BiVO 4 is a promising n-type semiconductor for water-splitting photoelectrochemical cells. We report here a new method to prepare BiVO 4 photoanodes that is based on an alkaline electrodeposition process, which avoids chemical etching of Bi. In addition, we present a simple and general method to prepare coatings of amorphous FeO x that behave as a co-catalyst on our BiVO 4 material, improving the water splitting photocurrent.The conversion of renewable energies into energy-rich fuels that can be stored, transported and used to generate electricity on-site and on-demand is a very attractive way to solve the main problem of renewables, namely their intermittency. [1] In this frame, water-splitting photoelectrochemical cells (PECs) are attracting a considerable amount of attention. [2][3][4][5] These devices are made of semiconductor (SC) photoelectrodes that are able to convert solar energy into H 2 (an energy-rich fuel) and O 2 . Upon light absorption, the charge carriers photogenerated in the SC are driven to the solid-liquid interface where they participate in the water splitting half-reactions: hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). [2][3][4][5] In this process, the OER is the most challenging reaction as it requires a considerable energy input [6] and also because most of SCs are subject to photocorrosion, which makes them unstable in photoelectrolysis conditions. [7] Among n-type SCs that have been investigated as photoanodes for OER, BiVO 4 stands out for several reasons: [8,9] first, it is composed of relatively abundant and non-toxic materials, [10] it has a bandgap narrow enough (2.4 eV) to absorb a significant part of the solar spectrum, [11] a valence band below the O 2 /H 2 O standard potential and a theoretical solar-to-hydrogen efficiency of~9 %. [12] However, the water splitting performance of BiVO 4 is still limited by its poor charge extraction [13] and its low catalytic activity for OER, which implies to employ additional chemical and surface engineering processes to improve its efficiency. [14] Among these methods, BiVO 4 doping [15,16] photocharging [17,18] cathodic polarization, [19] nanostructuring, [20,21] as well as its interfacing with: highly active OER co-catalysts (cocats) [22][23][24][25] another SC [26][27][28][29] and plasmonic materials [30,31] have shown great promise. The synthesis of photoelectrochemically active BiVO 4 on a conductive substrate is thus of great importance and can be performed by: i) spray-based, [13,18,29] or ii) hydrothermal [17,19] methods, iii) metal-organic decomposition, [21,28,30] iv) physical vapor deposition [26,32] and v) electrodeposition. [22,[33][34][35][36] The latter approach is very attractive due to its simplicity and its low cost [37,38] and electrodeposited BiVO 4 has already led to very important breakthroughs. [22,25] Furthermore, electrodeposition processes are generally easily tunable and can be applied to various types of conductive substrates, regardless of their composition and geometry, which is particula...