IrOx Nanoclusters Modified by BaCO3 Enable ″Two Birds with One Stone″ in Solar-Driven Direct Unbuffered Seawater Electrolysis

作者：Gan Du, Wei Sun, Yuling Hu, Jianjun Liao, Xinlong Tian, Hanqing Gao, Chengjun Ge · 发表于：ACS Applied Materials & Interfaces · 年份：2021 · DOI：10.1021/acsami.1c17587 · 被引用次数：17 · 研究领域：Advanced Photocatalysis Techniques、Electrocatalysts for Energy Conversion、Electronic and Structural Properties of Oxides

Direct seawater electrolysis (DSE) coupled with renewable energy can maximize the sustainability of hydrogen energy acquisition by effectively alleviating the dependence on pure water resources. In a practical sense, the parallel chlorine evolution reaction (CER) of DSE opens up an opportunity to hit ″two birds with one stone″ by the dual values of anode and cathode. However, the biggest challenge is how to control the selectivity of CER to balance its values and drawbacks. Here, we use the different nucleation rates of iridium and barium ions in a weak basic solution and subsequent acid etching to devise an IrO x nanocluster (IrO x -Cs) supported BaCO 3 . The catalyst–support interaction between IrO x -Cs and BaCO 3 enables repelling the Cl – near the electrode interface layer to achieve a controlled CER selectivity. Additionally, the mass activity of the prepared IrO x -Cs@BaCO 3 is as high as 1402 A g –1 Ir, which is 7.12 times higher than that of IrO 2 oxides in unbuffered seawater. The photovoltaic-electrolysis device paired by IrO x -Cs@BaCO 3 with controlled CER activity and Pt demonstrated that valuable active chlorine and H 2 can be simultaneously obtained, with the flexibility to bind to different ion exchange membranes.