<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>3(2)</volume><submitter>Sadeghi E</submitter><funding>T?rkiye Bilimler Akademisi</funding><pubmed_abstract>The security of future energy, hydrogen, is subject to designing high-performance, stable, and low-cost electrocatalysts for hydrogen and oxygen evolution reactions (HERs and OERs), for the realization of efficient overall water splitting. Two-dimensional (2D) metal-organic frameworks (MOFs) introduce a large family of materials with versatile chemical and structural features for a variety of applications, such as supercapacitors, gas storage, and water splitting. Herein, a series of nanocomposites based on NCM/Ni-BDC@NF (N=Ni, C=Co, M:F=Fe, C=Cu, and Z=Zn, BDC: benzene dicarboxylic acid, NF: nickel foam) were directly developed on NF using a facile yet scalable solvothermal method. After coupling, the electronic structure of metallic atoms was well-modulated. Based on the XPS results, for the NCF/Ni-BDC, cationic atoms shifted to higher oxidation states, favorable for the OER. Conversely, for the NCZ/Ni-BDC and NCC/Ni-BDC nanocomposites, cationic atoms shifted to lower oxidation states, advantageous for the HER. The as-prepared NCF/Ni-BDC demonstrated prominent OER performance, requiring only 1.35 and 1.68 V versus a reversible hydrogen electrode to afford 10 and 50 mA cm&lt;sup>-2&lt;/sup> current densities, respectively. On the cathodic side, NCZ/Ni-BDC exhibited the best HER activity with an overpotential of 170 and 350 mV to generate 10 and 50 mA cm&lt;sup>-2&lt;/sup>, respectively, under 1.0 M KOH medium. In a two-electrode alkaline electrolyzer, the assembled NCZ/Ni-BDC (cathode) ∥ NCF/Ni-BDC (anode) couple demanded a cell voltage of only 1.58 V to produce 10 mA cm&lt;sup>-2&lt;/sup>. The stability of NCF/Ni-BDC toward OER was also exemplary, experiencing a continuous operation at 10, 20, and 50 mA cm&lt;sup>-2&lt;/sup> for nearly 45 h. Surprisingly, the overpotential after OER stability at 50 mA cm&lt;sup>-2&lt;/sup> dropped drastically from 450 to 200 mV. Finally, the faradaic efficiencies for the overall water splitting revealed the respective values of 100 and 85% for the H&lt;sub>2&lt;/sub> and O&lt;sub>2&lt;/sub> production at a constant current density of 20 mA cm&lt;sup>-2&lt;/sup>.</pubmed_abstract><journal>ACS materials Au</journal><pagination>143-163</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9999482</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Designing In Situ Grown Ternary Oxide/2D Ni-BDC MOF Nanocomposites on Nickel Foam as Efficient Electrocatalysts for Electrochemical Water Splitting.</pubmed_title><pmcid>PMC9999482</pmcid><pubmed_authors>Peighambardoust NS</pubmed_authors><pubmed_authors>Chamani S</pubmed_authors><pubmed_authors>Sadeghi E</pubmed_authors><pubmed_authors>Aydemir U</pubmed_authors></additional><is_claimable>false</is_claimable><name>Designing In Situ Grown Ternary Oxide/2D Ni-BDC MOF Nanocomposites on Nickel Foam as Efficient Electrocatalysts for Electrochemical Water Splitting.</name><description>The security of future energy, hydrogen, is subject to designing high-performance, stable, and low-cost electrocatalysts for hydrogen and oxygen evolution reactions (HERs and OERs), for the realization of efficient overall water splitting. Two-dimensional (2D) metal-organic frameworks (MOFs) introduce a large family of materials with versatile chemical and structural features for a variety of applications, such as supercapacitors, gas storage, and water splitting. Herein, a series of nanocomposites based on NCM/Ni-BDC@NF (N=Ni, C=Co, M:F=Fe, C=Cu, and Z=Zn, BDC: benzene dicarboxylic acid, NF: nickel foam) were directly developed on NF using a facile yet scalable solvothermal method. After coupling, the electronic structure of metallic atoms was well-modulated. Based on the XPS results, for the NCF/Ni-BDC, cationic atoms shifted to higher oxidation states, favorable for the OER. Conversely, for the NCZ/Ni-BDC and NCC/Ni-BDC nanocomposites, cationic atoms shifted to lower oxidation states, advantageous for the HER. The as-prepared NCF/Ni-BDC demonstrated prominent OER performance, requiring only 1.35 and 1.68 V versus a reversible hydrogen electrode to afford 10 and 50 mA cm&lt;sup>-2&lt;/sup> current densities, respectively. On the cathodic side, NCZ/Ni-BDC exhibited the best HER activity with an overpotential of 170 and 350 mV to generate 10 and 50 mA cm&lt;sup>-2&lt;/sup>, respectively, under 1.0 M KOH medium. In a two-electrode alkaline electrolyzer, the assembled NCZ/Ni-BDC (cathode) ∥ NCF/Ni-BDC (anode) couple demanded a cell voltage of only 1.58 V to produce 10 mA cm&lt;sup>-2&lt;/sup>. The stability of NCF/Ni-BDC toward OER was also exemplary, experiencing a continuous operation at 10, 20, and 50 mA cm&lt;sup>-2&lt;/sup> for nearly 45 h. Surprisingly, the overpotential after OER stability at 50 mA cm&lt;sup>-2&lt;/sup> dropped drastically from 450 to 200 mV. Finally, the faradaic efficiencies for the overall water splitting revealed the respective values of 100 and 85% for the H&lt;sub>2&lt;/sub> and O&lt;sub>2&lt;/sub> production at a constant current density of 20 mA cm&lt;sup>-2&lt;/sup>.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Mar</publication><modification>2025-04-19T04:11:50.587Z</modification><creation>2025-04-19T04:11:50.587Z</creation></dates><accession>S-EPMC9999482</accession><cross_references><pubmed>38089730</pubmed><doi>10.1021/acsmaterialsau.2c00073</doi></cross_references></HashMap>