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窄带隙颗粒光催化剂用于一步激发整体水分解。

Narrow-Band-Gap Particulate Photocatalysts for One-Step-Excitation Overall Water Splitting.

机构信息

Research Initiative for Supra-Materials, Interdisciplinary Cluster for Cutting Edge Research, Shinshu University, Nagano-shi, Nagano 380-8553, Japan.

Office of University Professors, The University of Tokyo, 2-11-16 Yayoi, Bunkyo-ku, Tokyo 113-8656, Japan.

出版信息

Acc Chem Res. 2023 Apr 4;56(7):878-888. doi: 10.1021/acs.accounts.3c00011. Epub 2023 Mar 14.

Abstract

ConspectusSunlight-driven one-step-excitation overall water splitting (OWS) using a single particulate photocatalyst is a simple and cost-effective approach to producing sustainable hydrogen on a large scale, providing an important impetus to achieving a carbon-neutral society. Technoeconomic studies have determined that a minimum solar-to-hydrogen (STH) energy conversion efficiency of 5% must be achieved to allow this process to be economically competitive. Meeting this goal will require the fabrication of particulate photocatalysts comprising composites of semiconductors and cocatalysts that are sufficiently active under sunlight. A one-step-excitation OWS system based on a metal oxide semiconductor having a wide bandgap was first reported in 1980, and the performance of such systems has been improved significantly over the past decade. In particular, work by the authors' group increased the apparent quantum yield (AQY) obtainable for ultraviolet (UV)-active SrTiO to more than 90% in 2020. However, the STH conversion efficiency of a photocatalyst that absorbs only UV light (that is, λ < 400 nm) is limited to 1.7% even at an AQY of unity. It is therefore highly important to develop one-step-excitation OWS processes utilizing narrow bandgap photocatalysts having absorption edge wavelengths equal to or longer than 500 nm. Such systems would be expected to meet the desired 5% STH energy conversion efficiency once a constant AQY of approximately 63% is obtained.This Account summarizes the development and application of narrow-band-gap (oxy)nitride and oxysulfide photocatalysts in the authors' laboratory that are able to split water in response to wavelengths as high as 500 to 650 nm via single-step photoexcitation. At first, the authors briefly recount the key steps required to progress from the initial utilization of a UV-active SrTiO photocatalyst as an OWS-active material to the realization of an AQY of almost unity. Multiple design and refinement strategies applied to both the semiconductor and cocatalysts associated with this benchmark photocatalyst are summarized, providing insights into the rational design of narrow-band-gap OWS-active photocatalysts. Furthermore, the necessity, target, and current status of developing narrow-band-gap OWS-active photocatalysts are discussed, followed by a comprehensive discussion of progress in the fabrication of OWS-active (oxy)nitride and oxysulfide photocatalysts with absorption edge wavelengths at up to the range of 500-650 nm in our laboratory. Specific examples are used to show the importance of several factors. First, adjusting the properties of the semiconducting material based on designing appropriate precursors, optimizing the synthetic conditions and aliovalent doping is described. Second, loading of efficient dual cocatalysts is examined. Lastly, the effectiveness of coating the particulate photocatalysts with surface nanolayers is addressed. Deficits related to the performance of present-day photocatalysts are also evaluated. Expectations with regard to future improvements of (oxy)nitride- and oxysulfide-based photocatalysts as a means of increasing the AQY are considered. The strategies summarized in this Account are expected to promote the development of nonsacrificial long-wavelength-responsive photosynthesis systems using water as a hydrogen/oxygen source.

摘要

概述阳光驱动的一步激发整体水分解(OWS)使用单个颗粒光催化剂是大规模生产可持续氢气的一种简单且具有成本效益的方法,为实现碳中和社会提供了重要动力。技术经济研究确定,必须达到最小的太阳能到氢气(STH)能量转换效率 5%,才能使该过程具有经济竞争力。实现这一目标将需要制造由半导体和助催化剂组成的颗粒光催化剂,这些光催化剂在阳光下具有足够的活性。基于具有宽带隙的金属氧化物半导体的一步激发 OWS 系统于 1980 年首次报道,过去十年中,此类系统的性能得到了显著提高。特别是,作者小组的工作将紫外(UV)活性 SrTiO 的表观量子产率(AQY)提高到 2020 年的 90%以上。然而,仅吸收紫外线(即 λ < 400nm)的光催化剂的 STH 转换效率限制在 1.7%,即使 AQY 为 1。因此,开发利用具有等于或长于 500nm 的吸收边缘波长的窄带隙光催化剂的一步激发 OWS 工艺非常重要。一旦获得约 63%的恒定 AQY,预计此类系统将满足所需的 5% STH 能量转换效率。本账户总结了作者实验室中窄带隙(氧)氮化物和氧硫化物光催化剂的开发和应用,这些光催化剂能够通过单步光激发响应高达 500 至 650nm 的波长进行水分解。首先,作者简要回顾了从最初利用 UV 活性 SrTiO 光催化剂作为 OWS 活性材料到实现几乎为 1 的 AQY 所需的关键步骤。总结了应用于该基准光催化剂的半导体和助催化剂的多种设计和改进策略,为窄带隙 OWS 活性光催化剂的合理设计提供了见解。此外,讨论了开发窄带隙 OWS 活性光催化剂的必要性、目标和现状,随后全面讨论了我们实验室中吸收边缘波长可达 500-650nm 的 OWS 活性(氧)氮化物和氧硫化物光催化剂的制备进展。使用具体示例来说明几个因素的重要性。首先,根据设计合适的前体来调整半导体材料的性质、优化合成条件和同价掺杂进行了描述。其次,考察了高效双助催化剂的负载。最后,讨论了用表面纳米层涂覆颗粒光催化剂的效果。还评估了与当前光催化剂性能相关的缺陷。考虑了基于(氧)氮化物和氧硫化物的光催化剂作为提高 AQY 的手段的未来改进的预期。本账户中总结的策略有望促进使用水作为氢/氧源的非牺牲长波长响应光合作用系统的发展。

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