Sangsawang Pongpop, Wisuttirattanamanee Chayada, Aueng-Aree Nichaphat, Thivasasith Anawat, Ittisanronnachai Somlak, Kaiyasuan Chokchai, Ngamroj Pawarisa, Phophuttharaksa Natthakit, Tanalikhit Pattarapon, Chavanalikigorn Natputthiya, Mueanngern Yutichai
Department of Chemistry, Kamnoetvidya Science Academy 999 Moo 1, Pa Yup Nai, Wang Chan Rayong 21210 Thailand
Frontier Research Center (FRC), Vidyasirimedhi Institute of Science and Technology 555 Moo 1, Pa Yup Nai, Wang Chan Rayong 21210 Thailand.
RSC Adv. 2025 Mar 11;15(10):7758-7768. doi: 10.1039/d4ra08196j. eCollection 2025 Mar 6.
Biopolymer films derived from starch and chitosan were soaked in vanadium salt solutions to produce vanadium metallopolymer films. Visible light irradiation induces significant color shifts from yellow to green due to changes in the oxidation state of vanadium. The material was observed to undergo dramatic structural changes upon incorporation of vanadium, with further restructuring occurring after visible light illumination. Metallopolymer films exhibited enhanced hydrophobic properties, which were further amplified when the material was irradiated with visible light, resulting in water contact angles up to 103°. X-ray photoelectron spectroscopy (XPS) measurements reveal that photoirradiation reduces vanadium metal from the 5+ (VO ) oxidation state to lower oxidation states. Initially, V (VO ) interacts electrostatically with -NH moieties in chitosan. These interactions were diminished following photoreduction as the formation of reduced species such as V (VO) decreases the interaction of vanadium (previously V) with -NH . As the biopolymer chain breaks free from vanadium, interactions between neighboring polymer strands increase, leading to significant shifts in biopolymer surface structuring. Atomic force microscopy (AFM) measurements showed high root mean square (RMS) roughness values in starch-chitosan control films due to free interactions between biopolymer chains. Upon vanadium soaking, the chains were pulled inward by electrostatic attraction, which created a constraint that reduced the configurational states of the polymer and prevented the chains from interacting with neighboring polymer chains, significantly lowering RMS roughness. After photoirradiation, the electrostatic forces became repulsive, which released the polymer from this constraint and led to a slight increase in RMS roughness. The newly structured surface, dominated by high-frequency features, aligns well with the hydrophobicity model being developed in this work. To verify the reversible nature of the film's surface properties, irradiation and oxidative treatment cycles were conducted, and the contact angle of water was shown to drastically cycle from >100° following irradiation to ≈60° after oxidative treatments. This reversible property provides prospects and design parameters for the fabrication of future smart photo-switchable biopolymer films.
将由淀粉和壳聚糖制成的生物聚合物薄膜浸泡在钒盐溶液中,以制备钒金属聚合物薄膜。由于钒氧化态的变化,可见光照射会引起显著的颜色变化,从黄色变为绿色。观察到该材料在掺入钒后会发生剧烈的结构变化,在可见光照射后会进一步重构。金属聚合物薄膜表现出增强的疏水性能,当材料用可见光照射时,疏水性能会进一步增强,导致水接触角高达103°。X射线光电子能谱(XPS)测量表明,光辐照将钒金属从5 +(VO)氧化态还原为较低的氧化态。最初,V(VO)与壳聚糖中的-NH基团发生静电相互作用。光还原后,随着诸如V(VO)等还原物种的形成减少了钒(先前为V)与-NH的相互作用,这些相互作用减弱。随着生物聚合物链从钒中游离出来,相邻聚合物链之间的相互作用增加,导致生物聚合物表面结构发生显著变化。原子力显微镜(AFM)测量表明,由于生物聚合物链之间的自由相互作用,淀粉-壳聚糖对照薄膜的均方根(RMS)粗糙度值较高。钒浸泡后,链通过静电引力向内拉动,这产生了一种约束,降低了聚合物的构型状态,并阻止链与相邻聚合物链相互作用,显著降低了RMS粗糙度。光辐照后,静电力变得具有排斥性,这使聚合物从这种约束中释放出来,并导致RMS粗糙度略有增加。以高频特征为主的新结构表面与本工作中正在开发的疏水性模型非常吻合。为了验证薄膜表面性质的可逆性,进行了辐照和氧化处理循环,结果表明水的接触角从辐照后的>100°急剧循环到氧化处理后的≈60°。这种可逆性质为未来智能光开关生物聚合物薄膜的制造提供了前景和设计参数。