二硫化钼
串联
分解水
钼
催化作用
光电化学
材料科学
化学
无机化学
纳米技术
电化学
光催化
物理化学
冶金
有机化学
电极
复合材料
作者
Micha Ben‐Naim,Reuben J. Britto,Chase Aldridge,Rachel E. Mow,Myles A. Steiner,Adam C. Nielander,Laurie A. King,Daniel J. Friedman,Todd G. Deutsch,James L. Young,Thomas F. Jaramillo
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2020-07-30
卷期号:5 (8): 2631-2640
被引量:65
标识
DOI:10.1021/acsenergylett.0c01132
摘要
While photoelectrochemical (PEC) solar-to-hydrogen efficiencies have greatly improved over the past few decades, advances in PEC durability have lagged behind. Corrosion of semiconductor photoabsorbers in the aqueous conditions needed for water splitting is a major challenge that limits device stability. In addition, a precious-metal catalyst is often required to efficiently promote water splitting. Herein, we demonstrate unassisted water splitting using a nonprecious metal molybdenum disulfide nanomaterial catalytic protection layer paired with a GaInAsP/GaAs tandem device. This device was able to achieve stable unassisted water splitting for nearly 12 h, while a sibling sample with a PtRu catalyst was only stable for 2 h, highlighting the advantage of the nonprecious metal catalyst. In situ optical imaging illustrates the progression of macroscopic degradation that causes device failure. In addition, this work compares unassisted water splitting devices across the field in terms of the efficiency and stability, illustrating the need for improved stability.
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