Shao-Yu Yuan, Tian-Tian Li, Jun-Yuan Cui, Jian-Kun Sun, Yan-Shang Gong, Artur Braun, Hong Liu, Jian-Jun Wang
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引用次数: 0
摘要
光电化学(PEC)水分裂技术为利用太阳能持续生产清洁氢燃料提供了一条前景广阔的途径。提高光阳极材料在酸性电解质中的性能一直是一个主要障碍--这是推动 PEC 技术发展的一个关键方面。为了应对这一挑战,我们报告了一种在酸性条件下提高赤铁矿光阳极效能的方法,即在其表面锚定含有羟基的 IrOx 纳米粒子。在 1.23 V 的电压下,相对于 RHE 的光电流密度达到了 1.71 mA cm-2,这标志着赤铁矿在酸性介质中的 PEC 效率有了显著的飞跃。IrOx 层的引入明显扩大了电化学活性表面积,增加了活性位点,促进了电荷分离和转移。它还可作为有效的空穴捕获层,将赤铁矿中光生成的空穴吸引到活性位点,促进水氧化过程的快速迁移。这一进步有望充分利用赤铁矿光阳极在酸性环境中的能力,从而为通过 PEC 水分离技术更有效、更可持续地制氢铺平道路。
Unlocking the potential of hematite photoanodes in acidic electrolytes: Boosting performance with ultra-small IrOx nanoparticles for efficient water splitting
Photoelectrochemical (PEC) water splitting offers a promising route for harnessing solar energy to produce clean hydrogen fuel sustainably. A major hurdle has been boosting the performance of photoanode materials within acidic electrolytes—a critical aspect for advancing PEC technology. In response to this challenge, we report a method to augment the efficacy of hematite photoanodes under acidic conditions by anchoring IrOx nanoparticles, replete with hydroxyl groups, onto their surface. A remarkable and steady photocurrent density of 1.71 mA cm−2 at 1.23 V versus RHE was achieved, marking a significant leap in PEC efficiency of hematite in acidic media. The introduction of the IrOx layer notably expanded the electrochemically active surface area for more active sites, fostering improved charge separation and transfer. It also served as an effective hole capture layer, drawing photogenerated holes from hematite to facilitate swift migration to the active sites for the water oxidation process. This advancement has the potential to fully harness the capabilities of hematite photoanodes in acidic environments, thereby smoothing the path toward more effective and sustainable hydrogen production through PEC water splitting.