462500 Tandem Core-Shell Si-Ta3N5 Photoanodes for Photoelectrochemical Water Oxidation

Tuesday, November 15, 2016: 1:36 PM
Golden Gate 8 (Hilton San Francisco Union Square)
Ieva Narkeviciute1, Pongkarn Chakthranont2, Christopher Hahn1, A.J.M. Mackus3, Stacey F. Bent2 and Thomas F. Jaramillo2, (1)Department of Chemical Engineering, Stanford University, Stanford, CA, (2)Chemical Engineering, Stanford University, Stanford, CA, (3)Eindhoven University of Technology, Eindhoven, Netherlands

Tantalum nitride (Ta3N) is a promising photoanode material for photoelectrochemical water splitting due to its n-type doping, relatively small bandgap of 2.1 eV, and band positions that straddle the redox potentials of both the hydrogen and oxygen evolution reactions.1 However, there are other challenges associated with Ta3N5 including poor charge transport properties, late photocurrent onset and photodegradation. To address all of these challenges, we fabricated efficient and stable core-shell heterostructured Si-Ta3N5 nanowire photoanodes coated with CoTiOx and NiO oxygen evolution co-catalysts.

Previous device architecture strategies for metal oxide semiconductors with charge transport limitations have included nanostructuring or scaffolding. In this work, a similar approach was applied to Ta3N5 to make a nanostructured core-shell Si-Ta3N5 device where the Si is a semiconducting, nanowire scaffold and the Ta3N5 is coated onto Si as a thin shell through which charge extraction should be efficient. With n-type Si as the scaffold, a heterojunction between Si and Ta3N5 is formed enabling a dual-absorber configuration resulting in a 200 mV cathodic shift for photocurrent onset due to the photovoltage gained from Si and therefore improves the overall performance of the Si-Ta3N5 device. The Si nanostructures were fabricated by a pseudo-Bosch deep reactive ion etching process, then tantalum oxide (Ta2O5) was coated onto Si by atomic layer deposition (ALD), and finally the Ta2O5 was nitrided in pure ammonia gas at 900 °C.

To gain a deeper understanding of charge transport within the thin Ta3N5 shells and to optimize the electrode performance, we varied the thickness of the shell between 10 and 70 nm and tested for ferrocyanide oxidation as a facile photoelectrochemical reaction. We found that in a core-shell Si-Ta3N5 nanostructured device, photocurrent decreased with increasing Ta3N5 thickness, which indicates that charge extraction becomes problematic with thicker Ta3N5 films. To verify that decreasing photocurrent was due to poor charge transport in thicker films, we performed absorbed photon to current efficiency (APCE) measurements with Ta3N5 deposited on planar Si and quartz substrates. Again, we found that APCE decreased once the films were thicker than 30 nm, demonstrating that the minority carrier diffusion length is likely tens of nanometers.

Finally, to address the problem of Ta3N5 photodegradation and to demonstrate photoelectrochemical performance for water oxidation in basic electrolyte with the core-shell system, CoTiOx and NiO oxygen evolution catalysts were coated onto Si-Ta3N5 by dipcoating from a sol-gel and ALD, respectively. In terms of activity, we found that CoTiOx interfaces well with Ta3N5 and yields a high photocurrent density compared to NiO. With NiO we were able to achieve a photocurrent density close to that of CoTiOx after Fe incorporation into NiO (henceforth called Ni(Fe)O).2 However, with CoTiOx, the device is not stable; but with only ~1 nm of Ni(Fe)O we see a marked improvement in stability. The device loses 40-50% of its peak photocurrent over a 24 hour chronoamperometry test. Compared to the current Ta3N5 reports in the literature, the Ni(Fe)O catalyst affords noteworthy stability.3-5 Therefore, in this work, we demonstrate a heterostructured Ta3N5 system with a tandem core-shell Si-Ta3N5 configuration that enabled earlier onset of photocurrent, efficient charge extraction from Ta3N5 and relatively stable long term water oxidation with a Ni(Fe)O co-catalyst.

1. Chun, W.-J.; Ishikawa, A.; Fujisawa, H.; Takata, T.; Kondo, J. N.; Hara, M.; Kawai, M.; Matsumoto, Y.; Domen, K. The Journal of Physical Chemistry B 2003, 107, (8), 1798-1803.

2. Trotochaud, L.; Young, S. L.; Ranney, J. K.; Boettcher, S. W. J Am Chem Soc 2014, 136, (18), 6744-6753.

3. Li, Y.; Zhang, L.; Torres-Pardo, A.; González-Calbet, J. M.; Ma, Y.; Oleynikov, P.; Terasaki, O.; Asahina, S.; Shima, M.; Cha, D.; Zhao, L.; Takanabe, K.; Kubota, J.; Domen, K. Nat Commun 2013, 4.

4. Liao, M.; Feng, J.; Luo, W.; Wang, Z.; Zhang, J.; Li, Z.; Yu, T.; Zou, Z. Advanced Functional Materials 2012, 22, (14), 3066-3074.

5. Liu, G.; Fu, P.; Zhou, L.; Yan, P.; Ding, C.; Shi, J.; Li, C. Chemistry – A European Journal 2015, 21, (27), 9624-9628.

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