Inside‐and‐Out Semiconductor Engineering for CO2 Photoreduction: From Recent Advances to New Trends DOI Creative Commons
Shuobo Wang, Xu Han, Yihe Zhang

et al.

Small Structures, Journal Year: 2020, Volume and Issue: 2(1)

Published: Sept. 30, 2020

Photocatalytic CO 2 reduction attracts substantial interests for the production of chemical fuels via solar energy conversion, but activity, stability, and selectivity products were severely determined by efficiencies light harvesting, charge migration, surface reactions. Structural engineering is a promising tactic to address aforementioned crucial factors boosting photoreduction. Herein, timely comprehensive review focusing on recent advances in photocatalytic conversion based design strategies over nano‐/microstructure, crystalline band structure, structure interface provided, which covers both thermodynamic kinetic challenges photoreduction process. The key parameters essential tailoring size, morphology, porosity, bandgap, surface, or interfacial properties photocatalysts are emphasized toward efficient selective into valuable chemicals. New trends structural meet demands prominent activity also introduced. It expected furnish guideline inside‐and‐out state‐of‐the‐art with well‐defined structures conversion.

Language: Английский

S-Scheme Heterojunction Photocatalyst DOI Creative Commons
Quanlong Xu, Liuyang Zhang, Bei Cheng

et al.

Chem, Journal Year: 2020, Volume and Issue: 6(7), P. 1543 - 1559

Published: June 26, 2020

Language: Английский

Citations

2881

Particulate Photocatalysts for Light-Driven Water Splitting: Mechanisms, Challenges, and Design Strategies DOI
Qian Wang, Kazunari Domen

Chemical Reviews, Journal Year: 2019, Volume and Issue: 120(2), P. 919 - 985

Published: Aug. 8, 2019

Solar-driven water splitting provides a leading approach to store the abundant yet intermittent solar energy and produce hydrogen as clean sustainable carrier. A straightforward route light-driven is apply self-supported particulate photocatalysts, which expected allow be competitive with fossil-fuel-derived on levelized cost basis. More importantly, powder-based systems can lend themselves making functional panels large scale while retaining intrinsic activity of photocatalyst. However, all attempts generate via water-splitting date have unfortunately fallen short efficiency values required for practical applications. Photocatalysis photocatalyst particles involves three sequential steps: (i) absorption photons higher energies than bandgap excitation electron-hole pairs in particles, (ii) charge separation migration these photoexcited carriers, (iii) surface chemical reactions based carriers. In this review, we focus challenges each step summarize material design strategies overcome obstacles limitations. This review illustrates that it possible employ fundamental principles underlying photosynthesis tools materials science prepare photocatalysts overall splitting.

Language: Английский

Citations

2160

Dual Cocatalysts in TiO2 Photocatalysis DOI

Aiyun Meng,

Liuyang Zhang, Bei Cheng

et al.

Advanced Materials, Journal Year: 2019, Volume and Issue: 31(30)

Published: May 30, 2019

Abstract Semiconductor photocatalysis is recognized as a promising strategy to simultaneously address energy needs and environmental pollution. Titanium dioxide (TiO 2 ) has been investigated for such applications due its low cost, nontoxicity, high chemical stability. However, pristine TiO still suffers from utilization of visible light photogenerated‐charge‐carrier recombination rate. Recently, photocatalysts modified by dual cocatalysts with different functions have attracted much attention the extended absorption, enhanced reactant adsorption, promoted charge‐carrier‐separation efficiency granted various cocatalysts. Recent progress on component structural design in summarized. Depending their components, decorated can be divided into following categories: bimetallic cocatalysts, metal–metal oxide/sulfide metal–graphene metal oxide/sulfide–graphene architecture, they categorized randomly deposited binary facet‐dependent selective‐deposition core–shell Concluding perspectives challenges opportunities further exploration cocatalyst–modified are presented.

Language: Английский

Citations

1065

Product selectivity of photocatalytic CO2 reduction reactions DOI
Junwei Fu,

Kexin Jiang,

Xiaoqing Qiu

et al.

Materials Today, Journal Year: 2019, Volume and Issue: 32, P. 222 - 243

Published: July 18, 2019

Language: Английский

Citations

972

Industrial carbon dioxide capture and utilization: state of the art and future challenges DOI
Wanlin Gao,

Shuyu Liang,

Rujie Wang

et al.

Chemical Society Reviews, Journal Year: 2020, Volume and Issue: 49(23), P. 8584 - 8686

Published: Jan. 1, 2020

This review covers the sustainable development of advanced improvements in CO2capture and utilization.

Language: Английский

Citations

961

Understanding the Roadmap for Electrochemical Reduction of CO2 to Multi-Carbon Oxygenates and Hydrocarbons on Copper-Based Catalysts DOI
Yao Zheng, Anthony Vasileff, Xianlong Zhou

et al.

