Lipińska Wiktoria, Wolff Stefania, Dehm Katharina E, Hager Simon P, Gumieniak Justyna, Kramek Agnieszka, Crisp Ryan W, Coy Emerson, Grochowska Katarzyna, Siuzdak Katarzyna
Centre for Plasma and Laser Engineering, Institute of Fluid-Flow Machinery, Polish Academy of Sciences, Fiszera 14 Street, 80-231 Gdańsk, Poland.
Faculty of Applied Physics and Mathematics, Institute of Nanotechnology and Materials Engineering, Gdańsk University of Technology, Narutowicza 11/12 Street, 80-233 Gdańsk, Poland.
Nanoscale. 2024 Aug 15;16(32):15265-15279. doi: 10.1039/d4nr01440e.
Differences between photoelectrochemical and electrochemical activity were thoroughly investigated for the oxygen evolution reaction mediated by AgS deposited on two types of ordered titania substrates. Titanium dioxide nanotubes were fabricated by anodization of magnetron sputtered Ti films on ITO-coated glass substrates or directly from Ti foil. Further, AgS deposition on the nanotubes was carried out using successive ionic layer adsorption and reaction, known as SILAR, with 5, 25, and 45 cycles performed. Two types of nanotubes, one on transparent the other on non-transparent substrates were compared regarding their geometry, structure, optical, and electrochemical properties. It was demonstrated that the composite of AgS grown on transparent nanotubes exhibits higher catalytic activity compared to AgS grown on the nanotubes formed on Ti foil. The results showed that transparent nanotubes after modification with AgS by 25 SILAR cycles exhibit 3 times higher photocurrent under visible light illumination than non-transparent ones treated with the same number of cycles. Furthermore, transparent nanotubes after 45 SILAR cycles of AgS exhibit enhanced activity towards oxygen evolution reaction with 9.3 mA cm at 1.1 V Ag/AgCl/0.1 M KCl which is six times higher than titania alone on Ti foil.
针对沉积在两种有序二氧化钛基底上的硫化银介导的析氧反应,对光电化学活性和电化学活性之间的差异进行了深入研究。通过对涂覆有氧化铟锡(ITO)的玻璃基底上的磁控溅射钛膜进行阳极氧化,或直接从钛箔制备二氧化钛纳米管。此外,使用连续离子层吸附和反应(称为SILAR)在纳米管上进行硫化银沉积,分别进行了5、25和45个循环。比较了两种类型的纳米管,一种在透明基底上,另一种在非透明基底上,考察了它们的几何形状、结构、光学和电化学性质。结果表明,与生长在钛箔上形成的纳米管上的硫化银相比,生长在透明纳米管上的硫化银复合材料表现出更高的催化活性。结果表明,经过25个SILAR循环用硫化银改性后的透明纳米管在可见光照射下的光电流比经过相同循环次数处理的非透明纳米管高3倍。此外,经过45个SILAR循环的硫化银处理后的透明纳米管在1.1 V Ag/AgCl/0.1 M KCl条件下对析氧反应表现出增强的活性,电流密度为9.3 mA cm,这比钛箔上单独的二氧化钛高6倍。