废水
化学
制氢
锌
电解
海水
碳纤维
盐(化学)
污染物
水解
碳化作用
流出物
废物管理
可再生能源
氢
无机化学
环境化学
能量载体
制浆造纸工业
活性炭
资源回收
环境科学
污水处理
化学工程
作者
Muya Cai,Shiyu Wang,Hongya Wang,Fengyin Zhou,Mengyi Tang,Xiaodan Zhang,Xin Qu,Danfeng Wang,Dihua Wang,H. Yin
标识
DOI:10.1002/anie.202512441
摘要
Abstract The direct use of seawater/wastewater for H 2 production remains a challenge because impurities in the water compromise electrolyzer stability. Here, we propose a two‐step approach that uses seawater/wastewater for H 2 generation, salt recovery, and pollutant degradation. First, Zn hydrolysis occurs at 250 °C in a space‐isolated system, where vapor reacts with solid Zn to generate porous ZnO and H 2 at the Zn/vapor interface, achieving up to 99.8% H 2 production efficiency. The physical isolation ensures automatic separation of ZnO, salts, and H 2 while facilitating in situ hydrogenation that degrades 96.9% of organic phenol, demonstrating pollutant remediation. To close the materials‐loop, the produced ZnO is electrochemically reduced back to Zn with a 99.3% Faradaic efficiency. We validate scalability using a 72 Ah Zn electrolyzer coupled with a 1000 mL reactor, achieving batch production of 2.32 g H 2 and 0.92 g seasalt. LCA confirms this combined electrolysis–hydrolysis approach has fewer carbon emissions and environmental footprints. Beyond H 2 production, this system leverages Zn as both an energy carrier to mitigate renewable energy intermittency and a versatile agent for salt recovery and wastewater treatment.
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