<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ganguly A</submitter><funding>US-Ireland Research and Development Partnership Programme</funding><funding>Engineering and Physical Sciences Research Council</funding><pagination>12339-12352</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10941191</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(10)</volume><pubmed_abstract>Progress in electrochemical water-splitting devices as future renewable and clean energy systems requires the development of electrodes composed of efficient and earth-abundant bifunctional electrocatalysts. This study reveals a novel flexible and bifunctional electrode (&lt;i>&lt;b>NiO@CNTR&lt;/b>&lt;/i>) by hybridizing macroscopically assembled carbon nanotube ribbons (&lt;b>&lt;i>CNTRs&lt;/i>&lt;/b>) and atmospheric plasma-synthesized NiO quantum dots (QDs) with varied loadings to demonstrate bifunctional electrocatalytic activity for stable and efficient overall water-splitting (OWS) applications. Comparative studies on the effect of different electrolytes, e.g., acid and alkaline, reveal a strong preference for alkaline electrolytes for the developed &lt;i>&lt;b>NiO@CNTR&lt;/b>&lt;/i> electrode, suggesting its bifunctionality for both HER and OER activities. Our proposed &lt;i>&lt;b>NiO@CNTR&lt;/b>&lt;/i> electrode demonstrates significantly enhanced overall catalytic performance in a two-electrode alkaline electrolyzer cell configuration by assembling the same electrode materials as both the anode and the cathode, with a remarkable long-standing stability retaining ∼100% of the initial current after a 100 h long OWS run, which is attributed to the "synergistic coupling" between NiO QD catalysts and the CNTR matrix. Interestingly, the developed electrode exhibits a cell potential (&lt;i>E&lt;/i>&lt;sub>10&lt;/sub>) of only 1.81 V with significantly low NiO QD loading (83 μg/cm&lt;sup>2&lt;/sup>) compared to other catalyst loading values reported in the literature. This study demonstrates a potential class of carbon-based electrodes with single-metal-based bifunctional catalysts that opens up a cost-effective and large-scale pathway for further development of catalysts and their loading engineering suitable for alkaline-based OWS applications and green hydrogen generation.</pubmed_abstract><journal>ACS applied materials &amp; interfaces</journal><pubmed_title>Flexible Bifunctional Electrode for Alkaline Water Splitting with Long-Term Stability.</pubmed_title><pmcid>PMC10941191</pmcid><funding_grant_id>EP/M015211/1</funding_grant_id><funding_grant_id>EP/T016000/1</funding_grant_id><funding_grant_id>EP/V055232/1</funding_grant_id><funding_grant_id>EP/R008841/1</funding_grant_id><funding_grant_id>USI160</funding_grant_id><pubmed_authors>Ganguly A</pubmed_authors><pubmed_authors>Mariotti D</pubmed_authors><pubmed_authors>McGlynn RJ</pubmed_authors><pubmed_authors>Boies A</pubmed_authors><pubmed_authors>Maguire P</pubmed_authors><pubmed_authors>Chakrabarti S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Flexible Bifunctional Electrode for Alkaline Water Splitting with Long-Term Stability.</name><description>Progress in electrochemical water-splitting devices as future renewable and clean energy systems requires the development of electrodes composed of efficient and earth-abundant bifunctional electrocatalysts. This study reveals a novel flexible and bifunctional electrode (&lt;i>&lt;b>NiO@CNTR&lt;/b>&lt;/i>) by hybridizing macroscopically assembled carbon nanotube ribbons (&lt;b>&lt;i>CNTRs&lt;/i>&lt;/b>) and atmospheric plasma-synthesized NiO quantum dots (QDs) with varied loadings to demonstrate bifunctional electrocatalytic activity for stable and efficient overall water-splitting (OWS) applications. Comparative studies on the effect of different electrolytes, e.g., acid and alkaline, reveal a strong preference for alkaline electrolytes for the developed &lt;i>&lt;b>NiO@CNTR&lt;/b>&lt;/i> electrode, suggesting its bifunctionality for both HER and OER activities. Our proposed &lt;i>&lt;b>NiO@CNTR&lt;/b>&lt;/i> electrode demonstrates significantly enhanced overall catalytic performance in a two-electrode alkaline electrolyzer cell configuration by assembling the same electrode materials as both the anode and the cathode, with a remarkable long-standing stability retaining ∼100% of the initial current after a 100 h long OWS run, which is attributed to the "synergistic coupling" between NiO QD catalysts and the CNTR matrix. Interestingly, the developed electrode exhibits a cell potential (&lt;i>E&lt;/i>&lt;sub>10&lt;/sub>) of only 1.81 V with significantly low NiO QD loading (83 μg/cm&lt;sup>2&lt;/sup>) compared to other catalyst loading values reported in the literature. This study demonstrates a potential class of carbon-based electrodes with single-metal-based bifunctional catalysts that opens up a cost-effective and large-scale pathway for further development of catalysts and their loading engineering suitable for alkaline-based OWS applications and green hydrogen generation.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-06-28T03:18:06.893Z</modification><creation>2025-04-04T20:18:43.386Z</creation></dates><accession>S-EPMC10941191</accession><cross_references><pubmed>38425008</pubmed><doi>10.1021/acsami.3c12944</doi></cross_references></HashMap>