Literature DB >> 23530781

Roles of cocatalysts in photocatalysis and photoelectrocatalysis.

Jinhui Yang1, Donge Wang, Hongxian Han, Can Li.   

Abstract

Since the 1970s, splitting water using solar energy has been a focus of great attention as a possible means for converting solar energy to chemical energy in the form of clean and renewable hydrogen fuel. Approaches to solar water splitting include photocatalytic water splitting with homogeneous or heterogeneous photocatalysts, photoelectrochemical or photoelectrocatalytic (PEC) water splitting with a PEC cell, and electrolysis of water with photovoltaic cells coupled to electrocatalysts. Though many materials are capable of photocatalytically producing hydrogen and/or oxygen, the overall energy conversion efficiency is still low and far from practical application. This is mainly due to the fact that the three crucial steps for the water splitting reaction: solar light harvesting, charge separation and transportation, and the catalytic reduction and oxidation reactions, are not efficient enough or simultaneously. Water splitting is a thermodynamically uphill reaction, requiring transfer of multiple electrons, making it one of the most challenging reactions in chemistry. This Account describes the important roles of cocatalysts in photocatalytic and PEC water splitting reactions. For semiconductor-based photocatalytic and PEC systems, we show that loading proper cocatalysts, especially dual cocatalysts for reduction and oxidation, on semiconductors (as light harvesters) can significantly enhance the activities of photocatalytic and PEC water splitting reactions. Loading oxidation and/or reduction cocatalysts on semiconductors can facilitate oxidation and reduction reactions by providing the active sites/reaction sites while suppressing the charge recombination and reverse reactions. In a PEC water splitting system, the water oxidation and reduction reactions occur at opposite electrodes, so cocatalysts loaded on the electrode materials mainly act as active sites/reaction sites spatially separated as natural photosynthesis does. In both cases, the nature of the loaded cocatalysts and their interaction with the semiconductor through the interface/junction are important. The cocatalyst can provide trapping sites for the photogenerated charges and promote the charge separation, thus enhancing the quantum efficiency; the cocatalysts could improve the photostability of the catalysts by timely consuming of the photogenerated charges, particularly the holes; most importantly, the cocatalysts catalyze the reactions by lowering the activation energy. Our research shows that loading suitable dual cocatalysts on semiconductors can significantly increase the photocatalytic activities of hydrogen and oxygen evolution reactions, and even make the overall water splitting reaction possible. All of these findings suggest that dual cocatalysts are necessary for developing highly efficient photocatalysts for water splitting reactions.

Entities:  

Year:  2013        PMID: 23530781     DOI: 10.1021/ar300227e

Source DB:  PubMed          Journal:  Acc Chem Res        ISSN: 0001-4842            Impact factor:   22.384


  98 in total

Review 1.  Rational Design and Construction of Cocatalysts for Semiconductor-Based Photo-Electrochemical Oxygen Evolution: A Comprehensive Review.

Authors:  Xiao-Ting Xu; Lun Pan; Xiangwen Zhang; Li Wang; Ji-Jun Zou
Journal:  Adv Sci (Weinh)       Date:  2018-11-19       Impact factor: 16.806

Review 2.  Facet-Engineered Surface and Interface Design of Photocatalytic Materials.

Authors:  Song Bai; Lili Wang; Zhengquan Li; Yujie Xiong
Journal:  Adv Sci (Weinh)       Date:  2016-08-17       Impact factor: 16.806

Review 3.  Bridging electrocatalyst and cocatalyst studies for solar hydrogen production via water splitting.

Authors:  Masaki Saruyama; Christian Mark Pelicano; Toshiharu Teranishi
Journal:  Chem Sci       Date:  2022-02-08       Impact factor: 9.825

Review 4.  Recent development of organic-inorganic hybrid photocatalysts for biomass conversion into hydrogen production.

Authors:  Ashil Augustin; Chitiphon Chuaicham; Mariyappan Shanmugam; Balakumar Vellaichamy; Saravanan Rajendran; Tuan K A Hoang; Keiko Sasaki; Karthikeyan Sekar
Journal:  Nanoscale Adv       Date:  2022-04-19

Review 5.  Polymer Photoelectrodes for Solar Fuel Production: Progress and Challenges.

Authors:  Madasamy Thangamuthu; Qiushi Ruan; Peter Osei Ohemeng; Bing Luo; Dengwei Jing; Robert Godin; Junwang Tang
Journal:  Chem Rev       Date:  2022-06-14       Impact factor: 72.087

6.  Water Splitting on Multifaceted SrTiO3 Nanocrystals: Calculations of Raman Vibrational Spectrum.

Authors:  Veera Krasnenko; Leonid L Rusevich; Aleksander Platonenko; Yuri A Mastrikov; Maksim Sokolov; Eugene A Kotomin
Journal:  Materials (Basel)       Date:  2022-06-15       Impact factor: 3.748

7.  Semiconductor quantum dot-sensitized rainbow photocathode for effective photoelectrochemical hydrogen generation.

Authors:  Hongjin Lv; Congcong Wang; Guocan Li; Rebeckah Burke; Todd D Krauss; Yongli Gao; Richard Eisenberg
Journal:  Proc Natl Acad Sci U S A       Date:  2017-10-09       Impact factor: 11.205

8.  Green fabrication of nanoporous BiVO4 films on ITO substrates for photoelectrochemical water-oxidation.

Authors:  Sayuri Okunaka; Yutaka Hitomi; Hiromasa Tokudome
Journal:  RSC Adv       Date:  2018-09-10       Impact factor: 3.361

9.  Efficient photocatalytic hydrogen evolution on single-crystalline metal selenide particles with suitable cocatalysts.

Authors:  Shanshan Chen; Junie Jhon M Vequizo; Takashi Hisatomi; Mamiko Nakabayashi; Lihua Lin; Zheng Wang; Akira Yamakata; Naoya Shibata; Tsuyoshi Takata; Taro Yamada; Kazunari Domen
Journal:  Chem Sci       Date:  2020-04-01       Impact factor: 9.825

10.  Nanostructured TiO2 Sensitized with MoS2 Nanoflowers for Enhanced Photodegradation Efficiency toward Methyl Orange.

Authors:  Sagar V Kite; Abhijit Nanaso Kadam; Dattatraya J Sathe; Satish Patil; Sawanta S Mali; Chang Kook Hong; Sang Wha Lee; Kalyanrao M Garadkar
Journal:  ACS Omega       Date:  2021-06-23
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