TY - JOUR
T1 - Enabling highly efficient photocatalytic hydrogen generation and organics degradation
T2 - Via a perovskite solar cell-assisted semiconducting nanocomposite photoanode
AU - Liu, Xueqin
AU - Wang, Yang
AU - Cui, Xun
AU - Zhang, Meng
AU - Wang, Bing
AU - Rager, Matthew
AU - Shu, Zhu
AU - Yang, Yingkui
AU - Li, Zhen
AU - Lin, Zhiqun
N1 - Publisher Copyright:
© 2019 The Royal Society of Chemistry.
PY - 2019
Y1 - 2019
N2 - Organometal trihalide perovskite solar cells (PSCs) have been widely recognized as a promising photovoltaic device due to their impressive set of outstanding excellent optoelectronic properties. However, the instability and intermittent energy output caused by the intensity fluctuation and/or the daily cycle of sunlight have motivated the direct application of PSCs in other energy fields. Here, we report an integrated solar-energy-conversion/water-splitting device comprising a single-junction PSC and CdS-decorated TiO 2 nanorod array (i.e., semiconducting CdS/TiO 2 NRA nanocomposite) photoanode with excellent photoelectrochemical (PEC) performance. Intriguingly, the introduction of PSC is found to effectively suppress the recombination of electrons and holes during the PEC catalytic process. As a result, the integrated device yields an overall solar-to-hydrogen efficiency of 1.54% and exhibits a six-fold increase in the degradation rate of methylene blue over that of the CdS/TiO 2 NRAs alone. As such, the crafting of a perovskite solar cell-assisted nanocomposite semiconductor photoanode may represent a viable route to alleviating the electron-hole recombination in water splitting and the degradation of organic pollutants, thus rendering the effective implementation of PSCs.
AB - Organometal trihalide perovskite solar cells (PSCs) have been widely recognized as a promising photovoltaic device due to their impressive set of outstanding excellent optoelectronic properties. However, the instability and intermittent energy output caused by the intensity fluctuation and/or the daily cycle of sunlight have motivated the direct application of PSCs in other energy fields. Here, we report an integrated solar-energy-conversion/water-splitting device comprising a single-junction PSC and CdS-decorated TiO 2 nanorod array (i.e., semiconducting CdS/TiO 2 NRA nanocomposite) photoanode with excellent photoelectrochemical (PEC) performance. Intriguingly, the introduction of PSC is found to effectively suppress the recombination of electrons and holes during the PEC catalytic process. As a result, the integrated device yields an overall solar-to-hydrogen efficiency of 1.54% and exhibits a six-fold increase in the degradation rate of methylene blue over that of the CdS/TiO 2 NRAs alone. As such, the crafting of a perovskite solar cell-assisted nanocomposite semiconductor photoanode may represent a viable route to alleviating the electron-hole recombination in water splitting and the degradation of organic pollutants, thus rendering the effective implementation of PSCs.
UR - http://www.scopus.com/inward/record.url?scp=85058857333&partnerID=8YFLogxK
U2 - 10.1039/c8ta08998a
DO - 10.1039/c8ta08998a
M3 - Article
AN - SCOPUS:85058857333
SN - 2050-7488
VL - 7
SP - 165
EP - 171
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 1
ER -