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Single‐metal atomic sites and vacancies can accelerate the transfer of photogenerated electrons and enhance photocatalytic performance in photocatalysis. In this study, a series of nickel hydroxide nanoboards (Ni(OH)x NBs) with different loadings of single‐atomic Ru sites (w‐SA‐Ru/Ni(OH)x) were synthesized via a photoreduction strategy. In such catalysts, single‐atomic Ru sites are anchored to the vacancies surrounding the pits. Notably, the SA‐Ru/Ni(OH)x with 0.60 wt % Ru loading (0.60‐SA‐Ru/Ni(OH)x) exhibits the highest catalytic performance (27.6 mmol g−1 h−1) during the photocatalytic reduction of CO2 (CO2RR). Either superfluous (0.64 wt %, 18.9 mmol g−1 h−1; 3.35 wt %, 9.4 mmol−1 h−1) or scarce (0.06 wt %, 15.8 mmol g−1 h−1; 0.29 wt %, 21.95 mmol g−1 h−1; 0.58 wt %, 23.4 mmol g−1 h−1) of Ru sites have negative effect on its catalytic properties. Density functional theory (DFT) calculations combined with experimental results revealed that CO2 can be adsorbed in the pits; single‐atomic Ru sites can help with the conversion of as‐adsorbed CO2 and lower the energy of *COOH formation accelerating the reaction; the excessive single‐atomic Ru sites occupy vacancies that retard the completion of CO2RR. [ABSTRACT FROM AUTHOR]

The rational design and construction of efficient and inexpensive bifunctional oxygen electrocatalysts are highly desirable for the development of rechargeable Zn–air batteries (ZABs). Although single‐atom Fe sites anchored on N‐doped carbon catalysts (Fe1/NC) ensure high oxygen reduction reaction activity, their unitary atomically dispersed active center faces difficult condition in catalyzing oxygen evolution reaction simultaneously. Herein, a composite catalyst containing heterointerface between Fe1/NC and selenides ((Fe,Co)Se2) is constructed. The obtained (Fe,Co)Se2@Fe1/NC exhibits extremely narrow potential gap of 0.616 V and remarkable stability in alkaline media, outperforming the benchmark catalysts (Pt/C+RuO2: 0.720 V). Experimental results and density functional theory calculations reveal that heterointerface between Fe1/NC and (Fe,Co)Se2 accelerates the electron transfer and provides more moderate adsorption sites, which endow (Fe,Co)Se2@Fe1/NC with extremely high bifunctional oxygen catalytic activity. This study not only provides a superior bifunctional catalyst for ZABs, but also enriches the application of single‐atom catalysts in multifunctional energy storage and conversion devices. [ABSTRACT FROM AUTHOR]

Constructing electrocatalysts with p‐block elements is generally considered rather challenging owing to their closed d shells. Here for the first time, we present a p‐block‐element bismuth‐based (Bi‐based) catalyst with the co‐existence of single‐atomic Bi sites coordinated with oxygen (O) and sulfur (S) atoms and Bi nanoclusters (Biclu) (collectively denoted as BiOSSA/Biclu) for the highly selective oxygen reduction reaction (ORR) into hydrogen peroxide (H2O2). As a result, BiOSSA/Biclu gives a high H2O2 selectivity of 95 % in rotating ring‐disk electrode, and a large current density of 36 mA cm−2 at 0.15 V vs. RHE, a considerable H2O2 yield of 11.5 mg cm−2 h−1 with high H2O2 Faraday efficiency of ∼90 % at 0.3 V vs. RHE and a long‐term durability of ∼22 h in H‐cell test. Interestingly, the experimental data on site poisoning and theoretical calculations both revealed that, for BiOSSA/Biclu, the catalytic active sites are on the Bi clusters, which are further activated by the atomically dispersed Bi coordinated with O and S atoms. This work demonstrates a new synergistic tandem strategy for advanced p‐block‐element Bi catalysts featuring atomic‐level catalytic sites, and the great potential of rational material design for constructing highly active electrocatalysts based on p‐block metals. [ABSTRACT FROM AUTHOR]

