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用于在酸性环境中稳定产氢的光阴极上的光照射氧化还原处理的铑磷纳米颗粒

Photoilluminated Redox-Processed RhP Nanoparticles on Photocathodes for Stable Hydrogen Production in Acidic Environments.

作者信息

Choi Ji Hoon, Lee Hak Hyeon, Jeon Sungho, Sarker Swagotom, Kim Dong Su, Stach Eric A, Cho Hyung Koun

机构信息

School of Advanced Materials Science and Engineering, Sungkyunkwan University, 2066, Seobu-ro, Jangan-gu, Suwon-si, Gyeonggi-do 16419, Republic of Korea.

Department of Materials Science and Engineering, University of Pennsylvania, Philadelphia, Pennsylvania 19104, United States.

出版信息

ACS Appl Mater Interfaces. 2024 May 1;16(17):21953-21964. doi: 10.1021/acsami.4c02147. Epub 2024 Apr 17.

Abstract

While photoelectrochemical (PEC) cells show promise for solar-driven green hydrogen production, exploration of various light-absorbing multilayer coatings has yet to significantly enhance their hydrogen generation efficiency. Acidic conditions can enhance the hydrogen evolution reaction (HER) kinetics and reduce overpotential losses. However, prolonged acidic exposure deactivates noble metal electrocatalysts, hindering their long-term stability. Progress requires addressing catalyst degradation to enable stable, efficient, and acidic PEC cells. Here, we proposed a process design based on the photoilluminated redox deposition (PRoD) approach. We use this to grow crystalline RhP nanoparticles (NPs) with a size of 5-10 on 30 nm-thick TiO, without annealing. Atomically precise reaction control was performed by using several cyclic voltammetry cycles coincident with light irradiation to create a system with optimal catalytic activity. The optimized photocathode, composed of RhP/TiO/Al-ZnO/CuO/Sb-CuO/ITO, achieved an excellent photocurrent density of 8.2 mA cm at 0 V and a durable water-splitting reaction in a strong acidic solution. Specifically, the RhP-loaded photocathode exhibited a 5.3-fold enhancement in mass activity compared to that utilizing just a Rh catalyst. Furthermore, scanning transmission electron microscopy (STEM) was performed to observe the real-time growth process of RhP NPs in a liquid cell.

摘要

虽然光电化学(PEC)电池在太阳能驱动的绿色制氢方面展现出潜力,但对各种光吸收多层涂层的探索尚未显著提高其产氢效率。酸性条件可以增强析氢反应(HER)动力学并减少过电位损失。然而,长时间暴露在酸性环境中会使贵金属电催化剂失活,从而阻碍其长期稳定性。要取得进展,需要解决催化剂降解问题,以实现稳定、高效且能在酸性环境下工作的PEC电池。在此,我们提出了一种基于光照射氧化还原沉积(PRoD)方法的工艺设计。我们利用此方法在30纳米厚的TiO上生长尺寸为5 - 10的结晶RhP纳米颗粒(NPs),无需退火。通过使用与光照射同步的几个循环伏安法循环来进行原子精确的反应控制,以创建具有最佳催化活性的系统。由RhP/TiO/Al - ZnO/CuO/Sb - CuO/ITO组成的优化光阴极在0 V时实现了8.2 mA cm的优异光电流密度,并在强酸性溶液中实现了持久的水分解反应。具体而言,与仅使用Rh催化剂相比,负载RhP的光阴极在质量活性方面提高了5.3倍。此外,还进行了扫描透射电子显微镜(STEM)观察RhP NPs在液体池中实时生长过程。

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