Metaphotonic Catalysis: Amorphous silicon metasurfaces encode photochemical activity

Engineering notes

Engineering notes will be added by the Power for Solar editorial team.

Chinese explanation / 中文解读

中文解读待补充：本站会优先为光伏效率、钙钛矿太阳能电池、储能技术、太阳能热利用、BIPV、并网技术等高价值论文补充中文说明。

Original abstract

Solar-to-fuel conversion can benefit from photoelectrodes with engineered light-matter interactions, yet most nanostructured designs provide limited control over the spatial and spectral distribution of photochemical activity. Here, we present an all-dielectric amorphous-silicon metasurface photoelectrode that confines resonant light-matter interactions within a 220-nm-thick active layer. Tunable Mie-type and guided-mode resonances spectrally encode chemical reactivity and produce absorptance above 80% near the silicon band edge, compared with less than 30% for an unpatterned film of the same thickness. The metasurface simultaneously functions as the light absorber, carrier-transport layer, and catalytic interface without an added co-catalyst or engineered passivation layer. Operando photo-scanning electrochemical microscopy reveals wavelength- and structure-dependent redox activity and a tenfold enhancement in internal quantum efficiency near the silicon band edge relative to planar films. Power-dependent measurements support a photon-driven rather than nonlinear photothermal origin of the enhancement, while surface-sensitive ultrafast transient-reflectivity measurements probe the underlying carrier dynamics. Light-coupled scanning electrochemical cell microscopy further shows hydrogen-evolution enhancements of up to 21-fold under photocatalytic conditions and 15-fold under photoelectrochemical bias, corresponding to 11.2-fold and 7.7-fold enhancements after accounting for the estimated surface-area increase. The metasurfaces remain stable during more than 10 hours of immersion and prolonged laser illumination. These results establish amorphous silicon as a stable and versatile platform for resonantly programmed photocatalysis and solar-fuel generation.

Links and sources

• Official / arXiv page
• PDF from original source

Comments