{"title":"WO3/Nb2CT x MXene 2D-2D异质结作为光电化学水分解的高性能光阳极。","authors":"Maida Murtaza, Waqas Ali Shah, Amir Waseem","doi":"10.1039/d5na00345h","DOIUrl":null,"url":null,"abstract":"<p><p>Photoelectrochemical (PEC) water splitting plays a key role in the production of green hydrogen, which is a sustainable energy source and non-exploitative to the environment. Therefore, the development of efficient photocatalysts is essential for enabling green hydrogen generation. In this work, the synergistic effect between tungsten oxide (WO<sub>3</sub>) and Nb<sub>2</sub>CT <sub><i>x</i></sub> (MXene) was explored for PEC water oxidation, and a composite catalyst was prepared using a hydrothermal and sonication approach to obtain a 2D/2D WO<sub>3</sub>/Nb<sub>2</sub>CT <sub><i>x</i></sub> heterojunction. WO<sub>3</sub> is a promising photocatalyst owing to its optimal band gap, stability, and cost-effectiveness, but its efficiency is hindered by poor charge transfer, rapid recombination, and weak visible light absorption. Integrating Nb<sub>2</sub>CT <sub><i>x</i></sub> , a highly conductive MXene, enhances charge separation, reduces electron-hole recombination, and strengthens photocatalytic activity. This synergy increases the number of catalytic sites, improves visible light absorption, and stabilizes WO<sub>3</sub>, leading to a more efficient and durable material for solar energy conversion and water splitting. The Tauc plot of the composite shows a slightly lower bandgap (2.56 eV) than that of pristine WO<sub>3</sub> (2.74 eV), while the charge separation efficiency of the composite is confirmed by its lower photoluminescence intensity than that of pristine WO<sub>3</sub>. Among the synthesized catalysts, WO<sub>3</sub>@Nb<sub>2</sub>C3 showed improved PEC-OER activity by attaining a photocurrent density of 4.71 mA cm<sup>-2</sup> at 1.23 V <i>vs.</i> RHE compared to the pristine WO<sub>3</sub> that attained a photocurrent density of 2.15 mA cm<sup>-2</sup> at the same potential. This strategy appears promising for designing catalysts for PEC water oxidation in a solar-driven hydrogen-powered future.</p>","PeriodicalId":18806,"journal":{"name":"Nanoscale Advances","volume":" ","pages":""},"PeriodicalIF":4.6000,"publicationDate":"2025-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12150343/pdf/","citationCount":"0","resultStr":"{\"title\":\"WO<sub>3</sub>/Nb<sub>2</sub>CT <sub><i>x</i></sub> MXene 2D-2D heterojunction as a high performance photoanode for photoelectrochemical water splitting.\",\"authors\":\"Maida Murtaza, Waqas Ali Shah, Amir Waseem\",\"doi\":\"10.1039/d5na00345h\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Photoelectrochemical (PEC) water splitting plays a key role in the production of green hydrogen, which is a sustainable energy source and non-exploitative to the environment. Therefore, the development of efficient photocatalysts is essential for enabling green hydrogen generation. In this work, the synergistic effect between tungsten oxide (WO<sub>3</sub>) and Nb<sub>2</sub>CT <sub><i>x</i></sub> (MXene) was explored for PEC water oxidation, and a composite catalyst was prepared using a hydrothermal and sonication approach to obtain a 2D/2D WO<sub>3</sub>/Nb<sub>2</sub>CT <sub><i>x</i></sub> heterojunction. WO<sub>3</sub> is a promising photocatalyst owing to its optimal band gap, stability, and cost-effectiveness, but its efficiency is hindered by poor charge transfer, rapid