Yu Hao, Dongfang Chen*, Dongyi Pu, Song Hu, Pavese Doague Nguela, Pucheng Pei and Xiaoming Xu*,
{"title":"通过协同电子调制构建N和f双掺杂pt基异质结催化剂以增强析氢反应活性和CO耐受性","authors":"Yu Hao, Dongfang Chen*, Dongyi Pu, Song Hu, Pavese Doague Nguela, Pucheng Pei and Xiaoming Xu*, ","doi":"10.1021/acsaem.4c0335010.1021/acsaem.4c03350","DOIUrl":null,"url":null,"abstract":"<p >The development of efficient and durable hydrogen evolution reaction (HER) electrocatalysts is critical for sustainable energy conversion. Although platinum (Pt) serves as a benchmark HER catalyst, its practical application is hindered by the high cost, limited durability, and susceptibility to CO poisoning. In this work, we report a heterojunction Pt-based catalyst, Pt@NCL-MXene, synthesized by LiF etching of MXene and subsequent NH<sub>3</sub> calcination. This process introduces dual nitrogen (N) and fluorine (F) doping and yields a nitrogen-doped carbon layer (NCL) coating on Pt nanoparticles with an average size of only 3.4 nm. Compared with conventional Pt–C catalysts, Pt@NCL-MXene exhibits a larger specific surface area, enhanced electron transfer efficiency, and an optimized d-band center, thereby facilitating both H* adsorption and desorption. As a result, Pt@NCL-MXene achieves a significantly lower overpotential of 73 mV at a current density of 100 mA cm<sup>–2</sup>, alongside improved kinetics and stability under operational conditions. Furthermore, the 9 wt % F-rich MXene support effectively suppresses CO adsorption on Pt, reducing the CO uptake to 0.224 mmol g<sup>–1</sup>, which is purportedly lower than that of Pt–C (0.264 mmol g<sup>–1</sup>), thereby mitigating CO poisoning and prolonging the catalyst’s service life. These findings offer insights into the rational design of advanced CO-resistant Pt-based HER electrocatalysts.</p>","PeriodicalId":4,"journal":{"name":"ACS Applied Energy Materials","volume":"8 6","pages":"3745–3753 3745–3753"},"PeriodicalIF":5.4000,"publicationDate":"2025-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Constructing N- and F-Dual-Doped Pt-Based Heterojunction Catalysts via Synergistic Electronic Modulation for Enhanced Hydrogen Evolution Reaction Activity and CO Tolerance\",\"authors\":\"Yu Hao, Dongfang Chen*, Dongyi Pu, Song Hu, Pavese Doague Nguela, Pucheng Pei and Xiaoming Xu*, \",\"doi\":\"10.1021/acsaem.4c0335010.1021/acsaem.4c03350\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The development of efficient and durable hydrogen evolution reaction (HER) electrocatalysts is critical for sustainable energy conversion. Although platinum (Pt) serves as a benchmark HER catalyst, its practical application is hindered by the high cost, limited durability, and susceptibility to CO poisoning. In this work, we report a heterojunction Pt-based catalyst, Pt@NCL-MXene, synthesized by LiF etching of MXene and subsequent NH<sub>3</sub> calcination. This process introduces dual nitrogen (N) and fluorine (F) doping and yields a nitrogen-doped carbon layer (NCL) coating on Pt nanoparticles with an average size of only 3.4 nm. Compared with conventional Pt–C catalysts, Pt@NCL-MXene exhibits a larger specific surface area, enhanced electron transfer efficiency, and an optimized d-band center, thereby facilitating both H* adsorption and desorption. As a result, Pt@NCL-MXene achieves a significantly lower overpotential of 73 mV at a current density of 100 mA cm<sup>–2</sup>, alongside improved kinetics and stability under operational conditions. Furthermore, the 9 wt % F-rich MXene support effectively suppresses CO adsorption on Pt, reducing the CO uptake to 0.224 mmol g<sup>–1</sup>, which is purportedly lower than that of Pt–C (0.264 mmol g<sup>–1</sup>), thereby mitigating CO poisoning and prolonging the catalyst’s service life. 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Constructing N- and F-Dual-Doped Pt-Based Heterojunction Catalysts via Synergistic Electronic Modulation for Enhanced Hydrogen Evolution Reaction Activity and CO Tolerance
The development of efficient and durable hydrogen evolution reaction (HER) electrocatalysts is critical for sustainable energy conversion. Although platinum (Pt) serves as a benchmark HER catalyst, its practical application is hindered by the high cost, limited durability, and susceptibility to CO poisoning. In this work, we report a heterojunction Pt-based catalyst, Pt@NCL-MXene, synthesized by LiF etching of MXene and subsequent NH3 calcination. This process introduces dual nitrogen (N) and fluorine (F) doping and yields a nitrogen-doped carbon layer (NCL) coating on Pt nanoparticles with an average size of only 3.4 nm. Compared with conventional Pt–C catalysts, Pt@NCL-MXene exhibits a larger specific surface area, enhanced electron transfer efficiency, and an optimized d-band center, thereby facilitating both H* adsorption and desorption. As a result, Pt@NCL-MXene achieves a significantly lower overpotential of 73 mV at a current density of 100 mA cm–2, alongside improved kinetics and stability under operational conditions. Furthermore, the 9 wt % F-rich MXene support effectively suppresses CO adsorption on Pt, reducing the CO uptake to 0.224 mmol g–1, which is purportedly lower than that of Pt–C (0.264 mmol g–1), thereby mitigating CO poisoning and prolonging the catalyst’s service life. These findings offer insights into the rational design of advanced CO-resistant Pt-based HER electrocatalysts.
期刊介绍:
ACS Applied Energy Materials is an interdisciplinary journal publishing original research covering all aspects of materials, engineering, chemistry, physics and biology relevant to energy conversion and storage. 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 energy applications.