<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(15)</volume><submitter>Zhang L</submitter><pubmed_abstract>Development of a low cost, high activity, and stable nonprecious metal bifunctional catalyst for electrocatalytic water cracking is a hot topic and big challenge. In this paper, we prepared a nitrogen-doped carbon nanotube (NCNT)-enhanced three-dimensional self-supported electrocatalyst with CoP and Co&lt;sub>2&lt;/sub>P coexistence by a two-step strategy of high-temperature carbonization and low-temperature phosphorylation. Furthermore, the induced three-dimensional carbon network skeleton facilitates rapid charge transfer. In addition, the active sites of the carbon foam (CF) are greatly increased by the construction of hollow structures. As a bifunctional electrocatalyst, CoP/Co&lt;sub>2&lt;/sub>P/NCNT@CF exhibited excellent catalytic activity for both hydrogen evolution reaction and oxygen evolution reaction in alkaline media, requiring low overpotentials of 133 and 289 mV to obtain a current density of 10 mA cm&lt;sup>-2&lt;/sup>, respectively. Additionally, the synthesized catalysts also exhibit good long-term stability, maintaining high catalytic activity after 20 h of continuous operation. We also confirmed the main driving force to improve the electron transfer between the heterostructures of Co and P by XPS spectra. The excellent electrocatalytic performance can be attributed to the close synergy between the highly active CoP/Co&lt;sub>2&lt;/sub>P/NCNT and CF. This study provides a new strategy for the design of highly active bifunctional self-supporting electrocatalysts.</pubmed_abstract><journal>ACS omega</journal><pagination>12846-12855</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9026089</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Construction of CoP/Co&lt;sub>2&lt;/sub>P Coexisting Bifunctional Self-Supporting Electrocatalysts for High-Efficiency Oxygen Evolution and Hydrogen Evolution.</pubmed_title><pmcid>PMC9026089</pmcid><pubmed_authors>Tiwari SK</pubmed_authors><pubmed_authors>Wang N</pubmed_authors><pubmed_authors>Pang B</pubmed_authors><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Zhu Y</pubmed_authors><pubmed_authors>Ola O</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Liu S</pubmed_authors><pubmed_authors>Liu G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Construction of CoP/Co&lt;sub>2&lt;/sub>P Coexisting Bifunctional Self-Supporting Electrocatalysts for High-Efficiency Oxygen Evolution and Hydrogen Evolution.</name><description>Development of a low cost, high activity, and stable nonprecious metal bifunctional catalyst for electrocatalytic water cracking is a hot topic and big challenge. In this paper, we prepared a nitrogen-doped carbon nanotube (NCNT)-enhanced three-dimensional self-supported electrocatalyst with CoP and Co&lt;sub>2&lt;/sub>P coexistence by a two-step strategy of high-temperature carbonization and low-temperature phosphorylation. Furthermore, the induced three-dimensional carbon network skeleton facilitates rapid charge transfer. In addition, the active sites of the carbon foam (CF) are greatly increased by the construction of hollow structures. As a bifunctional electrocatalyst, CoP/Co&lt;sub>2&lt;/sub>P/NCNT@CF exhibited excellent catalytic activity for both hydrogen evolution reaction and oxygen evolution reaction in alkaline media, requiring low overpotentials of 133 and 289 mV to obtain a current density of 10 mA cm&lt;sup>-2&lt;/sup>, respectively. Additionally, the synthesized catalysts also exhibit good long-term stability, maintaining high catalytic activity after 20 h of continuous operation. We also confirmed the main driving force to improve the electron transfer between the heterostructures of Co and P by XPS spectra. The excellent electrocatalytic performance can be attributed to the close synergy between the highly active CoP/Co&lt;sub>2&lt;/sub>P/NCNT and CF. This study provides a new strategy for the design of highly active bifunctional self-supporting electrocatalysts.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2025-04-04T19:09:53.175Z</modification><creation>2025-04-04T19:09:53.175Z</creation></dates><accession>S-EPMC9026089</accession><cross_references><pubmed>35474771</pubmed><doi>10.1021/acsomega.2c00123</doi></cross_references></HashMap>