Search

Recently, lead halide perovskites have emerged as promising photoanode materials for efficient hydrogen production. However, the sluggish kinetics of the oxygen evolution reaction (OER) and interfacial defect‐mediated charge accumulation inevitably result in efficiency loss and degradation of perovskite photoanodes. Herein, a defect‐passivated electron transport layer‐based perovskite photoanode combined with a catalyst layer favorable is introduced for iodide oxidation reaction bearing a small thermodynamic barrier and rapid kinetics compared to OER for efficient solar fuel generation. The resulting perovskite photoanode revealed a saturated photocurrent density of 22.4 mA cm−2 at 0.3 V versus the reversible hydrogen electrode (VRHE) with an impressive onset potential of −0.2 VRHE as well as durability for 225 h in a neutral electrolyte. In addition, an unbiased hydrogen‐production device comprising a perovskite photoanode and Pt coil electrocatalyst is demonstrated, achieving a remarkable solar‐to‐chemical conversion efficiency of 11.45% and stable operation for 25 h. Moreover, a wireless artificial leaf‐structured device realizing solar‐driven hydrogen generation in natural sea water under outdoor sunlight is presented. [ABSTRACT FROM AUTHOR]

Recently, lead halide perovskites have attracted significant attention as promising absorber materials for photoelectrochemical (PEC) solar water splitting. However, charge‐accumulation‐induced ion migration at the interface causes perovskite degradation and efficiency loss. To suppress the charge accumulation and improve the PEC performance of the perovskite photoanode, a simple interface engineering is proposed by decorating the SnO2/perovskite interface with a mixture of polyethylenimine ethoxylated (PEIE) and chlorobenzenesulfonic acid (CBSA). The mixed CBSA+PEIE treatment effectively passivates the oxygen vacancies in SnO2 and adjusts the band alignment between SnO2 and the perovskite. The synergistic effects of the mixture treatment facilitate an effective carrier extraction at the SnO2/perovskite interface, enhance the PEC performance, and improve the stability of the device. The perovskite photoanode exhibits an impressive applied bias photon‐to‐current efficiency of 12.9% with an outstanding durability for 225 h. Furthermore, an unbiased solar water splitting is achieved using all the perovskite photoelectrodes, resulting in a remarkable unassisted solar‐to‐hydrogen efficiency of 10.9% and a continuous 22 h stable operation. [ABSTRACT FROM AUTHOR]