材料科学
制氢
阳极
电解
电化学
阴极
催化作用
电解水
化学工程
电催化剂
量子点
纳米技术
氢
析氧
电极
硫黄
分解水
电化学能量转换
氢燃料
无机化学
储能
法拉第效率
作者
Run Ran,Haoliang Huang,Qing Chen,Fei Lin,Zhipeng Yu,W. A. Su,Chenyue Zhang,Qingsen Jia,Jingwei Wang,Yang Zhao,Kaiyang Xu,Binwen Zeng,Ying Xu,Weimian Zhang,Zhijian Peng,L. Liu
标识
DOI:10.1002/adfm.202525588
摘要
ABSTRACT Sulfur quantum dots (SQDs) represent an emerging class of metal‐free, biocompatible luminescent nanomaterials, yet their synthesis remains challenged by harsh conditions, high energy consumption, and limited scalability. Herein, we report a highly value‐added strategy coupling SQD synthesis with hydrogen production through sulfion (S 2 − ) oxidation reaction (SOR) assisted alkaline‐modified seawater electrolysis (SWE). Such coupling substantially lowers the energy demand for electrolysis and effectively circumvents the interfering chlorine evolution at the anode. An efficient and stable cobalt single‐atom catalyst (Co‐SAs‐PNC) is developed to boost SOR, achieving a large current density of 500 mA cm − 2 at 0.536 V vs. reversible hydrogen electrode in alkaline‐modified natural seawater and operating stably for 116 h. A flow cell comprising Co‐SAs‐PNC as the anode catalyst and commercial Pt/C as the cathode catalyst requires only 1.01 V to reach 500 mA cm − 2 and shows outstanding durability of >450 h. Besides valuable hydrogen generated at the cathode, the polysulfides electrochemically derived at the anode can be readily converted to multicolor photoluminescent SQDs. Comprehensive in situ/operando experiments and theoretical calculations elucidate the SOR mechanism at isolated Co sites. This work not only opens a new avenue for sustainable SQD production but also remarkably enhances the economic viability of the SWE technology.
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