Journal of the American Chemical Society, Journal Year: 2019, Volume and Issue: 141(19), P. 7646 - 7659

Published: April 15, 2019

Electrochemical reduction of CO2 to high-energy-density oxygenates and hydrocarbons beyond CO is important for long-term large-scale renewable energy storage. However, the key step C-C bond formation needed generation C2 products induces an additional barrier on reaction. This inevitably creates larger overpotentials greater variety as compared conversion C1 products. Therefore, in-depth understanding catalytic mechanism required advancing design efficient electrocatalysts control reaction pathway desired Herein, we present a critical appraisal focusing connection between fundamentals electrocatalysts. An discussion mechanistic aspects various pathways copper-based catalysts presented together with consideration practical factors under electrocatalytic operating conditions. By providing some typical examples illustrating benefit merging theoretical calculations, surface characterization, electrochemical measurements, try address issues ongoing debate toward better at atomic level envisioning roadmap generation.

Language: Английский

Citations

887

Heterogeneous Single-Atom Photocatalysts: Fundamentals and Applications DOI
Chao Gao, Jingxiang Low, Ran Long

et al.

Chemical Reviews, Journal Year: 2020, Volume and Issue: 120(21), P. 12175 - 12216

Published: March 18, 2020

Single-atom photocatalysts have shown their compelling potential and arguably become the most active research direction in photocatalysis due to fascinating strengths enhancing light-harvesting, charge transfer dynamics, surface reactions of a photocatalytic system. While numerous comprehensions about single-atom recently been amassed, advanced characterization techniques vital theoretical studies are strengthening our understanding on these materials, allowing us forecast working mechanisms applications photocatalysis. In this review, we begin by describing general background definition photocatalysts. A brief discussion metal-support interactions is then provided. Thereafter, current available for summarized. After having some fundamental photocatalysts, advantages discussed. Finally, end review with look into remaining challenges future perspectives We anticipate that will provide inspiration discovery manifestly stimulating development emerging area.

Language: Английский

Citations

829

Surface strategies for catalytic CO2reduction: from two-dimensional materials to nanoclusters to single atoms DOI
Liming Wang, Wenlong Chen, Doudou Zhang

et al.

Chemical Society Reviews, Journal Year: 2019, Volume and Issue: 48(21), P. 5310 - 5349

Published: Jan. 1, 2019

This work constructively reviewed and predicted the surface strategies for catalytic CO2reduction with 2D material, nanocluster single-atom catalysts

Language: Английский

Citations

748

Core–shell structured catalysts for thermocatalytic, photocatalytic, and electrocatalytic conversion of CO2 DOI Creative Commons
Sonali Das, Javier Pérez‐Ramírez, Jinlong Gong

et al.

Chemical Society Reviews, Journal Year: 2020, Volume and Issue: 49(10), P. 2937 - 3004

Published: Jan. 1, 2020

Catalytic conversion of CO2 to produce fuels and chemicals is attractive in prospect because it provides an alternative fossil feedstocks the benefit converting cycling greenhouse gas on a large scale. In today's technology, converted into hydrocarbon Fischer-Tropsch synthesis via water shift reaction, but processes for direct such as methane, methanol, C2+ hydrocarbons or syngas are still far from large-scale applications processing challenges that may be best addressed by discovery improved catalysts-those with enhanced activity, selectivity, stability. Core-shell structured catalysts relatively new class nanomaterials allow controlled integration functions complementary materials optimised compositions morphologies. For conversion, core-shell can provide distinctive advantages addressing catalyst sintering activity loss reforming processes, insufficient product selectivity thermocatalytic hydrogenation, low efficiency photocatalytic electrocatalytic hydrogenation. preceding decade, substantial progress has been made synthesis, characterization, evaluation potential applications. Nonetheless, remain inexpensive, robust, regenerable this class. This review in-depth assessment these thermocatalytic, photocatalytic, valuable hydrocarbons.

Language: Английский

Citations

652

A Covalent Organic Framework Bearing Single Ni Sites as a Synergistic Photocatalyst for Selective Photoreduction of CO2 to CO DOI

Wanfu Zhong,

Rongjian Sa, Liuyi Li

et al.

Journal of the American Chemical Society, Journal Year: 2019, Volume and Issue: 141(18), P. 7615 - 7621

Published: April 18, 2019

Photocatalytic reduction of CO2 into energy-rich carbon compounds has attracted increasing attention. However, it is still a challenge to selectively and effectively convert desirable reaction product. Herein, we report design synergistic photocatalyst for selective CO by using covalent organic framework bearing single Ni sites (Ni-TpBpy), in which electrons transfer from photosensitizer production the activated under visible-light irradiation. Ni-TpBpy exhibits an excellent activity, giving 4057 μmol g-1 5 h with 96% selectivity over H2 evolution. More importantly, when partial pressure was reduced 0.1 atm, 76% obtained. Theoretical calculations experimental results suggest that promising catalytic activity are ascribed effects TpBpy, TpBpy not only serves as host molecules but also facilitates activation inhibits competitive

Language: Английский

Citations

637