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A robust ALD-protected silicon-based hybrid photoelectrode for hydrogen evolution under aqueous conditions

机译:鲁棒的ALD保护的硅基混合光电极可在水条件下析氢

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摘要

Hydrogen production through direct sunlight-driven water splitting in photo-electrochemical cells (PECs) is a promising solution for energy sourcing. PECs need to fulfill three criteria: sustainability, cost-effectiveness and stability. Here we report an efficient and stable photocathode platform for H2 evolution based on Earth-abundant elements. A p-type silicon surface was protected by atomic layer deposition (ALD) with a 15 nm TiO2 layer, on top of which a 300 nm mesoporous TiO2 layer was spin-coated. The cobalt diimine–dioxime molecular catalyst was covalently grafted onto TiO2 through phosphonate anchors and an additional 0.2 nm ALD-TiO2 layer was applied for stabilization. This assembly catalyzes water reduction into H2 in phosphate buffer (pH 7) with an onset potential of +0.47 V vs. RHE. The resulting current density is –1.3 ± 0.1 mA cm–2 at 0 V vs. RHE under AM 1.5 solar irradiation, corresponding to a turnover number of 260 per hour of operation and a turnover frequency of 0.071 s–1.
机译:通过直接在光电化学电池(PEC)中由阳光驱动的水分解产生氢气是一种有希望的能源采购解决方案。 PEC需要满足三个标准:可持续性,成本效益和稳定性。在这里,我们报告了一种基于地球丰富元素的高效,稳定的H2进化光阴极平台。通过15 nm TiO2层的原子层沉积(ALD)保护p型硅表面,在其顶部旋涂300 nm介孔TiO2层。通过膦酸酯锚定将二亚胺钴-二肟钴分子催化剂共价接枝到TiO2上,并另外施加0.2 nm ALD-TiO2层以稳定化。该组件在磷酸盐缓冲液(pH 7)中催化水还原为H2,相对于RHE的起始电位为+0.47V。相对于AM 1.5太阳辐射下的RHE,0 V下相对于RHE的结果电流密度为–1.3±0.1 mA cm –2 –1

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