材料科学
制氢
光伏系统
氢
海水
钙钛矿(结构)
生产(经济)
工程物理
化学工程
电气工程
工程类
有机化学
海洋学
化学
经济
地质学
宏观经济学
作者
Yixian Li,Yanlin Li,Zhu Ma,Kai Yue,Qiang Yang,Xiaoshan Li,Qian Zhang,Fuchun Gou,Hao Du,Can Cheng,Maozhu Mao,Dunfeng Xiang,Zhuo Lv,Kai Liu,Bo Chen,Ruoxuan Xu,Qiang Yin,Bin Luo,Junjie Zhan,Kuan Sun
标识
DOI:10.1021/acsami.5c05891
摘要
Photovoltaic (PV) hydrogen production from seawater enables solar energy to be stored as hydrogen fuel; highly active electrocatalysts for the oxygen evolution reaction (OER) are critical. The interplay between PV output and the OER performance is crucial for achieving cost-effective and efficient hydrogen production. Here, we detail the synthesis of transition metal oxide catalysts through a rapid electrodeposition technique. Notably, the CoFe/indium tin oxide (ITO) demonstrated superior OER activity in a simulated seawater environment, with an overpotential of merely 268 mV at 10 mA/cm2. Unassisted perovskite PV hydrogen production coupled by tandem perovskite solar cells (PSCs) and CoFe/ITO//Pt water splitting cell achieved a peak operating current density of about 11.53 mA/cm2 and a solar to hydrogen efficiency of 14.18%. Furthermore, we meticulously crafted an extensive perovskite solar module framework for hydrogen production by scrutinizing the operational mechanisms of various active areas within the PSCs and the OER catalysts throughout the electrolytic process. A comprehensive techno-economic analysis has been conducted, which has unveiled that the levelized cost of hydrogen for the perovskite PV hydrogen production system was approximated at 7.17 $/kg. This finding provides both theoretical underpinning and practical direction for the advancement of solar hydrogen fuel production, underscoring its potential as a sustainable energy solution.
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