Ko Myohwa, Lee Myounghyun, Kim Taehyeon, Jin Wonjoo, Jang Wonsik, Hwang Seon Woo, Kim Haneul, Kwak Ja Hun, Cho Seungho, Seo Kwanyong, Jang Ji-Wook
School of Energy and Chemical Engineering, Ulsan National Institute of Science and Technology (UNIST), Ulsan, Republic of Korea.
Department of Materials Science and Engineering, Ulsan National Institute of Science and Technology (UNIST), Ulsan, Republic of Korea.
Nat Commun. 2025 Mar 19;16(1):2701. doi: 10.1038/s41467-025-58000-4.
To commercialize the technology of photoelectrochemical hydrogen production, it is essential to surpass the US. Department of Energy target of 0.36 mmol h cm for 1-sun hydrogen production rate. In this study, we utilize crystalline silicon, which can exhibit the highest photocurrent density (43.37 mA cm), as the photoelectrode material. However, achieving bias-free water splitting (>1.6 V) remains challenging due to the intrinsic low photovoltage of crystalline silicon (0.6 V). To address this limitation, we replace water oxidation with low-potential furfural oxidation, enabling not only bias-free hydrogen production but also dual hydrogen production at both the cathodic and anodic sides. This approach results in a record 1-sun hydrogen production rate of 1.40 mmol h cm, exceeding the Department of Energy target by more than fourfold.
为了使光电化学制氢技术商业化,超越美国能源部制定的1个标准太阳光下产氢速率0.36 mmol h cm的目标至关重要。在本研究中,我们使用能够展现出最高光电流密度(43.37 mA cm)的晶体硅作为光电极材料。然而,由于晶体硅固有的低光电压(0.6 V),实现无偏压水分解(>1.6 V)仍然具有挑战性。为了解决这一限制,我们用低电位糠醛氧化取代水氧化,不仅实现了无偏压产氢,还在阴极和阳极两侧实现了双极产氢。这种方法产生了创纪录的1个标准太阳光下1.40 mmol h cm的产氢速率,超过能源部目标四倍多。