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类淀粉样蛋白修饰的碳氮化物作为一种仿生材料用于增强光催化 CO 还原。

Amyloid-Like Protein-Modified Carbon Nitride as a Bioinspired Material for Enhanced Photocatalytic CO Reduction.

机构信息

Key Laboratory of Applied Surface and Colloid Chemistry, Ministry of Education, Xi'an Key Laboratory of Organometallic Material Chemistry, Xi'an Key Laboratory of Polymeric Soft Matter, School of Chemistry and Chemical Engineering, Shaanxi Normal University, Xi'an 710119, P. R. China.

State Key Laboratory of Photocatalysis on Energy and Environment, Fuzhou University, Fuzhou 350002, P. R. China.

出版信息

ACS Appl Mater Interfaces. 2024 Nov 20;16(46):63495-63508. doi: 10.1021/acsami.4c12315. Epub 2024 Nov 7.

Abstract

Modification of g-CN with metal-free biomaterials through an environmentally friendly, low-energy, facile, and rapid single-step method is desired for the preparation of photocatalysts with efficient activity and high selectivity of CO reduction but remains a great challenge. Herein, we develop a phase-transitioned protein modification strategy for photocatalysts through superfast amyloid-like protein assembly on surfaces using a one-step sequential coating method. Metal-free carbon nitride/protein heterojunction composite photocatalysts (the phase-transitioned lysozyme (PTL), phase-transitioned bovine serum albumin (PTB), and phase-transitioned ovalbumin (PTO)-coated carbon nitride@SiO (CN@SiO) and bioinspired carbon nitride hollow nanospheres (CN-HS) obtained by etching of CN@SiO) are prepared using lysozyme, bovine serum albumin, and ovalbumin. The insulator-semiconductor heterojunctions formed at the protein-carbon nitride interface promote the migration and separation of photogenerated charges. The exposed hydrophobic alkyl and aryl groups of the surface-modified protein enable the formation of a CO-aqueous solution-photocatalyst three-phase interface on the catalyst surface and the exposed -NH groups provide sites for CO adsorption, which effectively increases CO mass transfer and its adsorption as well as hydrophobicity, promoting CO reduction and inhibiting hydrogen production. Therefore, protein modification effectively improves the CO reduction activity and CO selectivity. For instance, compared to CN-HS, the CO yield of the PTL-modified CN-HS (1346.5 μmol g) increased by 24.5 times and the CO selectivity reached 90.5%. These findings represent a critical advancement in the surface modification of carbon nitride for CO reduction and the design of bioinspired materials for various applications.

摘要

通过环保、低能耗、简便、快速的单步方法对无金属生物材料进行 g-CN 修饰,以制备具有高效活性和高 CO 还原选择性的光催化剂,但这仍然是一个巨大的挑战。在此,我们通过使用一步连续涂层法,在表面上超快地进行淀粉样蛋白组装,开发了一种用于光催化剂的相转变蛋白修饰策略。使用溶菌酶、牛血清白蛋白和卵清蛋白制备了无金属碳氮化物/蛋白异质结复合光催化剂(相转变溶菌酶(PTL)、相转变牛血清白蛋白(PTB)和相转变卵清蛋白(PTO)涂层的碳氮化物@SiO(CN@SiO)和通过蚀刻 CN@SiO 获得的仿生碳氮化物空心纳米球(CN-HS))。在蛋白-碳氮化物界面形成的绝缘体-半导体异质结促进光生电荷的迁移和分离。表面修饰蛋白暴露的疏水性烷基和芳基基团在催化剂表面形成 CO-水溶液-光催化剂三相界面,并暴露出的-NH 基团提供 CO 吸附位点,这有效地增加了 CO 的传质及其吸附以及疏水性,促进 CO 还原并抑制氢气生成。因此,蛋白修饰有效地提高了 CO 还原活性和 CO 选择性。例如,与 CN-HS 相比,PTL 修饰的 CN-HS(1346.5 μmol g)的 CO 产率增加了 24.5 倍,CO 选择性达到 90.5%。这些发现代表了碳氮化物 CO 还原表面修饰和仿生材料设计在各种应用中的重要进展。

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