In photosynthesis, solar energy is harvested by photosensitizers, and then, the excited electrons transfer via a Z‐Scheme mode to enzymatic catalytic centers to trigger redox reactions. Herein, we constructed a core–shell Z‐scheme heterojunction of semiconductor@single‐atom catalysts (SACs). The oxygen‐vacancy‐rich ZnO core and single‐atom Co−N4 sites supported on nitrogen‐rich carbon shell (SA‐Co‐CN) act as the photosensitizer and the enzyme‐mimicking active centers, respectively. Driven by built‐in electric field across the heterojunction, photoexcited electrons could rapidly (2 ps) transfer from the n‐type ZnO core to the p‐type SA‐Co‐CN shell, finally boosting the catalytic performance of the surface‐exposed single‐atom Co−N4 sites for peroxymonosulfate (PMS) activation under light irradiation. The synergies between photocatalysis and heterogeneous Fenton‐like reaction lead to phenomenally enhanced production of various reactive oxygen species for rapid degradation of various microcontaminants in water. Experimental and theoretical results validate that the interfacial coupling of SA‐Co‐CN with ZnO greatly facilitates PMS adsorption and activation by reducing the adsorption energy and enhancing the cascade electron transfer processes for the photo‐Fenton‐like reaction. [ABSTRACT FROM AUTHOR]

Due to the surface inhomogeneity of the solid supports, direct growth of uniform bimetallic nanoparticles (NPs) with controllable structure and size thereon is particularly challenging. Herein, a surface‐confinement strategy is reported to directly prepare ultrafine bimetallic PtM NPs (MFe, Cu, and Co) with structure of core‐shell or intermetallic compounds on an N functionalized carbon support (NC). It is found that the N species of NC support can atomically disperse metal cations of precursors, which largely renders uniform nucleation and growth of bimetallic NPs and fine structure modulation of them. In another regard, metal transfer is confined to a narrow region on NC via N‐mediation, hence greatly favoring localized particle growth and formation of ultrafine bimetallic NPs. Remarkably, the ultrafine 3.1 ± 0.7 nm intermetallic Pt3Fe NPs on NC displayed excellent catalytic activity and durability toward electrochemical hydrogen evolution reaction. [ABSTRACT FROM AUTHOR]

The two‐dimensional nanosheets are conducive to not only endow opened surfaces for loading active metal atoms but also boost the mass transfer for the heterogeneous reactions. The challenge is how to load and stabilize single‐atoms on nanosheets in high‐areal densities. This work reports an efficient micro‐gas blasting (MGB) strategy to access versatile noble metal single‐atoms/metal oxide nanosheets, including Ir1/CoOx, Pd1/CeO2, etc. Especially for Pt/CeO2 nanosheets (Pt1/CeO2−S), the Pt loading is increased to 15 at%. The Pt1/CeO2−S catalysts from MGB are revealed to possess superior reactivity and tolerance in the model reaction of water‐gas shift (WGS). The Pt1/CeO2−S catalyst exhibit 2–3 times reactivity that of their thicker counterpart, single‐atom Pt1/CeO2 microspheric catalyst. Moreover, the single‐atom sites in Pt1/CeO2−S (1–10 %) catalysts are stable in a harsh WGS reaction condition of 10 % CO. This work thus paves a way to access the practical single‐atom catalysts. [ABSTRACT FROM AUTHOR]

