Highly‐Tunable Nickel Cobalt Oxide as a Low‐Temperature P‐Type Contact in Organic Photovoltaic Devices. Issue 4 (26th November 2012)
- Record Type:
- Journal Article
- Title:
- Highly‐Tunable Nickel Cobalt Oxide as a Low‐Temperature P‐Type Contact in Organic Photovoltaic Devices. Issue 4 (26th November 2012)
- Main Title:
- Highly‐Tunable Nickel Cobalt Oxide as a Low‐Temperature P‐Type Contact in Organic Photovoltaic Devices
- Authors:
- Ndione, Paul F.
Garcia, Andres
Widjonarko, N. Edwin
Sigdel, Ajaya K.
Steirer, K. Xerxes
Olson, Dana C.
Parilla, Philip A.
Ginley, David S.
Armstong, Neal R.
Richards, Robin E.
Ratcliff, Erin L.
Berry, Joseph J. - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>We report on the investigation of nickel cobalt oxide (Ni<sub>x</sub>Co<sub>3−x</sub>O<sub>4</sub>) thin films grown by pulsed laser deposition as hole‐transport interlayers (HTL) in organic photovoltaic (OPV) devices. Films of 7 nm thickness were grown under various oxygen deposition pressures (pO<sub>2</sub>) in the range of 2–200 mTorr. We explore both bulk and surface properties of these thin films. The workfunction (ϕ) for each of the films was statistically similar (∼4.7 eV), regardless of pO<sub>2</sub>. There was not a strong dependence of the power conversion efficiency (η) on the conductivities of the HTLs varying between 0.009 ‐ 10 S/cm. The observed differences in OPV efficiencies (ranging from 1.16 to 2.46%) were correlated to the near surface chemical composition of the Ni<sub>x</sub>Co<sub>3−x</sub>O<sub>4</sub> HTL, as observed by differences in the relative surface hydroxyl concentration. The critical role of the near‐surface composition of the HTL at the HTL/organic interface was further explored by modifying the hydroxyl concentration using an oxygen plasma treatment. This treatment mitigated the impact of surface hydroxyl coverage, demonstrating either identical or increased values for ϕ and η, regardless of initial pO<sub>2</sub> in the creation of the Ni<sub>x</sub>Co<sub>3−x</sub>O<sub>4</sub> HTL. To further explore this we also employed a phosphonic acid surface modification<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>We report on the investigation of nickel cobalt oxide (Ni<sub>x</sub>Co<sub>3−x</sub>O<sub>4</sub>) thin films grown by pulsed laser deposition as hole‐transport interlayers (HTL) in organic photovoltaic (OPV) devices. Films of 7 nm thickness were grown under various oxygen deposition pressures (pO<sub>2</sub>) in the range of 2–200 mTorr. We explore both bulk and surface properties of these thin films. The workfunction (ϕ) for each of the films was statistically similar (∼4.7 eV), regardless of pO<sub>2</sub>. There was not a strong dependence of the power conversion efficiency (η) on the conductivities of the HTLs varying between 0.009 ‐ 10 S/cm. The observed differences in OPV efficiencies (ranging from 1.16 to 2.46%) were correlated to the near surface chemical composition of the Ni<sub>x</sub>Co<sub>3−x</sub>O<sub>4</sub> HTL, as observed by differences in the relative surface hydroxyl concentration. The critical role of the near‐surface composition of the HTL at the HTL/organic interface was further explored by modifying the hydroxyl concentration using an oxygen plasma treatment. This treatment mitigated the impact of surface hydroxyl coverage, demonstrating either identical or increased values for ϕ and η, regardless of initial pO<sub>2</sub> in the creation of the Ni<sub>x</sub>Co<sub>3−x</sub>O<sub>4</sub> HTL. To further explore this we also employed a phosphonic acid surface modification agent on the HTL, increasing ϕ to 5.2 eV producing the best η value of 3.4%, equivalent to the PEDOT:PSS control devices. These results indicate that nickel cobalt oxide is a promising p‐type oxide for carrier‐selective interlayers in organic solar cells; however, for this to be fully realized the specific surface chemistry at the oxide/polymer interface must be controlled to increase ϕ and optimize device performance.</p> </abstract> … (more)
- Is Part Of:
- Advanced energy materials. Volume 3:Issue 4(2013:Apr.)
- Journal:
- Advanced energy materials
- Issue:
- Volume 3:Issue 4(2013:Apr.)
- Issue Display:
- Volume 3, Issue 4 (2013)
- Year:
- 2013
- Volume:
- 3
- Issue:
- 4
- Issue Sort Value:
- 2013-0003-0004-0000
- Page Start:
- 524
- Page End:
- 531
- Publication Date:
- 2012-11-26
- Subjects:
- Energy harvesting -- Materials -- Periodicals
Energy conversion -- Materials -- Periodicals
Energy storage -- Materials -- Periodicals
Photovoltaics -- Periodicals
Fuel cells -- Periodicals
Thermoelectric materials -- Periodicals
621.31 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1614-6840/ ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/aenm.201200742 ↗
- Languages:
- English
- ISSNs:
- 1614-6832
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0696.850700
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4302.xml