| Literature DB >> 33651590 |
Cheng-Chu Chung1, Han Yeh2, Po-Hsien Wu1, Cheng-Chieh Lin3,4, Chia-Shuo Li5, Tien-Tien Yeh2, Yi Chou2, Chuan-Yu Wei1, Cheng-Yen Wen1,3, Yi-Chia Chou2, Chih-Wei Luo2, Chih-I Wu5, Ming-Yang Li6, Lain-Jong Li6, Wen-Hao Chang2,7,8, Chun-Wei Chen1,3,9.
Abstract
Platinum diselenide (PtSe2) is a group-10 two-dimensional (2D) transition metal dichalcogenide that exhibits the most prominent atomic-layer-dependent electronic behavior of "semiconductor-to-semimetal" transition when going from monolayer to bulk form. This work demonstrates an efficient photoelectrochemical (PEC) conversion for direct solar-to-hydrogen (H2) production based on 2D layered PtSe2/Si heterojunction photocathodes. By systematically controlling the number of atomic layers of wafer-scale 2D PtSe2 films through chemical vapor deposition (CVD), the interfacial band alignments at the 2D layered PtSe2/Si heterojunctions can be appropriately engineered. The 2D PtSe2/p-Si heterojunction photocathode consisting of a PtSe2 thin film with a thickness of 2.2 nm (or 3 atomic layers) exhibits the optimized band alignment and delivers the best PEC performance for hydrogen production with a photocurrent density of -32.4 mA cm-2 at 0 V and an onset potential of 1 mA cm-2 at 0.29 V versus a reversible hydrogen electrode (RHE) after post-treatment. The wafer-scale atomic-layer controlled band engineering of 2D PtSe2 thin-film catalysts integrated with the Si light absorber provides an effective way in the renewable energy application for direct solar-to-hydrogen production.Entities:
Keywords: PtSe2/p-Si heterojunction; atomic layered catalyst; atomic-layer-dependent electronic behavior; photoelectrochemical cell; solar-to-hydrogen conversion
Year: 2021 PMID: 33651590 DOI: 10.1021/acsnano.0c08970
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881