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Morphology induced defects and crystal facet engineering in CQD@CdS photocatalyst for efficient hydrogen generation
Journal article

Morphology induced defects and crystal facet engineering in CQD@CdS photocatalyst for efficient hydrogen generation

比沙爾納哈克 and 繁根 曾
Applied Surface Science
07/2024

Abstract

Morphology;hydrogen

has increased by an average of 1.7 %, which has attained 17.9 TW in

2017 [1]. Projections further estimate this into 22 TW by 2030, an

almost 25 % increase, with fossil fuels accounting for nearly 80 % of the

total [2,3]. The undeniable reliance of the world on fossil fuels has raised

concerns from a sustainability and environmental standpoint. While

thermo and electrocatalysts in the chemical industry have addressed

some issues by reducing energy input, achieving bias-free photocatalytic

overall water splitting (OWS) into hydrogen (H2) and oxygen (O2) remains

a long-term goal for sustainable fuel production [4–8].

Photocatalytic OWS, unlike its highly studied photo-electrochemical

counterpart, eliminates the need for conductive electrolytes

or strong acidic/alkaline solutions. This reduces utilization costs, which

in turn addresses multiple stability and safety concerns [9]. Nevertheless,

challenges exists which are directly related to its narrow visiblelight-

response range and undesirable charge carrier recombination,

resulting in a limited apparent quantum yield (AQY) efficiency (typically

below 15 %) that is reported from literature [10]. The reported

content of UV light in the 300–400 nm region in the solar spectrum is

less than 3 % [11]. Despite almost having 40 % of solar light falling

within the visible spectrum found at 400–700 nm [12], current visiblelight-

responsive (VLR) catalysts are typically limited to 400–485 nm,

hindering energy conversion efficiency [13]. To maximize the efficiency

of photocatalytic water splitting systems, the selection of an appropriate

photocatalyst that can efficiently absorb longer wavelengths of solar

spectrum is very crucial.

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