It is extremely challenging to controllably synthesize rare earth‐containing nanoalloys due to the ultralow standard reduction potential of rare earth metals. Here, a surface‐confined strategy to prepare ultrafine Pt‐rare earth nanoalloys on a series of N‐functionalized supports is reported. It proves that by surface N‐metal coordination, the metal cations of precursors are atomically dispersed on support, which greatly favors uniform nucleation and growth of particles upon reduction. Moreover, the moderate metal transfer barrier from N ensures particle growth in a confined region to form ultrafine nanoalloys. Using this method, ultrafine PtLa, PtY, and PtDy nanoalloys are prepared on N‐functionalized supports such as carbon, zeolite, and Al2O3. Notably, the PtLa nanoalloys on N‐functionalized zeolite show superior activity and durability for propane oxidation. The strategy is expected to provide guidelines for preparing highly efficient rare earth‐containing nanoalloys for catalysis applications. [ABSTRACT FROM AUTHOR]

Developing electrocatalytic reactions with high‐efficiency can make important contributions to carbon neutrality. However, poor long‐term stability of catalysts is a bottleneck for its practical application. Herein, an "in situ periodic regeneration of catalyst (PR‐C)" strategy is proposed to give long‐term high efficiency of CO2 electroreduction to generate C2+ products over Cu catalyst by applying a positive potential pulse for a short time periodically in the halide‐containing electrolyte. The high Faradaic efficiency (81.2 %) and current density (22.6 mA cm−2) could be maintained completely at least 36 h, while the activity and selectivity decreased continuously without using the PR‐C method. Control experiments and operando characterization demonstrated that the surface structure and oxidation state of Cu could be recovered periodically by the PR‐C method, which was beneficial for CO2 activation and C−C coupling. [ABSTRACT FROM AUTHOR]

Electroreduction of CO2 into valuable fuels and feedstocks offers a promising way for CO2 utilization. However, the commercialization is limited by the low productivity. Here, we report a strategy to enhance the productivity of CO2 electroreduction by improving diffusion of CO2 to the surface of catalysts using porous organic cages (POCs) as an additive. It was noted that the Faradaic efficiency (FE) of C2+ products could reach 76.1 % with a current density of 1.7 A cm−2 when Cu‐nanorod(nr)/CC3 (one of the POCs) was used, which were much higher than that using Cu‐nr. Detailed studies demonstrated that the hydrophobic pores of CC3 can adsorb a large amount of CO2 for the reaction, and the diffusion of CO2 in the CC3 to the nanocatalyst surface is easier than that in the liquid electrolyte. Thus, more CO2 molecules make contact with the nanocatalysts in the presence of CC3, enhancing CO2 reduction and inhibiting generation of H2. [ABSTRACT FROM AUTHOR]

Electrocatalytic reduction of CO2 (CO2RR) to value‐added chemicals is of great significance for CO2 utilization, however the CO2RR process involving multi‐electron and proton transfer is greatly limited by poor selectivity and low yield. Herein, We have developed an atomically dispersed monovalent zinc catalyst anchored on nitrogenated carbon nanosheets (Zn/NC NSs). Benefiting from the unique coordination environment and atomic dispersion, the Zn/NC NSs exhibit a superior CO2RR performance, featuring a high current density up to 50 mA cm−2 with an outstanding CO Faradaic efficiency of ≈95 %. The center ZnI atom coordinated with three N atoms and one N atom that bridges over two adjacent graphitic edges (Zn‐N3+1) is identified as the catalytically active site. Experimental results reveal that the twisted Zn‐N3+1 structure accelerates CO2 activation and protonation in the rate‐determining step of *CO2 to *COOH, while theoretical calculations elucidate that atomically dispersed Zn‐N3+1 moieties decrease the potential barriers for intermediate COOH* formation, promoting the proton‐coupled CO2RR kinetics and boosting the overall catalytic performance. [ABSTRACT FROM AUTHOR]

