Li Yong, Tong Jialu, Chai Zihao, Wu Yuanyuan, Wang Dongting, Li Hongbin
Engineering Research Center for Hemp and Product in Cold Region of Ministry of Education, School of Light Industry and Textile, Qiqihar University, Qiqihar 161006, China.
Heilongjiang Provincial Key Laboratory of Oilfield Applied Chemistry and Technology, School of Chemical Engineering, Daqing Normal University, Daqing 163712, China.
Polymers (Basel). 2025 May 21;17(10):1417. doi: 10.3390/polym17101417.
Linear conjugated polymer photocatalysts are still hampered by challenges involving low charge separation efficiency and poor water dispersibility, which are crucial factors during the photocatalytic water splitting process. Herein, we synthesized Poly thieno[3,2-b]thiophene (PTT) nanoparticles with excellent visible light response characteristic. Subsequently, we constructed the gun-bullet model PTT/graphitic carbon nitride (PTT/g-CN) heterojunctions for photocatalytic hydrogen production, where PTT with good visible light response characteristic serves as the bullets and g-CN with good water dispersibility serves as the guns. The as-prepared PTT/g-CN heterojunctions show greatly accelerated charge separation and excellent photocatalytic hydrogen production performance. Specifically, 10PTT/g-CN demonstrates extraordinary hydrogen production performance, reaching 6.56 mmol g h (2 wt% Pt loading, 0.1 M AA as sacrificial agent, > 420 nm), calculated to be 15.3 and 22.6 times those of PTT and g-CN, respectively. Mechanistic studies reveal that the significantly improved performance of PTT/g-CN heterojunctions is ascribed to the accelerated charge transfer, which originates from the C…S/N…S noncovalent interactions among PTT and g-CN. The C…S/N…S noncovalent interactions act as an efficient interface charge transmission channel (ICTC), accelerating the steady stream of excited electron transfer from the lowest unoccupied molecular orbital (LUMO) of PTT to that of g-CN. The gun-bullet model heterojunctions proposed here provide a practical strategy for achieving exceptional visible light photocatalytic hydrogen production by combining charge separation with water dispersibility in polymer/polymer heterojunctions via noncovalent interactions.
线性共轭聚合物光催化剂仍然受到低电荷分离效率和差的水分散性等挑战的阻碍,这些是光催化水分解过程中的关键因素。在此,我们合成了具有优异可见光响应特性的聚噻吩并[3,2-b]噻吩(PTT)纳米颗粒。随后,我们构建了用于光催化产氢的子弹-枪模型PTT/石墨相氮化碳(PTT/g-CN)异质结,其中具有良好可见光响应特性的PTT作为子弹,具有良好水分散性的g-CN作为枪。所制备的PTT/g-CN异质结显示出大大加速的电荷分离和优异的光催化产氢性能。具体而言,10PTT/g-CN表现出非凡的产氢性能,达到6.56 mmol g h(2 wt% Pt负载,0.1 M AA作为牺牲剂,>420 nm),经计算分别是PTT和g-CN的15.3倍和22.6倍。机理研究表明,PTT/g-CN异质结性能的显著提高归因于电荷转移的加速,这源于PTT和g-CN之间的C…S/N…S非共价相互作用。C…S/N…S非共价相互作用充当了一个有效的界面电荷传输通道(ICTC),加速了激发电子从PTT的最低未占分子轨道(LUMO)到g-CN的稳定流。这里提出的子弹-枪模型异质结通过非共价相互作用在聚合物/聚合物异质结中将电荷分离与水分散性相结合,为实现优异的可见光光催化产氢提供了一种实用策略。