaen
dc.subjectSelf-powered integrated systemsen
dc.subjectTENGen
dc.subjectElectrocatalysisen
dc.subjectAmmonia
dc.subjectSelf-powered integrated systems
dc.subjectTENG
dc.subjectElectrocatalysis
dc.titleMAX phase metal carbide-enabled triboelectric nanogenerator for integrated ammonia generationen
dc.title.alternativeMAX phase metal carbide-enabled triboelectric nanogenerator for integrated ammonia generationen
dc.type.driverarticleen
dc.type.statusPeer-revieweden
dc.type.versionpublishedVersionen
sync.item.dbidVAV-199451en
sync.item.dbtypeVAVen
sync.item.insts2026.01.22 08:54:03en
sync.item.modts2026.01.22 07:32:06en
thesis.grantorVysoké učení technické v Brně. Středoevropský technologický institut VUT. Energie budoucnosti a inovacecs

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