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一种富电子空穴的双位镍催化剂,用于高效光催化整体水分解。

An electron-hole rich dual-site nickel catalyst for efficient photocatalytic overall water splitting.

机构信息

School of Chemical Engineering and Technology, Xi'an Jiaotong University, 710049, Xi'an, P.R., China.

College of Physics and Optoelectronic Engineering, Shenzhen University, 518060, Shenzhen, P.R., China.

出版信息

Nat Commun. 2023 Mar 29;14(1):1741. doi: 10.1038/s41467-023-37358-3.

Abstract

Photocatalysis offers an attractive strategy to upgrade HO to renewable fuel H. However, current photocatalytic hydrogen production technology often relies on additional sacrificial agents and noble metal cocatalysts, and there are limited photocatalysts possessing overall water splitting performance on their own. Here, we successfully construct an efficient catalytic system to realize overall water splitting, where hole-rich nickel phosphides (NiP) with polymeric carbon-oxygen semiconductor (PCOS) is the site for oxygen generation and electron-rich NiP with nickel sulfide (NiS) serves as the other site for producing H. The electron-hole rich NiP based photocatalyst exhibits fast kinetics and a low thermodynamic energy barrier for overall water splitting with stoichiometric 2:1 hydrogen to oxygen ratio (150.7 μmol h H and 70.2 μmol h O produced per 100 mg photocatalyst) in a neutral solution. Density functional theory calculations show that the co-loading in NiP and its hybridization with PCOS or NiS can effectively regulate the electronic structures of the surface active sites, alter the reaction pathway, reduce the reaction energy barrier, boost the overall water splitting activity. In comparison with reported literatures, such photocatalyst represents the excellent performance among all reported transition-metal oxides and/or transition-metal sulfides and is even superior to noble metal catalyst.

摘要

光催化为升级 HO 为可再生燃料 H 提供了一种有吸引力的策略。然而,目前的光催化制氢技术通常依赖于额外的牺牲剂和贵金属助催化剂,并且自身具有整体水分解性能的光催化剂有限。在这里,我们成功构建了一种有效的催化体系来实现整体水分解,其中富空穴的镍磷化物(NiP)与聚合的碳-氧半导体(PCOS)是产氧的场所,而富电子的 NiP 与硫化镍(NiS)则作为产生 H 的另一个场所。基于电子空穴富 NiP 的光催化剂在中性溶液中表现出快速动力学和低热力学能量障碍,具有化学计量比为 2:1 的整体水分解,每 100mg 光催化剂产生 150.7 μmol h H 和 70.2 μmol h O。密度泛函理论计算表明,NiP 的共负载及其与 PCOS 或 NiS 的杂化可以有效地调节表面活性位点的电子结构,改变反应途径,降低反应能量障碍,提高整体水分解活性。与已报道的文献相比,这种光催化剂在所有报道的过渡金属氧化物和/或过渡金属硫化物中表现出优异的性能,甚至优于贵金属催化剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a3e/10060254/87e0cd4ffd16/41467_2023_37358_Fig1_HTML.jpg

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