Lin Wei-Cheng, Sun Yu-En, Zhuang Ying-Rang, Huang Tse-Fu, Lin Kuei-Jhong, Elsenety Mohamed M, Yen Jui-Chen, Hsu Hung-Kai, Chen Bo-Han, Chang Chen-Yu, Chang Je-Wei, Huang Hsin-Ni, Li Bing-Heng, Jungsuttiwong Siriporn, Haldar Toton, Wang Shin-Huei, Lin Wan-Chi, Wu Tien-Lin, Chen Chin-Wen, Yu Chi-Hua, Su An-Chung, Lin Kun-Han, Jeng U-Ser, Yang Shang-Da, Chou Ho-Hsiu
Department of Chemical Engineering, National Tsing Hua University, Hsinchu 300044, Taiwan.
Department of Chemistry, Faculty of Science, Al-Azhar University, Nasr City, Cairo 11884, Egypt.
J Am Chem Soc. 2025 Jan 22;147(3):2537-2548. doi: 10.1021/jacs.4c13856. Epub 2024 Dec 20.
Mini-emulsion and nanoprecipitation techniques relied on large amounts of surfactants, and unresolved miscibility issues of heterojunction materials limited their efficiency and applicability in the past. Through our molecular design and developed surfactant-free precipitation method, we successfully fabricated the best miscible bulk-heterojunction-particles (BHJP) ever achieved, using donor () and acceptor () polymers. The structural similarity ensures optimal miscibility, as supported by the interaction parameter of the / blend is positioned very close to the binodal curve. Experimental studies and molecular dynamics simulations further revealed that surfactants hinder electron output sites and reduce the concentration of sacrificial agents at the interface, slowing polaron formation. Multiscale experiments verified that these BHJP, approximately 12 nm in diameter, further form cross-linked fractal networks of several hundred nanometers. Transient absorption spectroscopy showed that BHJP facilitates polaron formation and electron transfer. Our BHJP demonstrated a superior hydrogen evolution rate (HER) compared to traditional methods. The most active BHJP achieved an HER of 251.2 mmol h g and an apparent quantum yield of 26.2% at 500 nm. This work not only introduces a practical method for preparing BHJP but also offers a new direction for the development of heterojunction materials.
过去,微乳液和纳米沉淀技术依赖大量表面活性剂,且异质结材料未解决的混溶性问题限制了它们的效率和适用性。通过我们的分子设计并开发出无表面活性剂沉淀法,我们成功制备出了有史以来最佳混溶性的本体异质结颗粒(BHJP),使用了给体()和受体()聚合物。结构相似性确保了最佳混溶性,/ 共混物的相互作用参数非常接近双节线曲线就证明了这一点。实验研究和分子动力学模拟进一步表明,表面活性剂会阻碍电子输出位点并降低界面处牺牲剂的浓度,减缓极化子的形成。多尺度实验证实,这些直径约为12 nm的BHJP进一步形成了数百纳米的交联分形网络。瞬态吸收光谱表明,BHJP促进极化子的形成和电子转移。与传统方法相比,我们的BHJP展现出优异的析氢速率(HER)。最具活性的BHJP在500 nm处实现了251.2 mmol h g的HER和26.2%的表观量子产率。这项工作不仅介绍了一种制备BHJP的实用方法,还为异质结材料的发展提供了新方向。