Using renewable electricity to drive CO2 electroreduction is an attractive way to achieve carbon‐neutral energy cycle and produce value‐added chemicals and fuels. As an important platform molecule and clean fuel, methanol requires 6‐electron transfer in the process of CO2 reduction. Currently, CO2 electroreduction to methanol suffers from poor efficiency and low selectivity. Herein, we report the first work to design atomically dispersed Sn site anchored on defective CuO catalysts for CO2 electroreduction to methanol. It exhibits high methanol Faradaic efficiency (FE) of 88.6 % with a current density of 67.0 mA cm−2 and remarkable stability in a H‐cell, which is the highest FE(methanol) with such high current density compared with the results reported to date. The atomic Sn site, adjacent oxygen vacancy and CuO support cooperate very well, leading to higher double‐layer capacitance, larger CO2 adsorption capacity and lower interfacial charge transfer resistance. Operando experiments and density functional theory calculations demonstrate that the catalyst is beneficial for CO2 activation via decreasing the energy barrier of *COOH dissociation to form *CO. The obtained key intermediate *CO is then bound to the Cu species for further reduction, leading to high selectivity toward methanol. [ABSTRACT FROM AUTHOR]

Guided by first‐principles calculations, it was found that Cd single‐atom catalysts (SACs) have excellent performance in activating CO2, and the introduction of axial coordination structure to Cd SACs cannot only further decrease the free energy barrier of CO2 reduction, but also suppress the hydrogen evolution reaction (HER). Based on the above discovery, we designed and synthesized a novel Cd SAC that comprises an optimized CdN4S1 moiety incorporated in a carbon matrix. It was shown that the catalyst exhibited outstanding performance in CO2 electroreduction to CO. The faradaic efficiency (FE) of CO could reach up to 99.7 % with a current density of 182.2 mA cm−2 in a H‐type electrolysis cell, and the turnover frequency (TOF) value could achieve 73000 h−1, which was much higher than that reported to date. This work shows a successful example of how to design highly efficient catalysts guided by theoretical calculations. [ABSTRACT FROM AUTHOR]

A dual‐site catalyst allows for a synergetic reaction in the close proximity to enhance catalysis. It is highly desirable to create dual‐site interfaces in single‐atom system to maximize the effect. Herein, we report a cation‐deficient electrostatic anchorage route to fabricate an atomically dispersed platinum–titania catalyst (Pt1O1/Ti1−xO2), which shows greatly enhanced hydrogen evolution activity, surpassing that of the commercial Pt/C catalyst in mass by a factor of 53.2. Operando techniques and density functional calculations reveal that Pt1O1/Ti1−xO2 experiences a Pt−O dual‐site catalytic pathway, where the inherent charge transfer within the dual sites encourages the jointly coupling protons and plays the key role during the Volmer–Tafel process. There is almost no decay in the activity of Pt1O1/Ti1−xO2 over 300 000 cycles, meaning 30 times of enhancement in stability compared to the commercial Pt/C catalysts (10 000 cycles). [ABSTRACT FROM AUTHOR]

Electroreduction of CO2 to liquid fuels such as ethanol and n‐propanol, powered by renewable electricity, offers a promising strategy for controlling the global carbon balance and addressing the need for the storage of intermittent renewable energy. In this work, we discovered that the composite composed of nitrogen‐doped graphene quantum dots (NGQ) on CuO‐derived Cu nanorods (NGQ/Cu‐nr) was an outstanding electrocatalyst for the reduction of CO2 to ethanol and n‐propanol. The Faradaic efficiency (FE) of C2+ alcohols could reach 52.4 % with a total current density of 282.1 mA cm−2. This is the highest FE for C2+ alcohols with a commercial current density to date. Control experiments and DFT studies show that the NGQ/Cu‐nr could provide dual catalytic active sites and could stabilize the CH2CHO intermediate to enhance the FE of alcohols significantly through further carbon protonation. The NGQ and Cu‐nr had excellent synergistic effects for accelerating the reduction of CO2 to alcohols. [ABSTRACT FROM AUTHOR]

