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Cu2O Photocathode for Low Bias Photoelectrochemical Water Splitting Enabled by NiFe-Layered Double Hydroxide Co-Catalyst

机译:NiFe层状双氢氧化物助催化剂实现低偏压光电化学水分解的Cu2O阴极

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摘要

Layered double hydroxides (LDHs) are bimetallic hydroxides that currently attract considerable attention as co-catalysts in photoelectrochemical (PEC) systems in view of water splitting under solar light. A wide spectrum of LDHs can be easily prepared on demand by tuning their chemical composition and structural morphology. We describe here the electrochemical growth of NiFe-LDH overlayers on Cu2O electrodes and study their PEC behavior. By using the modified Cu2O/NiFe-LDH electrodes we observe a remarkable seven-fold increase of the photocurrent intensity under an applied voltage as low as −0.2 V vs Ag/AgCl. The origin of such a pronounced effect is the improved electron transfer towards the electrolyte brought by the NiFe-LDH overlayer due to an appropriate energy level alignment. Long-term photostability tests reveal that Cu2O/NiFe-LDH photocathodes show no photocurrent loss after 40 hours of operation under light at −0.2 V vs Ag/AgCl low bias condition. These improved performances make Cu2O/NiFe-LDH a suitable photocathode material for low voltage H2 production. Indeed, after 8 hours of H2 production under −0.2 V vs Ag/AgCl the PEC cell delivers a 78% faradaic efficiency. This unprecedented use of Cu2O/NiFe-LDH as an efficient photocathode opens new perspectives in view of low biasd or self-biased PEC water splitting under sunlight illumination.
机译:层状双氢氧化物(LDHs)是双金属氢氧化物,鉴于太阳光下的水分解作用,目前作为光电化学(PEC)系统中的助催化剂受到了广泛关注。通过调节LDH的化学组成和结构形态,可以轻松地制备各种LDH。我们在此描述NiFe-LDH覆盖层在Cu2O电极上的电化学生长,并研究其PEC行为。通过使用改良的Cu2O / NiFe-LDH电极,我们观察到在低至-0.2 V的施加电压下,相对于Ag / AgCl,光电流强度显着增加了七倍。这种明显影响的起因是由于适当的能级对准,NiFe-LDH覆层带来的电子向电解质的转移得到改善。长期的光稳定性测试表明,相对于Ag / AgCl低偏压条件,Cu2O / NiFe-LDH光电阴极在−0.2 V的光照下工作40小时后无光电流损失。这些改进的性能使Cu2O / NiFe-LDH成为适合低压H2生产的光电阴极材料。实际上,在相对于Ag / AgCl的−0.2 V下H2产生8小时后,PEC电池的法拉第效率为78%。鉴于在阳光照射下低偏置或自偏置的PEC水分解,这种前所未有的使用Cu2O / NiFe-LDH作为有效的光电阴极开辟了新的视角。

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