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High Solar-to-Hydrogen Conversion Efficiency at pH 7 Based on a PV-EC Cell with an Oligomeric Molecular Anode
Author(s) -
Yuanyuan Shi,
TsungYu Hsieh,
Md Asmaul Hoque,
Werther Cambarau,
Stéphanie Narbey,
Carolina GimbertSuriñach,
Emilio Palomares,
Mario Lanza,
Antoni Llobet
Publication year - 2020
Publication title -
acs applied materials and interfaces
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.535
H-Index - 228
eISSN - 1944-8252
pISSN - 1944-8244
DOI - 10.1021/acsami.0c16235
Subject(s) - anode , materials science , catalysis , water splitting , photovoltaic system , hydrogen , electrochemistry , oxide , hydrogen production , chemical engineering , work (physics) , solar cell , energy conversion efficiency , solar energy , nanotechnology , inorganic chemistry , optoelectronics , electrode , chemistry , organic chemistry , metallurgy , thermodynamics , electrical engineering , physics , photocatalysis , engineering
In the urgent quest for green energy vectors, the generation of hydrogen by water splitting with sunlight occupies a preeminent standpoint. The highest solar-to-hydrogen (STH) efficiencies have been achieved with photovoltaic-electrochemical (PV-EC) systems. However, most PV-EC water-splitting devices are required to work at extreme conditions, such as in concentrated solutions of HClO 4 or KOH or under highly concentrated solar illumination. In this work, a molecular catalyst-based anode is incorporated for the first time in a PV-EC configuration, achieving an impressive 21.2% STH efficiency at neutral pH. Moreover, as opposed to metal oxide-based anodes, the molecular catalyst-based anode allows us to work with extremely small catalyst loadings (<16 nmol/cm 2 ) due to a well-defined metallic center, which is responsible for the fast catalysis of the reaction in the anodic compartment. This work paves the way for integrating molecular materials in efficient PV-EC water-splitting systems.

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