Single‐atom catalysts have attracted much attention. Reported herein is that regulating charge transfer of lattice oxygen atoms in serial single‐atom‐doped titania enables tunable hydrogen evolution reaction (HER) activity. First‐principles calculations disclose that the activity of lattice oxygen for the HER can be regularly promoted by substituting its nearest metal atom, and doping‐induced charge transfer plays an essential role. Besides, the realm of the charge transfer of the active site can be enlarged to the second nearest atom by creating oxygen vacancies, resulting in further optimization for the HER. Various single‐atom‐doped titania nanosheets were fabricated to validate the proposed model. Taking advantage of the localized charge transfer to the lattice atom is demonstrated to be feasible for realizing precise regulation of the electronic structures and thus catalytic activity of the nanosheets. [ABSTRACT FROM AUTHOR]

The Neoarchean basement rocks of the Qixingtai region in the northwest of western Shandong, eastern North China Craton are divided into western and eastern domains, separated by a ductile shear zone. The western domain is mainly composed of early Neoarchean tonalitic and supracrustal rocks, and the eastern domain is composed of late Neoarchean crustally‐derived granite with diverse early Neoarchean enclaves up to several kilometres long of supracrustal and gneissic TTG‐diorite rocks. This study reports an integrated field, whole‐rock geochemistry and zircon U–Pb‐Hf study on the granites and their enclaves in the eastern domain. The supracrustal enclaves are mainly composed of meta‐basaltic and meta‐ultramafic rocks and are the same in lithological association and formation time as the 2,750–2,700 Ma Liuhang "Formation" in the western area. The TTG‐diorite enclaves can be divided into early and late groups. Magmatic zircons from early TTG‐diorite samples have U–Pb ages of 2,731 ± 17 to 2,748 ± 13 Ma and εHf(t) values of +2.7 to +9.5, whereas trondhjemite samples of the late group have U–Pb zircon ages of 2,588 ± 18 to 2,606 ± 12 Ma and εHf(t) values of +0.6 to +6.5. The Hf isotopic signatures on magmatic zircon from the >2,700 Ma diorite‐tonalites indicate that they are predominantly juvenile crustal additions, probably with minor involvement of older crust in their genesis, as given by tDM (Hf) ages ranging back to 2.92 Ga. The eastern granites range from monzogranite to syenogranite in composition and commonly have negative Eu anomalies, indicating residual plagioclase in the source region. Magmatic zircons from two granite samples have U–Pb ages of 2,516 ± 24 and 2,527 ± 18 Ma and εHf(t) values of +1.0 to +7.0. A fine‐grained syenogranite dyke contains inherited early Neoarchean zircons with εHf(t) values of +1.6 to +7.4. The isotopic signatures of the late Neoarchean granites that dominate the eastern domain show that they were derived from partial melting recycling of older continental crust recognized in the region – early Neoarchean rocks formed as a result of juvenile crustal additions. This is a common signature for late Archean crustal evolution throughout much of the North China Craton, and is the hallmark of some other Archean terranes, such as the Dharwar Craton of south India. The geodynamic explanations for the formation globally of vast amounts of crustally‐derived late Neoarchean granite are discussed. [ABSTRACT FROM AUTHOR]

For electrocatalysts for the hydrogen evolution reaction (HER), encapsulating transition metal phosphides (TMPs) into nitrogen‐doped carbon materials has been known as an effective strategy to elevate the activity and stability. Yet still, it remains unclear how the TMPs work synergistically with the N‐doped support, and which N configuration (pyridinic N, pyrrolic N, or graphitic N) contributes predominantly to the synergy. Here we present a HER electrocatalyst (denoted as MoP@NCHSs) comprising MoP nanoparticles encapsulated in N‐doped carbon hollow spheres, which displays excellent activity and stability for HER in alkaline media. Results of experimental investigations and theoretical calculations indicate that the synergy between MoP and the pyridinic N can most effectively promote the HER in alkaline media. [ABSTRACT FROM AUTHOR]

