Affiliation:
1. Beijing National Laboratory for Molecular Sciences Laboratories of Organic Solids Structural Chemistry of Unstable and Stable Species Photochemistry and Polymer Physics and Chemistry Institute of Chemistry Chinese Academy of Sciences Beijing 100190 China
2. University of Chinese Academy of Sciences Beijing 100049 China
Abstract
AbstractEfficient in situ deposition of metallic cocatalyst, like zero‐valent platinum (Pt), on organic photovoltaic catalysts (OPCs) is the prerequisite for their high catalytic activities. Here we develop the OPC (Y6CO), by introducing carbonyl in the core, which is available to σ‐π coordinate with transition metals, due to the high‐energy empty π* orbital of carbonyl. Y6CO exhibits a stronger capability to anchor Pt species and reduce them to metallic state, resulting in more Pt0 deposition, relative to the control OPC without the central σ‐π anchor. Single‐component and heterojunction nanoparticles (NPs) employing Y6CO show enhanced average hydrogen evolution rates of 230.98 and 323.22 mmol h−1 g[OPC]−1, respectively, under AM 1.5G, 100 mW cm−2 for 10 h, and heterojunction NPs yield the external quantum efficiencies of ca. 10 % in 500–800 nm. This work demonstrates that σ‐π anchoring is one efficient strategy for integrating metallic cocatalyst and OPC for high‐performance photocatalysis.
Funder
National Natural Science Foundation of China
China Postdoctoral Science Foundation
Cited by
1 articles.
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