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Title: Undoped and Ni-doped CoOx surface modification of porous BiVO4 photoelectrodes for water oxidation

Journal Article · · Journal of Physical Chemistry. C
 [1];  [2];  [3];  [4];  [5]
  1. Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Xi'an Jiaotong Univ., Shaanxi (China)
  2. Univ. of California, San Diego, La Jolla, CA (United States)
  3. SLAC National Accelerator Lab., Menlo Park, CA (United States)
  4. Xi'an Jiaotong Univ., Shaanxi (China)
  5. Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States)

© 2016 American Chemical Society. Surface modification of photoanodes with oxygen evolution reaction (OER) catalysts is an effective approach to enhance water oxidation kinetics, to reduce external bias, and to improve the energy harvesting efficiency of photoelectrochemical (PEC) water oxidation. Here, the surface of porous BiVO 4 photoanodes was modified by the deposition of undoped and Ni-doped CoO x via nitrogen flow assisted electrostatic spray pyrolysis. This newly developed atmospheric pressure deposition technique allows for surface coverage throughout the porous structure with thickness and composition control. PEC testing of modified BiVO 4 photoanodes shows that after deposition of an undoped CoO x surface layer, the onset potential shifts negatively by ca. 420 mV and the photocurrent density reaches 2.01 mA cm -2 at 1.23 vs V RHE under AM 1.5G illumination. Modification with Ni-doped CoO x produces even more effective OER catalysis and yields a photocurrent density of 2.62 mA cm -2 at 1.23 V RHE under AM 1.5G illumination. The valence band X-ray photoelectron spectroscopy and synchrotron-based X-ray absorption spectroscopy results show the Ni doping reduces the Fermi level of the CoO x layer; the increased surface band bending produced by this effect is partially responsible for the superior PEC performance.

Research Organization:
SLAC National Accelerator Laboratory (SLAC), Menlo Park, CA (United States); Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES)
Grant/Contract Number:
AC02-76SF00515; SC0004993; 51302211; AC02-05CH11231
OSTI ID:
1350543
Alternate ID(s):
OSTI ID: 1379585
Journal Information:
Journal of Physical Chemistry. C, Vol. 120, Issue 41; ISSN 1932-7447
Publisher:
American Chemical SocietyCopyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 52 works
Citation information provided by
Web of Science

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The synergistic effect of cation mixing in mesoporous Bi x Fe 1−x VO 4 heterojunction photoanodes for solar water splitting journal January 2019
Electrodeposition of Cobalt Phosphosulfide Nanosheets on Carbon Fiber Paper as Efficient Electrocatalyst for Oxygen Evolution journal May 2018
Surface- and interface-engineered heterostructures for solar hydrogen generation journal March 2018
Ni-Doped CuS as an efficient electrocatalyst for the oxygen evolution reaction journal January 2019
Interface engineering of 3D BiVO 4 /Fe-based layered double hydroxide core/shell nanostructures for boosting photoelectrochemical water oxidation journal January 2017
Strategies for Semiconductor/Electrocatalyst Coupling toward Solar‐Driven Water Splitting journal March 2020
Photoelectrochemical Performance of BiVO 4 Photoanodes Integrated with [NiFe]-Layered Double Hydroxide Nanocatalysts: Photoelectrochemical Performance of BiVO 4 Photoanodes Integrated with [NiFe]-Layered Double Hydroxide Nanocatalysts journal December 2017
New Iron-Cobalt Oxide Catalysts Promoting BiVO 4 Films for Photoelectrochemical Water Splitting journal June 2018
Photoelectrochemical Performance of BiVO 4 Photoanodes Integrated with [NiFe]‐Layered Double Hydroxide Nanocatalysts journal January 2018