Electrochemical reduction of CO2 into energy‐dense chemical feedstock and fuels provides an attractive pathway to sustainable energy storage and artificial carbon cycle. Herein, we report the first work to use atomic Ir electrocatalyst for CO2 reduction. By using α‐Co(OH)2 as the support, the faradaic efficiency of CO could reach 97.6 % with a turnover frequency (TOF) of 38290 h−1 in aqueous electrolyte, which is the highest TOF up to date. The electrochemical active area is 23.4‐times higher than Ir nanoparticles (2 nm), which is highly conductive and favors electron transfer from CO2 to its radical anion (CO2.−). Moreover, the more efficient stabilization of CO2.− intermediate and easy charge transfer makes the atomic Ir electrocatalyst facilitate CO production. Hence, α‐Co(OH)2‐supported atomic Ir electrocatalysts show enhanced CO2 activity and stability. High‐density atomic Ir supported on α‐Co(OH)2 had outstanding performance for CO2 reduction to CO. The faradaic efficiency can reach 97.6 % with a TOF of 38 290 h−1. The high catalytic activity is attributed to more active sites for CO2 adsorption and activation and the higher efficiency in stabilizing the CO2.− intermediate. [ABSTRACT FROM AUTHOR]

Herein, we designed and prepared a novel Fe/Fe2O3‐based catalyst, in which a remarkable synergistic effect has been revealed between Fe and Fe2O3 encapsulated in N‐doping porous carbon. The Fe‐based catalysts were fabricated via pyrolysis a mixture of MIL‐101(Fe) and melamine. The catalyst exhibits exceptionally high catalytic activity (TOFs up to 8898 h−1 which is about 100 times higher than the similar kinds of catalysts) and chemoselectivity for nitroarene reduction under mild conditions. Catalysis magic! Fe‐based NPs catalyst encapsulated in N‐doping porous carbon exhibits high catalytic active (with TOF=8898 h−1 which is about 100 of times higher than the similar catalysts) and chemoselectivity for nitro compounds reduction. [ABSTRACT FROM AUTHOR]

Abstract: Developing an efficient single‐atom material (SAM) synthesis and exploring the energy‐related catalytic reaction are important but still challenging. A polymerization–pyrolysis–evaporation (PPE) strategy was developed to synthesize N‐doped porous carbon (NPC) with anchored atomically dispersed Fe‐N4 catalytic sites. This material was derived from predesigned bimetallic Zn/Fe polyphthalocyanine. Experiments and calculations demonstrate the formed Fe‐N4 site exhibits superior trifunctional electrocatalytic performance for oxygen reduction, oxygen evolution, and hydrogen evolution reactions. In overall water splitting and rechargeable Zn–air battery devices containing the Fe‐N4 SAs/NPC catalyst, it exhibits high efficiency and extraordinary stability. This current PPE method is a general strategy for preparing M SAs/NPC (M=Co, Ni, Mn), bringing new perspectives for designing various SAMs for catalytic application. [ABSTRACT FROM AUTHOR]

Abstract: The practical use of overall water electrolysis is largely hindered by the need for precious noble metal‐based catalysts. Here, the colloidal synthesis of earth‐abundant electrocatalysts of Mo–Ni nanoparticles for efficient water splitting by thermal decomposition of Ni(acac)2 and Mo(CO)6 in the presence of 1‐octadecene and oleylamine at 320 °C is reported. It is shown that the optimized catalysts (Mo0.6Ni0.4) only require low overpotentials of 0.065 V for the hydrogen evolution reaction (HER) and of 290 mV for the oxygen evolution reaction (OER) to deliver a current density of 10 mA cm−2 in KOH (1.0 m). The as‐prepared Mo–Ni alloy nanoparticles also show extraordinary durability for both the HER and OER. A low potential of ≈1.62 V is required to yield a current density of 10 mA cm−2 when utilizing the alloy nanoparticles as bifunctional catalysts in a two‐electrode electrolyzer system. The ease of preparing either rigid or flexible high‐performance electrodes by making use of the alloy nanoparticle electrocatalysts without the need for binder further suggests the attractive application of colloidally stable nanoparticles in the field of electrochemical water splitting. [ABSTRACT FROM AUTHOR]