recombination, and weak visible light absorption. Integrating Nb<sub>2</sub>CT <sub><i>x</i></sub> , a highly conductive MXene, enhances charge separation, reduces electron-hole recombination, and strengthens photocatalytic activity. This synergy increases the number of catalytic sites, improves visible light absorption, and stabilizes WO<sub>3</sub>, leading to a more efficient and durable material for solar energy conversion and water splitting. The Tauc plot of the composite shows a slightly lower bandgap (2.56 eV) than that of pristine WO<sub>3</sub> (2.74 eV), while the charge separation efficiency of the composite is confirmed by its lower photoluminescence intensity than that of pristine WO<sub>3</sub>. Among the synthesized catalysts, WO<sub>3</sub>@Nb<sub>2</sub>C3 showed improved PEC-OER activity by attaining a photocurrent density of 4.71 mA cm<sup>-2</sup> at 1.23 V <i>vs.</i> RHE compared to the pristine WO<sub>3</sub> that attained a photocurrent density of 2.15 mA cm<sup>-2</sup> at the same potential. 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引用次数: 0
摘要
绿色氢是一种可持续的、对环境无害的能源,光电化学水分解在绿色氢生产中起着关键作用。因此,开发高效的光催化剂对于实现绿色制氢至关重要。本文探讨了氧化钨(WO3)与Nb2CT x (MXene)在PEC水氧化中的协同作用,并采用水热法和超声法制备了复合催化剂,得到了2D/2D WO3/Nb2CT x异质结。WO3具有良好的带隙、稳定性和成本效益,是一种很有前途的光催化剂,但其效率受到电荷转移差、复合速度快和可见光吸收弱的阻碍。集成高导电性MXene的Nb2CT x,可以增强电荷分离,减少电子-空穴复合,增强光催化活性。这种协同作用增加了催化位点的数量,提高了可见光吸收,并稳定了WO3,从而导致更有效和耐用的太阳能转换和水分解材料。Tauc图显示,复合材料的带隙(2.56 eV)略低于原始WO3 (2.74 eV),其光致发光强度低于原始WO3,证实了复合材料的电荷分离效率。在合成的催化剂中,WO3@Nb2C3在1.23 V / RHE下的光电流密度为4.71 mA cm-2,而原始WO3在相同电位下的光电流密度为2.15 mA cm-2,其PEC-OER活性有所提高。在太阳能驱动的氢动力未来,这一策略似乎有望为PEC水氧化设计催化剂。
WO3/Nb2CT x MXene 2D-2D heterojunction as a high performance photoanode for photoelectrochemical water splitting.
Photoelectrochemical (PEC) water splitting plays a key role in the production of green hydrogen, which is a sustainable energy source and non-exploitative to the environment. Therefore, the development of efficient photocatalysts is essential for enabling green hydrogen generation. In this work, the synergistic effect between tungsten oxide (WO3) and Nb2CT x (MXene) was explored for PEC water oxidation, and a composite catalyst was prepared using a hydrothermal and sonication approach to obtain a 2D/2D WO3/Nb2CT x heterojunction. WO3 is a promising photocatalyst owing to its optimal band gap, stability, and cost-effectiveness, but its efficiency is hindered by poor charge transfer, rapid recombination, and weak visible light absorption. Integrating Nb2CT x , a highly conductive MXene, enhances charge separation, reduces electron-hole recombination, and strengthens photocatalytic activity. This synergy increases the number of catalytic sites, improves visible light absorption, and stabilizes WO3, leading to a more efficient and durable material for solar energy conversion and water splitting. The Tauc plot of the composite shows a slightly lower bandgap (2.56 eV) than that of pristine WO3 (2.74 eV), while the charge separation efficiency of the composite is confirmed by its lower photoluminescence intensity than that of pristine WO3. Among the synthesized catalysts, WO3@Nb2C3 showed improved PEC-OER activity by attaining a photocurrent density of 4.71 mA cm-2 at 1.23 V vs. RHE compared to the pristine WO3 that attained a photocurrent density of 2.15 mA cm-2 at the same potential. This strategy appears promising for designing catalysts for PEC water oxidation in a solar-driven hydrogen-powered future.