4.7 Article

Insight into the whole characteristics of (Pd/WP)/CdS for photocatalytic hydrogen evolution

Journal

JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume 633, Issue -, Pages 649-656

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2022.11.084

Keywords

( Pd; WP); CdS; Ternary photocatalyst; Synergistic effect; CB position; Hydrogen evolution

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(Noble metal/non-noble metal)/semiconductor ternary photocatalysts show high efficiency and attractiveness for photocatalytic hydrogen evolution. This study focuses on the physicochemical characteristics of (Pd/WP)/CdS ternary photocatalysts. The (0.05%Pd/4%WP)/CdS exhibits significantly improved hydrogen evolution activity compared to other catalysts, and it also demonstrates good capacitance, conductivity, and catalytic ability.
The (noble metal/non-noble metal)/semiconductor are efficient and attractive ternary photocatalysts for photocatalytic hydrogen evolution. To deeply understand the advantages of ternary photocatalysts, the physicochemical characteristics of both the whole ternary photocatalysts and each part of that must be revealed. Herein, we design (Pd/WP) as a co-catalyst loaded on CdS to form ternary photocat-alysts (Pd/WP)/CdS. The (0.05%Pd/4%WP)/CdS exhibits a high hydrogen evolution activity of 18.0 mmol/ h/g, which is 1.5 times of WP/CdS, 2.2 times of Pd/CdS, and 6.4 times of pure CdS. Additionally, pho-toelectrochemical tests demonstrate that (Pd/WP)/CdS has appropriate capacitance, excellent conduc-tivity and strong catalytic ability, which can inhibit the recombination of photo-excited carries and boost hydrogen evolution. Especially, ultraviolet photoelectron spectroscopy (UPS) tests show that the conduction band (CB) position of (Pd/WP)/CdS can be regulated successfully through synergistic effect of Pd, WP, and CdS. This study not only reveals the physicochemical properties of ternary pho-tocatalysts from a holistic perspective, but also provides a pathway for hydrogen evolution of scientific and economic interest. (c) 2022 Published by Elsevier Inc.

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