Jason Scott

Dr. Jason Scott

Particles and Catalysis Research Group, School of Chemical Engineering, The University of New South Wales, Sydney, NSW 2052, Australia

Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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19 October 2020 in Chemical Society Reviews
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Journal Article
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WGWanlin Gao
Wanlin Gao
SLShuyu Liang
Shuyu Liang
RWRujie Wang
Rujie Wang
QJQian Jiang
Qian Jiang
YZYu Zhang
Yu Zhang
SPSang-Eon Park
Sang-Eon Park
This review covers the sustainable development of advanced improvements in CO 2 capture and utilization.

17 February 2012 in The Journal of Physical Chemistry Letters
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Journal Article
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WTWey Yang Teoh
Wey Yang Teoh
Jason ScottJason Scott
Jason Scott
RARose Amal
Rose Amal

12 April 2017 in Journal of Materials Chemistry A
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Journal Article
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Helena Yuan WangHelena Yuan Wang
Helena Yuan Wang
HAHamidreza Arandiyan
Hamidreza Arandiyan
Jason ScottJason Scott
Jason Scott
ABAli Bagheri
Ali Bagheri
Hongxing DaiHongxing Dai
Hongxing Dai
RARose Amal
Rose Amal
The present review article highlights the preparation, characterization, properties, and recent developments in porous metal oxide catalysts for heterogeneous catalysis.

9 December 2019 in Advanced Materials
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Journal Article
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Hao WuHao Wu
Hao Wu
HTHui Ling Tan
Hui Ling Tan
Cui Ying ToeCui Ying Toe
Cui Ying Toe
Jason ScottJason Scott
Jason Scott
Liang WangLiang Wang
Liang Wang
YNYun Hau Ng
Yun Hau Ng

22 August 2018 in Angewandte Chemie International Edition
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Journal Article
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Cui Ying ToeCui Ying Toe
Cui Ying Toe
Zhaoke ZhengZhaoke Zheng
Zhaoke Zheng
Hao WuHao Wu
Hao Wu
Jason ScottJason Scott
Jason Scott
RARose Amal
Rose Amal
YNYun Hau Ng
Yun Hau Ng

16 February 2021 in Energy & Environmental Science
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Journal Article
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Cui Ying ToeCui Ying Toe
Cui Ying Toe
CTConstantine Tsounis
Constantine Tsounis
JZJiajun Zhang
Jiajun Zhang
HMHassan Masood
Hassan Masood
DGDenny Gunawan
Denny Gunawan
RARose Amal
Rose Amal
Photoreforming is a process that harnesses the redox ability of photocatalysts upon illumination, to simultaneously drive the reduction of H+ into hydrogen gas and oxidation of organic compounds. Over the past few decades, significant effort has been devoted to improving the photocatalytic hydrogen evolution efficiency, while substantially less focus has been directed towards the oxidation reactions. More recently, the realization of the potential for simultaneous hydrogen production with value-added organics has inspired researchers to use photooxidation pathways to tune the selectivity of oxidized products. As a distinct benefit, the less energetically demanding organic reforming is highly favorable when compared to the slow kinetics of oxygen evolution which negates the need for expensive and/or harmful hole scavengers. Photocatalyst modifications, such as secondary component deposition, doping, defect, phase and morphology engineering, have been the main strategies adopted to tune the photooxidation pathways and oxidation products. Direct control of the process conditions, including pH, temperature and reactant concentration, and favorable reactor designs can further improve the selectivity towards desired products. While other published reviews focus on the types of photocatalysts or feedstocks used to enhance the hydrogen evolution efficiency, this review highlights the importance of controlling the selectivity of the photoreforming reaction, particularly as an alternative path for waste abatement or valorization for industry. This review links the strategies used to improve the selectivity of photoreforming of organic waste into high-value and desirable chemicals, as well as offers an outlook on the future research direction required to deliver highly selective photocatalyst. A holistic strategy that comprises photocatalyst and system designs, appropriate characterizations and implementation of artificial intelligence has also been proposed and discussed to further aid establishment of the structure–mechanism–function relationship, thereby accelerating the discovery of optimum selective photoreforming systems.