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High performance III-V photoelectrodes for solar water splitting via synergistically tailored structure and stoichiometry

机译:通过协同定制的结构和化学计量比的高性能III-V光电极用于太阳能水分解

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摘要

Catalytic interface of semiconductor photoelectrodes is critical for high-performance photoelectrochemical solar water splitting because of its multiple roles in light absorption, electrocatalysis, and corrosion protection. Nevertheless, simultaneously optimizing each of these processes represents a materials conundrum owing to conflicting requirements of materials attributes at the electrode surface. Here we show an approach that can circumvent these challenges by collaboratively exploiting corrosion-resistant surface stoichiometry and structurally-tailored reactive interface. Nanoporous, density-graded surface of ‘black’ gallium indium phosphide (GaInP2), when combined with ammonium-sulfide-based surface passivation, effectively reduces reflection and surface recombination of photogenerated carriers for high efficiency photocatalysis in the hydrogen evolution half-reaction, but also augments electrochemical durability with lifetime over 124 h via strongly suppressed kinetics of corrosion. Such synergistic control of stoichiometry and structure at the reactive interface provides a practical pathway to concurrently enhance efficiency and durability of semiconductor photoelectrodes without solely relying on the development of new protective materials.
机译:半导体光电极的催化界面对于高性能光电化学太阳能水分解至关重要,因为它在光吸收,电催化和腐蚀防护方面具有多种作用。然而,由于电极表面的材料属性的矛盾要求,同时优化这些工艺中的每一个都代表了材料难题。在这里,我们展示了一种可以通过共同开发耐腐蚀表面化学计量和结构定制的反应界面来克服这些挑战的方法。 “黑色”磷化铟镓镓(GaInP2)的纳米多孔,密度渐变的表面与基于硫化铵的表面钝化结合使用时,可有效减少光生载流子的反射和表面重组,从而在制氢半反应中实现高效光催化。通过强烈抑制腐蚀的动力学,还可延长电化学寿命,使用寿命超过124 augmenth。这种在反应界面上化学计量和结构的协同控制提供了一条实用的途径,可以同时提高半导体光电极的效率和耐用性,而不必完全依靠新的保护材料的开发。

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