Prof. Ho-Hsiu ChouTaiwan
Department of Chemical Engineering, National Tsing Hua University (NTHU)
| 2023/08 to present | | Professor, Department of Chemical Engineering, NTHU |
| 2022/08 to present | | Director, Administrative Affair Division, Operations Center for Industry Collaboration, NTHU |
| 2021/07 to present | | Jointly Appointed Professor, College of Semiconductor Research, NTHU |
| 2006/09 - 2010/06 | | PhD: Department of Chemistry, NTHU |
| 2001/09 - 2005/06 | | BSc: Department of Chemistry, NTHU |
| 2013/10 - 2016/02 | | Postdoc Fellow, Department of Chemical Engineering, Stanford University |
| 2013/02 - 2013/05 | | Visiting Researcher, Engineering Science, IMEC (Belgium) |
| 2010/08 - 2013/02 | | Postdoc Fellow, Department of Chemistry, NTHU |
| 2025 | | NSTC Outstanding Research Award |
| 2024 | | The Polymer Society, Taipei Outstanding Polymer Research Award |
| 2024 | | The SCEJ Award for Outstanding Asian Researcher and Engineer |
Molecular Design and Interfacial Science of Functional Polymers for Sustainable Energy, Flexible Electronics, and Recyclable Materials.
Molecularly Engineered Semiconducting Polymers for Solar-Driven Hydrogen Evolution and Circular Waste Upcycling via Photoreforming
TBA TBA
Green and Sustainable Polymer Materials/TBA
Harnessing sunlight to drive chemical transformations represents one of the most promising routes toward a sustainable energy future. Among various approaches, molecularly engineered polymeric photocatalysts, encompassing conjugated polymers, conjugated microporous polymers, polymer dots, and covalent organic frameworks (COFs), provide unique advantages for solar-driven hydrogen evolution. Their molecular versatility—offering structural tunability, abundant design space, and compatibility with low-temperature, solution-based fabrication—enables precise control of energy levels and charge dynamics critical for efficient charge separation and hydrogen production. However, polymer-based photocatalysts still face challenges in aqueous environments due to their intrinsic hydrophobicity, which limits interfacial charge transfer and suppresses hydrogen evolution efficiency. Our research focuses on enhancing the polymer–water interface through rational control of backbone conjugation, donor–acceptor interactions, and interfacial properties, achieving highly efficient hydrogen evolution in the presence of sacrificial reagents. Building on this foundation, our recent research expands polymer photocatalysis beyond conventional water splitting toward circular waste upcycling via photoreforming. These semiconducting polymers exhibit exceptional design flexibility and controllable energy levels, yet their interfacial characteristics remain crucial for achieving stable performance. To address this, we incorporated hydrophilic building blocks into discontinuously conjugated backbones, markedly improving interfacial hydrophilicity and charge accessibility while maintaining desirable semiconducting features. Furthermore, by evaluating photocatalytic behavior in natural and simulated seawater, we reveal how ionic species and interfacial barriers influence activity and durability. Extending beyond pure-water systems, we further employ these materials for solar-driven photoreforming, coupling the oxidation of plastics, biomass, and food waste into value-added organics with the concurrent reduction to hydrogen fuel, thereby establishing a sustainable and circular waste-to-energy platform. This presentation will highlight the molecular design principles and interfacial engineering strategies that goven both hydrogen evolution and photoreforming systems, offering new insights into how polymer chemistry can bridge solar energy conversion and chemical production.