4.8 Article

Efficient charge carrier separation and excellent visible light photoresponse in Cu2O nanowires

Journal

NANO ENERGY
Volume 50, Issue -, Pages 118-125

Publisher

ELSEVIER
DOI: 10.1016/j.nanoen.2018.05.028

Keywords

Cu2O nanowire; Tunable electronic structure; Carrier separation; Photodiode; First-principles

Funding

  1. National Natural Science Foundation of China [11674042, 61574024]
  2. Thousand Youth Talents Program of China [0210001104136]
  3. Key Program Science Foundation of Natural Science Foundation of Chongqing [cstc2017jcyjBX0054, cstc2015jcyjA50023]
  4. Fundamental Research Funds of the Central Universities [106112016CDJXY120001, 106112017CDJXY120005]
  5. Chongqing Innovation Fund for Graduate Students [CYS17015]

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Last decade has witnessed a surge of research pertaining to Cu2O nanowires for fields of photocatalysts, sensors, solar cells and rechargeable battery systems owing to their unique physicochemical properties. Their atomic properties, especially the size dependent electronic structures, however, remain unknown. Herein, by combining systematic first-principles calculations with material synthesis, characterization, device fabrication and measurement, we investigated physical properties of Cu2O nanowires and their applications in visible light photodiodes. We explored Cu2O nanowires with triangular and hexagonal cross sections of a series of diameter size, and found that they have favorable formation energies, indicative of facile synthesis. These nanowires have tunable direct band gap ranging from 2.2 to 5.4 eV, and a simple model is derived to effectively predict gap size. Remarkably, obvious spatially separated charge distribution of conduction and valance band edges was observed, ensuring long lifetime of excited electron-hole pairs that may greatly benefit performance of optoelectronic devices. Experimentally, we synthesized well-crystallized Cu2O nanowires and fabricated photodiodes, which exhibit a fast rise time of 9.86 ms, decay time of 27.37 ms, and high responsivity of 10 A/W. We expect these results to shed new light on Cu2O nanostructures for scalable, versatile and high-performance optoelectronic devices.

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