Details

Autor(en) / Beteiligte

• Xu, Weiwei
• Gao, Wenchao
• Meng, Linxing
• Tian, Wei
• Li, Liang

Titel

Incorporation of Sulfate Anions and Sulfur Vacancies in ZnIn2S4 Photoanode for Enhanced Photoelectrochemical Water Splitting

Ist Teil von

• Advanced energy materials, 2021-07, Vol.11 (26), p.n/a

Ort / Verlag

Weinheim: Wiley Subscription Services, Inc

Erscheinungsjahr

2021

Quelle

Wiley Online Library All Journals

Beschreibungen/Notizen

• Severe charge recombination and slow surface water oxidation kinetics seriously limit the practical application of ZnIn2S4 photoanodes for photoelectrochemical water splitting. Herein, an in situ strategy to introduce sulfate (SO42−) anions and controlled bulk sulfur vacancies (Sv) into a ZnIn2S4 photoanode is developed, and its PEC performance is remarkably enhanced, achieving a photocurrent density of 3.52 mA cm−2 at 1.23 V versus reversible hydrogen electrode (VRHE) and negatively shifted onset potential of 0.01 VRHE in phosphate buffer without a sacrificial agent under AM 1.5G illumination. The experimental characterizations and density functional theory calculations reveal that the SO42− groups enhance the oxygen evolution reaction kinetics, while bulk Sv improves the bulk carrier separation. The remarkable bulk carrier separation efficiency of 75.01% and surface carrier injection efficiency of 79.69% are achieved at 1.23 VRHE. This work provides a new route to design efficient photoanodes by the simultaneous manipulation of metal‐free anions and sulfur vacancies. In situ nonmetallic SO42− anions and modulated bulk sulfur vacancies are introduced into ZnIn2S4 photoanodes for photoelectrochemical water splitting. The SO42− groups help to reduce the oxygen evolution reaction (OER) overpotential, thus enhancing OER activity. In addition, the control of sulfur vacancies can promote the bulk charge separation and alleviate surface carrier recombination.