Abundant mafic‐ultramafic blocks and dikes occur in the area north of Zunhua City, eastern Hebei Province, and were previously suggested to be part of a late Archean ophiolitic assemblage. We employed SHRIMP zircon dating and a geochemical study on these mafic and surrounding rocks to test the ophiolite hypothesis. The SHRIMP data suggest that three metagabbro samples were metamorphosed at ∼1.8 Ga. Numerous ∼2.5 Ga zircons display strong oscillatory zoning, characteristic of zircons from granitoid rocks but not from gabbro, so we suggest that these are xenocrystic grains. The age of these xenocrystic zircons and their metamorphic rims suggests that these mafic blocks formed in Paleoproterozoic. The surrounding gneiss of intermediate composition also contains 2.5 Ga zircons with oscillatory zoning and 1.8 Ga metamorphic rims. Fractionated REE patterns and Nb, Ta, Zr, Hf negative anomalies to variable extent were observed in the mafic blocks and surrounding rocks, also supporting a significant difference in the chemistry of ophiolitic rocks. Our data suggest that many mafic blocks in northern Zunhua are not part of a late Archean ophiolite complex but part of a tectonically dismembered Paleoproterozoic intrusive gabbro complex. This study shows that late Paleoproterozoic metamorphism occurred in the western part of eastern Hebei Province. [ABSTRACT FROM AUTHOR]

The Daqingshan area in the North China Craton (NCC) incorporates several suites of magmatic intrusives including gabbros, granodiorites, charnockites and syenogranites, which were overprinted by subsequent metamorphic events. In this study, we report detailed morphological and textural characteristics as well as sensitive high resolution ion microprobe (SHRIMP) U-Pb ages of zircons from ten representative samples of the magmatic suites including syenogranites, charnockites and granodiorites. The zircons in these rocks are characterized by typical magmatic crystallization features including elongate prismatic grains with angular to sub-angular faces which are overprinted by a variety of reworked textures indicating strong recrystallization. These structures are terminated by thin and variable metamorphic overgrowths. U-Pb analyses of the zircons reveal multiple tectono-thermal events including magmatic crystallization at 2.30-2.00, 1.96-1.94 and 1.85-1.82 Ga and metamorphic overprint at 1.97-1.94 and 1.87-1.82 Ga. The episodic magmatism and regional metamorphism recorded in our study show a complex sequence of tectonic processes during the early to late Palaeoproterozoic associated with the amalgamation of crustal blocks within the NCC, with the youngest episode of the syenogranites representing regional extension at the end of the final cratonization of the NCC. Copyright © 2012 John Wiley & Sons, Ltd. [ABSTRACT FROM AUTHOR]

Constructing well defined nanostructures is promising but still challenging for high‐efficiency catalysts for hydrogen evolution reaction (HER) and energy storage. Herein, utilizing the differences in surface energies between (111) facets of CoP and NiCoP, a novel CoP/NiCoP heterojunction is designed and synthesized with a nanotadpoles (NTs)‐like morphology via a solid‐state phase transformation strategy. By effective interface construction, the disorder in terms of electronic structure and coordination environment at the interface in CoP/NiCoP NTs is created, which leads to dramatically elevated HER performance within a wide pH range. Theoretical calculations prove that an optimized proton chemisorption and H2O dissociation are achieved by an optimized phosphide polymorph at the interface, accelerating the HER reaction. The CoP/NiCoP NTs are also proved to be excellent candidates for use in supercapacitors (SCs) with a high specific capacitance (1106.2 F g−1 at 1 A g−1) and good cycling stability (nearly 100% initial capacity retention after 1000 cycles). An asymmetric supercapacitor shows a high energy density (145 F g−1 at 1 A g−1) and good cycling stability (capacitance retention is 95% after 3200 cycles). This work provides new insights into the catalyst design for electrocatalytic and energy storage applications. [ABSTRACT FROM AUTHOR]