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Synergizing aliovalent doping and interface in heterostructured NiV nitride@oxyhydroxide core-shell nanosheet arrays enables efficient oxygen evolution

An earth-abundant and highly efficient oxygen evolution reaction (OER) electrocatalyst has long been the holy grail in the entire energy conversion chain. Despite the considerable efforts in advancing non-precious-metal candidates by multiscale structural engineering, an adequate structural integrat...

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Published in:Nano energy 2021-07, Vol.85, p.105961, Article 105961
Main Authors: Gao, Xiaorui, Li, Xin, Yu, Yong, Kou, Zongkui, Wang, Pengyan, Liu, Ximeng, Zhang, Jie, He, Jiaqing, Mu, Shichun, Wang, John
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container_title Nano energy
container_volume 85
creator Gao, Xiaorui
Li, Xin
Yu, Yong
Kou, Zongkui
Wang, Pengyan
Liu, Ximeng
Zhang, Jie
He, Jiaqing
Mu, Shichun
Wang, John
description An earth-abundant and highly efficient oxygen evolution reaction (OER) electrocatalyst has long been the holy grail in the entire energy conversion chain. Despite the considerable efforts in advancing non-precious-metal candidates by multiscale structural engineering, an adequate structural integration remains a significant challenge in achieving an efficient OER, largely bottlenecked by a low population of active sites and limited synergistic effect. Herein, we propose a synergistic strategy of effectively combining aliovalent doping and interface in the NiV nitride@oxyhydroxide (NiVN@OOH) heterostructured nanosheet arrays, successfully developed by in-situ electrochemical surface reconfiguration (ESR) from the core-shell nanostructured Ni3N@Ni3VN aiming for enabling OER kinetics. The thus-optimized NiVN@OOH with abundant core-shell interfaces, vertically aligned nanosheet arrays and purposely-chosen V-doping, demonstrates superior OER activity with an ultralow overpotential of 233 mV at the current density of 50 mA cmgeo−2, 64-fold rise in catalytic current density at 1.47 V vs. reversible hydrogen electrode (RHE) and 37-fold increase in turn-over frequency at an overpotential of 240 mV, over those of Ni3N@OOH, together with a robust long-term stability in 1 M KOH. Our DFT calculations further reveal that the synergistic effects of the aliovalent V-doping and interface engineering have boosted the intrinsic OER activity on adjacent oxygen active sites. The discovery in the present work provides a new paradigm of multiscale-controlled synergy for much enhanced electrocatalysis. [Display omitted] •NiV nitride@oxyhydroxide heterostructured nanosheet arrays was proposed.•An in-situ electrochemical surface reconfiguration (ESR) on Ni3N@Ni3VN takes place.•Aliovalent V-doping and abundant core-shell interfaces lead to a high OER activity.•NiVN@OOH delivers an ultralow overpotential of 233 mV at 50 mA cm–2.•DFT calculations were performed to identify the synergistic effect in multiscale structure.
doi_str_mv 10.1016/j.nanoen.2021.105961
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subjects In-situ electrochemical surface reconfiguration
NiVN@OOH core-shell
OER electrolysis
Synergy of aliovalent V-doping and interface
title Synergizing aliovalent doping and interface in heterostructured NiV nitride@oxyhydroxide core-shell nanosheet arrays enables efficient oxygen evolution
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