分解水
杰纳斯
材料科学
电场
纳米技术
跨坐
领域(数学)
光电子学
氧化还原
可见光谱
色散(光学)
清水
作者
Mostafa Torkashvand,Saeedeh Sarabadani Tafreshi,Caterina Cocchi,Surender Kumar
出处
期刊:Nanoscale
[Royal Society of Chemistry]
日期:2026-01-01
卷期号:18 (30): 16007-16016
被引量:1
摘要
Identifying materials that simultaneously straddle the water redox potentials and possess an intrinsic electric field is crucial for achieving high solar-to-hydrogen (STH) efficiency. Using state-of-the-art first-principles calculations, including a range-separated hybrid functional and spin-orbit coupling, we investigate MoXY/WXY (X, Y = S, Se) Janus bilayers for overall water splitting. We find a critical competition between the metal-to-metal chemical potential difference and the intrinsic dipoles at the interface between the Janus monolayers. The Se-Se interfaced heterobilayer is intrinsically capable of driving water splitting, while its S-S counterpart can meet the redox requirements through pH modulation. For both configurations, a remarkable STH efficiency of 17.1% is anticipated. Furthermore, we predict a threshold of 1.0 eV for the built-in potential gradient to govern the transition from overall water splitting to band-edge pinning. Compared to homobilayers, heterobilayers benefit from the reciprocity between layer-specific dipoles and the Mo/W chemical potential difference, which promotes spatial separation and suppresses recombination, overall enhancing hydrogen production. Our results establish specific electronic descriptors for Janus heterostructures, providing a rational design rule for maximizing solar-driven hydrogen production in asymmetric two-dimensional materials.
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