Strategic Doping for Precise Structural Control and Intense Photocurrents Under Visible Light in Ba(2)M(0.4)Bi(1.6)O(6) (M = La, Ce, Pr, Pb, Y) Double Perovskites

通过策略性掺杂实现 Ba(2)M(0.4)Bi(1.6)O(6) (M = La, Ce, Pr, Pb, Y) 双钙钛矿的精确结构控制和可见光下强光电流。

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Abstract

Developing functional perovskites is important for advancing solar energy conversion technologies. This study investigates the effects of dopants on the structural, optical, electronic, and solar conversion performances of Ba(2)M(0.4)Bi(1.6)O(6) double perovskites. X-ray diffraction (XRD) and Rietveld refinement confirm crystallization in the I2/m space group (M = La, Ce, Pr, Pb), and Fm3¯m and I2/m space groups (M = Y). The B1-O-B2 structure modulates to highly ordered (M = La, Y), partially ordered (M = Pr), or disordered (M = Ce, Pb). UV-vis spectra show strong light absorption, with Tauc plots estimating ~1.57 eV (M = La) and ~1.73 eV (M = Pr) optical band gaps. Under AM 1.5G illumination, the M = La photoelectrode generates photocurrents of 1 mA cm(-2) at 0.3 V(RHE), surpassing M = Ce and Pb (1 μm, 4-times spin-coating). Increasing its thickness to 7.7 μm (4-times dip-coating) further enhances the photocurrents to 2.3 mA cm(-2) at 0.2 V(RHE), outperforming all counterparts due to improved stability. Fine-tuning crystal and electronic structures via strategic B-site doping provides a new route for engineering Ba(2)Bi(2)O(6)-based double perovskites for broad solar energy conversion applications.

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