2022
DOI: 10.1039/d2sc04585k
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Synergistic effect of p-type and n-type dopants in semiconductors for efficient electrocatalytic water splitting

Abstract: Co-substituting a stable material, e.g. TiO2, with both n- and p-type dopants, allows tuning its reactivity to activate the material for oxygen evolution. This opens up a new design avenue for acid water electrolysis electrocatalysts.

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Cited by 5 publications
(5 citation statements)
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References 68 publications
(114 reference statements)
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“…Outstanding efficiencies were demonstrated with membrane electrode assemblies (MEAs), where a gas diffusion electrode (GDE), functioning as the cathode, and a zero gap anode are directly mated on a polymer electrolyte membrane. With the MEA, the distance between the electrodes is minimized to the thickness of the membrane, leading to a reduction of transport resistance and thus to an increase in energy efficiency. High-performing flow cells, containing the MEA, operate with a single aqueous electrolyte or even only H 2 O at the anode. Here, the oxygen evolution reaction (OER) takes place, oftentimes on an Ir-MMO catalyst surface which is a stable catalyst for the OER in various conditions. , The cathode provides a Ag catalyst layer, a highly selective and stable catalyst for the CO 2 -to-CO reaction, and is fed with humidified CO 2 gas from the rear side of the electrode. , …”
Section: Introductionmentioning
confidence: 99%
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“…Outstanding efficiencies were demonstrated with membrane electrode assemblies (MEAs), where a gas diffusion electrode (GDE), functioning as the cathode, and a zero gap anode are directly mated on a polymer electrolyte membrane. With the MEA, the distance between the electrodes is minimized to the thickness of the membrane, leading to a reduction of transport resistance and thus to an increase in energy efficiency. High-performing flow cells, containing the MEA, operate with a single aqueous electrolyte or even only H 2 O at the anode. Here, the oxygen evolution reaction (OER) takes place, oftentimes on an Ir-MMO catalyst surface which is a stable catalyst for the OER in various conditions. , The cathode provides a Ag catalyst layer, a highly selective and stable catalyst for the CO 2 -to-CO reaction, and is fed with humidified CO 2 gas from the rear side of the electrode. , …”
Section: Introductionmentioning
confidence: 99%
“…13−15 Here, the oxygen evolution reaction (OER) takes place, oftentimes on an Ir-MMO catalyst surface which is a stable catalyst for the OER in various conditions. 3,16 The cathode provides a Ag catalyst layer, a highly selective and stable catalyst for the CO 2 -to-CO reaction, and is fed with humidified CO 2 gas from the rear side of the electrode. [13][14][15]17 Reportedly, the highest selectivities are reached with MEAs containing anion exchange membranes (AEMs).…”
Section: ■ Introductionmentioning
confidence: 99%
“…The OER is confined to oxide-like surfaces, which often re-structure under operando conditions. Experimental development of oxygen evolving catalysts is done separately for acidic water electrolysis [2][3][4] and alkaline media electrolysis [5][6][7]. State of the art OER catalysts for acidic electrolysis are based on noble metal oxides such as RuO 2 and IrO 2 , the scarcity of which adversely affects large scale deployment of this technology.…”
Section: Introductionmentioning
confidence: 99%
“…The most common one, which is generally used as a foundation for the computational screening of prospective oxygen evolving catalysts conforms to a Volmer-Heyrovsky type of mechanism and can be described as a sequence of four consecutive concerted one electron/proton transfer reactions as outlined in eqs. (1)(2)(3)(4):…”
Section: Introductionmentioning
confidence: 99%
“…To facilitate photoinduced •OH generation, we here modify the electronic states of TiO2 by doping it with magnesium, which has a smaller formal charge (+2 in MgO) compared to Ti (+4 in TiO2). Previous studies indicate that low-valence element doping can effectively weaken the binding strength of * O-containing species (such as * O and * OH) on the TiO2 surfaces [18,19]. Consequently, this may facilitate the •OH generation.…”
mentioning
confidence: 99%