4.8 Article

Highly efficient and stable p-type ZnO nanowires with piezotronic effect for photoelectrochemical water splitting

Journal

NANO ENERGY
Volume 61, Issue -, Pages 550-558

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.nanoen.2019.04.098

Keywords

P-type ZnO; Nanowires; Piezotronic effect; Photoelectrochemical; Hydrogen evolution

Funding

  1. National Natural Science Foundation of China [51462008, 61764003]
  2. Key Research and Development Program of Hainan Province [ZDYF2017166]
  3. US Department of Energy, Basic Energy Sciences, Division of Materials Science and Engineering [DE-AC02-07CH11358]

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Unremitting efforts have been made to develop high-performance photoelectrochemical (PEC) water-splitting system to produce clean hydrogen fuel using sunlight. In this work, a novel way, combining highly-ordered nanowires (NWs) structure and piezotronic effect of p-type ZnO has been demonstrated to dramatically enhance PEC hydrogen evolution performance. Systematic characterizations indicate that the Sb atoms uniformly dope into ZnO NWs and substitute Zn sites with the introduction of two zinc vacancies to form the shallow acceptor Sb-Zn-2V(Zn) complex. Detailed synchrotron-based X-ray absorption near-edge structure (XANES) experiments in O K-edge and Zn L-edge further confirm the formation of the complex, and theoretical calculation verifies the Sb5+ state dominating the complex. The optimal photocurrent density of the 0.2Sb/ZnO-anneal NWs can reach -0.85 mA/cm(2) (0 V-RHE) which is 17.2 times larger than that of the n-ZnO NWs under sunlight illumination (100 mW/cm(2)). Furthermore, the piezotronic effect can be introduced to regulate the charge separation and transfer in the ZnO NWs through modulating the band structure near the interface. The photocurrent density can further increase to -1.08 mA/cm(2) (0 V-RHE) under a 0.6% tensile strain, which is 27.4% enhancement with respect to the ZnO sample without strain. These results provide an efficient way to design and develop high-performance photoelectrodes toward PEC hydrogen evolution.

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