Porphyrins‐Assisted Cocatalyst Engineering with CoOV Bond in BiVO4 Photoanode for Efficient Oxygen Evolution Reaction

Abstract The application of photoelectrochemical (PEC) water splitting is limited by the sluggish surface oxygen evolution reaction (OER) kinetics. OER kinetics can be effectively improved through cocatalyst engineering. However, the tardy transfer process and serious recombination of carriers are t...

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Main Authors: Linxing Meng, Zunyan Lv, Weiwei Xu, Wei Tian, Liang Li
Format: Article
Language:English
Published: Wiley 2023-03-01
Series:Advanced Science
Subjects:
Online Access:https://doi.org/10.1002/advs.202206729
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author Linxing Meng
Zunyan Lv
Weiwei Xu
Wei Tian
Liang Li
author_facet Linxing Meng
Zunyan Lv
Weiwei Xu
Wei Tian
Liang Li
author_sort Linxing Meng
collection DOAJ
description Abstract The application of photoelectrochemical (PEC) water splitting is limited by the sluggish surface oxygen evolution reaction (OER) kinetics. OER kinetics can be effectively improved through cocatalyst engineering. However, the tardy transfer process and serious recombination of carriers are the key factors restricting the cocatalyst development. Taking BiVO4 as an example, a Co‐modified heme film rich in large conjugated ring structures is introduced onto the photoanode surface using a solvothermal method. This film functions as an efficient cocatalyst. It considerably reduces the surface overpotential, promotes the transfer of photogenerated holes, and boosts the kinetics of OER by specifically affecting the formation of OOH*. Simultaneously, the formed CoOV bonds induce strong interaction at the photoanode/cocatalyst interfaces, reducing the recombination of photogenerated carriers. Consequently, the onset potential of the optimized photoanode decreases from 0.45 to 0.07 V and the photocurrent density at 1.23 V versus reversible hydrogen electrode boosts to 5.3 mA cm−2. This work demonstrates a facile strategy for designing cocatalysts to obtain rapid hole transfer capability and reduced carrier recombination for improved PEC performance.
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spelling doaj.art-e0db81f047cc4de39f1f54586f774ace2023-03-15T13:19:15ZengWileyAdvanced Science2198-38442023-03-01108n/an/a10.1002/advs.202206729Porphyrins‐Assisted Cocatalyst Engineering with CoOV Bond in BiVO4 Photoanode for Efficient Oxygen Evolution ReactionLinxing Meng0Zunyan Lv1Weiwei Xu2Wei Tian3Liang Li4School of Physical Science and Technology Jiangsu Key Laboratory of Thin Films Center for Energy Conversion Materials and Physics (CECMP) Soochow University Suzhou 215006 P. R. ChinaSchool of Physical Science and Technology Jiangsu Key Laboratory of Thin Films Center for Energy Conversion Materials and Physics (CECMP) Soochow University Suzhou 215006 P. R. ChinaSchool of Physical Science and Technology Jiangsu Key Laboratory of Thin Films Center for Energy Conversion Materials and Physics (CECMP) Soochow University Suzhou 215006 P. R. ChinaSchool of Physical Science and Technology Jiangsu Key Laboratory of Thin Films Center for Energy Conversion Materials and Physics (CECMP) Soochow University Suzhou 215006 P. R. ChinaSchool of Physical Science and Technology Jiangsu Key Laboratory of Thin Films Center for Energy Conversion Materials and Physics (CECMP) Soochow University Suzhou 215006 P. R. ChinaAbstract The application of photoelectrochemical (PEC) water splitting is limited by the sluggish surface oxygen evolution reaction (OER) kinetics. OER kinetics can be effectively improved through cocatalyst engineering. However, the tardy transfer process and serious recombination of carriers are the key factors restricting the cocatalyst development. Taking BiVO4 as an example, a Co‐modified heme film rich in large conjugated ring structures is introduced onto the photoanode surface using a solvothermal method. This film functions as an efficient cocatalyst. It considerably reduces the surface overpotential, promotes the transfer of photogenerated holes, and boosts the kinetics of OER by specifically affecting the formation of OOH*. Simultaneously, the formed CoOV bonds induce strong interaction at the photoanode/cocatalyst interfaces, reducing the recombination of photogenerated carriers. Consequently, the onset potential of the optimized photoanode decreases from 0.45 to 0.07 V and the photocurrent density at 1.23 V versus reversible hydrogen electrode boosts to 5.3 mA cm−2. This work demonstrates a facile strategy for designing cocatalysts to obtain rapid hole transfer capability and reduced carrier recombination for improved PEC performance.https://doi.org/10.1002/advs.202206729BiVO4cocatalystsphotoanodewater splitting
spellingShingle Linxing Meng
Zunyan Lv
Weiwei Xu
Wei Tian
Liang Li
Porphyrins‐Assisted Cocatalyst Engineering with CoOV Bond in BiVO4 Photoanode for Efficient Oxygen Evolution Reaction
Advanced Science
BiVO4
cocatalysts
photoanode
water splitting
title Porphyrins‐Assisted Cocatalyst Engineering with CoOV Bond in BiVO4 Photoanode for Efficient Oxygen Evolution Reaction
title_full Porphyrins‐Assisted Cocatalyst Engineering with CoOV Bond in BiVO4 Photoanode for Efficient Oxygen Evolution Reaction
title_fullStr Porphyrins‐Assisted Cocatalyst Engineering with CoOV Bond in BiVO4 Photoanode for Efficient Oxygen Evolution Reaction
title_full_unstemmed Porphyrins‐Assisted Cocatalyst Engineering with CoOV Bond in BiVO4 Photoanode for Efficient Oxygen Evolution Reaction
title_short Porphyrins‐Assisted Cocatalyst Engineering with CoOV Bond in BiVO4 Photoanode for Efficient Oxygen Evolution Reaction
title_sort porphyrins assisted cocatalyst engineering with coov bond in bivo4 photoanode for efficient oxygen evolution reaction
topic BiVO4
cocatalysts
photoanode
water splitting
url https://doi.org/10.1002/advs.202206729
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AT zunyanlv porphyrinsassistedcocatalystengineeringwithcoovbondinbivo4photoanodeforefficientoxygenevolutionreaction
AT weiweixu porphyrinsassistedcocatalystengineeringwithcoovbondinbivo4photoanodeforefficientoxygenevolutionreaction
AT weitian porphyrinsassistedcocatalystengineeringwithcoovbondinbivo4photoanodeforefficientoxygenevolutionreaction
AT liangli porphyrinsassistedcocatalystengineeringwithcoovbondinbivo4photoanodeforefficientoxygenevolutionreaction