{"title":"Electron Transfer in Heterojunctions Comprised of Co3O4 Nanorods Decorated with CoP Nanoparticles for Electrocatalytic Water Splitting","authors":"Wenjuan Lu, Xiaodong Cai*, Danhua Jiao*, Tianxue Li, Weiwei Xu, Liangliang Xu, Yue Wang* and Qizhao Wang*, ","doi":"10.1021/acsanm.5c00547","DOIUrl":null,"url":null,"abstract":"<p >Heterostructure design has been employed for electrocatalytic water splitting, nevertheless, the correlation between charge distribution at the active sites and the electrochemical processes remains ambiguous. In this study, bifunctional nanoarrayed CoP/Co<sub>3</sub>O<sub>4</sub> nanosheets on carbon cloth (CC) heterostructure nanoparticles were systematically synthesized to enhance electrical transmission at the interface. The CoP/Co<sub>3</sub>O<sub>4</sub> coupling CC substrate increases the electron transport efficiency and prevents catalyst aggregation and corrosion during catalytic operations. The synthesized materials exhibited expected hydrogen evolution reaction/oxygen evolution reaction (HER/OER) performance under alkaline circumstances, attaining 10 mA cm<sup>–2</sup> with overpotentials of 58 and 273 mV, respectively. Meanwhile, just 1.61 V is required for the two-electrode configuration to attain 10 mA cm<sup>–2</sup>, exceeding earlier recorded Co<sub>3</sub>O<sub>4</sub>-based electrocatalysts. Experimental and density functional theory (DFT) studies confirm that CoOOH/Co<sub>3</sub>O<sub>4</sub> functions as the true active site for the reconstructive formation of CoP/Co<sub>3</sub>O<sub>4</sub>, hence diminishing the adsorption energy of the intermediate and accelerating the reaction kinetics. This technique is anticipated to facilitate efficient charge transfer in water splitting and be applicable to other energy transformation processes.</p>","PeriodicalId":6,"journal":{"name":"ACS Applied Nano Materials","volume":"8 9","pages":"4899–4910 4899–4910"},"PeriodicalIF":5.5000,"publicationDate":"2025-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Nano Materials","FirstCategoryId":"88","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsanm.5c00547","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Heterostructure design has been employed for electrocatalytic water splitting, nevertheless, the correlation between charge distribution at the active sites and the electrochemical processes remains ambiguous. In this study, bifunctional nanoarrayed CoP/Co3O4 nanosheets on carbon cloth (CC) heterostructure nanoparticles were systematically synthesized to enhance electrical transmission at the interface. The CoP/Co3O4 coupling CC substrate increases the electron transport efficiency and prevents catalyst aggregation and corrosion during catalytic operations. The synthesized materials exhibited expected hydrogen evolution reaction/oxygen evolution reaction (HER/OER) performance under alkaline circumstances, attaining 10 mA cm–2 with overpotentials of 58 and 273 mV, respectively. Meanwhile, just 1.61 V is required for the two-electrode configuration to attain 10 mA cm–2, exceeding earlier recorded Co3O4-based electrocatalysts. Experimental and density functional theory (DFT) studies confirm that CoOOH/Co3O4 functions as the true active site for the reconstructive formation of CoP/Co3O4, hence diminishing the adsorption energy of the intermediate and accelerating the reaction kinetics. This technique is anticipated to facilitate efficient charge transfer in water splitting and be applicable to other energy transformation processes.
异质结构设计已被用于电催化水分解,然而,活性位点的电荷分布与电化学过程之间的关系仍然不明确。在本研究中,系统地合成了碳布(CC)异质结构纳米颗粒上的双功能纳米阵列CoP/Co3O4纳米片,以增强界面上的电传输。CoP/Co3O4耦合CC衬底提高了电子传递效率,防止了催化过程中的催化剂聚集和腐蚀。合成的材料在碱性条件下表现出预期的析氢/析氧反应(HER/OER)性能,可达到10 mA cm-2,过电位分别为58和273 mV。同时,双电极配置只需1.61 V即可达到10 mA cm-2,超过先前记录的基于co3o4的电催化剂。实验和密度泛函理论(DFT)研究证实CoOOH/Co3O4是CoP/Co3O4重构的真正活性位点,从而降低了中间体的吸附能,加速了反应动力学。该技术有望促进水分解过程中有效的电荷转移,并适用于其他能量转换过程。
期刊介绍:
ACS Applied Nano Materials is an interdisciplinary journal publishing original research covering all aspects of engineering, chemistry, physics and biology relevant to applications of nanomaterials. The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrate knowledge in the areas of materials, engineering, physics, bioscience, and chemistry into important applications of nanomaterials.