TY - JOUR AU - Dong Su Kim AU - Kun Woong Lee AU - Su Yeon Jung AU - Ji Hoon Choi AU - Hak Hyeon Lee AU - Won Seok Yang AU - Yun Seong Cho AU - Jin Wook Yang AU - Joohoon Kang AU - Shannon W Boettcher AU - Hyung Koun Cho AB -

Although monoclinic bismuth vanadate (BiVO4) is a promising photoanode for solar water splitting, its practical use is hindered by imperfect photocurrent generation/collection, low photovoltage compared to the bandgap, and corrosion side reactions that limit durability. Here, we introduce a controlled-annealing sol–gel process for BiVO4 thin-film photoanodes along with an optimized linear-sweep-voltammetry photodeposition of CoFeOxHy cocatalysts. The resulting BiVO4 films annealed at 550 °C exhibited a photocurrent density of 4.1 mA/cm2 at 1.23 VRHE under 1 sun AM 1.5G solar simulation and a low onset potential of 0.26 VRHE due to high majority carrier conductivity, a crystalline bulk with reduced defects as evidenced by x-ray photoelectron spectroscopy and photoluminescence lifetime analysis, and thus enhanced photocarrier collection. However, significant degradation in performance was found due to interfacial photocorrosion. To protect the surface and speed the oxygen-evolution reaction CoFeOxHy cocatalyst layers were deposited. By varying the number of consecutive sweeps and adjusting the applied bias range, an ultra-thin (∼15 nm) CoFeOxHy cocatalyst layer was uniformly grown deposited over 30 cycles on the BiVO4 surface. The resulting BiVO4/CoFeOxHy yielded 4.03 mA/cm2 at 1.23 VRHE and onset potential of 0.24 VRHE, with stable operation (∼15 % loss in photocurrent at 1.23 VRHE relative to ∼60 % loss in the uncatalyzed control sample). These conformal CoFeOxHy catalytic layers function simultaneously to selectively collect photoexcited holes from the BiVO4, catalyze the water-oxidation reaction, and protect the BiVO4 from photodegradation.

BT - Applied Surface Science DA - 04/2025 DO - 10.1016/j.apsusc.2025.162470 N2 -

Although monoclinic bismuth vanadate (BiVO4) is a promising photoanode for solar water splitting, its practical use is hindered by imperfect photocurrent generation/collection, low photovoltage compared to the bandgap, and corrosion side reactions that limit durability. Here, we introduce a controlled-annealing sol–gel process for BiVO4 thin-film photoanodes along with an optimized linear-sweep-voltammetry photodeposition of CoFeOxHy cocatalysts. The resulting BiVO4 films annealed at 550 °C exhibited a photocurrent density of 4.1 mA/cm2 at 1.23 VRHE under 1 sun AM 1.5G solar simulation and a low onset potential of 0.26 VRHE due to high majority carrier conductivity, a crystalline bulk with reduced defects as evidenced by x-ray photoelectron spectroscopy and photoluminescence lifetime analysis, and thus enhanced photocarrier collection. However, significant degradation in performance was found due to interfacial photocorrosion. To protect the surface and speed the oxygen-evolution reaction CoFeOxHy cocatalyst layers were deposited. By varying the number of consecutive sweeps and adjusting the applied bias range, an ultra-thin (∼15 nm) CoFeOxHy cocatalyst layer was uniformly grown deposited over 30 cycles on the BiVO4 surface. The resulting BiVO4/CoFeOxHy yielded 4.03 mA/cm2 at 1.23 VRHE and onset potential of 0.24 VRHE, with stable operation (∼15 % loss in photocurrent at 1.23 VRHE relative to ∼60 % loss in the uncatalyzed control sample). These conformal CoFeOxHy catalytic layers function simultaneously to selectively collect photoexcited holes from the BiVO4, catalyze the water-oxidation reaction, and protect the BiVO4 from photodegradation.

PB - Elsevier BV PY - 2025 EP - 162470 T2 - Applied Surface Science TI - Efficient BiVO4/CoFeO H photoanodes using controlled annealing and conformal linear-sweep electrocatalyst photodeposition UR - https://doi.org/10.1016/j.apsusc.2025.162470 VL - 689 SN - 0169-4332 ER -